Therapeutic compounds and related methods of use
Technical Field The exposed to one or more of the embodiment is related to a kind of fused ring compounds containing and has its organic light-emitting device. Background Art Organic light-emitting device (organic light emitting device) as a spontaneous-emitting device, such as a wide viewing angle, excellent contrast, rapid reaction, high-brightness, the advantages of fine driving voltage characteristics, and can provide multi-color Image. Organic light-emitting device may comprise an anode, cathode and an organic layer, the organic layer includes launching resettlement layerly between the anode and the cathode. Organic light-emitting device can include between the anode and the emissive layer of a hole conveying region between the emitting layer and the cathode is interposed between between area of electronic transmission. Self-anode into the hole via the hole conveying region moves to the emitting layer, since the cathode injecting electrons by electronic transmission area mobile to the emitting layer. Such as cavity and electronic in the carrier in the emitting layer, generating excitons (exciton). When the exciton self-excited state to the ground state, the light-emitting. Content of the invention Technical problem The exposed to one or more of the embodiment includes a novel fused ring compounds containing and has its organic light-emitting device. Light-emitting device, which comprises, for example, of different compounds each other as the main body, and so has a relatively low driving voltage, high efficiency, long service life and the characteristic of the radiance. Compounds in for electronic transmission to provide a layer with a low driving voltage, high efficiency, long service life and the characteristic of the radiance of the light-emitting device. Technical solution According to the present invention one or more embodiments, provides a formula 1 expresses the fused ring compounds: In the formula 1 in, ring A1 by formula 1A expressed, Wherein X1 to N-[ (L1)a1-(R1)b1], S, O or Si (R4) (R5); L1 to L3 by the independently substituted or not substituted C6-C60 arylene selected from, A1 to a3 on the various independently 0 to 5 in the selected integer, R1 to R5 all independently each selected from the following: hydrogen, deuterium, -F (fluorine-based), -Cl (chlorine-based), -Br (bromo), -I (iodine-based), hydroxy, a substituted or an unsubstituted C1-C60 alkyl, a substituted or an unsubstituted C1-C60 alkoxy, a substituted or an unsubstituted C3-C10 cycloalkyl, a substituted or an unsubstituted C6-C60 aryl, a substituted or an unsubstituted C6-C60 aryloxy group, a substituted or an unsubstituted C6-C60 arylthio and substituted or not substituted by a monovalent non-aromatic gathers many thickly cyclic group, wherein R2 and R3 by at least one of the substituted or non-substituted C6-C60 aryl group and the substituted or non-substituted monovalent non-aromatic gathers many thickly cyclic group selected from, R11 to R14 all independently each selected from the following: hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, a substituted or an unsubstituted C1-C60 alkyl, a substituted or an unsubstituted C1-C60 alkoxythiophene, C3-C10 cycloalkyl, C6-C60 aryl, C6-C60 aryloxy, C6-C60 arylthio and gathers many thickly monovalent non-aromatic cyclic group, and B1 to b3 on the various independently 1 to 3 an integer selected, When the R2 is a substituted or an unsubstituted phenyl, R3 each selected from the following: hydrogen, a substituted or an unsubstituted phenyl, a substituted or an unsubstituted biphenyl, substituted or not substituted terphenyl base, a substituted or an unsubstituted luen four phenyl, a substituted or an unsubstituted naphthyl, a substituted or an unsubstituted anthryl, a substituted or an unsubstituted [...], substituted or not substituted hydrazo three phenyl, a substituted or an unsubstituted Pyren, a substituted or an unsubstituted Fikki, a substituted or an unsubstituted [...] and a substituted or an unsubstituted qu Ji ; Substituted C6-C60 aryl, substituted C1-C60 alkyl, substituted C1-C60 alkoxy, substituted C3-C10 cycloalkyl, substituted C6-C60 aryl, substituted C6-C60 aryloxy, substituted C6-C60 substituted arylthio and of a monovalent non-aromatic gathers many thickly in substituent of cyclic group of at least one of each selected from the following: Deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C60 alkyl and C1-C60 alkoxy, C1-C60 alkyl and C1-C60 alkoxy, all after deuterium, -F, -Cl, -Br, -I, hydroxy, C3-C10 cycloalkyl, C6-C60 aryl, C6-C60 aryloxy, C6-C60 arylthio and univalent non-aromatic gathers many thickly at least one of the cyclic group in substituted, C3-C10 cycloalkyl, C6-C60 aryl, C6-C60 aryloxy, C6-C60 arylthio and gathers many thickly monovalent non-aromatic cyclic group, C3-C10 cycloalkyl, C6-C60 aryl, C6-C60 aryloxy, C6-C60 arylthio and gathers many thickly monovalent non-aromatic cyclic group, all after deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C60 alkyl, C1-C60 alkoxythiophene, C3-C10 cycloalkyl, C6-C60 aryl, C6-C60 aryloxy, C6-C60 arylthio and univalent non-aromatic gathers many thickly at least one of the cyclic group in substituted, and R2 and R3 substituted base by selected from the following: Deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C60 alkyl, C1-C60 alkoxythiophene, C3-C10 cycloalkyl, C6-C60 aryl, C6-C60 aryloxy, C6-C60 arylthio and gathers many thickly monovalent non-aromatic cyclic group. According to the present invention one or more embodiments, the organic light-emitting device includes a 1st electrode, is placed in 1st and 2nd electrodes of the electrode opposite the electrode between the electrode and the 1st 2nd the organic layer, the organic layer as defined above comprising the fused ring compound. Fused ring compounds can be contained in the organic layer in the emitting layer or the electron transport layer, the emissive layer may also comprises a dopant. In the emitting layer fused ring compounds can be used as a main body. According to the exposure of one or more embodiments, the organic light-emitting device includes an organic layer containing the following two: i) by the following formula 1 expresses the fused ring compound; and ii) by formula 41 with the 1st compound expressed by following formula 61 in the 2nd of said at least one of the compounds. In formula 41 in, X41 to N-[ (L42)a42-(R42)b42], S, O, S (=O), S (=O)2, C (=O), C (R43) (R44), Si (R43) (R44), P (R43), P (=O) (R43) or C=N (R43); In the type 61 in, ring A61 by formula 61A expressed; In the type 61 in, ring A62 by formula 61B expressed; X61 to N-[ (L62)a62-(R62)b62], S, O, S (=O), S (=O)2, C (=O), C (R63) (R64), Si (R63) (R64), P (R63), P (=O) (R63) or C=N (R63); X71 to C (R71) or N, X72 to C (R72) or N, X73 to C (R73) or N, X74 to C (R74) or N, X75 to C (R75) or N, X76 to C (R76) or N, X77 to C (R77) or N, and X78 to C (R78) or N; Ar41, L41, L42, L61 and L62 each is independently substituted or not substituted C3-C10asian link alkyl, a substituted or an unsubstituted C2-C10 jaya heterocyclic alkyl, a substituted or an unsubstituted C3-C10 jaya cycloalkenyl, substituted or not substituted C2-C10asia is mixed cycloalkenyl, substituted or not substituted C6-C60 jaya aryl, a substituted or an unsubstituted C2-C60 heteroarylidenyl, a substituted or an unsubstituted divalent non-aromatic gathers many thickly cyclic group or a substituted or an unsubstituted divalent non-aromatic gathers many thickly mixed cyclic group; N1 and n2 on the various independently 0 to 3 in the selected integer; A41, a42, a61 and a62 on the various independently 0 to 5 in the selected integer; R41 to R44, R51 to R54, R61 to R64 and R71 to R79 each is independently hydrogen, deuterium, -F (fluorine-based), -Cl (chlorine-based), (polybromide yl)-Br, -I (iodine-based), hydroxy, cyano, amino, amidino, a substituted or an unsubstituted C1-C60 alkyl, a substituted or an unsubstituted C2-C60 alkenyl, a substituted or an unsubstituted C2-C60 alkynyl, substituted or not substituted C1-C60 alkoxy, a substituted or an unsubstituted C3-C10 cycloalkyl, a substituted or an unsubstituted C2-C10 heterocyclic alkyl, a substituted or an unsubstituted C3-C10 cycloalkenyl, substituted or not substituted C2-C10 heterocyclic alkenyl, a substituted or an unsubstituted C6-C60 aryl, a substituted or an unsubstituted C6-C60 aryloxy group, a substituted or an unsubstituted C6-C60 arylthio, a substituted or an unsubstituted C2-C60 heteroaryl, a substituted or an unsubstituted monovalent non-aromatic gathers many thickly cyclic group, substituted or not substituted by a monovalent non-aromatic gathers the multi-link base thickly mixed, -N (Q1) (Q2), -Si (Q3) (Q4) (Q5) or-B (Q6) (Q7); B41, b42, b51 to b54, b61, b62 and b79 on the various independently 1 to 3 in the selected integer. According to another aspect, the organic layer of the organic light-emitting device in the auxiliary layer of electronic transmission includes fused ring compounds, and also containing the compounds represented by general formula 2 that the hole transmission layer of a compound. In the formula 2 in, L201 is a substituted or an unsubstituted C6 to C30 arylene or a substituted or an unsubstituted C2 to C30 heteroarylidenyl, n101 is 1 to 5 an integer that is elected in, R201 to R212 each is independently hydrogen, deuterium, a substituted or an unsubstituted C1 to C20 alkyl, a substituted or an unsubstituted C6 to C50 aryl group, a substituted or an unsubstituted C2 to C50 heteroaryl, or combinations thereof, and R201 to R212 the exist independently, or fused to each other, form the ring. Advantageous functions Fused ring compound having excellent electric characteristics and thermal stability, and thus an organic layer containing the above-mentioned fused ring compound, organic light-emitting device can have a low drive voltage, high efficiency and long service life. Description of drawings Figure 1 to Figure 3 is the schematic view of the disclosed according to one embodiment of the organic light-emitting device. < 符号说明 > 1: organic photoelectric device 11 : 1st electrode 15: organic layer 19 : 2nd electrode 31: hole transport layer 32: emitting layer 33: hole transport layer 34: electron transport layer 35: electronic transmission auxiliary layer 36: electron injection layer 37:a hole injection layer Mode of execution According to one embodiment of this disclosure, to provide a kind of the compounds represented by general formula 1 the fused ring compounds: In the formula 1 in, ring A1may by the type 1A expressed: In the formula 1A in, X1 can be N-[ (L1)a1-(R1)b1], S, O or Si (R4) (R5), L1 to L3 by the independently substituted or not substituted C6-C60 arylene selected from, A1 to a3 on the various independently 0 to 5 in the selected integer, R1 to R5 all independently each selected from the following: hydrogen, deuterium, -F (fluorine-based), -Cl (chlorine-based), -Br (bromo), -I (iodine-based), hydroxy, a substituted or an unsubstituted C1-C60 alkyl, a substituted or an unsubstituted C1-C60 alkoxy, a substituted or an unsubstituted C3-C10 cycloalkyl, a substituted or an unsubstituted C6-C60 aryl, a substituted or an unsubstituted C6-C60 aryloxy group, a substituted or an unsubstituted C6-C60 arylthio and substituted or not substituted by a monovalent non-aromatic gathers many thickly cyclic group, wherein R2 and R3 by at least one of the substituted or non-substituted C6-C60 aryl group and the substituted or non-substituted monovalent non-aromatic gathers many thickly cyclic group selected from, R11 to R14 all independently each selected from the following: hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, a substituted or an unsubstituted C1-C60 alkyl, a substituted or an unsubstituted C1-C60 alkoxythiophene, C3-C10 cycloalkyl, C6-C60 aryl, C6-C60 aryloxy, C6-C60 arylthio and gathers many thickly monovalent non-aromatic cyclic group, and B1 to b3 on the various independently 1 to 3 an integer selected, When the R2 is a substituted or an unsubstituted phenyl, R3 each selected from the following: hydrogen, a substituted or an unsubstituted phenyl, a substituted or an unsubstituted biphenyl, substituted or not substituted terphenyl base, a substituted or an unsubstituted luen four phenyl, a substituted or an unsubstituted naphthyl, a substituted or an unsubstituted anthryl, a substituted or an unsubstituted [...], substituted or not substituted hydrazo three phenyl, a substituted or an unsubstituted Pyren, a substituted or an unsubstituted Fikki, a substituted or an unsubstituted [...] and a substituted or an unsubstituted qu Ji. L1, a1, R1, b1, R4 and R5 with the definition of these groups of the definition of below the same. In some embodiment, X1 can be S, O or Si (R4) (R5), but not limited to this. In some other embodiment, X1 can be S or O, but is not limited to this. Ring A1 with shared with two adjacent carbon atoms is 6-membered ring fused. Therefore, also 1 condensed ring compound may by the type 1-1 of the formula 1-2 said one of: In the formula 1-1 to 1-2 in, X1, L2, L3, a2, a3, R2, R3, R11 to R14, b2 and b3 with the following definitions can be of the formula 1 the same. In the above formula, L1 to L3 each by independently substituted or not substituted C6-C60 arylene selected. For example, L1 to L3 can all independently each selected from the following: Phenylene (phenylene), sub-biphenyl (biphenylene), asian association triphenylporphyrin (terphenylene), four phenyltheophylline (quaterphenylene) asian association, subnaphthyl (naphthylene), (fluorenylene) [...], [...], asian phenanthryl (phenanthrenylene), inferior anthryl (anthracenylene), (fluoranthrenylene) anthryl asian firefly, asia unites Asia triphenylporphyrin (triphenylenylene), (pyrenylene) asian pyrenyl, phenyl (naphthacenylene) (chrysenylene) and four asia is thickasia Qu Ji ; and Phenylene, biphenylene (biphenylene), asian association triphenylporphyrin (terphenylene), four phenyltheophylline (quaterphenylene) asian association, subnaphthyl (naphthylene), (fluorenylene) [...], [...], asian phenanthryl (phenanthrenylene), inferior anthryl (anthracenylene), (fluoranthrenylene) anthryl asian firefly, asia unites Asia triphenylporphyrin (triphenylenylene), (pyrenylene) asian pyrenyl, phenyl (naphthacenylene) (chrysenylene) and four asia is thickasia Qu Ji, all after deuterium atom, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl, C1-C20 alkoxythiophene, C6-C20 aryl and univalent non-aromatic gathers many thickly in cyclic group of at least one substituted. In some other embodiments, the upper in the formula, L1 to L3 each formula independently 2-1 to 2-15 said one of: In the formula 2-1 to 2-15 in, Z1 to Z4 can all independently each selected from the following: hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl, C1-C20 alkoxy, phenyl, biphenyl, terphenyl base, luen four phenyl, naphthyl, anthryl, [...], hydrazo three phenyl, Pyren, Fikki, qu Ji[...] and; D1 can be 1 to 4 an integer that is elected in the; d2 can be 1 to 3 an integer that is elected in the; d3 can be 1 to 6 an integer that is elected in the; d4 can be 1 to 8 selected in the integer; d6 can be 1 to 5 an integer that is elected in the; and * and *' independently for each of the binding site of the adjacent atoms. In some other embodiments, the upper in the formula, L1 to L3 each formula independently 3-1 to 3-37 said one of, but not limited to this: Teachings in 1 in, indicating L1 number of a1 can be 0, 1, 2, 3, 4 or 5, and in some embodiments, is 0,1 or 2, and in some other embodiments, to 0 or 1. When the a1 to 0 time, * - (L1)a1-*' can be a single bond. When the a1 is 2 or greater, at least two L1 can be identical or different to each other. A2 and a3 can be based on a1 among description of 1 to understand the structure. In some embodiments, a1, a2 and a3 each of them is independently 0,1 or 2. In the, R1 to R5 can all independently each selected from the following: hydrogen, deuterium, -F (fluorine-based), -Cl (chlorine-based), -Br (bromo), -I (iodine-based), hydroxy, a substituted or an unsubstituted C1-C60 alkyl, a substituted or an unsubstituted C1-C60 alkoxy, a substituted or an unsubstituted C3-C10 cycloalkyl, a substituted or an unsubstituted C6-C60 aryl, a substituted or an unsubstituted C6-C60 aryloxy group, a substituted or an unsubstituted C6-C60 arylthio and substituted or not substituted by a monovalent non-aromatic gathers many thickly cyclic group, wherein R2 and R3 by at least one of the substituted or non-substituted C6-C60 aryl group and the substituted or non-substituted monovalent non-aromatic cyclic group selected gathers many thickly. In some embodiments, in the, R1 to R5 can all independently each selected from the following: Hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl and C1-C20 alkoxy, C1-C20 alkyl and C1-C20 alkoxy, all after deuterium atom, -F, -Cl, -Br, -I and at least one of the hydroxyl groups substituted, Phenyl (phenyl), biphenyl (biphenyl), (terphenyl) terphenyl base, luen four phenyl (quaterphenyl), (pentalenyl) and cyclopentadienyl, indenyl-based (indenyl), naphthyl (naphthyl), (azulenyl) [...], and cycloheptatriene -based (heptalenyl), dicyclopentadiene and phenyl (indacenyl), acenaphthene-based (acenaphthyl), luxuriant growth-based (fluorenyl), [...], benzocarbazoles [...], dibenzo [...], propylene gathers the naphthyl (phenalenyl), (phenanthrenyl) Fikki, anthryl (anthracenyl), luxuriant growth anthryl (fluoranthenyl), hydrazo triphenylporphyrin (triphenylenyl), Pyren (pyrenyl), (chrysenyl) qu Ji, thick four phenyl (naphthacenyl), [...] -based (picenyl), (perylenyl) [...], luen five phenyl (pentaphenyl), thick six phenyl (hexacenyl), thick five phenyl (pentacenyl), bastide-based (rubicenyl), (ovalenyl) cronene base[...] (coronenyl) and, Phenyl, biphenyl, terphenyl base, luen four phenyl, and cyclopentadienyl, indenyl, naphthyl, [...], and cycloheptatriene base, dicyclopentadiene and phenyl, [...], [...], [...], benzocarbazoles [...], dibenzo [...], propylene gathers the naphthyl, Fikki, anthryl, [...], hydrazo three phenyl, Pyren, qu Ji, thick four phenyl, Pyren, [...], luen five phenyl, thick six phenyl, phenyl thick five, ru Ji, [...]cronene base and, via the following various in the selected at least one substituted: deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl, C1-C20 alkoxythiophene, -Si (Q33) (Q34) (Q35), phenyl, biphenyl, terphenyl base, luen four phenyl, and cyclopentadienyl, indenyl, naphthyl, [...], and cycloheptatriene base, dicyclopentadiene and phenyl, [...], [...], [...], benzocarbazoles [...], dibenzo [...], propylene gathers the naphthyl, Fikki, anthryl, [...], hydrazo three phenyl, Pyren, qu Ji, thick four phenyl, Pyren, [...], luen five phenyl, thick six phenyl, phenyl thick five, ru Ji, [...]cronene base and, Wherein i) R2 and R3 at least one and in ii) R1 can all independently each selected from the following: Phenyl, biphenyl, terphenyl base, luen four phenyl, and cyclopentadienyl, indenyl, naphthyl, [...], and cycloheptatriene base, dicyclopentadiene and phenyl, [...], [...], [...], benzocarbazoles [...], dibenzo [...], propylene gathers the naphthyl, Fikki, anthryl, [...], hydrazo three phenyl, Pyren, qu Ji, thick four phenyl, [...], [...], luen five phenyl, thick six phenyl, phenyl thick five, ru Ji, [...]cronene base and; Phenyl, biphenyl, terphenyl base, luen four phenyl, and cyclopentadienyl, indenyl, naphthyl, [...], and cycloheptatriene base, dicyclopentadiene and phenyl, [...], [...], [...], benzocarbazoles [...], dibenzo [...], propylene gathers the naphthyl, Fikki, anthryl, [...], hydrazo three phenyl, Pyren, qu Ji, thick four phenyl, Pyren, [...], luen five phenyl, thick six phenyl, phenyl thick five, ru Ji, [...]cronene base and, via the following various in the selected at least one substituted: deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl, C1-C20 alkoxy, phenyl, biphenyl, terphenyl base, luen four phenyl, and cyclopentadienyl, indenyl, naphthyl, [...], and cycloheptatriene base, dicyclopentadiene and phenyl, [...], [...], [...], benzocarbazoles [...], dibenzo [...], propylene gathers the naphthyl, Fikki, anthryl, [...], hydrazo three phenyl, Pyren, qu Ji, thick four phenyl, Pyren, [...], luen five phenyl, thick six phenyl, phenyl thick five, ru Ji, and cronene base[...]. In some other embodiment, R1 to R5 can all independently each selected from the following: Hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl and C1-C20 alkoxy, C1-C20 alkyl and C1-C20 alkoxy, all after deuterium, -F, -Cl, -Br, -I, or hydroxyl substituted at least one of, Phenyl, biphenyl, terphenyl base, luen four phenyl, naphthyl, propylene gathers the naphthyl, Fikki, anthryl, [...], hydrazo three phenyl, Pyren, qu Ji, [...][...] and; Phenyl, biphenyl, terphenyl base, luen four phenyl, naphthyl, propylene gathers the naphthyl, Fikki, anthryl, [...], hydrazo three phenyl, Pyren, qu Ji, [...][...] and, via the following various in the selected at least one substituted: deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl, C1-C20 alkoxy, phenyl, biphenyl, terphenyl base, luen four phenyl, naphthyl, propylene gathers the naphthyl, Fikki, anthryl, [...], hydrazo three phenyl, Pyren, qu Ji, and [...][...] ; and i) R2 and R3 at least one and in ii) R1 can all independently each selected from the following: Phenyl, biphenyl, terphenyl base, luen four phenyl, naphthyl, propylene gathers the naphthyl, Fikki, anthryl, [...], hydrazo three phenyl, Pyren, qu Ji, and [...][...] ; or Phenyl, biphenyl, terphenyl base, luen four phenyl, naphthyl, propylene gathers the naphthyl, Fikki, anthryl, [...], hydrazo three phenyl, Pyren, qu Ji, [...][...] and, via the following various in the selected at least one substituted: deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl, C1-C20 alkoxy, phenyl, biphenyl, terphenyl base, luen four phenyl, naphthyl, propylene gathers the naphthyl, Fikki, anthryl, [...], hydrazo three phenyl, Pyren, qu Ji, and [...][...]