COMPOUND AND ORGANIC ELECTRONIC DEVICE INCLUDING SAME
The Korean application number and filing date for displaying an e-mail to the 30 March 2016 patent Korean patent application number 10 - 2016 - 0038453 call it will dance and blue, all the specification content to multiple myelomas are included. The specification is compound and including organic electronic devices are disclosed. Organic electronic devices include organic light emitting typical flow tides. The means by which electrical energy using organic material generally organic light emitting phenomenon to light installed on the pipe body. Organic light emitting phenomena between an anode and a cathode and a solvent including conventional organic light emitting devices has a meshed structure. The organic compound layer is formed of organic light-emitting material in order to enhance stability and different multilayered structure of which is in many cases, e.g. hole injection layer, hole transport layer, light emitting layer, metal-containing fullerene, can be made with an or the like. Such an organic light-emitting device structure a voltage between two electrodes on the liquid crystal in the solution with holes, and the process is organic electronics is cathode, electrons are injected and when meeting the OLEDs (exciton) is formed, is equal to 1000 ppm when a light again falls into the ground state. Said development of novel materials such as organic light emitting continuously etc. required. In particular an improvement in color purity of blue organic electronic devices connected power supply includes chromatic reappearance coat (a low reflective emission wavelength) is crucial metals and Sn-SB. Light emitting layer most representative american roh blood [leyn derivative which is used as a light emitting dopant materials include diaryl are disclosed. In particular aryl group having electron-attractive group having blue light emitting short-wavelength introducing flushes can be obtained due to aggregation of hydrogen when hydrogen fluorine but instead directly substituted at both sidewalls of the then easily occur between door number, lowering the efficiency of door number organic of an electronic component to or presented as a substrate. The specification includes isolating a high efficiency organic electronic devices can be obtained compound comprises a monomer including a broadcast receiver number [...] organic electronic devices. The specification by the formula 1 is represented by compound number [...] substrate. [Formula 1] In said formula 1, R1 To R7 Hereinafter and R2 represent same or different, are independently hydrogen; deuterium; for halogen; nitrile group; nitro; hydroxy; neel carbonate; ester; for imide; amide group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted fluoroalkyl group; a substituted or unsubstituted cycloalkyl; substituted or nonsubstituted substituted between the light-emitting; a substituted or unsubstituted silyl group; a substituted or unsubstituted to boron; substituted or unsubstituted phosphine [...]; substituted or a substituted or unsubstituted amine group; a substituted or unsubstituted [...]; substituted or nonsubstituted a substituted aryl group; or a substituted or non-substituted R and, R8 Fluorine; or a fluoroalkyl group and a substituted or unsubstituted, R8 Wherein at least one of the fluorine, R1 is integer number of 1 to 4, R2 is positive numbers of 1 to 5, R3 is integer number of 1 to 4, R4 is positive numbers of 1 to 2, R5 is integer number of 1 to 2, R6 is positive numbers of 1 to 4, R7 is integer number of 1 to 5, R8 is positive numbers of 1 to 5, R1 is 2 or more, a plurality of R1 Hereinafter or and on each other, R2 is 2 or more, a plurality of R2 Hereinafter or which on each other, R3 is 2 or more, a plurality of R3 Hereinafter or and on each other, R4 is 2 or more, a plurality of R4 On which aids to hereinafter, R5 is 2 or more, a plurality of R5 Hereinafter or and on each other, R6 is 2 or more, a plurality of R6 Hereinafter or which on each other, R7 is 2 or more, a plurality of R7 Hereinafter or and on each other, R8 is 2 or more, a plurality of R8 As each other or different hereinafter disclosed. In addition, the specification includes a number 1 electrode; said number 1 number 2 opposite electrode having