. In some other embodiment, R1 to R5 can all independently each selected from the following: Hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl and C1-C20 alkoxy, C1-C20 alkyl and C1-C20 alkoxy, all after deuterium, -F, -Cl, -Br, -I, or hydroxyl substituted at least one of, Formula 4-1 to 4-5 among 4-34 to 4-37 said one of the groups, and i) R2 and R3 at least one and in ii) R1 the formula illustrated independently 4-1 to 4-5 among 4-34 to 4-37 group expressed in one of. According to another embodiment, in the present invention in the condensed ring compound, X1 to S or O, R1 to R5 each is independently hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl or C1-C20 alkoxy; C1-C20 alkyl and C1-C20 alkoxy, all after deuterium atom, -F, -Cl, -Br, -I, or hydroxyl substituted at least one of the; or Compounds represented by general formula 4-1 to 4-5 among 4-34 to 4-37 one; R2 and R3 in at least one of the independent of the compounds represented by general formula 4-1 to 4-5 among 4-34 to 4-37 said one of: In the formula 4-1 to 4-37 in, Y31 can be O, S, C (Z33) (Z34), N (Z35) or Si (Z36) (Z37), (its Chinese 4-23 of in Y31 can be is not NH), Z31 to Z37 can all independently each selected from the following: hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, cyano, amino, amidino, C1-C20 alkyl, C1-C20 alkoxy, phenyl, naphthyl, anthryl, Fikki, [...], qu Ji, benzocarbazoles carbazolyl, dibenzo carbazolyl, b benzofuranyl, dibenzo thienyl, pyridyl, pyrimidinyl, carbazolyl, triazinyl, quinolyl, isoquinolyl, quinazolinyl, [...], biphenyl, terphenyl base and luen four phenyl, Z38 to Z41 can all independently each selected from the following: hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl, C1-C20 alkoxy, phenyl, naphthyl, anthryl, Pyren, Fikki, [...], qu Ji, biphenyl, terphenyl base and luen four phenyl, E1 can be 1 to 5 an integer selected, e2 can be 1 to 7 in an integer selected, e3 can be 1 to 3 an integer selected, e4 can be 1 to 4 an integer selected, e6 can be 1 to 6 an integer selected, and * the binding site of the adjacent atoms. Z31 can all independently each selected from the following: hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, cyano, amino, amidino, C1-C20 alkyl, C1-C20 alkoxy, phenyl, naphthyl, anthryl, Fikki, [...], qu Ji, benzocarbazoles carbazolyl, dibenzo carbazolyl, b benzofuranyl, dibenzo thienyl, pyridyl, pyrimidinyl, carbazolyl, triazinyl, quinolyl, isoquinolyl, quinazolinyl, [...], biphenyl, terphenyl base and luen four phenyl, In some other embodiment, R1 can be made by the following various selected from: Phenyl, biphenyl, terphenyl base, luen four phenyl, naphthyl, propylene gathers the naphthyl, Fikki, anthryl, [...], [...], hydrazo three phenyl, Pyren, and qu Ji[...], and Phenyl, biphenyl, terphenyl base, luen four phenyl, naphthyl, propylene gathers the naphthyl, Fikki, anthryl, [...], [...], hydrazo three phenyl, Pyren, [...]qu Ji and, via the following various in the selected at least one substituted: deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl, C1-C20 alkoxy, phenyl, biphenyl, terphenyl base, luen four phenyl, naphthyl, propylene gathers the naphthyl, Fikki, anthryl, [...], [...], hydrazo three phenyl, Pyren, and qu Ji[...]. In some other embodiments, the formula 1 a in R2 and R3 can be at least one of each selected from the following: Phenyl, biphenyl, terphenyl base, luen four phenyl, naphthyl, Fikki, anthryl, [...], hydrazo [...] and three phenyl, and Phenyl, biphenyl, terphenyl base, luen four phenyl, naphthyl, Fikki, anthryl, [...], hydrazo [...] and three phenyl, via the following various in the selected at least one substituted: deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl, C1-C20 alkoxythiophene, -Si (Q33) (Q34) (Q35), phenyl, biphenyl, terphenyl base, luen four phenyl, naphthyl, propylene gathers the naphthyl, Fikki, anthryl, hydrazo [...] and three phenyl. In the above equation 1 in, R11 to R14 can all independently each selected from the following: hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, a substituted or an unsubstituted C1-C60 alkyl, a substituted or an unsubstituted C1-C60 alkoxythiophene, C3-C10 cycloalkyl, C6-C60 aryl, C6-C60 aryloxy, C6-C60 arylthio and gathers many thickly monovalent non-aromatic cyclic group. In some embodiments, the formula 1 a in R11 to R14 can all independently each selected from the following: Hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl and C1-C20 alkoxy, C1-C20 alkyl and C1-C20 alkoxy, all after deuterium atom, -F, -Cl, -Br, -I, or hydroxyl substituted at least one of, Phenyl, biphenyl, terphenyl base, luen four phenyl, naphthyl, [...], [...], benzocarbazoles [...], dibenzo [...], Fikki, anthryl, [...], hydrazo three phenyl, qu Ji Pyren and. In some other embodiments, the formula 1 a in R11 to R14 can all independently each selected from the following: Hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl and C1-C20 alkoxy, Phenyl, biphenyl, terphenyl base, luen four phenyl, naphthyl, [...], [...], Fikki, anthryl, [...], hydrazo three phenyl, qu Ji Pyren and. In some other embodiments, in the above equation 1 in, R11 to R14 each independently can be hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl and C1-C20 elected alkoxy, but is not limited to this. In some other embodiments, the formula 1 a in R11 to R14 can be hydrogen. In some other embodiments, the aboving R1 to R5 can all independently each selected from the following: Hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl and C1-C20 alkoxy, C1-C20 alkyl and C1-C20 alkoxy, all after deuterium atom, -F, -Cl, -Br, -I, or hydroxyl substituted at least one of, and Formula 5-1 to 5-9, type 5-18 to 5-21 formula 5-45 to 5-66 said one of the groups, and i) R2 and R3 at least one and in ii) R1 all independently each selected from the following: by formula 5-1 to 5-9, type 5-18 to 5-21 formula 5-45 to 5-66 group expressed in one of; and R11 to R14 can all independently each selected from the following: Hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl and C1-C20 alkoxy, Formula 5-1 to 5-9, type 5-18 to 5-21 formula 5-45 to 5-66 group expressed in one of, but not limited to this. According to another embodiment, X1 to S or O, R1 to R5 each is independently Hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl or C1-C20 alkoxy; C1-C20 alkyl and C1-C20 alkoxy, all after deuterium atom, -F, -Cl, -Br, -I, or hydroxyl substituted at least one of the; or Compounds represented by general formula 5-1 to 5-9, type 5-18 to 5-21 formula 5-45 to 5-66 one; R2 and R3 in at least one of the independent of the compounds represented by general formula 5-1 to 5-9, type 5-18 to 5-21 formula 5-45 to 5-66 said one of, R11 to R14 each is independently Hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl or C1-C20 alkoxy; or Compounds represented by general formula 5-1 to 5-9, type 5-18 to 5-21 formula 5-45 to 5-66 one of: when type 1 of in R2 can be substituted or not substituted phenyl, R3 each selected from the following: hydrogen, a substituted or an unsubstituted phenyl, a substituted or an unsubstituted biphenyl, substituted or not substituted terphenyl base, a substituted or an unsubstituted luen four phenyl, a substituted or an unsubstituted naphthyl, a substituted or an unsubstituted anthryl, a substituted or an unsubstituted [...], substituted or not substituted hydrazo three phenyl, a substituted or an unsubstituted Pyren, a substituted or an unsubstituted Fikki, a substituted or an unsubstituted [...] and a substituted or an unsubstituted qu Ji. Indicating R1 number of b1 can be 1 to 3 an integer of, and in some embodiments, b1 can be 1 or 2. For example, b1 can be 1. When the b1 is 2 or greater, at least two R1 can be identical or different to each other. B2 and b3 can be based on b1 among description of 1 to understand the structure. In some embodiments, the in this text in any type, substituted C6-C60 arylene substituents can be at least one of each selected from the following: Deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C60 alkyl and C1-C60 alkoxy, C1-C60 alkyl and C1-C60 alkoxy, all after deuterium, -F, -Cl, -Br, -I and at least one of the hydroxyl groups substituted, C3-C10 cycloalkyl, C6-C60 aryl, C6-C60 aryloxy, C6-C60 arylthio and gathers many thickly monovalent non-aromatic cyclic group, C3-C10 cycloalkyl, C6-C60 aryl, C6-C60 aryloxy, C6-C60 arylthio and gathers many thickly monovalent non-aromatic cyclic group, all after deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C60 alkyl, C1-C60 alkoxythiophene, C3-C10 cycloalkyl, C6-C60 aryl, C6-C60 aryloxy, C6-C60 arylthio and univalent non-aromatic gathers many thickly in cyclic group of at least one substituted. In some other embodiments, the in this text in any type, substituted C6-C60 arylene substituents can be at least one of each selected from the following: C1-C60 alkyl and C1-C60 alkoxy, all after deuterium, -F, -Cl, -Br, -I, hydroxy, naphthyl, [...], [...], benzocarbazoles [...], dibenzo [...], Fikki, anthryl, [...], hydrazo three phenyl, qu Ji Pyren and replace at least one of, Phenyl, biphenyl, terphenyl base, luen four phenyl, naphthyl, [...], [...], benzocarbazoles [...], dibenzo [...], Fikki, anthryl, [...], hydrazo three phenyl, qu Ji Pyren and, Phenyl, biphenyl, terphenyl base, luen four phenyl, naphthyl, [...], [...], benzocarbazoles [...], dibenzo [...], Fikki, anthryl, [...], hydrazo three phenyl, qu Ji Pyren and, various after deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C60 alkyl, C1-C60 alkoxy, phenyl, biphenyl, terphenyl base, luen four phenyl, naphthyl, [...], [...], benzocarbazoles [...], dibenzo [...], Fikki, anthryl, [...], hydrazo three phenyl, Pyren and in qu Ji at least one substituted. In some embodiments, the above-mentioned fused ring compound can be the following one of the compounds, but is not limited to this: [Group I] Type 1-1 in X1 =S interethni Type 1-1 in X1 =O interethni Type 1-1 in X1 =Si (R4) (R5) interethni (R4 and R5 are described in the specification) Type 1-1 in X1 =N-[ (L1)a1-(R1)b1] interethni (L1, a1, R1 and b1 are described in the specification) Type 1-2 in X1 =O interethni Type 1-2 in X1 =S interethni Type 1-2 in X1 =Si (R4) (R5) interethni (R4 and R5 are described in the specification) Type 1-2 in X1 =N-[ (L1) a1 - (R1) b1] interethni, (L1, a1, R1 and b1 are described in the specification) Teachings in 1 in, R2 and R3 can be at least one of the substituted or non-substituted C6-C60 aryl group and the substituted or non-substituted monovalent non-aromatic cyclic group selected gathers many thickly. Therefore, also 1 condensed ring compound may have is suitable for use in the material of the organic light-emitting device, such as the main material for the emitting layer (for example, comprises a body with dopant main body material of the emitting layer) of the steps can to HOMO, LUMO energy step, T1 can be meta-and S1 can order. Type 1 can be the fused ring compound having an excellent heat stability and electrical stability, and therefore, the use of fused ring compound of the organic light-emitting device can have high efficiency and long-life characteristic. Teachings 1 condensed ring compound has wherein the pyrimidine ring and a benzene ring with the ring and respectively A1 condensed the opposite side of the core (also refer to 1'), and therefore can be acted on it is fit for organic light-emitting device is placed between a pair of electrodes of the material of the organic layer (e.g., for the material of the emitting layer) of the steps can to HOMO, LUMO energy step, T1 can be meta-and S1 can order, and has excellent heat stability and electrical stability. For example, when the teachings 1 condensed ring compound is used as an organic light-emitting device when the body is in the emitting layer, on the basis of the body-dopant energy transfer mechanisms, organic light-emitting device can have high efficiency and long life. Although not limited to any particular theory, the following compounds, however, can have too B electronic transmission capability of the transmission of the cavity can not be realized with the balance between the electronic transmission. Therefore, containing the compound B organic light-emitting device may have a bad efficiency characteristic. C [...] the following compounds containing condensed ring in the core instead of pyrimidine ring, and can be with bad heat stability and electrical stability. The use of Gaussian analog measuring compound 30, compound 29, compound 27, compound b-41, compound b-71, compound b-116, compound a-30, compound a-40, compound a-41, compound a-42, compound a-46, compound a-56, compound a-70, compound a-71, compound a-74, compound a-75, compound a-82, compound a-84, compound a-108, compound a-110, compound a-112, compound a-114, compound a-116, compound e-70, compound e-71, compound e-74, compound e-82, compound e-84, compound e-88, compound e-114, compound f-70, compound f-71, compound f-74, compound f-75, compound f-82, compound f-84, compound compound f-114 and B f-88 and compound, compound HOMO D C and of the compound, the tri-state LUMO and (T1) can order (the use of super-computer GAIA (IBM power 6) with gauss 09 method to calculate the substance of each energy-level). Results for display in the following table 1 in. [Table 1] Reference table 1, compound B the absolute value of the LUMO energy-level of more than compound 30, compound 29, compound 27, compound b-41, compound b-71, compound b-116, compound a-30, compound a-40, compound a-41, compound a-42, compound a-46, compound a-56, compound a-70, compound a-71, compound a-74, compound a-75, compound a-82, compound a-84, compound a-108, compound a-110, compound a-112, compound a-114, compound a-116, compound e-70, compound e-71, compound e-74, compound e-82, compound e-84, compound e-88, compound e-114, compound f-70, compound f-71, compound f-74, compound f-75, compound f-82, compound f-84, compound compound f-114 f-88 and can order of the absolute value of the LUMO, indicating too capacity of electronic transmission. C and compounds D of the compounds can be less than the absolute value of the LUMO-compound 30, compound 29, compound 27, compound b-41, compound b-71, compound b-116, compound a-30, compound a-40, compound a-41, compound a-42, compound a-46, compound a-56, compound a-70, compound a-71, compound a-74, compound a-75, compound a-82, compound a-84, compound a-108, compound a-110, compound a-112, compound a-114, compound a-116, compound e-70, compound e-71, compound e-74, compound e-82, compound e-84, compound e-88, compound e-114, compound f-70, compound f-71, compound f-74, compound f-75, compound f-82, compound f-84, compound compound f-114 f-88 and can order of the absolute value of the LUMO, indicating too weak ability of electronic transmission. Therefore, found that with compound 30, compound 29, compound 27, compound b-41, compound b-71, compound b-116, compound a-30, compound a-40, compound a-41, compound a-42, compound a-46, compound a-56, compound a-70, compound a-71, compound a-74, compound a-75, compound a-82, compound a-84, compound a-108, compound a-110, compound a-112, compound a-114, compound a-116, compound e-70, compound e-71, compound e-74, compound e-82, compound e-84, compound e-88, compound e-114, compound f-70, compound f-71, compound f-74, compound f-75, compound f-82, compound f-84, compound compound f-88 and f-114 comparison, compound B, compound compound C and D is not possible to realize the transmission of the cavity of a balance between the electronic transmission. Examples of synthesizing based on the following description, the technical personnel in this field also can be easy to understand 1 synthesis of the fused-ring compound. As mentioned above, also 1 condensed ring compound can be suitable for use as the main body of the emitting layer of the organic layer or the hole transport layer. Because the organic layer containing the above-described compounds of formula 1 the fused ring compound, therefore organic light-emitting device can have a low drive voltage, high efficiency and long service life. Teachings 1 condensed ring compound can be used for the organic light-emitting device between a pair of electrodes. For example, fused-ring compound can be included in the emitting layer, the emitting layer between the electrode and the 1st of a hole conveying region (for example, hole conveying region can include a hole injection layer, hole transport layer and electron barrier layer in at least one of) 2nd emitting layer between the electrodes and the area of electronic transmission (for example, electronic transmission zone may comprise a hole blocking layer, electron transport layer and electron injection layer in at least one of) in at least one of the in. For example, teachings 1 can be included in the fused ring compound of the emitting layer, wherein the emissive layer may also comprises a dopant, and in the emitting layer fused ring compounds can be used as a main body. For example, the emitting layer can be a green light emitting layer, the dopant can be a phosphorescent dopant. As used herein, "(for example organic layer) containing at least one fused ring compound" means "(organic layer) also comprising a 1 condensed ring compound or at least two kinds of different teachings 1 condensed ring compound". For example, an organic light-emitting device can be only an organic layer comprising compound 1 as a fused ring compound. For example, compound 1 can comprise the emitting layer in an organic light-emitting device. In some embodiments, can be the organic layer of the organic light-emitting device containing the compound 1 or compound 2 as a condensed ring compound. For example, compound 1, compound 2 can be contained in the layer thereon (such as containing the compound 1, compound 2 in transmitting layer) or in different layers. For example, can include fused ring compounds as organic layer contained in transmission of electronic transmission of the main body or in the auxiliary layer. For example, the anode electrode is the 1st, 2nd electrode is the cathode, and the organic layer can comprise i) emitting layer disposed between the electrode and the 1st and includes a hole injection layer, a hole transporting layer and the electron barrier layer in at least one of a hole conveying region; and ii) is placed between electrodes and 2nd emitting layer comprising the hole blocking layer, electron transport layer, the electron injecting layer and at least one of the area of electronic transmission. As used herein, the term "organic layer" refers to an organic light-emitting device is placed on the electrode and the 1st 2nd single between the electrodes and/or a plurality of layers. "Organic layer" may include, for example, an organic compound or organic metal complex containing a metal of the composition. According to another embodiment of the present invention, organic light-emitting device, which comprises the electrode 1st, 2nd 1st electrode opposite to the electrode of the electrode and the 1st and 2nd organic layer between electrodes, and comprises the emitting layer and the at least more than one fused ring compound. Figure 1 to Figure 3 is the schematic view of the disclosed according to one embodiment of the organic light-emitting device (10). In the below, the reference view 1, according to the present disclosure to describe one embodiment of the structure of the organic light-emitting device and method of manufacturing the same. Organic light-emitting device (10) has the following structure, wherein the 1st electrode (11), an organic layer (15) and 2nd electrodes (19) are sequentially stacked in this order. 1st electrode can be arranged in the base plate (11) or 2nd electrode (19) is. The base plate can be used for existing in the organic light emitting device of any of the base plate. In some embodiments, base plate is has strong mechanical strength, thermal stability, transparency, surface smoothness, easy handleability and the water resistance of the glass substrate or transparent plastic substrate. 1st electrode (11) can pass 1st electrode forming material is deposited or formed on the substrate by sputtering. 1st electrode (11) can be the anode. The material can be selected as the material with work function in order to promote hole injection. 1st electrode (11) can be a reflective electrode, the semi-transmissive electrode or a transmissive electrode. For example, for the 1st electrode material can be indium tin oxide (ITO), indium-zinc oxide (IZO), stannic oxide (SnO2) or zinc oxide (ZnO). In some embodiments, material can be a metal, such as magnesium (mg), aluminum (Al), aluminum-lithium (Al-Li), calcium (Ca), magnesium-indium (mg-In), magnesium-silver (mg-Ag) or analogues thereof. 1st electrode (11) may have a single-layer structure or a multilayer structure of at least two layers. Organic layer (15) can be placed in the 1st electrode (11) the upper. Organic layer (15) may comprise a hole conveying region (hole transport region), the emitting layer (emissionlayer) and electronic transmission at least one of the (electron transport region). Hole conveying region can be placed in the 1st electrode (11) and the emitting layer. Hole conveying region can include a hole injection layer, hole transport layer, the buffer layer in the electron barrier layer and at least one. For example, reference view 2, according to the present invention the following description of one embodiment of the organic light-emitting device. Organic layer (15) comprises a hole transport layer (31), the emitting layer (32) and is inserted in hole transport layer (31) and the emitting layer (32) between the auxiliary transmission of the cavity (33). Hole conveying region can comprise at least two hole transport layer, a hole-transporting layer and contact the emitting layer is defined as a hole transport layer. Hole conveying region can comprise only a hole injection layer or a hole transport layer. In some embodiments, electronic transmission area may have containing hole injection layer (37)/ a hole transport layer (31) or a hole injection layer (37)/ a hole transport layer (31)/ electron barrier layer structure, wherein the forming the electronic transmission of the structure of the layers can be sequentially stacked in the order of 1st electrode (11) the upper. For example, further include a hole injection layer (37) and an electron injecting layer (36) and the 1st electrode (11)/ a hole injection layer (37)/ a hole transport layer (31)/ hole transmission layer (33)/ emitting layer (32)/ electronic transmission auxiliary layer (35)/ electron transport layer (34)/ electron injection layer (37)/ 2nd electrode (19) as shown in Figure 3 are shown in the stack. A hole injection layer (37) can be improved with the ITO as the anode for a hole transport layer (31) between the interface characteristic of the organic material, and coating the ITO so that the planarization of the surface of the ITO and planarization. For example, a hole injection layer (37) can be included in the work function of the ITO and the hole transport layer (31) of the median between HOMO the conductivity of the material of the particular need, in order to adjust the work function of the ITO as the anode and the hole transporting layer (31) of the difference of HOMO. Together with this invention, a hole injection layer (37) can include N4, N4 '-diphenyl-N4, N4' -bis-(9-phenyl -9H-carbazole-3-yl) phenylbenzene -4,4 '-diamine (N4, N4' -diphenyl-N4, N4 '-bis (9-phenyl -9H-carbazol-3-yl) biphenyl-4,4' -diamine), but is not limited to this. Furthermore, a hole injection layer (37) can also include the existing material, such as copper phthalocyanine (CuPc), N, N '-dinaphthyl-N, N' -phenyl-(1,1 '-biphenyl) - 4,4' -diamine, NPD), 4,4 ', 4 "-tris [methylphenyl (phenyl) amino] three benzyl amine (m-MTDATA), 4,4', 4"-tris [1-naphthyl (phenyl) amino] three benzyl amine (1-TNATA), 4,4 ', 4"-tris [2-naphthyl (phenyl) amino] three benzyl amine (2-TNATA), 1, 3, 5-tri [N-(4-diphenyl amino phenyl) phenyl-amino] phenylethyl (p-DPA-TDAB) and its analogues, such as 4,4' -bis [N-[ 4 - {N, N-bis (3-methyl phenyl) amino} phenyl]-N-phenyl-amino] biphenyl (DNTPD), six azabenzene and phenanthrene-rokko nitriles (HAT-CN) and its analogue compound, poly (3,4-ethylenedioxy-thiophene)-poly (styrene sulfonate) (PEDOT) as a conductive polymer. A hole injection layer (37) can be used, for example, is coated on the ITO as the anode, the thickness of 10 angstroms to 300 angstroms. Electron injection layer (36) is stacked in the electron-transport layer on the electron injection to the anode in order to promote and improve the power efficiency. The electron injection layer can be any known material in the field, is not limited to such as LiF, Liq, NaCl, CsF, Li2 O, BaO and its analogue. When the hole conveying region containing hole injection layer (37) at the time, the hole injection layer (HIL) 1st electrode (11), for example, by the vacuum deposition, spin coating, casting, lb deposition method or the like in a plurality of method for forming any one of a. When using the vacuum deposition to form a hole injection layer, a vacuum deposition conditions used for forming the hole injection layer to be formed and the material of the hole injection layer of the desired structural and thermal changes. For example, vacuum deposition can be at about 100 °C to about 500 °C temperature, about 10-8 taintor to about 10-3 and pressure of about 0.01 ANGSTROM/second to about 100 ANGSTROM/second under the deposition rate. However, is not limited to the deposition conditions. When using the rotary coating to form a hole injection layer, coating conditions visual used for forming the hole injection layer to be formed and the material of the hole injection layer of the desired structural and thermal changes. For example, coating rate can be at about 2000rpm to about 5000rpm range, and the coating after heat treatment in order to remove the solvent, the temperature of which is about 80 °C to about 200 °C range. However, coating conditions are not limited to this. Can be based on the above-mentioned hole injecting layer forming conditions, defined is used for forming the hole transport layer and electron barrier layer conditions. In some embodiments, hole conveying region can comprise m-MTDATA, TDATA, 2-TNATA, NPB, β-NPB, TPD, spiro-TPD, spiro-NPB, α-NPB, TAPC, HMTPD, TCTA (4,4 ', 4 "-tri (N-carbazolyl) triphenylamine (4,4', 4"-tris (N-carbazolyl) triphenylamine)), Pani/DBSA (Polyaniline/Dodecylbenzenesulfonicacid: polyaniline/dodecyl benzenesulfonic acid), PEDOT/PSS (Poly (3,4-ethylenedioxythiophene)/ Poly (4-styrenesulfonate): poly (3,4-ethylenedioxy-thiophene)/ poly (4-styrene sulfonate)), Pani/CSA (Polyaniline/Camphor sulfonicacid: polyaniline/camphor sulfonic acid), (Polyaniline)/ Poly PANI/PSS (4-styrenesulfonate): polyaniline)/ poly (4-styrene sulfonate)), is represented by following type 201 and of a compound represented by the following formula 202 in that at least one of the compounds. Teachings in 201 in, Ar101 and Ar102 can all independently each selected from the following: Phenylene, Asia and cyclopentadienyl, [...], subnaphthyl, [...], Asia and cycloheptatriene base, [...], [...], jaya propylene gathers the naphthyl, asian phenanthryl, jaya anthryl, [...] anthryl, asian association jaya three phenyl, asian pyrenyl, asia Qu Ji, asia is thick four phenyl, [...], and five asia is thick[...] phenyl, and Phenylene, Asia and cyclopentadienyl, [...], subnaphthyl, [...], Asia and cycloheptatriene base, [...], [...], jaya propylene gathers the naphthyl, asian phenanthryl, jaya anthryl, [...] anthryl, asian association jaya three phenyl, asian pyrenyl, asia Qu Ji, asia is thick four phenyl, [...], and five asia is thick[...] phenyl, all after deuterium, -F, -Cl, -Br, -I, hydroxy, cyano, nitro, amino, amidino, hydrazine, [...], carboxylic acid or salt thereof, sulfonic acid or its salt, phosphoric acid group or its salt phosphonate, C1-C60 alkyl, C2-C60 ene yl, C2-C60 alkynyl, C1-C60 alkoxythiophene, C3-C10 cycloalkyl, C3-C10 cycloalkenyl, C2-C10 heterocyclic alkyl, C2-C10 heterocyclic alkenyl, C6-C60 aryl, C6-C60 aryloxy, C6-C60 arylthio, C2-C60 hetero aryl group, a monovalent non-aromatic gathers many thickly cyclic group and univalent non-aromatic fused hetero cyclic group of at least one substituted. In the formula 201 in, the and xa xb is independently 0 to 5 an integer of, for example can be 0,1 or 2. For example, for xa 1 and xb can be 0, but is not limited to this. In the formula 201 among 202 in, R101 to R108, R111 to R119 and R121 to R124 can all independently each selected from the following: Hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, cyano, nitro, amino, amidino, hydrazine, [...], a carboxylic acid group or its salt, sulfonic acid group or its salt, phosphoric acid group or its salt phosphonate, C1-C10 alkyl (for example methyl, ethyl, propyl, butyl, pentyl, hexyl or its similar group) and C1-C10 alkoxy (such as methoxy, ethoxy, propoxy, butoxy, pentoxy or its similar group); C1-C10 alkyl and C1-C10 alkoxy, all after deuterium, -F, -Cl, -Br, -I, hydroxy, cyano, nitro, amino, amidino, hydrazine, [...], a carboxylic acid group or its salt, sulfo group or its salt phosphonate and its base or phosphate salt of at least one substituted; Phenyl, naphthyl, anthryl, and [...] Pyren; and Phenyl, naphthyl, anthryl, and [...] Pyren, all after deuterium, -F, -Cl, -Br, -I, hydroxy, cyano, nitro, amino, amidino, hydrazine, [...], a carboxylic acid group or its salt, sulfonic acid group or its salt, phosphoric acid group or its salt phosphonate, C1-C10 alkyl and C1-C10 at least one of the alkoxy substituted. However, the embodiment of the invention is not limited to this. Teachings in 201 in, R109 can be made by the following various selected from: phenyl, naphthyl, anthryl and pyridyl, and Phenyl, naphthyl, anthryl and pyridyl, all after deuterium, -F, -Cl, -Br, -I, hydroxy, cyano, nitro, amino, amidino, hydrazine, [...], a carboxylic acid group or its salt, sulfonic acid group or its salt, phosphoric acid group or its salt phosphonate, C1-C20 alkyl and C1-C20 at least one of the alkoxy substituted. In some embodiments, formula 201 compound may by the type 201A expressed, but is not limited to this: In the formula 201A in, R101, R111, R112 and R109 can be the same as the above defined. For example, type 201 among the compound 202 can include the following compounds a compound HT1 HT20 to the compound, but is not limited to this: The thickness of the transmission of the cavity may be about 100 egypt to approximately 10000 angstroms, and in some embodiments, is about 100 egypt to approximately 1000 angstroms. When the hole conveying region containing hole injection layer, hole transport layer, the thickness of the hole injection layer may be about 100 egypt to approximately 10,000 angstroms, and in some embodiments, is about 100 egypt to approximately 1,000 angstroms, and the thickness of the hole transport layer may be about 50 egypt to approximately 2,000 angstroms, and in some embodiments, about 100 egypt to approximately 1,500 angstroms. When the hole conveying region, hole injection layer and the thickness of the hole transport layer is within the range, the drive voltage has no substantive on the following obtain satisfactory transmission characteristics of the cavity. In addition to the above material, hole conveying region can also include a charge-generating material in order to improve conductivity. Charge generating material can be uniform or non-uniform dispersion in the hole transport region. For example, charge generating material p-type dopant. The P-type dopant can be quinine derivatives, metal oxide and one of the compounds containing cyano, but is not limited to this. P-type dopant for quinone derivative non-limiting example, two methane (TCNQ), such as four cyano quinone, 2, 3, 5, 6-tetra-fluoro-four cyano -1,4- benzene and quinone b methane (F4-TCNQ) and the like; metal oxide, such as tungsten oxide, molybdenum oxide and the like; and cyano-containing compound, such as the following compound HT-D1. Hole conveying region can also include a buffer layer. The buffer layer can be spontaneous layer according to the wavelength of the light emitted from the optical resonance of the compensation light, and therefore can increase efficiency. The emitting layer (EML) can be through the use of vacuum deposition, spin coating, casting, lb deposition method or the like in the hole transport region is formed. When the emitting layer using vacuum deposition or spin coat formed, for depositing and coating conditions can be similar to those used for the conditions for forming the hole injection layer, however for depositing and coating of the visual condition of the material used for forming the emitting layer. The emitting layer can include body and dopant. Teachings can include a main body 1 in the fused ring compound of at least one. For example, the body can include the 1st and 2nd main body of the main body, the main 1st and 2nd main body are different from each other. In some embodiments, divided by aboving 1 outside the fused ring compounds, the organic layer of the organic light-emitting device can only include the above-mentioned fused ring compound (1st main body), or also includes the compounds represented by general formula 41 with the 1st compound expressed by following formula 61 of the said two kinds of compound 2nd compound in at least one of. 2nd comprising the main body can be represented by formula 41 with 1st compound of formula 61 in the 2nd of said at least one of the compounds. In the compounds represented by general formula 61 in, ring A61 by the following formulae 61A expressed, and the compounds represented by general formula 61 in, ring A62 by the following formulae 61B expressed. In the compounds represented by general formula 61 in, ring A61enjoys the carbon the thick and the adjacent 5-membered ring and ring A62, and the compounds represented by general formula 61 in, ring A62enjoys the carbon the thick and the adjacent ring A62 and 6 membered ring. Also in 41 in, X41 can be N-[ (L42)a42-(R42)b42], S, O, S (=O), S (=O)2, C (=O), C (R43) (R44), Si (R43) (R44), P (R43), P (=O) (R43) or C=N (R43); Type 61 of the ring in A61 can be are represented by the formulas 61A expressed; Type 61 of the ring in A62 can be are represented by the formulas 61B expressed; X61 can be N-[ (L62)a62-(R62)b62], S, O, S (=O), S (=O)2, C (=O), C (R63) (R64), Si (R63) (R64), P (R63), P (=O) (R63) or C=N (R63); X71 can be C (R71) or N; X72 can be C (R72) or N; X73 can be C (R73) or N; X74 can be C (R74) or N; X75 can be C (R75) or N; X76 can be C (R76) or N; X77 can be C (R77) or N; X78 can be C (R78) or N; Ar41, L41, L42, L61 and L62 can all independently each selected from the following: a substituted or an unsubstituted C3-C10asian link alkyl, a substituted or an unsubstituted C2-C10 jaya heterocyclic alkyl, a substituted or an unsubstituted C3-C10 jaya cycloalkenyl, substituted or not substituted C2-C10asia is mixed cycloalkenyl, substituted or not substituted C6-C60 jaya aryl, a substituted or an unsubstituted C2-C60 heteroarylidenyl, a substituted or an unsubstituted divalent non-aromatic gathers many thickly cyclic group and a substituted or an unsubstituted divalent non-aromatic fused hetero cyclic group; N1 and n2 can all independently from 0 to 3 in the selected integer; R41 to R44, R51 to R54, R61 to R64 and R71 to R79 can all independently each selected from the following: hydrogen, deuterium, -F (fluorine-based), -Cl (chlorine-based), (polybromide yl)-Br, -I (iodine-based), hydroxy, cyano, nitro, amino, amidino, a substituted or an unsubstituted C1-C60 alkyl, a substituted or an unsubstituted C2-C60 alkenyl, a substituted or an unsubstituted C2-C60 alkynyl, substituted or not substituted C1-C60 alkoxy, a substituted or an unsubstituted C3-C10 cycloalkyl, a substituted or an unsubstituted C2-C10 heterocyclic alkyl, a substituted or an unsubstituted C3-C10 cycloalkenyl, substituted or not substituted C2-C10 heterocyclic alkenyl, a substituted or an unsubstituted C6-C60 aryl, a substituted or an unsubstituted C6-C60 aryloxy group, a substituted or an unsubstituted C6-C60 arylthio, a substituted or an unsubstituted C2-C60 heteroaryl, a substituted or an unsubstituted monovalent non-aromatic gathers many thickly cyclic group, substituted or not substituted by a monovalent non-aromatic fused hetero cyclic group, -N (Q1) (Q2), -Si (Q3) (Q4) (Q5) and-B (Q6) (Q7); and A41, a42, a61 and a62 can all independently from 0 to 3 in the selected integer; B41, b42, b51 to b54, b61, b62 and b79 that can all independently 1 to 3 in the selected integer. In some embodiment, R41 to R44, R51 to R54, R61 to R64 and R71 to R79 can all independently each selected from the following: hydrogen, deuterium atom, -F, -Cl, -Br, -I, hydroxy, cyano, amino, amidino, C1-C20 alkyl, C1-C20 alkoxythiophene, C3-C10 cycloalkyl, C3-C10 cycloalkenyl, C6-C20 aryl and gathers many thickly monovalent non-aromatic cyclic group, In some other embodiments, the teachings 41 among 61 in, R41 to R44, R51 to R54, R61 to R64 and R71 to R79 can all independently each selected from the following: Hydrogen, deuterium atoms, -F, -Cl, -Br, -I, hydroxy, cyano, amino, amidino, C1-C20 alkyl and C1-C20 alkoxy; Phenyl, and cyclopentadienyl, naphthyl, [...], [...], benzocarbazoles [...], dibenzo [...], propylene gathers the naphthyl, Fikki, anthryl, [...], hydrazo three phenyl, Pyren, qu Ji, [...], [...], luen five phenyl, carbazolyl, benzofuranyl, benzothienyl, b benzofuranyl, dibenzo thienyl, benzo carbazyl and b benzocarbazoles carbazolyl; and Phenyl, and cyclopentadienyl, naphthyl, [...], [...], benzocarbazoles [...], dibenzo [...], propylene gathers the naphthyl, Fikki, anthryl, [...], hydrazo three phenyl, Pyren, qu Ji, [...], [...], luen five phenyl, carbazolyl, benzofuranyl, benzothienyl, b benzofuranyl, dibenzo thienyl, benzo carbazyl and b benzocarbazoles carbazolyl, via the following various in the selected at least one substituted: deuterium, -F, -Cl, -Br, -I, hydroxy, cyano, amino, amidino, C1-C20 alkyl, C1-C20 alkoxy, phenyl, and cyclopentadienyl, naphthyl, [...], [...], benzocarbazoles [...], dibenzo [...], propylene gathers the naphthyl, Fikki, anthryl, [...], hydrazo three phenyl, Pyren, qu Ji, [...], [...], luen five phenyl, carbazolyl, benzofuranyl, benzothienyl, b benzofuranyl, dibenzo thienyl, benzo carbazyl and b benzocarbazoles carbazolyl, but is not limited to this. For example, L61 and L62 each is independently substituted or not substituted C6-C60 jaya aryl, a substituted or an unsubstituted C2-C60 heteroarylidenyl or a substituted or an unsubstituted divalent non-aromatic gathers the multi-link base thickly, R51 to R54, R61 to R64 and R71 to R79 each is independently hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, cyano, amino, amidino, a substituted or an unsubstituted C1-C20 alkyl, a substituted or an unsubstituted C1-C20 alkoxy, a substituted or an unsubstituted C3-C10 cycloalkyl, a substituted or an unsubstituted C3-C10 cycloalkenyl, substituted or not substituted C6-C20 aryl group or a substituted or an unsubstituted monovalent non-aromatic fused hetero cyclic group. In some embodiments, formula 41 of in R51, R53 and R54 of formula 61 of in R71 to R79 can all independently each selected from the following: hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, cyano, nitro, amino, amidino, C1-C20 alkyl, C2-C20 ene yl, C2-C20 alkynyl and C1-C20 alkoxy. In some other embodiments, type 41 of in R51, R53 and R54 of formula 61 of in R71 to R79 can be hydrogen. Formula 41 of in R41, R42 and R52 of formula 61 of in R61 and R62 that the teachings can be independently 1, type 4-1 to 4-33 group expressed in one of. In some embodiments, formula 41 of in R41, R42 and R52 of formula 61 of in R61 and R62 the teachings is independently from about 1, type 4-1 to 4-5 formula 4-26 to 4-33 group expressed in one of. In some other embodiments, type 41 of in R41, R42 and R52 of formula 61 of in R61 and R62 the teachings is independently from about 1, type 5-1 to 5-27 among 5-40 to 5-44 group expressed in one of. However, embodiments of the present invention is not limited to this. According to another embodiment, the organic light emitting device can be containing the main 1st, and 2nd emitting layer of dopant of the main body, wherein the main body and the 1st 2nd main body are different from each other, 1st main body comprises the formula 1 expresses the fused ring compound, and 2nd main body comprises the compounds represented by general formula 41 with the 1st compound expressed by following formula 61 in the 2nd of said at least one of the compounds. In some other embodiments, the above-mentioned 1st compound can be by following formula 41-1 to 41-12 said one of, and the above 2nd compound can be by following formula 61-1 to 61-6 said one of. However, embodiments of the present invention is not limited to this. In the formula 41-1 to 41-12 formula 61-1 to 61-6 in, X41, X61, L41, a41, L61, a61, R41, R51 to R54, b41, b51 to b54, R61, b61, R71 to R79 and b79 can be the same as the above defined. Represented by formula 1 includes fused ring compounds expressed by one of the compounds of group I. In some embodiments, also 41 of the 1st compounds can include the following compound A1 to compound A111 of one, and the type 61 of 2nd compounds can include the following compound B1 to compound B20 of one. However, embodiments of the present invention is not limited to this. For example, the main body and the 1st 2nd main body can be in the weight ratio of about 1:99 to about 99:1 range, and in some embodiments, in about 10:90 to about 90:10 within range. When the weight ratio is in these ranges, the 1st and 2nd is electronic transmission of the transmission characteristics of the cavity of the main body of the balance can be achieved, so that the organic light-emitting device and the emission efficiency can be improved service life. When the emitting layer includes the main body when the with dopant, the dopant in the amount of 100 parts by weight of the body from about 0.01 parts by weight to about 15 parts by weight. However, the amount of dopant is not limited to this range. Examples of synthesizing based on the following description, the technical personnel in this field also can be easily aware 1 condensed ring compound, teachings 41 and 1st of the above compound of formula 61 of the synthetic method of the compound of 2nd. When the organic light-emitting device is a full-color organic light-emitting device, the emitting layer can be patterned in a red light emitting layer, green light emitting layer and a blue light emitting layer. In some embodiments, the emitting layer can have a stacked structure, which includes a red light emitting layer, green light emitting layer and/or a blue light emitting layer, but is not limited to this, these layer above stacked on each other, emit a white light. A red light emitting layer, a blue light emitting layer and the green light emitting layer can include one of the teachings of the main body 1 of the fused ring compound. For example, the main body of the green light emitting layer can be of the formula 1 the fused ring compound. Furthermore, a blue light emitting layer can include auxiliary layer of electronic transmission represented by formula 1 expresses the fused ring compound. Emitting layer of the light-emitting device can include a dopant, which can be based on fluorescence mechanisms luminous fluorescent dopant or based on phosphorescence mechanism light emitting phosphorescent dopants. In some embodiments, the emitting layer can contains at least a compound of formula 1 with the fused ring compound of the main body of the phosphorescent dopant. Containing phosphorescent dopant can be transition metal (for example, iridium (Ir), platinum (Pt), osmium (Os) or rhodium (Rh)) organic metal complex. Phosphorescent dopant can include the compounds represented by general formula 81 of the organic metal compound that: In the formula 81 in, M can be iridium (Ir), platinum (Pt), osmium (Os), titanium (Ti), zirconium (Zr), hafnium (Hf), europium (Eu), terbium (Tb) or thulium (Tm); Y1 to Y4 each of them is independently carbon (C) or nitrogen (N); Y1 and Y2 can be bound to each other via a single bond or double bond, and Y3 and Y4 can be bound to each other via a single bond or double bond; CY1 and CY2 can all independently is benzene, naphthalene, luxuriant