electrode; and said number 1 electrode with said number 2 electrode 1 as organic electronic devices including at least one layer of a solvent, said organic layer including an organic electronic device is at least one layer 1 these compounds a number [...] substrate. The specification according to one embodiment state organic light emitting electrical component including organic compounds are used, organic of the electrical component of barrier, and improving photo, compound thermal stability by heat can be pixel. Figure 1 shows a specification of an organic electronic device according to the invention embodiment state (10) timing a are disclosed. Figure 2 shows a specification of an organic electronic device according to the invention in another embodiment state (11) timing a are disclosed. Hereinafter, the specification more detailed as follows. The specification of the substituted example are described below but, limited to are not correct. In the specification, The connection portion positioned between the big. The term "substituted" that the compounds other hydrogen atom coupled carbon atoms substituted International dispersing medium, substituted hydrogen atom locations position i.e., substituted substituted if possible location does not define, when 2 or more substituted, 2 or more substituents may be the same or different each other. The specification that the term "substituted or unsubstituted" in deuterium; for halogen; nitrile group; nitro; hydroxy; neel carbonate; ester; for imide; amino group; alkoxy; alkyl; cycloalkyl; the light-emitting; silyl group; to boron; amine; phosphine [...]; aryl; and N, O, S, Se and Si atoms constituting the at least one selected from the group consisting 1 a 1 or 2 or more heterocyclic substituted with allyl including the steps of example 2 or more substituents substituted or substituted during said connected, or any substituted airway does not have a means other. In the specification, examples of halogen fluorine, chlorine, bromine, or iodine flow tides. In the specification, particularly but not limited to carbon number neel carbonate, preferably in 1 to 30 carbon atoms. Specifically to the compounds of the following structure such as but, limited to are not correct. In the specification, a process for carbon number particularly but not limited to, 1 to 30 carbon atoms preferably disclosed. Specifically, compounds represented by formula but, limited to are not correct. In the specification, particularly but not limited to carbon number of imide, 1 to 30 carbon atoms preferably disclosed. Specifically to the compounds of the following structure such as but, limited to are not correct. In the specification, the amide nitrogen of amide hydrogen, 1 to 30 carbon atoms of straight, branched or dendrimeric polymer backbone chain of 6 to 30 carbon atoms can be substituted with allyl phenyl or benzyl ring. Specifically, compounds represented by formula but, limited to are not correct. In the specification, and [...] straight or branched alkyl groups, particularly preferably 1 to 40 carbon but not limited in number. Specific examples include methyl, ethyl, propyl, n - propyl, isopropyl, butyl, n - butyl, isobutyl, tert - butyl, sec - butyl, 1 - methyl - butyl, 1 - ethyl - butyl, neopentyl, n - neopentyl, cyclopentyl isocyanate, neopentyl, tert - neopentyl, hexyl, n - hexyl, 1 - methyl neopentyl, cyclopentyl methyl 2 -, 4 - methyl - 2 - neopentyl, 3, 3 - dimethylbutyl, 2 - ethylbutyl, [...], n - [...], 1 - methyl hexyl, pen [thil methyl cycloalkyl, cyclo [heyk thread methyl, octyl, n - octyl, tert - octyl, 1 - methyl [...], 2 - ethylhexyl, 2 - propyl neopentyl, n - nonyl, 2, 2 - dimethyl [...], 1 - ethyl - propyl, 1, 1 - dimethyl - propyl, hexyl isocyanate, 2 - methyl neopentyl, cyclohexyl 4 - methyl, 5 - methyl hexyl is provided to be used, is not limited to. In the specification, particularly but not limited to cycloalkyl, preferably 3 carbon atoms to 6300 and, specifically cyclopropyl, cyclobutyl, cyclopentyl cycloalkyl, of sodium 3 - methyl, 2, 3 - dimethyl of sodium, cyclohexyl, methyl 3 - hour claw [heyk thread, methyl 4 - hour claw [heyk thread, 2, 3 - dimethyl hour claw [heyk thread, 3, 4, 5 - methyl hour claw [heyk thread tree, 4 a-tert - butyl hour claw [heyk thread, cyclo [...], cyclo-octyl is