growth, [...], indenyl, pyrrole, thiophene, furan (furan), imidazole, pyrazole, thiazole, isothiazole, oxazole, isoxazole (isooxazole), pyridine, pyrazine, pyrimidine, pyridazine, quinoline, isoquinoline, [...], [...], quinazoline, oxazole, benzimidazole, benzofuran (benzofuran), benzothiophene, benzothiophene different benzene, benzoxazol, diozaiole different benzene, triazole, tetrazole, [...], triazine, b benzofuranacetic (dibenzofuran) or dibenzothiophenes, wherein CY1 and CY2 visual situation via the (optionally) single bond or organic bonding group (organic linking group) bound to each other; R81 and R82 can all independently each selected from the following: hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, cyano, nitro, amino, amidino, hydrazine, hydrazone, a carboxylic acid group or its salt, sulfonic acid group or its salt, phosphoric acid group or its salt, a substituted or an unsubstituted C1-C60 alkyl, a substituted or an unsubstituted C2-C60 alkenyl, a substituted or an unsubstituted C2-C60 alkynyl, substituted or not substituted C1-C60 alkoxy, a substituted or an unsubstituted C3-C10 cycloalkyl, a substituted or an unsubstituted C2-C10 heterocyclic alkyl, a substituted or an unsubstituted C3-C10 cycloalkenyl, substituted or not substituted C2-C10 heterocyclic alkenyl, a substituted or an unsubstituted C6-C60 aryl, a substituted or an unsubstituted C6-C60 aryloxy group, a substituted or an unsubstituted C6-C60 arylthio, a substituted or an unsubstituted C2-C60 heteroaryl, a substituted or an unsubstituted monovalent non-aromatic gathers many thickly cyclic group, substituted or not substituted by a monovalent non-aromatic fused hetero cyclic group, -N (Q1) (Q2), -Si (Q3) (Q4) (Q5) and-B (Q6) (Q7); A81 and a82 independently on the 1 to 5 selected in an integer; N81 can be 0 to 4 selected in an integer; N82 can be 1,2 or 3; L81 can be made by the following various selected from: univalent organic ligands, bivalent organic ligands and trivalent organic ligands. R81 and R82 on the above definition R11 the same. Phosphorescent dopant can be PD1 containing compound to compound PD78 in at least one of, but not limited to this (PD1 the following compounds for Ir (ppy)3): In some embodiments, a phosphorescent dopant can be or PtOEP comprising the following expressed PhGD. In some other embodiments, a phosphorescent dopant can be of the following said DPVBi, DPAVBi, TBPe, DCM, DCJTB, coumarin 6 and C545T at least one of the in. When the emitting layer includes the main body when the with dopant, the dopant in the amount of 100 parts by weight of the body from about 0.01 parts by weight to about 20 parts by weight. However, the amount of dopant is not limited to this range. The thickness of the emitting layer may be about 100 egypt to approximately 1000 angstroms, and in some embodiments, may be about 200 egypt to approximately 600 angstroms. When the emitting layer with the thickness of these range, the driving voltage has no real following on the emitting layer can have improved light emitting capability. Subsequently, the emission can be placed on the electronic transmission. Electronic transmission zone may comprise a hole blocking layer, electron transport layer and electron injection layer in at least one of. In some embodiments, electronic transmission area may have include an electron transport layer, a hole blocking layer/electron transport layer/electron injection layer or electron transporting layer/electron injection layer structure, wherein the forming the electronic transmission of the structure in the layer can be stacked in the stated order on the emitting layer. However, embodiments of the present invention is not limited to this. For example, according to one embodiment of the organic light-emitting device in the hole conveying region can include at least two hole transport layer, and in this case, contact emitting layer is defined as a hole transport layer of the hole transport layer. Electronic transport layer may have a single-layer structure or comprises at least two different multi-layer structure of the material. Electronic transmission area can include are represented by the formulas 1 the fused ring compound. For example, electronic transmission zone can comprise an electron transport layer, electron transport layer can include teachings and 1 the fused ring compound. In other words more specific, comprising electronic transmission auxiliary layer can be represented by formula 1 expresses the fused ring compound. Organic light-emitting device can also include the compounds represented by general formula 2 compound expressed by the hole transport layer, wherein the electron-transport layer includes fused ring compounds. In the formula 2 in, L201 is a substituted or an unsubstituted C6 to C30 arylene or a substituted or an unsubstituted C2 to C30 heteroarylidenyl, N101 to 1 to 5 an integer of, R201 to R212 each is independently hydrogen, deuterium, a substituted or an unsubstituted C1 to C20 alkyl, a substituted or an unsubstituted C6 to C50 aryl group, a substituted or an unsubstituted C2 to C50 heteroaryl, or combinations thereof, and R201 to R212 the exist independently, or fused to each other, form the ring. In the formula 2 in, "substituted" means after deuterium, halogen, hydroxy, amino, a substituted or an unsubstituted C1 to C30 amino, nitro, a substituted or an unsubstituted C1 to C40 silicon alkyl, C1 to C30 alkyl, C3-C30 cycloalkyl, C2 to C30 heterocyclic alkyl, C6 to C30 aryl group, C2 to C30 heteroaryl, C1 to C20 alkoxy, fluoro, C1-C10 three fluoro alkyl or cyano substituted, instead of at least one hydrogen. According to one embodiment of the hole transmission layer can include the compounds represented by general formula P-1 to P-5 one of the compounds expressed by the. Based on the above-mentioned hole injecting layer forming conditions, can define electronic transmission used for forming the hole blocking layer, electron transport layer and electron injection layer conditions. When the electronic transmission area comprises the hole blocking layer, hole blocking layer BCP and Bphen the following may be included in at least one of. However, embodiments of the present invention is not limited to this. The cavity may be about the thickness of the barrier layer 20 egypt to approximately 1000 angstroms, and in some embodiments, about 30 egypt to approximately 300 angstroms. When the thickness of the HBL in these range, the driving voltage has no real following on the hole blocking layer can have improved hole blocking ability. BCP described above and in addition outside of Bphen, electronic transmission area can also include the following Alq3, Balq, TAZ and NTAZ at least one of the in. In some embodiments, the electron transport layer of the compound can include the following said ET1 and ET2 compound in at least one of, but not limited to this. In some other embodiments, the electron transport layer also may contain 1 condensed ring compound, but is not limited to this. The thickness of the electron transporting layer may be about 100 egypt to approximately 1000 angstroms, and in some embodiments, about 150 egypt to approximately 500 angstroms. When the thickness of the electron transporting layer in these range, the driving voltage has no real following on the electron transport layer can have a satisfactory capacity of electronic transmission. In some embodiments, in addition to the above material, an electron transport layer can also include metal-containing material. Metal-containing material can comprise lithium wrong composition. Lithium complexes of the following non-limiting example, compound ET-D1 ( [...], LiQ) or the following compound ET-D2. Electronic transmission area electronic self-promotion can include 2nd electrode (19) (EIL) injected into the electron injection layer. The electron injection layer may contain LiF, NaCl, CsF, Li2 O and BaO in at least one of the elected. The thickness of the electron injecting layer may be about 1 egypt to approximately 100 angstroms, and in some embodiments, about 3 egypt to approximately 90 angstroms. When the electron injection layer has a thickness of the range, the driving voltage has no real following on the electron injection layer can have satisfactory electron injection ability. 2nd electrode (19) is arranged on the organic layer (15) is. 2nd electrode (19) can be a cathode. For 2nd electrode (19) of the material can be a metal, alloy or with low work function of the conductive compound or a combination thereof. For 2nd electrode (19) of the non-limiting example, the material is lithium (Li), magnesium (mg), aluminum (Al), aluminum-lithium (Al-Li), calcium (Ca), magnesium-indium (mg-In) and magnesium-silver (mg-Ag), or analogues thereof. In some embodiments, the manufacture of a top-emission type light-emitting device, 2nd electrode (19) can be made of, for example, ITO or IZO is formed a transmissive electrode. While the above-described Figure 1 of the organic light-emitting device, however, the embodiment of the invention is not limited to this. As used in this text, C1-C60 alkyl are those with 1 to 60 carbon atoms in straight chain or branched chain univalent (monovalent) aliphatic hydrocarbyl. Non-limiting example, is methyl, ethyl, propyl, isobutyl, butyl 2nd, 3rd-butyl, pentyl, isoamyl and hexyl. C1-C60 with alkylene means C1-C60 of the same structure as the divalent (divalent) alkyl group. As used in this text, C1-C60 alkoxy means the-OA101 a monovalent radical (wherein A101 is aforementioned C1-C60 alkyl). Non-restrictive example is methoxy, ethoxy and isopropoxy. As used in this text, C2-C60 alkenyl means C2-C60 alkyl intermediate or end comprising at least one carbon double bond structure. For non-limiting example, vinyl, propenyl and butene-based. C2-C60 alkenylene means with the C2-C60 alkenyl same bivalent group of the structure. As used in this text, C2-C60 alkynyl means C2-C60 alkyl or carbon three comprising at least one of the tail end of the structure. Non-restrictive example is ethynyl (ethynyl) and propynyl (propynyl). The use in this text C2-C60 with asian alkyne base means C2-C60 alkynyl same bivalent group of the structure. As used in this text, C3-C10 cycloalkyl are those with 3 to 10 carbon atoms of a monovalent monocyclic alkyl. Non-restrictive example is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and cycloheptyl. C3-C10 with alkyl means asian link C3-C10 cycloalkyl same bivalent group of the structure. As used in this text, C2-C10 heterocyclic alkyl are those with 2 to 10 carbon atoms of a monovalent monocyclic group, comprising at least one of them by N, O, P and S elected in the hetero-atom as a ring atom. Non-restrictive example is tetrahydrofuryl (tetrahydrofuranyl) and tetrahydrofurfuroxy thienyl. C2-C10 jaya heterocyclic alkyl means with the C2-C10 heterocyclic alkyl divalent group of the same structure. As used in this text, C3-C10 refers to cycloalkenyl having 3 to 10 carbon atoms of a monovalent monocyclic group, in the ring thereof comprising at least one double bond, but does not have aromatic (aromacity). Non-restrictive example is cyclopentenyl, cyclohexenyl and cycloheptaene base. C3-C10 jaya cycloalkenyl means with the C3-C10 cycloalkenyl same bivalent group of the structure. As used herein, use of herein C2-C10 heterocyclic alkenyl are those with 2 to 10 carbon atoms of a monovalent monocyclic group, the ring thereof comprising at least one double bond in the comprising at least one of them by N, O, P and S elected in the hetero-atom as a ring atom. C2-C10 heterocyclic alkenyl of non-restrictive example is 2,3-dihydro furan group and 2,3-tetrahydrothiophene base. The use in this text C2-C10 jaya heterocyclic alkenyl means with the C2-C10 heterocyclic alkenyl same bivalent group of the structure. As used in this text, C6-C60 aryl are those with 6 to 60 carbon atoms (monovalent) of a monovalent aromatic carbocyclic aromatic-based, and C6-C60 arylene are those with 6 to 60 carbon atoms of an aromatic homocyclic ring base of a divalent (divalent). C6-C60 aryl non-restrictive example is phenyl, naphthyl, anthryl, Fikki, qu Ji Pyren and. When the C6-C60 aryl and C6-C60 arylene comprises at least two ring, two of the rings can be fused to each other. As used in this text, C2-C60 heteroaryl are those with 2 to 60 carbon atoms of a monovalent aromatic carbocyclic aromatic group, comprising at least one of them by N, O, P and S elected in the hetero-atom as a ring atom. C2-C60 heteroarylidenyl are those with 2 to 60 carbon atoms, divalent aromatic homocyclic ring base, comprising at least one of them by N, O, P and S elected in the hetero-atom as a ring atom. C2-C60 heteroaryl of non-restrictive example is pyridyl, pyrimidinyl, pyrazinyl, pyridazinyl, triazinyl, quinolyl and isoquinolyl. When the C2-C60 heteroaryl and C2-C60 heteroarylidenyl comprises at least two ring, two of the rings can be fused to each other. As used in this text, C6-C60 aryloxy indicating-OA102 (wherein A102 is aforementioned C6-C60 aryl), and C6-C60 arylthio (arylthio) indicating-SA103 (wherein A103 is aforementioned C6-C60 aryl). As used herein, a monovalent non-aromatic condensed polycyclic group is (non-aromatic condensedpolycyclic group) with at least two mutually fused ring a monovalent radical, wherein comprise only carbon atom (for example, 8 to 60 carbon atoms) as ring atoms and aromatic (non-aromacity) without the entire molecule. Non-restrictive example is [...]. Divalent non-aromatic condensed polycyclic group is a with a monovalent non-aromatic condensed polycyclic group is a divalent group of the same structure. As used herein, a monovalent non-aromatic fused Heteropolycyclic group refer to (non-aromatic condensedheteropolycyclic group) with at least two mutually fused ring a monovalent radical, wherein the carbon atom (for example 2 to 60 carbon atoms) by N and, O, P and S as the hetero-atom is elected in ring forming atoms and aromatic (non-aromacity) without the entire molecule. A monovalent non-aromatic fused Heteropolycyclic group of non-restrictive example is carbazolyl. Divalent non-aromatic fused Heteropolycyclic group is a with a monovalent non-aromatic fused Heteropolycyclic group of the same structure as the divalent group. "Biphenyl" means "phenyl is phenyl substituted". Examples will now be reference to the following detailed description includes fused ring compounds and organic light-emitting device containing the same of the present invention of one or more embodiments. However, these examples only for a purpose of the note and do not wish to limit the invention to one or more of the scope of the embodiment. In the following synthetic example, statements "the use of 'B' instead of 'A' " means the equivalent 'B' under 'A' of the amount is the same. [Experimental example] In the below, unless the special reference to, for example, the initial material and synthetic examples and reaction material purchase from Sigma - [...] limited or TCI Company. [Embodiment] (Synthesis of boric acid ester) According to the following synthetic examples of the borate KR10-2014-0135524A section 35 page by the same method as described on the method of synthesis of synthetic, and for the reaction process of the boric acid ester [formula A] and [formula B]. [General formula A] (In the formula A in, "L" is a substituted or an unsubstituted C6 to C60 arylene) [General formula B] (In the above formula in B, Ar1 and Ar2 is independently a substituted or an unsubstituted C6-C30 aryl group. For example, can be a substituted or an unsubstituted phenyl, a substituted or an unsubstituted biphenyl, substituted or not substituted terphenyl base, a substituted or an unsubstituted luen four phenyl, a substituted or an unsubstituted naphthyl, a substituted or an unsubstituted anthryl, a substituted or an unsubstituted [...], a substituted or an unsubstituted qu Ji and its similar group. ) In the below, through the embodiment to display as used in the present invention the response of the method for synthesis of borate ester of the material for the better understanding. (Synthesis of compound main body 1st) Synthesis example 1: synthesis of compound 29 A synthetic intermediate (1) (benzo -1H-thieno [3,2-d] pyrimidine -2,4-dione) The benzo-3-amino-2-thiophene carboxylic acid methyl ester (47.5 g, 0 . 23 mol) with urea (79.4 g, 1 . 15 mol) the mixture of 2000 ml round bottom flask in about 200 °C lower stirring for about 2 hours. In cooling high temperature reaction product to the room temperature, wherein added to the sodium hydroxide solution is then filtered to remove impurities, and acidification (HCl, 2N). Drying of the precipitate, A to obtain intermediate (1) (35 g, 75%). C10 H6 N2 O2 S the calculated value: C, 55.04; H, 2.77 ; N, 12.84; O, 14.66 ; S, 14.69; content: C, 55.01 ; H, 2.79; N, 12.81 ; O, 14.69; S, 14.70 A synthetic intermediates (benzo -2,4-dichloro-thieno [3,2-d] pyrimidine) A mixed intermediate (1) (benzo -1H-thieno [3,2-d] pyrimidine -2,4-dione) (35 g, 0 . 16 mol) and phosphorus oxychloride (600 ml) in a 1000 ml round-bottom flask to reflux the stirring for about 6 hours. Cooling the reaction product to and room temperature under stirring in the ice/water, get precipitation. Filtering the resulting reaction precipitation, in the form of a white solid is obtained intermediate A (benzo -2,4-dichloro-thieno [3,2-d] pyrimidine) (35 g, 85%, white solid). The use of elemental analysis and differentiation intermediate A NMR. The results are as follows. C10 H4 Cl2 N2 S the calculated value: C, 47.08; H, 1.58 ; Cl, 27.79; N, 10.98 ; S, 12.57; content: C, 47.03 ; H, 1.61; Cl, 27.81 ; N, 10.98; S, 12.60 300MHz (CDCl3, PPM): 7.63 (t, 1H), 7.76 (t, 4H), 7.95 (d, 1H), 8.53 (d, 1H) A-29 synthetic intermediates Add 20.0 g (78.4 mmol) intermediate A, 11.0 g (90.15 mmol) phenyl boronic acid (manufacturer: Beijing auspicious Dongfang chemical technology, ltd.), 27.09 g (195.99 mmol) potassium carbonate and 4.53 g (3.9 mmol) Pd (PPh3)4 (four-(triphenylphosphine) palladium (0)) to 1000 ml of flask in 300 ml of 1,4-dioxane and 150 ml in the nitrogen atmosphere under improved in about 60 °C lower heating about 12 hours. The resulting mixture is added to 1000 ml of methanol, to obtain crystalline solid powder by filtration. The resulting products are dissolved for single paradichlorbenzene and to filter using silica gel/diatomaceous earth, then removed and a proper amount of organic solvent recrystallization with methanol, to obtain intermediate A-29 (13.9 g, yield 60%). C16 H9 ClN2 S the calculated value: C, 64.75; H, 3.06 ; Cl, 11.95; N, 9.44 ; S, 10.80; content: C, 63.17 ; H, 3.08; Cl, 12.13 ; N, 9.37; S, 10.82 Synthesis of compound 29 Added 13.9 g (46.8 mmol) intermediate A-29,23.2 g (53.86 mmol) borate (1) (Sanya phenyl-phenyl-borate, manufacturing: KR10-2014-0135524A section 36 page), 16.2 g (117.1 mmol) potassium carbonate and 2.7 g (2.3 millimoles) Pd (PPh3)4 (four-(triphenylphosphine) palladium (0)) to 500 ml round bottom flask in the 150 ml of 1,4-dioxane and 75 ml in the nitrogen atmosphere of the improved reflux under heating for about 6 hours. To the resulting mixture is added 500 ml of methanol, to obtain crystalline solid powder by filtration. The resulting products are dissolved for single paradichlorbenzene and to filter using silica gel/diatomaceous earth, then removed and a proper amount of organic solvent recrystallization with methanol, to obtain compound 29 (16.7 g, yield 64%). The use of elemental analysis, NMR identification compound 29. The results are as follows. C40 H24 N2 S the calculated value: C, 85.08; H, 4.28 ; N, 4.96; S, 5.68 ; content: C, 84.95; H, 4.18 ; N, 5.17; S, 5.72 300MHz (CDCl3, PPM): 7.61-7.73 (m, 10H), 8.07 (t, 2H), 8.16 (d, 1H), 8.28 (d, 1H), 8.65 (t, 1H), 8.74 (s, 3H), 8.85-8.92 (m, 2H), 9.04 (s, 2H) Synthetic example 2: synthesis of compound 30 Add 10.0 g (33.7 mmol) intermediate A-29,19.6 g (38.8 mmol) borate (2) (Sanya phenyl-biphenyl-borate, synthetic: KR10-2014-0135524 section 37 described in page), 11.6 g (84.2 mmol) potassium carbonate, 1.9 g (1.68 mmol) Pd (PPh3)4 (four-(triphenylphosphine) palladium (0)) to the 250 ml round-bottom flask of 100 ml of 1,4-dioxane and 50 ml in the nitrogen atmosphere improved under heating to reflux for about 6 hours. The resulting mixture is added to 300 ml of methanol, to obtain crystalline solid powder by filtration. The resulting products are dissolved for single paradichlorbenzene and to filter using silica gel/diatomaceous earth, then removed and a proper amount of organic solvent with methanol recrystallizaiton, get compound 30 (14.0 g, yield 65%). The use of elemental analysis, NMR identification compound 30. The results are as follows. C46 H28 N2 S the calculated value: C, 86.22; H, 4.40 ; N, 4.37; S, 5.00 ; content: C, 85.95; H, 4.58 ; N, 4.17; S, 5.02 300MHz (CDCl3, PPM): 7.63-7.91 (m, 12H), 8.05 (d, 1H), 8.10 (d, 1H), 8.18 (d, 1H), 8.27 (d, 1H), 8.33 (s, 1H), 8.39 (dd, 2H), 8.77 (t, 2H), 8.81-8.92 (m, 3H), 8.95 (d, 1H), 9.08-9.12 (m, 2H), 9.20 (s, 1H) Synthetic example 3: synthesis of compound 27 A-27 synthetic intermediates In addition to using borate (2) (Sanya phenyl-biphenyl-borate) instead of phenyl boronic acid outer, with the synthetic example 1 synthesis of intermediate A-29 A-27 synthetic intermediates in the same manner as (25.34 g, yield 68%). C40 H23 ClN2 S the calculated value: C, 80.19; H, 3.87 ; Cl, 5.92; N, 4.68 ; S, 5.35; content: C, 78.57 ; H, 3.39; Cl, 5.68 ; N, 4.32; S, 5.15 Synthesis of compound 27 In addition to the use of intermediate respectively A-27 and phenyl boronic acid instead of intermediate A-29 and Sanya phenyl-biphenyl-borate outer, with the synthetic example 1 synthesis of compound 29 in the same manner as synthesis of compound 27 (15.37 g, yield 56%). C46 H28 N2 S the calculated value: C, 86.22; H, 4.40 ; N, 4.37; S, 5.00 ; content: C, 85.18; H, 4.28 ; N, 4.14; S, 4.83 300MHz (CDCl3, PPM): 7.41-7.57 (m, 10H), 7.70-7.88 (m, 7H), 7.98-8.18 (m, 6H), 8.28 (d, 2H), 8.93 (d, 2H), 9.15 (s, 1H) Synthetic example ad-1: synthesis of compound a-30 Synthesis of compound a-30 The 3.0 g (11.8 mmol) intermediate A, 8.8 g (24.7 mmol) of boric acid (3), 4.1 g (29.4 mmol) potassium carbonate and 0.6 g (0.6 mmol) four (triphenylphosphine) palladium (0) placed in 100 ml round-bottom flask of in 40 ml of 1,4-dioxane and 20 ml of water and then in the nitrogen atmosphere under heating to reflux 6 hours. Furthermore, the mixture thus obtained is added to 150 ml of methanol and crystalline solid, used for dissolved in the single paradichlorbenzene and silica gel/diatomaceous earth filter, and then the a proper amount of the solvent is removed, the re-crystallization with methanol, obtain compound a-30 (5.7 g, yield 75%). Compound a-30 the elemental analysis results are as follows. The calculated value of C46H30N2S: C, 85.95 ; H, 4.70; N, 4.36 ; S, 4.99; content: C, 85.91 ; H, 4.69; N, 4.31 ; S, 4.94 Synthetic example ad-2: synthesis of compound a-40 Synthesis of compound a-40 In addition to the use of intermediate respectively A-29 and borate (4) the outer, according to with compound 29 synthesis example 1 synthesis of compound a-40 the same method (11.4 g, yield 74%). Compound a-40 to the elemental analysis results are as follows. The calculated value of C40H26N2S: C, 84.77 ; H, 4.62; N, 4.94 ; S, 5.66; content: C, 84.71 ; H, 4.59; N, 4.92 ; S, 5.60 Synthetic example ad-3: synthesis of compound a-41 A-a-41 synthetic intermediates Add 10.0 g (39.2 mmol) intermediate A, 12.1 g (43.1 mmol) borate (5), 13.5 g (98.0 mmol) potassium carbonate and 2.3 g (43.1 mmol) four (triphenylphosphine) palladium (0) to 500 ml round-bottom flask of in 140 ml of 1,4-dioxane and 70 ml of water and then in the nitrogen atmosphere in the 60 °C the reflux under heating under 12 hours. Then the mixture obtained by the added to 500 ml of methanol and crystalline solid, used for dissolved in the single paradichlorbenzene and silica gel/diatomaceous earth filter, and then in a proper amount of solvent is removed from the re-crystallization with methanol, to obtain intermediate A-a-41 (10.1 g, yield 69%). The calculated value of C22H13ClN2S: C, 70.87 ; H, 3.51; Cl, 9.51 ; N, 7.51; S, 8.60 ; content: C, 70.80; H, 3.50 ; Cl, 9.47; N, 7.49 ; S, 8.60 Synthesis of compound a-41 Add 5.0 g (13.4 mmol) intermediate A-a-41,6.4 g (14.8 mmol) borate (4), 4.6 g (33.5 mmol) potassium carbonate and 0.8 g (0.7 mmol) four (triphenylphosphine) palladium (0) to 500 ml round bottom flask in a 50 ml of 1,4-dioxane and 25 ml of water and then in the nitrogen atmosphere under heating to reflux 8 hours. Then the mixture obtained by the added to 150 ml of methanol and crystalline solid, used for dissolved in the single paradichlorbenzene and silica gel/diatomaceous earth filter, and then in a proper amount of solvent is removed from the re-crystallization with methanol, obtain compound a-41 (6.2 g, yield 72%). Compound a-41 the elemental analysis results are as follows. The calculated value of C46H30N2S: C, 85.95 ; H, 4.70; N, 4.36 ; S, 4.99; content: C, 85.90 ; H, 4.68; N, 4.31 ; S, 4.93 Synthetic example ad-4: synthesis of compound a-42 A-a-42 synthetic intermediates In addition to the biphenyl boric acid intermediate (manufacturer: Beijing auspicious Dongfang chemical technology, ltd.) instead of phenyl boronic acid outer, intermediate A-29 in accordance with the synthetic example 1 synthesis of intermediate A-a-42 the same method (7.3 g, yield 68%). The calculated value of C22H13ClN2S: C, 70.87 ; H, 3.51; Cl, 9.51 ; N, 7.51; S, 8.60 ; content: C, 70.81; H, 3.46 ; Cl, 9.50; N, 7.49 ; S, 8.60 Synthesis of compound a-42 In addition to the use of intermediate respectively A-a-42 and borate (4) replace the intermediate A-29 and borate (1) an outer, according to with compound 29 synthesis example 1 synthesis of compound a-42 the same method (15.7 g, yield 56%). Compound a-42 to the elemental analysis results are as follows. The calculated value of C46H30N2S: C, 85.95 ; H, 4.70; N, 4.36 ; S, 4.99; content: C, 85.93 ; H, 4.62; N, 4.33 ; S, 4.98 Synthetic example ad-5: synthesis of compound a-46 A-a-46 synthetic intermediates In addition to using borate (6) intermediate instead of phenyl boronic acid outer, intermediate A-29 in accordance with the synthetic example 1 synthesis of intermediate A-a-46 the same method (6.1 g, yield 70%). The calculated value of C28H17ClN2S: C, 74.91 ; H, 3.82; Cl, 7.90 ; N, 6.24; S, 7.14 ; content: C, 74.91; H, 3.76 ; Cl, 7.87; N, 6.21 ; S, 7.11 Synthesis of compound a-46 In addition to the use of intermediate respectively A-a-46 and borate (4) intermediate to replace intermediate A-29 and borate (1) intermediate the outer, according to with compound 29 synthesis example 1 synthesis of compound a-46 the same method (4.4 g, yield 64%). Compound a-46 to the elemental analysis results are as follows. The calculated value of C52H34N2S: C, 86.88 ; H, 4.77; N, 3.90 ; S, 4.46; content: C, 86.80 ; H, 4.73; N, 3.87 ; S, 4.43 Synthetic example ad-6: synthesis of compound a-56 Synthesis of compound a-56 In addition to using borate (4) intermediate replace the boronic acid (3) intermediate the outer, a-30 with the compounds according to examples of synthesizing ad-1 a-56 the same method to synthesize compound (8.3 g, yield 74%). Compound a-56 to the elemental analysis results are as follows. The calculated value of C58H38N2S: C, 87.63 ; H, 4.82; N, 3.52 ; S, 4.03; content: C, 87.61 ; H, 4.80; N, 3.52 ; S, 4.02 Synthetic example ad-7: synthesis of compound a-70 Synthesis of compound a-70 In addition to using borate (7) to replace the borate (4) the outer, a-40 with the compounds according to examples of synthesizing ad-2 a-70 the same method to synthesize compound (7.7 g, yield 70%). Compound a-70 to the elemental analysis results are as follows. The calculated value of C46H30N2S: C, 85.95 ; H, 4.70; N, 4.36 ; S, 4.99; content: C, 85.90 ; H, 4.70; N, 4.32 ; S, 4.90 Synthetic example ad-8: synthesis of compound a-71 Synthesis of compound a-71 In addition to using borate (7) to replace the borate (4) the outer, a-41 with the compounds according to examples of synthesizing ad-3 a-71 the same method to synthesize compound (10.2 g, yield 78%). Compound a-71 to the elemental analysis results are as follows. The calculated value of C52H34N2S: C, 86.88 ; H, 4.77; N, 3.90 ; S, 4.46; content: C, 86.82 ; H, 4.75; N, 3.87 ; S, 4.42 Synthetic example ad-9: synthesis of compound a-74 A-a-74 synthetic intermediates Add 10.0 g (39.2 mmol) intermediate A, 21.9 g (43.1 mmol) borate (7), 13.5 g (98.0 mmol) potassium carbonate and 2.3 g (2.0 mmol) of four (triphenylphosphine) palladium (0) to 500 ml round-bottom flask of in 140 ml of 1,4-dioxane and 70 ml of water and then in the nitrogen atmosphere in the 60 °C the reflux under heating under 16 hours. Then the mixture obtained by the added to 300 ml of methanol and crystalline solid, used for dissolved in the single paradichlorbenzene and silica gel/diatomaceous earth filter, and then in a proper amount of solvent is removed from the re-crystallization with methanol, obtain compound A-a-74 (16.5 g, yield 70%). C40H25ClN2 the calculated value: C, 79.92; H, 4.19 ; Cl, 5.90; N, 4.66 ; S, 5.33; content: C, 79.90 ; H, 4.19; Cl, 5.89 ; N, 4.65; S, 5.31 Synthesis of compound a-74 Add 10.0 g (16.6 mmol) intermediate A-a-74,2.2 g (18.3 mmol) phenyl boronic acid, 5.8 g (41.6 mmol) potassium carbonate and 1.0 g (0.8 mmol) of four (triphenylphosphine) palladium (0) to 500 ml round bottom flask in a 50 ml of 1,4-dioxane and 25 ml of water and then in the nitrogen atmosphere under heating to reflux 8 hours. Then the mixture obtained by the added to 150 ml of methanol and crystalline solid, used for dissolved in the single paradichlorbenzene and silica gel/diatomaceous earth filter, and then in a proper amount of solvent is removed from the re-crystallization with methanol, obtain compound a-74 (6.8 g, yield 64%). Compound a-74 the elemental analysis results are as follows. The calculated value of C46H30N2S: C, 85.95 ; H, 4.70; N, 4.36 ; S, 4.99; content: C, 85.91 ; H, 4.69; N, 4.33 ; S, 4.94 Synthetic example ad-10: synthesis of compound a-75 Synthesis of compound a-75 In addition to using borate (5) instead of phenyl boronic acid outside the intermediate, compound a-74 according to the examples of synthesis of ad-9 a-75 the same method to synthesize compound (6.2 g, yield 73%). Compound a-75 to the elemental analysis results are as follows. The calculated value of C52H34N2S: C, 86.88 ; H, 4.77; N, 3.90 ; S, 4.46; content: C, 86.88 ; H, 4.73; N, 3.85 ; S, 4.45 Synthetic example ad-11: synthesis of compound a-82 In addition to using borate (8) instead of borate (7) intermediate the outer, a-70 with the compounds according to examples of synthesizing ad-7 a-82 the same method to synthesize compound (6.7 g, yield 67%). Compound a-82 to the elemental analysis results are as follows. The calculated value of C52H34N2S: C, 86.88 ; H, 4.77; N, 3.90 ; S, 4.46; content: C, 86.85 ; H, 4.76; N, 3.87 ; S, 4.46 Synthetic example ad-12: synthesis of compound a-84 In addition to using borate (9) instead of the intermediate ester (7) intermediate the outer, a-70 with the compounds according to examples of synthesizing ad-7 a-84 the same method to synthesize compound (9.3 g, yield 76%). Compound a-84 to the elemental analysis results are as follows. The calculated value of C52H34N2S: C, 86.88 ; H, 4.77; N, 3.90 ; S, 4.46; content: C, 86.84 ; H, 4.77; N, 3.89 ; S, 4.45 Synthetic example ad-13: synthesis of compound a-114 In addition to using borate (10) instead of the intermediate ester (7) intermediate the outer, a-70 with the compounds according to examples of synthesizing ad-7 a-114 the same method to synthesize compound (10.9 g, yield 75%). Compound a-114 to the elemental analysis results are as follows. The calculated value of C46H30N2S: C, 85.95 ; H, 4.70; N, 4.36 ; S, 4.99; content: C, 85.94 ; H, 4.68; N, 4.30 ; S, 4.87 Synthetic example ad-14: synthesis of compound a-108 In addition to using borate (11) instead of the intermediate ester (7) intermediate the outer, a-70 with the compounds according to examples of synthesizing ad-7 a-108 the same method to synthesize compound (8.4 g, yield 70%). Compound a-108 to the elemental analysis results are as follows. The calculated value of C44H26N2S: C, 85.96 ; H, 4.26; N, 4.56 ; S, 5.22; content: C, 85.94 ; H, 4.21; N, 4.50 ; S, 5.22 Synthetic example ad-15: synthesis of compound a-110 In addition to using borate (12) instead of the intermediate ester (7) intermediate the outer, a-70 with the compounds according to examples of synthesizing ad-7 a-110 the same method to synthesize compound (6.7 g, yield 65%). Compound a-110 to the elemental analysis results are as follows. The calculated value of C42H26N2S: C, 85.39 ; H, 4.44; N, 4.74 ; S, 5.43; content: C, 85.30 ; H, 4.44; N, 4.73 ; S, 5.42 Synthetic example ad-16: synthesis of compound a-112 In addition to using borate (13) instead of the intermediate ester (7) intermediate, compound a-70 according to the examples of synthesis of ad-7 a-112 the same method to synthesize compound (7.9 g, yield 67%). Compound a-112 to the elemental analysis results are as follows. The calculated value of C48H30N2S: C, 86.46 ; H, 4.53; N, 4.20 ; S, 4.81; content: C, 86.45 ; H, 4.52; N, 4.18 ; S, 4.80 Synthetic example ad-17: synthesis of compound a-116 Add 5.0 g (10.8 mmol) intermediate A-a-116, intermediate AA-a-116 (10.8 mmol), 3.7 g (53.8 mmol) potassium carbonate and 0.6 g (0.5 mmol) of four (triphenylphosphine) palladium (0) to 100 ml round-bottom flask of in 40 ml of 1,4-dioxane and 20 ml of water and then in the nitrogen atmosphere under heating to reflux 12 hours. Then the mixture thus obtained is added to 120 ml of methanol and crystalline solid, used for dissolved in the single paradichlorbenzene and silica gel/diatomaceous earth filter, and then in a proper amount of solvent is removed from the re-crystallization with methanol, obtain compound a-116 (6.1 g, yield 64%). The calculated value of C47H30N2S: C, 86.21 ; H, 4.62; N, 4.28 ; S, 4.90; content: C, 86.21 ; H, 4.60; N, 4.25 ; S, 4.89 (Reference reaction process: intermediate A-a-116 synthetic procedure) (Reference reaction process: intermediate AA-a-116 synthetic procedure) Synthetic example ad-18: synthesis of compound b-41 B synthetic intermediate (1) (benzo-3-ureido-furan-2-carboxylic acid methyl ester) Adding way Proecss isocyanic acid chlorine to dropwise (33.4 ml, 0.38 mol) to -78 ° C the lower round-bottom flask (1000 ml) containing the benzo-3-amino-furan-2-carboxylic acid methyl ester (49.0 g, 0 . 25 mol) in 1000 ml of methylene chloride in solution. Slow heating the reactants to the room temperature and the stirring 2 hours. Concentrated agition reactant, adding concentrated hydrochloric acid (100 ml) to the residue and the 100 °C the mixture is stirred for one hour. Cooling the reaction mixture to room temperature and saturated NaHCO3 aqueous solution and on. Then filtering the solid, takes the form of a beige solid obtained B the intermediate (1) (benzo-3-ureido-furan-2-carboxylic acid methyl ester) (52.1 g, 87%). C11 H10 N2 O4 the calculated value: C, 56.41; H, 4.30 ; N, 11.96; O, 27.33 ; content: C, 56.45; H, 4.28 ; N, 11.94; O, 27.32 B synthetic intermediate (2) (benzo-furo [3,2-d] pyrimidine -2,4-diol) B the intermediate (1) (benzo-3-ureido-furan-2-carboxylic acid methyl ester) (50.0 g, 0 . 21 mole) suspended in 2000 ml of round-bottom flask in 1000 ml of methanol and adding way to dropwise 2M NaOH to the (300 ml). Reflux the reaction mixture and the stirring 3 hours. Cooling the produce to the room temperature and the use of concentrated hydrochloric acid acidified to pH 3. After the concentrated mixture, slowly dropwise added to methanol to residue manner in order to make the solid precipitation. Filtering the generated solid and drying, to obtain intermediate B (2) (benzo-furo [3,2-d] pyrimidine -2,4-diol) (38.0 g, 88%). C10 H6 N2 O3 the calculated value: C, 59.41; H, 2.99 ; N, 13.86; O, 23.74 ; content: C, 59.41; H, 2.96 ; N, 13.81; O, 23.75 Intermediate B (benzo -2,4-dichloro-furo [3,2-d] pyrimidine) B the intermediate (2) (benzo-furo [3,2-d] pyrimidine -2,4-diol) (37.2 g, 0 . 18 mol) is dissolved in 1000 ml round-bottom flask phosphorus oxychloride in in (500 ml). Cooling the mixture to -30 ° C and slowly adding N, N-diisopropyl ethylamine (52 ml, 0.36 mol) to its. The reactant reflux and the stirring 36 hours and cooled to the room temperature is kept. Reactant in the ice/water, and then extracting with ethyl acetate. Furthermore, using NaHCO3 washing aqueous solution of the organic layer thus obtained then by Na2 SO4 drying. Concentrating the organic layer of the obtained, obtain intermediate B (benzo -2,4-dichloro-furo [3,2-d] pyrimidine) (20.4 g, 46%). Intermediate B element analysis and NMR analysis the results are as follows. C10 H4 Cl2 N2 O the calculated value: C, 50.24; H, 1.69 ; Cl, 29.66; N, 11.72 ; O, 6.69; content: C, 50.18 ; H, 1.79; Cl, 29.69 ; N, 11.69; O, 6.70; 300MHz (CDCl3, PPM): 7.55 (t, 1H), 7.71-7.82 (m, 2H), 8.25 (d, 1H) B-37 synthetic intermediates In the nitrogen flow in the 40 °C the 40.0 g (167.3 mmol) intermediate B, 22.4 g (184.1 mmol) phenyl boronic acid, 57.8 g (418.3 mmol) potassium carbonate and 9.7 g (8.4 mmol) Pd (PPh3)4 (four (triphenylphosphine) palladium (0)) into 2000 ml of flask in 500 ml of 1,4-dioxane and 250 ml of water for 8 hours. Adding the mixture to 1500 ml of methanol and filtered in the wherein the crystalline solid, used for dissolved in the single paradichlorbenzene and silica gel/diatomaceous earth filter, and then the self-its removing a proper amount of organic solvent recrystallization with methanol, to obtain intermediate B-37 (31.0 g, yield 66%). C16 H9 ClN2 O the calculated value: C, 68.46; H, 3.23 ; Cl, 12.63; N, 9.98 ; O, 5.70; content: C, 68.95 ; H, 3.08; Cl, 12.17 ; N, 10.01; O, 5.62 Synthesis of compound b-41 Added 10.2 g (36.5 mmol) intermediate B-37,8.5 g (19.6 mmol) borate (4), 6.2 g (44.5 mmol) potassium carbonate and 1.0 g (0.9 mmol) four (triphenylphosphine) palladium (0) to 500 ml round-bottom flask the in 60 ml of 1,4-dioxane and 30 ml of water in a nitrogen atmosphere and then the reflux under heating under 12 hours. The mixture is added to 200 ml of methanol and filtered in the wherein the crystalline solid, dissolved in the single paradichlorbenzene and silica gel/diatomaceous earth for the filter and then a proper amount of organic solvent removed re-crystallization with methanol, obtain compound b-41 (7.0 g, yield 71%). Compound b-41 the elemental analysis results are as follows. The calculated value of C40H26N2O: C, 87.25 ; H, 4.76; N, 5.09 ; O, 2.91; content: C, 87.22 ; H, 4.71; N, 5.08 ; O, 2.90 Synthetic example ad-19: synthesis of compound b-71 Add 5.0 g (intermediate B-37 (17.8 mmol), 10.0 g (19.6 mmol) borate (7), 6.2 g (44.5 mmol) potassium carbonate and 1.0 g (0.9 mmol) four (triphenylphosphine) palladium (0) to 500 ml round-bottom flask the in 60 ml of 1,4-dioxane and 30 ml of water in a nitrogen atmosphere and then the reflux under heating under 12 hours. The mixture is added to 200 ml of methanol and filtered in the wherein the crystalline solid, used for dissolved in the single paradichlorbenzene and silica gel/diatomaceous earth filter, and then the self-its removing a proper amount of organic solvent recrystallization with methanol, obtain compound b-71 (7.5 g, yield 67%). Compound b-71 the elemental analysis results are as follows. The calculated value of C46H30N2O: C, 88.15 ; H, 4.82; N, 4.47 ; O, 2.55; content: C, 88.11 ; H, 4.81; N, 4.43 ; O, 2.52 Synthetic example ad-20: synthesis of compound b-116 B-b-116 synthetic intermediates Add 30.0 g (125.5 mmol) intermediate B, 23.7 g (138.0 mmol) naphthalene-1-yl-boronic acid, 43.4 g (313.7 mmol) potassium carbonate and 7.3 g (6.3 mmol) four (triphenylphosphine) palladium (0) to 1000 ml of flask in 400 ml of 1,4-dioxane and 200 ml of water, and then the flow of nitrogen in the 55 °C lower heating 16 hours. The mixture obtained is added to 1200 ml of methanol and filtering wherein the crystalline solid, used for dissolved in the single paradichlorbenzene and silica gel/diatomaceous earth filter, and then the self-its removing a proper amount of organic solvent recrystallization with methanol, to obtain intermediate B-b-116 (29.1 g, yield 70%). The calculated value of C20H11ClN2O: C, 72.62 ; H, 3.35; Cl, 10.72 ; N, 8.47; O, 4.84 ; content: C, 72.60; H, 3.35 ; Cl, 10.71; N, 8.40 ; O, 4.83 Synthesis of compound b-116 Add 5.0 g (15.1 mmol) intermediate B-b-116,8.5 g (16.6 mmol) borate (7), 5.2 g (37.8 mmol) potassium carbonate and 0.9 g (0.8 mmol) of four (triphenylphosphine) palladium (0) to a 250 ml round bottom flask in a 50 ml of 1,4-dioxane and 25 ml of water in a nitrogen atmosphere and then the reflux under heating under 12 hours. The mixture obtained is added to 150 ml of methanol, and filtered in the wherein the crystalline solid, used for dissolved in the single paradichlorbenzene and silica gel/diatomaceous earth filter, and then remove the a proper amount of organic solvent recrystallization with methanol, obtain compound b-116 (7.1 g, yield 69%). Compound b-116 the elemental analysis results are as follows. The calculated value of C50H32N2O: C, 88.73 ; H, 4.77; N, 4.14 ; O, 2.36; content: C, 88.70 ; H, 4.76; N, 4.07 ; O, 2.19 Synthetic example ad-21:C synthetic intermediates C-2 synthetic intermediates Adding 45.0 g intermediate C-1 (171.7 mmol), 30.0 g (163.5 mmol) 2, 4, 6-trichloro-pyrimidine, 56.5 g (408.9 mmol) potassium carbonate and 9.5 g (8.2 mmol) four (triphenylphosphine) palladium to 2000 ml of flask in 540 ml of 1,4-dioxane and 270 ml of water and then in the nitrogen atmosphere under heating to reflux 12 hours. The mixture obtained is added to 1000 ml of methanol, and filtered in the wherein the crystalline solid, dissolved in toluene and with silica gel/diatomaceous earth filter, and then remove the a proper amount of organic solvent recrystallization with methanol, to obtain intermediate C-2 (37.0 g, yield 76%). C12H12Cl2 N2Si the calculated value: C, 50.89; H, 4.27 ; Cl, 25.03; N, 9.89 ; Si, 9.92; content: C, 50.32 ; H, 4.22; Cl, 24.98 ; N, 9.73; Si, 9.84; C synthetic intermediates The 37.0 g (130.6 mmol) intermediate C-2 and 2.4 g (2.6 mmol) chlorine three (triphenylphosphine) rhodium (I) into the 1000 ml flask, adding way dropwise to 600 ml of 1,4-dioxane to and in the nitrogen atmosphere the mixture is heated to reflux under 8 hours. At the end of the reaction, the organic layer is removed the residue obtained after the chromatography treatment administered by column level, obtain intermediate C (20.2 g, yield 55%). C12H10Cl2 N2Si the calculated value: C, 51.25; H, 3.58 ; Cl, 25.21; N, 9.96 ; Si, 9.99; content: C, 51.15 ; H, 3.53; Cl, 25.16 ; N, 9.90; Si, 9.93 Synthetic example ad-22: synthesis of compound c-40 C-54 synthetic intermediates Add 20.0 g (71.1 mmol) intermediate C, 9.5 g (78.2 mmol) phenyl boronic acid, 24.6 g (177.8 mmol) potassium carbonate and 4.1 g (3.6 mmol) four (triphenylphosphine) palladium (0) to 500 ml of flask 200 ml of 1,4-dioxane and 100 ml of water and then in 55 °C heated in a nitrogen flow under 16 hours. The mixture obtained is added to 600 ml of methanol and filtered in the wherein the crystalline solid, used for dissolved in the single paradichlorbenzene and silica gel/diatomaceous earth filter, and then remove the a proper amount of organic solvent recrystallization with methanol, to obtain intermediate C-54 (17.2 g, yield 75%). The calculated value of C18H15ClN2Si: C, 66.96 ; H, 4.68; Cl, 10.98 ; N, 8.68; Si, 8.70 ; content: C, 66.92; H, 4.63 ; Cl, 10.96; N, 8.67 ; Si, 8.65 Synthesis of compound c-40 Add 5.0 g (15.5 mmol) intermediate C-54,7.4 g (17.0 mmol) borate (4), 5.4 g (38.7 mmol) potassium carbonate and 0.9 g (0.8 mmol) of four (triphenylphosphine) palladium (0) to 100 ml round-bottom flask of in 40 ml of 1,4-dioxane and 20 ml of water and then in the nitrogen atmosphere under heating to reflux 8 hours. The mixture obtained is added to 120 ml of methanol, and filtered in the wherein the crystalline solid, used for dissolved in the single paradichlorbenzene and silica gel/diatomaceous earth filter, and then remove the a proper amount of organic solvent recrystallization with methanol, obtain compound c-40 (6.5 g, yield 71%). Compound c-40 the elemental analysis results are as follows. The calculated value of C42H32N2Si: C, 85.10 ; H, 5.44; N, 4.73 ; Si, 4.74; content: C, 85.07 ; H, 5.42; N, 4.70 ; Si, 4.74 Synthetic example ad-23: synthesis of compound c-70 In addition to using borate (7) to replace the borate (4), with compound c-40 according to examples of synthesizing ad-22 c-70 the same method to synthesize compound (7.1 g, yield 69%). Compound c-70 the elemental analysis results are as follows. The calculated value of C48H36N2Si: C, 86.19 ; H, 5.42; N, 4.19 ; Si, 4.20; content: C, 86.18 ; H, 5.40; N, 4.16 ; Si, 4.16 Synthetic example ad-24: synthesis of compound d-119 Compounds of this invention to provide particular examples of compound d-119 by the following four step synthesis. D-2 synthetic intermediates Add 50.0 g (222.2 mmol) intermediate D-1 (manufacturer: TCI Company), 50.1 g (233.3 mmol) 4, 4, 5, 5-tetramethyl-2 - (2-nitro-phenyl) - 1, 3, 2- two oxygen mixed boron heterocyclic pentane, 76.8 g (555.4 mmol) potassium carbonate and 12.8 g (11.1 mmol) four (triphenylphosphine) palladium to 2000 ml of flask in 700 ml of 1,4-dioxane and 350 ml of water, and then in the nitrogen atmosphere under heating to reflux 12 hours. The mixture obtained is added to 2000 ml of methanol and filtered in the wherein the crystalline solid, dissolved in toluene and with silica gel/diatomaceous earth filter, and then remove the a proper amount of organic solvent recrystallization with methanol, to obtain intermediate D-2 (54.5 g, yield 75%). C16H10ClN3 O2 calculated value of:C, 61.65; H, 3.23 ; Cl, 11.37; N, 13.48 ; O, 10.27; content: C, 61.23 ; H, 3.15; Cl, 11.37 ; N, 13.21; O, 10.20; D-3 synthetic intermediates Add 20.0 g (64.2 mmol) intermediate D-2,29.1 g (67.4 mmol) borate (4), 22.2 g (160.4 mmol) potassium carbonate and 3.7 g (3.2 mmol) of four (triphenylphosphine) palladium to 500 ml of flask 200 ml of 1,4-dioxane and 100 ml of water and then in the nitrogen atmosphere under heating to reflux 12 hours. The mixture obtained is added to 600 ml of methanol and filtered in the wherein the crystalline solid, dissolved in toluene and silica gel/bergmeal and filtration used, then a proper amount of organic solvent in the re-crystallization with methanol, to obtain intermediate D-3 (23.9 g, yield 61%). C40H27N3 O2 calculated value of:C, 82.60; H, 4.68 ; N, 7.22; O, 5.50 ; content: C, 82.60; H, 4.63 ; N, 7.21; O, 5.49; D-4 synthetic intermediates D-3 the intermediates (20.0 g, 34.4 millimoles) and PPh3 (27.1 g, 103.2 mmol) in 250 ml flask, add 80 ml of 1,2-dichlorobenzene (DCB) to the exchange with nitrogen and after the 150 °C the mixture is stirred 12 hours. In cooling after the distillation is removed to produce the DCB and at room temperature, dissolved in a small amount of toluene and via column chromatography purification (hexane), to obtain intermediate D-4 (10.3 g, yield 54%). C40H27N3 the calculated value: C, 87.40; H, 4.95 ; N, 7.64; content: C, 87.40 ; H, 4.93; N, 7.59; Synthesis of compound d-119 Add 10.0 g (27.3 mmol) intermediate D-4,4.5 g (28.6 mmol) of bromobenzene, 5.2 g (54.5 mmol) 3rd sodium butylate, 1.6 g (2.7 mmol) Pd (dba)2 and 2.2 ml butyl phosphine three 3rd (50% in toluene for) to 500 ml round-bottom flask of in 180 ml of xylene and then in the nitrogen atmosphere under heating to reflux 15 hours. The mixture obtained is added to 360 ml of methanol and filtered in the wherein the crystalline solid, used for dissolved in the single paradichlorbenzene and silica gel/diatomaceous earth filter, and then remove the a proper amount of organic solvent recrystallization with methanol, obtain compound d-40 (11.8 g, yield 69%). Compound d-119 the elemental analysis results are as follows. C46H31N3 the calculated value: C, 88.29; H, 4.99 ; N, 6.72; content: C, 88.20 ; H, 4.95; N, 6.71 Synthetic example ad-25: synthesis of compound e-70 E-2 synthetic intermediates Adding way Proecss isocyanic acid chlorine to dropwise (23.7 ml, 274.6 mmol) to -78 ° C lower 2000 ml round-bottom flask containing intermediates in E-1 (35.0 g, 183.1 mmol) in dichloromethane (1000 ml) in solution. Slow heating the reactants to the room temperature and the stirring 2 hours. After the concentration of the reactant, adding 6N (300 ml) to the residue and the 100 °C the mixture is stirred 1 hour. Cooling the reaction mixture to room temperature and saturated NaHCO3 and in an aqueous solution. Then filtering the solid, takes the form of a beige solid is obtained intermediate E-2 (43.2 g, yield 88%). C10H9NO3 the calculated value: C, 62.82; H, 4.74 ; N, 7.33; O, 25.11 ; content: C, 62.82; H, 4.74 ; N, 7.33; O, 25.11 (Reference reaction process: intermediate E-1 synthetic procedure) E-3 synthetic intermediates E-2 the intermediates (40.0 g, 0 . 19 mol) is suspended in 1000 ml round-bottom flask of in 1000 ml of methanol and adding way to dropwise 2M NaOH to the (300 ml). Reflux the reaction mixture and the stirring 3 hours. Cooling the produce to the room temperature and the use of concentrated hydrochloric acid acidified to pH 3. After the concentrated mixture, slowly dropwise added to methanol to residue manner in order to make the solid precipitation. Filtering solid and drying, to obtain intermediate E-3 (39.0 g, yield 85%). C11H10N2 O4 the calculated value: C, 56.41; H, 4.30 ; N, 11.96; O, 27.33 ; content: C, 56.40; H, 4.20 ; N, 11.92; O, 27.31 E-4 synthetic intermediates In the 500 ml round-bottom flask E-3 the intermediates (39.0 g, 191.0 mmol) with 200 ml of a mixture of phosphorus oxychloride reflux and the stirring 8 hours. Cooling the reaction mixture to room temperature and then at the same time the strong agitation of the ice/water in order to precipitate. Filtering the obtained reactant, to obtain intermediate E-4 (40.7 g, 89%, white solid). C10H4Cl2 N2O the calculated value: C, 50.24; H, 1.69 ; Cl, 29.66; N, 11.72 ; O, 6.69; content: C, 50.21 ; H, 1.65; Cl, 29.63 ; N, 11.64; O, 6.62 E-5 synthetic intermediates Add 10.0 g intermediate E-4 (41.8 mmol), 5.4 g (43.9 mmol) phenyl boronic acid, 14.5 g (104.6 mmol) potassium carbonate and 2.4 g (2.1 mmol) of four (triphenylphosphine) palladium (0) to 500 ml of flask in 140 ml of 1,4-dioxane and 70 ml of water and then in the 60 °C in the nitrogen flows down under heating 10 hours. The obtained mixture is added to 450 ml of methanol and filtered in the wherein the crystalline solid, used for dissolved in the single paradichlorbenzene and silica gel/diatomaceous earth filter, and then remove the a proper amount of organic solvent recrystallization with methanol, to obtain intermediate E-5 (8.0 g, yield 65%). The calculated value of C16H9ClN2O: C, 68.46 ; H, 3.23; Cl, 12.63 ; N, 9.98; O, 5.70 ; content: C, 68.40; H, 3.22 ; Cl, 12.61; N, 9.94 ; O, 5.70 Synthesis of compound e-70 Add 5.0 g (17.8 mmol) intermediate E-5,9.5 (18.7 mmol) borate (7), 6.2 g (44.5 mmol) potassium carbonate and 1.0 g (0.9 mmol) four (triphenylphosphine) palladium (0) to the 250 ml round-bottom flask the in 60 ml of 1,4-dioxane and 30 ml of water in a nitrogen atmosphere and then the reflux under heating under 12 hours. The obtained mixture is added to 200 ml of methanol and filtered in the wherein the crystalline solid, used for dissolved in the single paradichlorbenzene and silica gel/diatomaceous earth filter, and then remove the a proper amount of organic solvent recrystallization with methanol, obtain compound e-70 (8.1 g, yield 67%). Compound e-70 the elemental analysis results are as follows. The calculated value of C46H30N2O: C, 88.15 ; H, 4.82; N, 4.47 ; O, 2.55; content: C, 88.14 ; H, 4.80; N, 4.39 ; O, 2.53 Synthetic example ad-26: synthesis of compound f-70 F-2 synthetic intermediates In a 250 ml round bottom flask in the 200 °C F-1 under intermediate agitation (35.0 g, 0 . 17 mol) with urea (50.7 g, 0 . 84 mol) mixture of 2 hours. Cooling high-temperature the reaction mixture to room temperature and the sodium hydroxide solution, the mixtures are filtered to remove impurities and then acidified (HCl, 2N) and drying the precipitate obtained, obtain intermediate F-2 (18.9 g, 51%). C10H6N2 O2S the calculated value: C, 55.04; H, 2.77 ; N, 12.84; O, 14.66 ; S, 14.69; content: C, 55.01 ; H, 2.77; N, 12.83 ; O, 14.65; S, 14.63 (Reference reaction process: intermediate F-1 the procedure of the synthesis reaction) F-3 synthetic intermediates The 250 ml round-bottom flask thing F-2 in the (18.9 g, 99.2 mmol) with (100 ml in) the mixture of phosphorus oxychloride reflux and the stirring 6 hours. Cooling the reaction mixture to room temperature and then at the same time the strong stirring in the ice/water, get precipitation. Filtering the obtained reactant, to obtain intermediate F-3 (17.5 g, 85%, white solid). C10H4Cl2 N2S the calculated value: C, 47.08; H, 1.58 ; Cl, 27.79; N, 10.98 ; S, 12.57; content: C, 47.04 ; H, 1.53; Cl, 27.74 ; N, 10.96; S, 12.44 F-4 synthetic intermediates Add 10.0 g (39.2 mmol) intermediate F-3,5.3 g (43.1 mmol) phenyl boronic acid, 13.5 g (98.0 mmol) potassium carbonate and 2.3 g (2.0 mmol) of four (triphenylphosphine) palladium (0) to 500 ml of flask in 140 ml of 1,4-dioxane and 70 ml of water and then in the 60 °C in the nitrogen flows down under heating 10 hours. The obtained mixture is added to 450 ml of methanol and filtered in the wherein the crystalline solid, used for dissolved in the single paradichlorbenzene and silica gel/diatomaceous earth filter, and then remove the a proper amount of organic solvent recrystallization with methanol, to obtain intermediate F-4 (8.0 g, yield 69%). The calculated value of C16H9ClN2S: C, 64.75 ; H, 3.06; Cl, 11.95 ; N, 9.44; S, 10.80 ; content: C, 64.72; H, 3.06 ; Cl, 11.94; N, 9.42 ; S, 10.77 Synthesis of compound f-70 Add 5.0 g (16.9 mmol) intermediate F-4,9.4 g (18.5 mmol) borate (7), 5.8 g (42.1 mmol) potassium carbonate and 1.0 g (0.8 mmol) of four (triphenylphosphine) palladium (0) to the 250 ml round-bottom flask the in 60 ml of 1,4-dioxane and 30 ml of water in a nitrogen atmosphere and then the reflux under heating under 12 hours. The obtained mixture is added to 200 ml of methanol and filtered in the wherein the crystalline solid, used for dissolved in the single paradichlorbenzene and silica gel/diatomaceous earth filter, and then remove the a proper amount of organic solvent recrystallization with methanol, obtain compound f-70 (7.9 g, yield 73%). Compound f-70 the elemental analysis results are as follows. The calculated value of C46H30N2O: C, 88.15 ; H, 4.82; N, 4.47 ; O, 2.55; content: C, 88.12 ; H, 4.76; N, 4.44 ; O, 2.52 Synthetic example ad-27: synthesis of compound e-71 E-71 synthetic intermediates In addition to using borate (5) instead of phenyl boronic acid outer, intermediate E-5 according to the examples of synthesis of ad-25 e-71 the same method to synthetic intermediates (8.1 g, yield 70%). The calculated value of C22H13ClN2O: C, 74.06 ; H, 3.67; Cl, 9.94 ; N, 7.85; O, 4.48 ; content: C, 74.01; H, 3.65 ; Cl, 9.89; N, 7.84 ; O, 4.42 Synthesis of compound e-71 In addition to using intermediate e-71 E-5 replace the intermediate outer, e-70 with the compounds according to examples of synthesizing ad-25 e-71 the same method to synthesize compound (7.5 g, yield 72%). The calculated value of C52H34N2O: C, 88.86 ; H, 4.88; N, 3.99 ; O, 2.28; content: C, 88.81 ; H, 4.87; N, 3.96 ; O, 2.23 Synthetic example ad-28: synthesis of compound e-74 E-74 synthetic intermediates In addition to using borate (7) instead of phenyl boronic acid outer, intermediate E-5 according to the examples of synthesis of ad-25 e-74 the same method to synthetic intermediates (10.5 g, yield 78%). The calculated value of C40H25ClN2O: C, 82.11 ; H, 4.31; Cl, 6.06 ; N, 4.79; O, 2.73 ; content: C, 82.10; H, 4.28 ; Cl, 6.05; N, 4.75 ; O, 2.70 Synthesis of compound 74 In addition to using intermediate e-74 E-5 replace the intermediate, compound e-70 according to the examples of synthesis of ad-25 e-74 the same method to synthesize compound (5.3 g, yield 65%). The calculated value of C46H30N2O: C, 88.15 ; H, 4.82; N, 4.47 ; O, 2.55; content: C, 88.15 ; H, 4.82; N, 4.47 ; O, 2.55 Synthetic example ad-29: synthesis of compound e-75 Synthesis of compound e-75 In addition to using borate (5) instead of phenyl boronic acid outer, e-74 with the compounds according to examples of synthesizing ad-28 e-75 the same method to synthesize compound (7.0 g, yield 69%). The calculated value of C52H34N2O: C, 88.86 ; H, 4.88; N, 3.99 ; O, 2.28; content: C, 88.85 ; H, 4.84; N, 3.97 ; O, 2.28 Synthetic example ad-30: synthesis of compound e-82 Synthesis of compound e-82 In addition to using borate (8) instead of borate (7), with compound e-70 according to examples of synthesizing ad-25 e-82 the same method to synthesize compound (8.4 g, yield 70%). The calculated value of C52H34N2O: C, 88.86 ; H, 4.88; N, 3.99 ; O, 2.28; content: C, 88.80 ; H, 4.81; N, 3.91 ; O, 2.27 Synthetic example ad-31: synthesis of compound e-84 Synthesis of compound e-84 In addition to using borate (9) replace the borate (7), with compound e-70 according to examples of synthesizing ad-25 e-84 the same method to synthesize compound (11.2 g, yield 71%). The calculated value of C52H34N2O: C, 88.86 ; H, 4.88; N, 3.99 ; O, 2.28; content: C, 88.86 ; H, 4.85; N, 3.93 ; O, 2.21 Synthetic example ad-32: synthesis of compound e-88 Synthesis of compound e-88 In addition to using borate (14) instead of borate (7) the outer, e-70 with the compounds according to examples of synthesizing ad-25 e-88 the same method to synthesize compound (6.2 g, yield 67%). The calculated value of C52H34N2O: C, 88.86 ; H, 4.88; N, 3.99 ; O, 2.28; content: C, 88.83 ; H, 4.88; N, 3.98 ; O, 2.26 Synthetic example ad-33: synthesis of compound e-114 Synthesis of compound e-114 In addition to using borate (10) to replace the borate (7) the outer, e-70 with the compounds according to examples of synthesizing ad-25 e-114 the same method to synthesize compound (9.8 g, yield 69%). The calculated value of C46H30N2O: C, 88.15 ; H, 4.82; N, 4.47 ; O, 2.55; content: C, 88.13 ; H, 4.81; N, 4.40 ; O, 2.51 Synthetic example ad-35: synthesis of compound f-71 F-71 synthetic intermediates In addition to using borate (5) instead of phenyl boronic acid outer, intermediate F-4 according to the examples of synthesis of ad-26 f-71 the same method to synthetic intermediates (11.3 g, yield 74%). The calculated value of C22H13ClN2S: C, 70.87 ; H, 3.51; Cl, 9.51 ; N, 7.51; S, 8.60 ; content: C, 70.83; H, 3.50 ; Cl, 9.89; N, 7.47 ; S, 8.59 Synthesis of compound f-71 In addition to using intermediate f-71 F-4 replace the intermediate, compound f-70 according to the examples of synthesis of ad-26 f-71 the same method to synthesize compound (9.4 g, yield 72%). The calculated value of C52H34N2S: C, 86.88 ; H, 4.77; N, 3.90 ; S, 4.46; content: C, 86.84 ; H, 4.74; N, 3.88 ; S, 4.43 Synthetic example ad-36: synthesis of compound f-74 F-74 synthetic intermediates In addition to using borate (7) instead of phenyl boronic acid outer, intermediate F-4 according to the examples of synthesis of ad-26 f-74 the same method to synthetic intermediates (8.9 g, yield 74%). The calculated value of C40H25ClN2S: C, 79.92 ; H, 4.19; Cl, 5.90 ; N, 4.66; S, 5.33 ; content: C, 79.89; H, 4.18 ; Cl, 5.87; N, 4.65 ; S, 5.30 Synthesis of compound f-74 In addition to using intermediate f-74 F-4 replace the intermediate, compound f-70 according to the examples of synthesis of ad-26 f-74 the same method to synthesize compound (7.6 g, yield 68%). The calculated value of C46H30N2S: C, 85.95 ; H, 4.70; N, 4.36 ; S, 4.99; content: C, 85.92 ; H, 4.68; N, 4.35 ; S, 4.95 Synthetic example ad-37: synthesis of compound f-75 In addition to using borate (5) instead of phenyl boronic acid outer, f-74 with the compounds according to examples of synthesizing ad-36 f-75 the same method to synthesize compound (6.3 g, yield 66%). The calculated value of C52H34N2S: C, 86.88 ; H, 4.77; N, 3.90 ; S, 4.46; content: C, 86.87 ; H, 4.75; N, 3.89 ; S, 4.40 Synthetic example ad-38: synthesis of compound f-82 Synthesis of compound f-82 In addition to using borate (8) instead of borate (7) the outer, f-70 with the compounds according to examples of synthesizing ad-26 f-82 the same method to synthesize compound (6.3 g, yield 72%). The calculated value of C52H34N2S: C, 86.88 ; H, 4.77; N, 3.90 ; S, 4.46; content: C, 86.86 ; H, 4.75; N, 3.88 ; S, 4.45 Synthetic example ad-39: synthesis of compound f-84 Synthesis of compound f-84 In addition to using borate (9) replace the borate (7) the outer, f-70 with the compounds according to examples of synthesizing ad-26 f-84 the same method to synthesize compound (9.3 g, yield 69%). The calculated value of C52H34N2S: C, 86.88 ; H, 4.77; N, 3.90 ; S, 4.46; content: C, 86.86 ; H, 4.76; N, 3.85 ; S, 4.42 Synthetic example ad-40: synthesis of compound f-88 Synthesis of compound f-88 In addition to using borate (14) instead of borate (7) the outer, f-70 with the compounds according to examples of synthesizing ad-26 f-88 the same method to synthesize compound (7.6 g, yield 73%). The calculated value of C52H34N2S: C, 86.88 ; H, 4.77; N, 3.90 ; S, 4.46; content: C, 86.86 ; H, 4.73; N, 3.89 ; S, 4.44 Synthetic example ad-41: synthesis of compound f-114 Synthesis of compound f-114 In addition to using borate (10) to replace the borate (7) the outer, f-70 with the compounds according to examples of synthesizing ad-26 f-114 the same method to synthesize compound (7.6 g, yield 67%). The calculated value of C46H30N2S: C, 85.95 ; H, 4.70; N, 4.36 ; S, 4.99; content: C, 85.90 ; H, 4.69; N, 4.33 ; S, 4.96 (Synthetic 2nd main compound) Synthesis example 4: synthesis of compound A1 Under the nitrogen atmosphere of 16.62 g (51.59 mmol) 3-bromo-N-phenyl carbazole, 17.77 g (61.91 mmol) N-phenyl carbazole-3-yl boronic acid and 200 ml of tetrahydrofuran: toluene (1:1) mixture and 100 ml 2M-potassium carbonate aqueous solution equipped with a stirrer into 500 ml round-bottom flask, and in added 2.98 g (2.58 mmol) four (triphenylphosphine) palladium (0) to and in the nitrogen atmosphere under heating to reflux for about 12 hours. After the end of the reaction, the methanol is added to the reaction product, to obtain the solid by filtration. Water and methanol fully wash this solid, and then drying. By heating, the resulting product is dissolved in 1 liter of chlorobenzene in, then use silica gel filtering and removing the solvent. By heating, the resulting product is dissolved in 500 ml in toluene, then re-crystallization, get compound A1 16.05 g (yield 64%). C36 H24 N2 the calculated value: C, 89.23; H, 4.99 ; N, 5.78; content: C, 89.45 ; H, 4.89; N, 5.65 Synthesis example 5: synthesis of compound A2 Under the nitrogen atmosphere of 20.00 g (50.21 mmol) 3-bromo-N-biphenyl diphenylenimine, 18.54 g (50.21 mmol)) N-phenyl carbazole-3-borate and 175 ml of tetrahydrofuran: toluene (1:1) mixture of the and 75 ml 2M-potassium carbonate aqueous solution equipped with a stirrer into 500 ml round-bottom flask and add in 2.90 g (2.51 mmol) four (triphenylphosphine) palladium (0) to and in the nitrogen atmosphere under heating to reflux for about 12 hours. After the end of the reaction, the methanol is added to the reaction product, to obtain the solid by filtration. Water and methanol fully wash this solid, and then drying. By heating, the resulting product is dissolved in 700 ml of chlorobenzene in, then use silica gel filtering and removing the solvent. By heating, the resulting product is dissolved in 400 ml of chlorobenzene in, then re-crystallization, get compound A219.15 g (yield 68%). C42 H28 N2 the calculated value: C, 89.97; H, 5.03 ; N, 5.00; content: C, 89.53 ; H, 4.92; N, 4.89 Synthesis example 6: synthesis of compound A5 Adding 12.81 g (31.36 mmol) N-phenyl -3,3-luen diphenylenimine, 8.33 g (31.36 mmol) 2-chloro-bis -4,6-phenyl-pyridine, 6.03 g sodium butylate 3rd (62.72 mmol), 1.80 g (3.14 mmol) three (dibenzylidene acetone) two palladium and 2.6 ml of three -3rd butyl phosphine (50% in toluene for) to 500 ml of round-bottom flask 200 ml of xylene and in the nitrogen atmosphere to reflux under heating for about 15 hours. To the resulting mixture is added 600 ml of methanol, to obtain crystalline solid powder by filtration. The resulting product is dissolved in dichlorobenzene and to filter using silica gel/diatomaceous earth, then removed and a proper amount of organic solvent with methanol recrystallizaiton, get compound A5 (13.5 g, yield 68%). C47 H31 N3 the calculated value: C, 88.51; H, 4.90 ; N, 6.59; content: C, 88.39 ; H, 4.64; N, 6.43 Synthetic example 7: synthesis of compound A15 Under the nitrogen atmosphere of 10.00 g (31.04 mmol) 3-bromo-N-phenyl carbazole, 10.99 g (31.04 mmol) 2-Sanya phenyl borate, 150 ml of tetrahydrofuran: toluene (1:1) mixture of the and 75 ml 2M-potassium carbonate aqueous solution equipped with a stirrer into 500 ml round-bottom flask, and in added 1.79 g (1.55 mmol) four (triphenylphosphine) palladium (0) to and in the nitrogen atmosphere under heating to reflux for about 12 hours. After the end of the reaction, the methanol is added to the reaction product, to obtain the solid by filtration. Water and methanol fully wash this solid, and then drying. By heating, the resulting product is dissolved in 400 ml of chlorobenzene in, then use silica gel filtering and removing the solvent. By heating, the resulting product is dissolved in 300 ml in toluene, then re-crystallization, get compound A1 58.74 g (yield 60%). C36 H23 N the calculated value: C, 92.08; H, 4.94 ; N, 2.98; content: C, 92.43 ; H, 4.63; N, 2.84 Synthetic example 8: synthesis of compound A17 Under the nitrogen atmosphere of 15.00 g (37.66 mmol) 3-bromo-N-methyl biphenyl diphenylenimine, 16.77 g (37.66 mmol) 3-borate-N-biphenyl diphenylenimine, 200 ml of tetrahydrofuran: toluene (1:1) mixture and 100 ml 2M-potassium carbonate aqueous solution equipped with a stirrer into 500 ml round-bottom flask, and in added 2.18 g (1.88 mmol) of four (triphenylphosphine) palladium (0) to and in the nitrogen atmosphere under heating to reflux for about 12 hours. After the end of the reaction, the methanol is added to the reaction product, to obtain the solid by filtration. Water and methanol fully wash this solid, and then drying. By heating, the resulting product is dissolved in 500 ml of chlorobenzene in, then filtering using and silica gel remove the solvent. By heating, the resulting product is dissolved in 400 ml in toluene, then re-crystallization, get compound A1 16.07 g (yield 67%). C48 H32 N2 the calculated value: C, 90.54; H, 5.07 ; N, 4.40; content: C, 90.71 ; H, 5.01; N, 4.27 Synthetic example ad-42: synthesis of compound A63 The 6.3 g (15.4 mmol) N-phenyl -3,3-luen diphenylenimine, 5.0 g (15.4 mmol) 4 - (4-bromophenyl) dibenzo [b, d] furan, 3.0 g (30.7 mmol) 3rd sodium butylate, 0.9 g (1.5 mmol) three (dibenzalacetone) palladium II and 1.2 ml butyl phosphine three 3rd (50% in toluene for) with 100 ml of xylene in the 250 ml round-bottom flask and then mixed in the in the nitrogen atmosphere under heating to reflux 15 hours. The resulting mixture is added to 300 ml of methanol in order to make the solid crystalline, and filtering solid, dissolved in dichlorobenzene, and the use of silica gel/diatomaceous earth is used to filter, and then the self-its removing a proper amount of organic solvent recrystallization with methanol, to obtain intermediate A63 (7.3 g, yield 73%). The calculated value of C48H30N2O: C, 88.59 ; H, 4.65; N, 4.30 ; O, 2.46; content: C, 88.56 ; H, 4.62; N, 4.20 ; O, 2.43 Synthetic example ad-43: synthesis of compound A64 The 6.1 g (15.0 mmol) N-phenyl -3,3-luen diphenylenimine, 5.1 g (15.0 mmol) 4 - (4-bromophenyl) dibenzo [b, d] thiophene, 2.9 g (30.0 mmol) 3rd sodium butylate, 0.9 g (1.5 mmol) three (dibenzalacetone) palladium II and 1.2 ml butyl phosphine three 3rd (50% in toluene for) with 100 ml of xylene in 250 ml round bottom flask in mixed, and then in the nitrogen atmosphere under heating to reflux 15 hours. The resulting mixture is added to 300 ml of methanol in order to make the solid crystalline, and filtering solid, dissolved in the single paradichlorbenzene and the use of silica gel/diatomaceous earth filter material to the filter, and then remove the a proper amount of organic solvent recrystallization with methanol, to obtain intermediate A64 (6.7 g, yield 67%). The calculated value of C48H30N2S: C, 86.46 ; H, 4.53; N, 4.20 ; S, 4.81; content: C, 86.41 ; H, 4.51; N, 4.18 ; S, 4.80 Synthetic example 9: synthesis of compound B2 Synthetic intermediate B2 Adding 39.99 g (156.01 mmol) indole and diphenylenimine, 26.94 g bromobenzene (171.61 mmol), 22.49 g sodium butylate 3rd (234.01 mmol), 4.28 g (4.68 mmol) three (dibenzylidene acetone) two palladium and 2.9 ml of three -3rd butyl phosphine (50% in toluene for) to 1000 ml round-bottom flask of 500 ml of xylene, and in the nitrogen atmosphere and mix reflux under heating for about 15 hours. The resulting mixture is added to 1000 ml of methanol, to obtain crystalline solid powder by filtration. The resulting product is dissolved in dichlorobenzene and to filter using silica gel/diatomaceous earth, then removed and a proper amount of organic solvent recrystallization with methanol, to obtain intermediate B2 (23.01 g, yield 44%). C24 H16 N2 the calculated value: C, 86.72; H, 4.85 ; N, 8.43; content: C, 86.72 ; H, 4.85; N, 8.43 Synthesis of compound B2 Adding 22.93 g (69.03 mmol) intermediate B2,11.38 g bromobenzene (72.49 mmol), 4.26 g (75.94 mmol) potassium hydroxide, 13.14 g (69.03 mmol) cuprous iodide and 6.22 g (34.52 mmol) 1,10- [...] to 500 ml round-bottom flask of in 230 ml of dimethyl formamide and in the nitrogen atmosphere to reflux under heating for about 15 hours. The resulting mixture is added to 1000 ml of methanol, to obtain crystalline solid powder by filtration. The resulting product is dissolved in dichlorobenzene and to filter using silica gel/diatomaceous earth, then removed and a proper amount of organic solvent with methanol recrystallizaiton, get compound B2 (12.04 g, yield 43%). C30 H20 N2 the calculated value: C, 88.21; H, 4.93 ; N, 6.86; content: C, 88.21 ; H, 4.93; N, 6.86 Assessment example 1: synthesis of compound assessment HOMO, LUMO and the tri-state (T1) can be meta- According to in table 2 the method described in the synthesis of chemical compounds to assess stepses HOMO, LUMO energy-level and T1 can order. Display the results in table 1 and table 3 in. [Table 2] [Table 3] Reference table 1 and table 3, synthetic compounds with suitable for organic light-emitting device of the electrical characteristic of the material. Assessment example 2: compound heat characteristic evaluation Each kind of synthesis of chemical compounds using thermal analysis TGA (thermogravimetric analysis) and DSC (differential scanning calorimetry) for (N2 atmosphere, temperature range: room temperature to 800 °C (10 °C/minutes)-TGA, room temperature to 400 °C-DSC, the disc type; disposable Al Pt disk (TGA) in the plate, disposable Al disk (DSC)). The results show in table 4 in. Reference table 4, synthetic compounds with excellent thermal stability. [Table 4] Fabricating organic light emitting device (emitting layer device (1)-a single body) Example ad-1 The glass substrate with the ITO electrode is cut to 50 mm × 50 mm × 0.5 mm size, the acetone, isopropanol and the acoustic wave in the pure water washing treatment, each washing 15 minutes, and UV ozone washing for 30 minutes. To m-MTDATA 1 ANGSTROM/second deposition rate vacuum deposition on the glass substrate on the ITO electrode, so as to form with 600 angstroms of the thickness of the hole injection layer, and then to α-NPB 1 ANGSTROM/second the deposition rate of the vacuum deposition to form a hole injecting layer 300 angstroms of the thickness of the hole transport layer. Subsequently Ir (ppy)3 (dopant) and compounds b-41 respectively (main body) by about 0.1 ANGSTROM/second and about 1 ANGSTROM/second the deposition rate of co-deposition on the hole transport layer, in order to form and has about 400 angstroms of the thickness of the emitting layer. BAlq to about 1 ANGSTROM/second the deposition rate of the vacuum deposition of the reflective layer, in order to form with the 50 angstroms of the thickness of the hole barrier layer, and then Alq3 vacuum deposition to form the hole blocking layer having 300 angstroms of the thickness of the hole transport layer. In the vacuum deposition on the electron transport layer about 10 angstroms thickness (electron injection layer) LiF and 2000 angstroms thickness Al (cathode), thereby manufacturing the organic light-emitting device. Example ad-2 In addition to using compound b-71 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example 1 In addition to using compound 29 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example 2 In addition to the use of compound 30 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-3 In addition to using compound 27 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-4 In addition to using compound a-30 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-5 In addition to using compound a-40 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-6 In addition to using compound a-41 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-7 In addition to using compound a-42 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-8 In addition to using compound a-46 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-9 In addition to using compound a-56 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-10 In addition to using compound a-70 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-11 In addition to using compound a-71 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-12 In addition to using compound a-74 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-13 In addition to using compound a-75 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-14 In addition to using compound a-82 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-15 In addition to using compound a-84 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-16 In addition to using compound a-114 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-17 In addition to using compound a-110 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-18 In addition to using compound a-112 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-19 In addition to using compound c-40 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-20 In addition to using compound c-50 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-21 In addition to using compound d-119 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-22 In addition to using compound e-70 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-23 In addition to using compound f-70 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-24 In addition to using compound e-71 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-25 In addition to using compound e-74 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-26 In addition to using compound e-75 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-27 In addition to using compound e-82 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-28 In addition to using compound e-84 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-29 In addition to using compound e-88 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-30 In addition to using compound e-114 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-31 In addition to using compound f-71 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-32 In addition to using compound f-74 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-33 In addition to using compound f-75 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-34 In addition to using compound f-82 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-35 In addition to using compound f-84 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-36 In addition to using compound f-88 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-37 In addition to using compound f-114 compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Fabricating organic light emitting device (device-mixed body emitting layer) Example ad-38 Apart from Ir (ppy)3 (dopant), compound a-70 compound (1st main body) and A1 (2nd main body) to 10:45:45 weight ratio of co-deposited on the hole transport layer to form a 400 angstroms of the thickness of the transmitting layer, in order to instantiate ad-1 the same manner as in the production of organic light-emitting device. Example ad-39 In addition to the use of compound A2 instead of compound A1 forming the layer, and examples ad-38 in the same manner as in the production of organic light-emitting device. Example ad-40 In addition to the use of compound A5 instead of compound A1 forming the layer, and examples ad-38 in the same manner as in the production of organic light-emitting device. Example ad-41 In addition to the compound A15 instead of compound A1 forming the layer, and examples ad-38 in the same manner as in the production of organic light-emitting device. Example ad-42 In addition to the use of compound A17 instead of compound A1 forming the layer, and examples ad-38 in the same manner as in the production of organic light-emitting device. Example ad-43 In addition to using compound A63 instead of compound A1 forming the layer, and examples ad-38 in the same manner as in the production of organic light-emitting device. Example ad-44 In addition to using compound A64 instead of compound A1 forming the layer, and examples ad-38 in the same manner as in the production of organic light-emitting device. Example ad-45 In addition to the use of compound B2 instead of compound A1 forming the layer, and examples ad-38 in the same manner as in the production of organic light-emitting device. Example ad-46 Apart from Ir (ppy)3 (dopant), compound a-40 compound (1st main body) and A17 (2nd main body) to 10:45:45 the weight ratio of the co-deposited in order to form the hole transport layer has about 400 angstroms of the thickness of the transmitting layer, and examples ad-38 in the same manner as in the production of organic light-emitting device. Example ad-47 In addition to using compound a-71 a-40 replace the compound forming the emission layer, the example ad-46 in the same manner as in the production of organic light-emitting device. Example ad-48 In addition to using compound a-74 a-40 replace the compound forming the emission layer, the example ad-46 in the same manner as in the production of organic light-emitting device. Example ad-49 In addition to using compound a-75 a-40 replace the compound forming the emission layer, the example ad-46 in the same manner as in the production of organic light-emitting device. Example ad-50 In addition to using compound a-82 a-40 replace the compound forming the emission layer, the example ad-46 in the same manner as in the production of organic light-emitting device. Example ad-51 In addition to using compound a-84 a-40 replace the compound forming the emission layer, the example ad-46 in the same manner as in the production of organic light-emitting device. Example ad-52 Apart from Ir (ppy)3 (dopant), compound a-75 compound (1st main body) and A63 (2nd main body) to 10:45:45 the weight ratio of the co-deposited in order to form the hole transport layer has about 400 angstroms of the thickness of the transmitting layer, and examples ad-38 in the same manner as in the production of organic light-emitting device. Example ad-53 In addition to using compound A64 replace compound A63 forming the layer, and examples ad-52 in the same manner as in the production of organic light-emitting device. Example ad-54 In addition to using compound e-75 a-40 replace the compound forming the emission layer, the example ad-46 in the same manner as in the production of organic light-emitting device. Example ad-55 In addition to using compound e-114 a-40 replace the compound forming the emission layer, the example ad-46 in the same manner as in the production of organic light-emitting device. Example ad-56 In addition to using compound f-75 a-40 replace the compound forming the emission layer, the example ad-46 in the same manner as in the production of organic light-emitting device. Example ad-57 In addition to using compound f-114 a-40 replace the compound forming the emission layer, the example ad-46 in the same manner as in the production of organic light-emitting device. Example ad-58 In addition to using compound A64 instead of compound A17 forming the layer, and examples ad-54 in the same manner as in the production of organic light-emitting device. Example ad-59 In addition to using compound A64 instead of compound A17 forming the layer, and examples ad-55 in the same manner as in the production of organic light-emitting device. Example ad-60 In addition to using compound A64 instead of compound A17 forming the layer, and examples ad-56 in the same manner as in the production of organic light-emitting device. Example ad-61 In addition to using compound A64 instead of compound A17 forming the layer, and examples ad-57 in the same manner as in the production of organic light-emitting device. Comparative example 1 In addition to the compounds of compound A b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Comparative example 2 In addition to the compounds of compound B b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Comparative example 3 C in addition to the compounds of compound b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Comparative example 4 In addition to the compounds of compound D b-41 replaced as the main body forming the layer, and examples ad-1 in the same manner as in the production of organic light-emitting device. Example ad-62 (emitting layer device (2)-a single body) According to the synthesis examples by using ad-20 b-116 of the main body and as (piq)2 Ir (acac) making organic light-emitting device as a dopant. Use of 1000 angstroms thick the ITO as the anode, and the use is 1000 angstroms thick aluminum (Al) as a cathode. Specific tokiyuki, a method of fabricating organic light emitting device using an anode, said ITO anode having a 15 ohm/square centimeter of the sheet resistance of the glass substrate is cut into 50 mm × 50 mm × 0.7 mm in size, are respectively with acetone, isopropanol and the pure water ultrasonic cleaning 15 minutes and UV ozone cleaning its 30 minutes to obtain. On the substrate, the 650×10-7 pahi vacuum degree in a 0.1 nanometer/sec to 0.3 nano meters/sec deposition rate N4, N4 '-di (naphthalene-1-yl)-N4, N4' -diphenyl-biphenyl -4,4 '-diamine (N4, N4' -di (naphthalene-1-yl)-N4, N4 '-diphenylbiphenyl-4,4' -diamine: NPB) (80 nm) form 800 angstroms thick hole transport layer. Subsequently, in the same vacuum deposition conditions through the use of synthetic example ad-20 b-116 of forming 300 angstroms thick emitting layer, and in this text, together at the same time depositing the phosphorescent dopant (piq)2 Ir (acac). In this text, to 100% by weight of the emitting layer is 3% by weight of the phosphorescent dopant to deposit the deposition rate. Subsequently, in the emitting layer, in the same vacuum deposition conditions through the use of double (2-methyl-8-quinoline) - 4 - (foundation benzyl phenol ) aluminum (bis (2-methyl-8-quinolinolate) - 4 - (phenylphenolato) aluminium: BAlq) forming 50 angstroms thick of the hole barrier layer. Subsequently, in the same vacuum deposition conditions of the next deposition Alq3 form 200 angstroms thick electron transport layer. On the electron transport layer, and LiF Al by sequentially depositing forming a cathode, thereby producing organic photoelectric device. The structure of the organic optoelectronic device for ITO/NPB (80 nm)/ EML (b-116 (97 weight %) + (piq)2 Ir (acac) (3 weight %), 30 nanometer)/ Balq (5 nanometer)/ Alq3 (20 nm)/ LiF (1 nanometer)/ Al (100 nanometer). Example ad-63 In addition to using synthetic example ad-14 a-108 the compound of synthetic example replaced ad-20 compound b-116 outer, according to the example ad-62 the same method for manufacturing organic light-emitting device. Ad-1 comparative examples In addition to using has the following structure instead of CBP ad-62 of example compound b-116 outer, according to the example ad-62 the same method for manufacturing organic light-emitting device. Organic light-emitting device used for making the NPB, BAlq, CBP and (piq)2 Ir (acac) has the following structure. Assessment example 3: characteristic evaluation of the organic light-emitting device (I) Using PR650 spectrum scan source quantity sensing unit (self-optical research assurers) measurement example 1, example 2, example ad-1 to embodiment examples ad-17 and ad-21 ad-63 and comparison example to example 1 to the comparison example 4 and comparison examples ad-1 of the driving voltage of the organic light-emitting device, and the current efficiency of the lightness, the use of auspicious moment arrives (Kethley SMU236) natural resources quantity sensing unit power supply. Described below in specific amount measured, and the results shown in table 5 to table 7 in. (1) the voltage change the gauging regards the change in the density of the current Through the use of current-voltmeter (keithley 2400), since the voltage to 0 volt to 10 volts to each of the organic light-emitting device for measuring the current, the current value and the measured divided by the area in order to provide a result. (2) the voltage change the gauging regards the lightness change By using brilliance idea (Minolta Cs-1000A), since the voltage to 0 volt to 10 volts to measuring each of brightness of the organic light-emitting device. (3) measuring the light-emitting efficiency The use of self-the above-mentioned (1) and (2) the lightness and current density obtained voltage calculation and the same current density (10 milliampere/square centimeter) of the current efficiency under (cd/A). (4) life In measuring the lightness (cd/m2) maintained at 5000cd/m2 (cd/A) under at the same time reduce the current efficiency of 90% to obtain the time-consuming. [Table 5] Reference table 5, the discovery and the comparative example 1 to comparative example 4 is compared to the organic light-emitting device, embodiment 1, embodiment 2, embodiment ad-1 to embodiment examples ad-17 and ad-21 ad-37 to examples of the organic light-emitting device having a low driving voltage and high current efficiency. [Table 6] Reference table 6, and comparative example 1 to comparative example 4 is compared to the organic light-emitting device, instance ad-38 ad-61 to examples of the organic light-emitting device exhibiting low driving voltage, high efficiency and long service life. [Table 7] Reference table 7, and comparative examples ad-1 compared to an organic light emitting device, instance ad-62 ad-63 and examples of the organic light-emitting device exhibiting improved driving voltage, light emitting efficiency and/or power efficiency aspects and features. Fabricating organic light emitting device (ETB device) Example ad-64 The ultrasonic washing with distilled water/1500 angstroms thick of the thin film of ITO (indium tin oxide) coated glass substrate. Such as isopropyl alcohol, acetone, methanol and the like of the ultrasonic washing solvent glass substrate washing, drying, is transmitted to the plasma cleaner, oxygen plasma through the use of the cleaning, cleaning its 10 minutes, and is transmitted to the vacuum depositor. Thus-obtained ITO transparent electrode is used as ITO anode, and by the deposition HT13 formed on in the 1400 angstroms thick hole injection and transport layer. Subsequently, on the hole transport layer, through to 5% by weight of the doped amount of limited preparation of the SFC BH113 and BD370 as the blue fluorescent light-emitting body and dopant to form Thick emitting layer. Subsequently, in the emitting layer, ad-18 by depositing the synthesis of example compound b-41 forming 50 angstroms thick layer of electronic transmission. On the electron transport layer, by vacuum deposition three (8-hydroxy-quinoline) aluminum (Alq3) form 310 angstroms thick electron transport layer, the electron-transporting layer by vacuum deposition in order 15 angstroms thick of and Liq 1200 angstroms thick of forming a cathode Al, making organic light-emitting device. Organic light-emitting device has five layer of the organic thin film layer structure, specific tokiyuki, ITO/HT13 (1400 angstroms)/ / EML [BH113: BD370=95:5 weight %] (200 angstroms)/ compound b-41 (50 angstroms)/ Alq3 (310 heydon)/ Liq (15 angstroms)/ Al (1200 angstroms) Example ad-65 In addition to using synthetic example ad-19 b-71 compounds of examples ad-42 replaced b-41 the compound, according to the example ad-64 the same method for manufacturing organic light-emitting device. Example ad-66 In addition to using synthetic example ad-2 a-40 compounds of examples ad-42 replaced b-41 the compound, according to the example ad-64 the same method for manufacturing organic light-emitting device. Example ad-67 In addition to using synthetic example ad-7 a-70 compounds of examples ad-42 replaced b-41 the compound, according to the example ad-64 the same method for manufacturing organic light-emitting device. Example ad-68 In addition to using synthetic example ad-8 a-71 compounds of examples ad-42 replaced b-41 the compound, according to the example ad-64 the same method for manufacturing organic light-emitting device. Example ad-69 In addition to using synthetic example ad-9 a-74 compounds of examples ad-42 replaced b-41 the compound, according to the example ad-64 the same method for manufacturing organic light-emitting device. Example ad-70 In addition to using synthetic example ad-10 a-75 compounds of examples ad-42 replaced b-41 the compound, according to the example ad-64 the same method for manufacturing organic light-emitting device. Example ad-71 In addition to using synthetic example ad-11 a-82 compounds of examples ad-42 replaced b-41 the compound, according to the example ad-64 the same method for manufacturing organic light-emitting device. Example ad-72 In addition to using synthetic example ad-12 a-84 compounds of examples ad-42 replaced b-41 the compound, according to the example ad-64 the same method for manufacturing organic light-emitting device. Example ad-73 In addition to using synthetic example ad-28 e-74 compounds of examples ad-42 replaced b-41 the compound, according to the example ad-64 the same method for manufacturing organic light-emitting device. Example ad-74 In addition to using synthetic example ad-29 e-75 compounds of examples ad-42 replaced b-41 the compound, according to the example ad-64 the same method for manufacturing organic light-emitting device. Example ad-75 In addition to using synthetic example ad-33 e-114 compounds of examples ad-42 replaced b-41 the compound, according to the example ad-64 the same method for manufacturing organic light-emitting device. Example ad-76 In addition to using synthetic example ad-36 f-74 compounds of examples ad-42 replaced b-41 the compound, according to the example ad-64 the same method for manufacturing organic light-emitting device. Example ad-77 In addition to using synthetic example ad-37 f-75 compounds of examples ad-42 replaced b-41 the compound, according to the example ad-64 the same method for manufacturing organic light-emitting device. Example ad-78 In addition to using synthetic example ad-41 f-114 compounds of examples ad-42 replaced b-41 the compound, according to the example ad-64 the same method for manufacturing organic light-emitting device. Ad-2 comparative examples In addition to not using an electronic transmitting the auxiliary layer is, according to the example ad-64 the same method for manufacturing organic light-emitting device. Example ad-79 In addition to the formed 1350 angstroms thick hole injection and transport layer instead of 1400 angstroms thick hole injection and transport layer, and by vacuum deposition compound P-5 formed on the hole transport layer 50 angstroms thick hole transport layer, and then by vacuum deposition synthesis example ad-5 a-46 the compound is formed on the emitting layer 50 angstroms thick electronic transmitting the auxiliary layer is, according to the example ad-64 the same method for manufacturing organic light-emitting device. Organic light-emitting device has the six-layer structure of the organic thin layer, specific tokiyuki, ITO/HT13 (1350 angstroms)/ P-5 (50 angstroms)/ EML [BH113: BD370=95:5 weight %] (200 angstroms)/ compound a-46 (50 angstroms)/ Alq3 (310 heydon)/ Liq (15 angstroms)/ Al (1200 angstroms). Example ad-80 In addition to using synthetic example ad-19 b-71 compounds of examples ad-79 replaced a-46 the compound, according to the example ad-79 the same method for manufacturing organic light-emitting device. Ad-3 comparative examples In addition to not using an electronic transmitting the auxiliary layer is, according to the example ad-79 the same method for manufacturing organic light-emitting device. Assessment example 4 : (II) the characteristics of the organic light-emitting device Measurement according to example ad-64 ad-80 and comparison example to example ad-2 ad-3 and comparison examples of the organic light-emitting device depending on voltage, light emitting efficiency and the service life of the current density and the lightness change of, and the results in table 8 and table 9 in. Measuring (1) the voltage changes depending on the change in the density of electric current, (2) depending on the voltage change and the lightness change (3) method for evaluation of the light-emitting efficiency by example 3. Specific tokiyuki, the following service life of the measuring. Life Measuring system for measuring example pula Nix life ad-64 ad-80 and comparison example to example ad-2 ad-3 and comparison examples of the organic light-emitting device for T97 life, to 750cd/m2 as the initial lightness (cd/m2) the gauging regards light-emitting and time after its lightness is reduced, relative to the initial lightness, its lightness reduced to 97% of the time. [Table 8] Reference table 8, according to the example ad-64 ad-78 to examples of the organic light-emitting device according to the comparative examples exhibited ad-2 compared to an organic light emitting device, the extension of the life. Therefore, confirmed that the electron transport layer to improve life characteristic of an organic light-emitting device. [Table 9] Reference table 9, example ad-79 ad-80 and examples of the organic light emitting device display ad-3 with the comparison example is compared to the organic light-emitting device, the driving voltage of the fine, light-emitting efficiency and in service life. Salinomycin analogs and pharmaceutically acceptable compositions containing salinomycin analogs. Dosage forms and kits comprising salinomycin analogs and pharmaceutically acceptable compositions containing salinomycin analogs. Methods of using salinomycin analogs, pharmaceutically acceptable compositions, dosage forms, and kits for the treatment of proliferative diseases, e.g., cancer, or microbial infections in a subject 1. A fused ring compound, its formula 1 expresses: <式1> <式1A> In the formula 1 in, ring A1 by formula 1A expressed, X1 to N-[ (L1)a1-(R1)b1], S, O or Si (R4) (R5); L1 to L3 by the independently substituted or not substituted C6-C60 arylene selected from, A1 to a3 on the various independently 0 to 5 selected integer, R1 to R5 all independently each selected from the following: hydrogen, deuterium, -F (fluorine-based), -Cl (chlorine-based), -Br (bromo), -I (iodine-based), hydroxy, a substituted or an unsubstituted C1-C60 alkyl, a substituted or an unsubstituted C1-C60 alkoxy, a substituted or an unsubstituted C3-C10 cycloalkyl, a substituted or an unsubstituted C6-C60 aryl, a substituted or an unsubstituted C6-C60 aryloxy group, a substituted or an unsubstituted C6-C60 arylthio and substituted or not substituted by a monovalent non-aromatic gathers many thickly cyclic group, Wherein R2 and R3 by at least one of the substituted or non-substituted C6-C60 aryl group and the substituted or non-substituted monovalent non-aromatic gathers many thickly cyclic group selected from, R11 to R14 all independently each selected from the following: hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, a substituted or an unsubstituted C1-C60 alkyl, a substituted or an unsubstituted C1-C60 alkoxythiophene, C3-C10 cycloalkyl, C6-C60 aryl, C6-C60 aryloxy, C6-C60 arylthio and gathers many thickly monovalent non-aromatic cyclic group, and B1 to b3 on the various independently 1 to 3 an integer selected, When the R2 is a substituted or an unsubstituted phenyl, R3 each selected from the following: hydrogen, a substituted or an unsubstituted phenyl, a substituted or an unsubstituted biphenyl, substituted or not substituted terphenyl base, a substituted or an unsubstituted luen four phenyl, a substituted or an unsubstituted naphthyl, a substituted or an unsubstituted anthryl, a substituted or an unsubstituted [...], substituted or not substituted hydrazo three phenyl, a substituted or an unsubstituted Pyren, a substituted or an unsubstituted Fikki, a substituted or an unsubstituted [...] and a substituted or an unsubstituted qu Ji. 2. Fused ring compound according to Claim 1, wherein the compounds are represented by type states the fused ring 1-1 of the formula 1-2 said one of: <式1-1> <式1-2> Wherein in the formula 1-1 to 1-2 in, X1, L2, L3, a2, a3, R2, R3, R11 to R14, b2 and b3 with claim 1 are as defined in the. 3. Fused ring compound according to Claim 1, wherein X1 to S or O. 4. Fused ring compound according to Claim 1, wherein L1 to L3 each independently represented by formula 2-1 to 2-15 said one of: Wherein in the formula 2-1 to 2-15 in, Z1 to Z4 all independently each selected from the following: hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl, C1-C20 alkoxy, phenyl, biphenyl, terphenyl base, luen four phenyl, naphthyl, anthryl, hydrazo three phenyl, Pyren, Fikki, qu Ji[...] and; D1 is 1 to 4 an integer that is elected in the; d2 is 1 to 3 an integer that is elected in the; d3 is 1 to 6 an integer that is elected in the; d4 is 1 to 8 selected in the integer; d6 is 1 to 5 an integer that is elected in the; and * and*' each independently and the adjacent atom binding site. 5. Fused ring compound according to Claim 1, Wherein L1 to L3 each independently represented by formula 3-1 to 3-37 said one of: Wherein in the formula 3-1 to 3-37 in, And ** ' each independently and the adjacent atom binding site. 6. Fused ring compound according to Claim 1, Wherein R1 to R5 all independently each selected from the following: Hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl and C1-C20 alkoxy, C1-C20 alkyl and C1-C20 alkoxy, all after deuterium atom, -F, -Cl, -Br, -I and at least one of the hydroxyl groups substituted, and Formula 4-1 to 4-5 among 4-34 to 4-37 group expressed in one of; and i) R2 and R3 at least one and in ii) R1 all independently each selected from the following: by formula 4-1 to 4-5 formula 4-34 to 4-37 group expressed in one of: Wherein in the formula 4-1 to 4-5 among 4-34 to 4-37 in, Z31 and Z38 to Z41 all independently each selected from the following: hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl, C1-C20 alkoxy, phenyl, naphthyl, anthryl, Pyren, Fikki, [...], qu Ji, biphenyl, terphenyl base and luen four phenyl, E1 is 1 to 5 an integer selected, e2 is 1 to 7 in an integer selected, e3 is 1 to 3 an integer selected, e4 is 1 to 4 an integer selected, and * the binding site of the adjacent atoms. 7. Fused ring compound according to Claim 1, Wherein X1 to S or O, R1 to R5 all independently each selected from the following: Hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl and C1-C20 alkoxy, C1-C20 alkyl and C1-C20 alkoxy, all after deuterium atom, -F, -Cl, -Br, -I and at least one of the hydroxyl groups substituted, and Formula 4-1 to 4-5 among 4-34 to 4-37 group expressed in one of; and R2 and R3 the at least one of the independently each selected from the following: by formula 4-1 to 4-5 among 4-34 to 4-37 group expressed in one of: Wherein in the formula 4-1 to 4-5 among 4-34 to 4-37 in, Z31 and Z38 to Z41 all independently each selected from the following: hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl, C1-C20 alkoxy, phenyl, naphthyl, anthryl, Pyren, Fikki, [...], qu Ji, biphenyl, terphenyl base and luen four phenyl, E1 is 1 to 5 an integer selected, e2 is 1 to 7 in an integer selected, e3 is 1 to 3 an integer selected, e4 is 1 to 4 an integer selected, and * the binding site of the adjacent atoms. 8. Fused ring compound according to Claim 1, Wherein R2 and R3 at least one of each selected from the following: Phenyl, biphenyl, terphenyl base, luen four phenyl, naphthyl, Fikki, anthryl, hydrazo [...] and three phenyl, and Biphenyl, terphenyl base, luen four phenyl, naphthyl, Fikki, anthryl, hydrazo [...] and three phenyl, via the following various in the selected at least one substituted: deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl, C1-C20 alkoxy, phenyl, naphthyl, propylene gathers the naphthyl, Fikki, anthryl, [...], hydrazo three phenyl, qu Ji Pyren and. 9. Fused ring compound according to Claim 1, Wherein R11 to R14 all independently each selected from the following: Hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl and C1-C20 alkoxy, and Phenyl, biphenyl, terphenyl base, luen four phenyl, naphthyl, [...], [...], benzocarbazoles [...], dibenzo [...], propylene gathers the naphthyl, Fikki, anthryl, [...], hydrazo three phenyl, qu Ji Pyren and. 10. Fused ring compound according to Claim 1, Wherein R1 to R5 all independently each selected from the following: Hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl and C1-C20 alkoxy, C1-C20 alkyl and C1-C20 alkoxy, all after deuterium atom, -F, -Cl, -Br, -I and at least one of the hydroxyl groups substituted, by formula 5-1 to 5-9, type 5-18 to 5-21 formula 5-45 to 5-66 said one of the groups, and i) R2 and R3 at least one and in ii) R1 all independently each selected from the following: by formula 5-1 to 5-9, type 5-18 to 5-21 formula 5-45 to 5-66 group expressed in one of, Wherein R11 to R14 all independently each selected from the following: Hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl and C1-C20 alkoxy, and Formula 5-1 to 5-9, type 5-18 to 5-21 formula 5-45 to 5-66 group expressed in one of: Wherein in the formula 5-1 to 5-9, type 5-18 to 5-21 formula 5-45 to 5-66 in, * Adjacent atoms in the binding site. 11. Fused ring compound according to Claim 1, Wherein X1 to S or O, R1 to R5 all independently each selected from the following: Hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl and C1-C20 alkoxy, C1-C20 alkyl and C1-C20 alkoxy, all after deuterium atom, -F, -Cl, -Br, -I and at least one of the hydroxyl groups substituted, and Formula 5-1 to 5-9, type 5-18 to 5-21 formula 5-45 to 5-66 group expressed in one of; and R2 and R3 the at least one of the independently each selected from the following: by formula 5-1 to 5-9, type 5-18 to 5-21 formula 5-45 to 5-66 group expressed in one of, Wherein R11 to R14 all independently each selected from the following: Hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, C1-C20 alkyl and C1-C20 alkoxy, and Formula 5-1 to 5-9, type 5-18 to 5-21 formula 5-45 to 5-66 group expressed in one of: Wherein in the formula 5-1 to 5-9, type 5-18 to 5-21 formula 5-45 to 5-66 in, * Adjacent atoms in the binding site. 12. Fused ring compound according to Claim 1, Wherein the compound is the following groups states the fused ring 1 list of one of the compounds: [Group 1] 13. An organic light-emitting device, including: 1st electrode; 2nd electrode, placed in the stated 1st opposite electrode; and Organic layer, placed in the stated 1st 2nd between the electrodes with the electrode, and comprises at least one as in claim 1 to 12 to any one of the fused ring compound. 14. Organic light-emitting device according to Claim 13, wherein the compound as the main body states the fused ring included in the organic layer in the emitting layer, or contained in electronic transmission in the auxiliary layer. 15. Organic light-emitting device according to Claim 14, wherein the emitting layer further comprises the main body of the represented by formula 41 with 1st compound of formula 61 in said 2nd compound of at least one of: <式41> <式61> Wherein in the formula 41 in, X41 to N-[ (L42)a42-(R42)b42], S, O, S (=O), S (=O)2, C (=O), C (R43) (R44), Si (R43) (R44), P (R43), P (=O) (R43) or C=N (R43); Type 61 of the ring in A61 by formula 61A expressed; Type 61 of the ring in A62 by formula 61B expressed; X61 to N-[ (L62)a62-(R62)b62], S, O, S (=O), S (=O)2, C (=O), C (R63) (R64), Si (R63) (R64), P (R63), P (=O) (R63) or C=N (R63); X71 to C (R71) or N; X72 to C (R72) or N; X73 to C (R73) or N; X74 to C (R74) or N; X75 to C (R75) or N; X76 to C (R76) or N; X77 to C (R77) or N; X78 to C (R78) or N; Ar41, L41, L42, L61 and L62 all independently each selected from the following: a substituted or an unsubstituted C3-C10asian link alkyl, a substituted or an unsubstituted C2-C10 jaya heterocyclic alkyl, a substituted or an unsubstituted C3-C10 jaya cycloalkenyl, substituted or not substituted C2-C10asia is mixed cycloalkenyl, substituted or not substituted C6-C60 jaya aryl, a substituted or an unsubstituted C2-C60 heteroarylidenyl, a substituted or an unsubstituted divalent non-aromatic gathers many thickly cyclic group and a substituted or an unsubstituted divalent non-aromatic fused hetero cyclic group; N1 and n2 on the various independently 0 to 3 in the selected integer; R41 to R44, R51 to R54, R61 to R64 and R71 to R79 all independently each selected from the following: hydrogen, deuterium, -F (fluorine-based), -Cl (chlorine-based), (polybromide yl)-Br, -I (iodine-based), hydroxy, cyano, amino, amidino, a substituted or an unsubstituted C1-C60 alkyl, a substituted or an unsubstituted C2-C60 alkenyl, a substituted or an unsubstituted C2-C60 alkynyl, substituted or not substituted C1-C60 alkoxy, a substituted or an unsubstituted C3-C10 cycloalkyl, a substituted or an unsubstituted C2-C10 heterocyclic alkyl, a substituted or an unsubstituted C3-C10 cycloalkenyl, substituted or not substituted C2-C10 heterocyclic alkenyl, a substituted or an unsubstituted C6-C60 aryl, a substituted or an unsubstituted C6-C60 aryloxy group, a substituted or an unsubstituted C6-C60 arylthio, a substituted or an unsubstituted C2-C60 heteroaryl, a substituted or an unsubstituted monovalent non-aromatic gathers many thickly cyclic group, substituted or not substituted by a monovalent non-aromatic fused hetero cyclic group, -N (Q1) (Q2), -Si (Q3) (Q4) (Q5) and-B (Q6) (Q7); A41, a42, a61 and a62 on the various independently 0 to 3 in the selected integer; and B41, b42, b51 to b54, b61, b62 and b79 on the various independently 1 to 3 in the selected integer. 16. Organic light-emitting device according to Claim 15, Wherein the emitting layer includes the main 1st, and 2nd dopant of the main body, Wherein said main body and said 1st 2nd main body are different from each other, The 1st main body comprises at least one formula 1 compound states the fused ring of, and The main body comprises a 2nd represented by formula 41 with the 1st compound of formula 61 in the 2nd of said at least one of the compounds. 17. Organic light-emitting device according to Claim 15, L61 and L62 all independently each selected from the following: a substituted or an unsubstituted C6-C60 jaya aryl, a substituted or an unsubstituted C2-C60 heteroarylidenyl and without a substituted or non-substituted divalent aromatic gathers many thickly cyclic group; R51 to R54, R61 to R64 and R71 to R79 all independently each selected from the following: hydrogen, deuterium, -F, -Cl, -Br, -I, hydroxy, cyano, amino, amidino, a substituted or an unsubstituted C1-C20 alkyl, a substituted or an unsubstituted C1-C20 alkoxy, a substituted or an unsubstituted C3-C10 cycloalkyl, a substituted or an unsubstituted C3-C10 cycloalkenyl, substituted or not substituted C6-C20 aryl and substituted or not substituted by a monovalent non-aromatic gathers many thickly mixed cyclic group. 18. Organic light-emitting device according to Claim 15, wherein said 1st compound represented by formula 41-1 to 41-12 said one of, and the 2nd compound represented by formula 61-1 to 61-6 said one of: Wherein in the formula 41-1 to 41-12 among 61-1 to 61-6 in, X41, X61, L41, a41, L61, a61, R41, b41, R61, R51 to R54, b51 to b54, b61, R71 to R79 and b79 with claim 15 is the same as defined in the. 19. Organic light-emitting device according to Claim 15, Wherein the compound is the following groups states the fused ring 1 one of the compounds set out, and Wherein the 1st and the 2nd compound is the compound of the following group 2 list of one of the compounds: [Group 1] [Group 2] 20. Organic light-emitting device according to Claim 14, wherein The said compound is contained in the states the fused ring of the organic layer in the electron transport layer, and The organic light-emitting device also includes the compounds represented by general formula 2 compound expressed by: <式2> Wherein in the formula 2 in, L201 is a substituted or an unsubstituted C6 to C30 arylene or a substituted or an unsubstituted C2 to C30 heteroarylidenyl, n101 is 1 to 5 is selected in an integer of, R201 to R212 each is independently hydrogen, deuterium, a substituted or an unsubstituted C1 to C20 alkyl, a substituted or an unsubstituted C6 to C50 aryl group, a substituted or an unsubstituted C2 to C50 heteroaryl, or combinations thereof, and R201 to R212 the exist independently, or fused to each other, form the ring. Compound number Tg Tc Tm 30 128 246 261 29 116 185 250 27 129 223 267 Device Electron transport layer Color coordinates of (x, y) T97 life (hours) @ 750 knitt Example ad-64 Compound b-41 (0.133,0 . 148) 163 Example ad-65 Compound b-71 (0.132,0 . 149) 170 Example ad-66 Compound a-40 (0.132,0 . 148) 175 Example ad-67 Compound a-70 (0.133,0 . 147) 190 Example ad-68 Compound a-71 (0.133,0 . 148) 195 Example ad-69 Compound a-74 (0.132,0 . 149) 180 Example ad-70 Compound a-75 (0.132,0 . 148) 197 Example ad-71 Compound a-82 (0.133,0 . 149) 190 Example ad-72 Compound a-84 (0.133,0 . 149) 183 Example ad-73 Compound e-74 (0.133,0 . 148) 184 Example ad-74 Compound e-75 (0.133,0 . 149) 189 Example ad-75 Compound e-114 (0.133,0 . 148) 187 Example ad-76 Compound f-74 (0.133,0 . 148) 185 Example ad-77 Compound f-75 (0.133,0 . 148) 191 Example ad-78 Compound f-114 (0.133,0 . 149) 188 Ad-2 comparative examples Not used (0.133,0 . 146) 120