provided to be used, is not limited. In the specification, alkoxy and at least one linear, branched or ring [...] be. Alkoxy carbon number not limited specially but, preferably 1 to 20 carbon atoms in. Specifically, methoxy, ethoxy, n - propoxy, isopropoxy, i - propyl oxy, n - butoxy, isobutoxy, tert - butoxy, sec - butoxy, n - pen [thil jade city, neopentylglycol pen [thil jade city, ISO pen [thil jade city, Serial n -, 3, 3 - dimethyl butyl jade city, 2 - ethyl butyl jade city, n - jade [thil jade city, n - nonyloxy, n - it will be burnt oxy, benzyloxy, but it cuts the qualitative jade city like p - methyl, limited to are not correct. In the specification, and neel the [khey which it will know it crawls straight or branched [...], particularly but not limited to carbon number, preferably 2 to 40 in. Specific examples are vinyl, 1 - propenyl, pro-phenyl isocyanate, 1 - butenyl, 2 - butenyl, 3 - butenyl, 1 - [...], [...] 2 -, 3 - [...], 3 - methyl - 1 - butenyl, 1, 3 - buta to d neel, allyl, 1 - phenyl vinyl - 1 - yl, 2 - phenyl vinyl - 1 - yl, 2, 2 - diphenylvinyl - 1 - yl, 2 - phenyl - 2 - (naphthyl - 1 - yl) vinyl - 1 - yl, 2, 2 - bis (diphenyl - 1 - yl) vinyl - 1 - yl, steel hemp cloth neel, [su mote [ley neel is provided to be used is not limited to them. In the specification, and said Si atoms [...] Si and connected directly as radical substituted group, - SiR104 R105 R106 And represented, R104 To R106 Which are equal to each other or different from the hereinafter, are independently hydrogen; deuterium; for halogen; alkyl; the light-emitting; alkoxy; cycloalkyl; aryl; and new [...] comprising at least one of substituents disclosed. Specific examples thread reel [...] tree, tree [thil it will be recorded, the d methyl it will be recorded t - butyl, vinyl the d methyl it will be recorded, profile the d methyl it will be recorded, tree phenyl thread reel, the d phenyl it will be recorded, phenyl silyl group is provided to be used, the pieces are not correct. In the specification, the boron - BR100 R101 Can have a, said R100 , And R101 Assigns the same and or different hereinafter, are independently hydrogen; deuterium; halogen; nitrile group; or a substituted or unsubstituted cycloalkyl group of 3 to 30 only annularity [...] C12; 1 to 30 C12 of straight or branched chain substituted or unsubstituted alkyl group; or a substituted or unsubstituted aryl group of 6 to 30 only annularity [...] C12; and a substituted or unsubstituted hetero with allyl 2 to 30 selected from the group consisting of C12 or [...] only annularity can be. The specification only annularity in carbon number but not limited particularly if it is an allyl trianthracene, 6 to 30 carbon atoms preferably disclosed. Specifically only annularity aryl group include phenyl, non-phenyl, [...], but like quarter phenyl, limited to are not correct. It is an allyl carbon number but not limited particularly when said trianthracene electrically. 10 to 30 carbon atoms preferably disclosed. Specifically polycyclic aryl group include me [phu, [...], lung difficulty [thu reel, fine [ley neel, vinyl [ley neel, three neel cryo, but like the flue five [ley neel, limited to are not correct. In the specification, process for preparation thereof said neel five [ley it crawls can be substituted, can be adjacent substituents in combination forms a ring. Process for preparation thereof when said five [ley neel gigas substituted, , , , , , But like, limited to are not correct. In the specification, heterogeneous reactor N hetero aryl, O, S, Si and at least one of the hetero [...] Se 1 as including, but not limited to carbon number 2 to 50 carbon atoms particularly preferably disclosed. Examples for hetero [...] thiophene, furan to, a pyrrole, an imidazole, thiazole dozing,, oxa dozing,, to oxadiazole, triazole dozing,, [...] pyridazinone, gate [...], pyrimido [...], dust triazole, triazole dozing,, arc [...], multivibrator pyridazinone, pyrazole [...], [...], quinazoline to, the [khwi stipend neel it will live, it will keep phthalides, pyrido pyrimido [...], pyrido pyrazole [...], pyrazole roh [...] antagonist activity, ISO quinoline, indole to, cover dozing,, oxa dozing, benzimidazole, benzthiazole is already dozing,, benzo the mote oh dozing,, benzo cover dozing,, benzo [...], dibenzo [...], benzo [...], lung difficulty [ssu roll phosphorus (phenanthroline), thia [...], ISO the jade company it will become sleepy, oxadiazole [...], d oh it will become sleepy thiazole, benzo the mote oh it will become sleepy, and dibenzo [...] is provided to be used, these exclusively are not correct. In the specification, the amine amino group (- NH2 ) Hydrogen atoms substituted with at least one other substituent means 1 which is of amine, - NR107 R108 And represented, R107 And R108 Which are equal to each other or different from the hereinafter, are independently hydrogen; deuterium; for halogen; alkyl; the light-emitting; alkoxy; cycloalkyl; aryl; and new [...] comprising at least one of substituents disclosed (stage, R107 And R108 At least one of the hydrogen is endured). For example, - NH2 ; Mono [...]; d alkyl amine; N - alkyl [...]; mono [...]; reel amine diaryl; N - [...]; N - alkyl [...], mono [...] d hetero biting amine crossroad and can be selected from the group consisting, particularly but not limited to carbon number, preferably in 1 to 30. Specific examples hydroxybutyrolactone methyl amine, dimethyl hydroxybutyrolactone, ethyl hydroxybutyrolactone, d ethyl amine, phenyl hydroxybutyrolactone, naphthylamine to, non-phenyl amine, do not sprout three neel amine, 9 - methyl - do not sprout three neel amine, d phenyl amine, d [thol reel amine, N - phenyl [thol reel amine, phenyl amine tree, N - phenyl non-phenyl amine; N - phenyl me [phu amine; N - non-phenyl or [phu amine; N - [...]; N - phenyl [...]; N - non-phenyl lung difficulty [thu neel amine; N - phenyl [...]; N - phenyl [...]; N - [...]; N - non-phenyl [phul base five [ley neel amine is provided to be used, limited to are not correct. In the specification, phosphine oxide specifically d phenyl gun spin oxide, the resulting [phu gun spin oxide is provided to be used, the pieces are not correct. In the specification, examples substituted or nonsubstituted substituted mono amine it will be biting [...], diaryl reel amine substituted or unsubstituted, or a substituted or unsubstituted triazoles reel amine giga 2000. Only annularity [...][...] and during said aryl, polycyclic [...] be. 2 or more including only annularity [...] trianthracene said aryl, polycyclic aryl, polycyclic aryl group or only annularity group can be simultaneously. For example, the aryl of said aforementioned [...][...] example can be selected. Examples amine it will be biting specific amine, naphthylamine, biphenyl amine, do not sprout three neel amines, amine - 3 - methyl, 4 - methyl - naphthylamine, 2 - methyl - biphenyl amine, 9 - methyl - do not sprout three neel amines, diphenyl amine, phenyl naphthyl amine, amine [...], tolyl phenyl amine, carbazole and triphenyl amine is provided to be used, limited to are not correct. In the specification, a substituted or unsubstituted heterocyclic amine it will be biting mono [...] examples, a d hetero amine it will be biting a substituted or unsubstituted, or a substituted or unsubstituted hetero biting amine giga tree 2000. Said heteroaryl group including 2 or more hetero trianthracene hetero [...] only annularity, polycyclic heteroaryl group, heterocyclic group or polycyclic heteroaryl group only annularity can be simultaneously. For example, said hetero aryl can be selected from a variety of the aforementioned hetero [...] example during [...]. In the specification, it will be a multi annularity or aromatic ring which only annularity, and can be selected from a number 1 of the plug not [...][...] said example. The specification is represented by said formula 1 compound number [...] substrate. The specification of embodiment in the condition, R1 To R7 Hydrogen; deuterium; C12 alkyl substituted or unsubstituted 1 to 30; C12 6 60 to a substituted or unsubstituted aryl; substituted or unsubstituted silyl group; or a substituted or unsubstituted heterocyclic inhibitors of [...] be C12 2 to 60. Another one embodiment in the condition, R1 To R7 Hydrogen; a substituted or unsubstituted alkyl 1 to 10 C12; C12 6 to 30 substituted or unsubstituted aryl; substituted or unsubstituted silyl group; or a substituted or unsubstituted heterocyclic inhibitors of C12 [...] be 2 to 30. Another one embodiment in the condition, R1 To R7 Hydrogen; alkyl of 1 to 10 carbon atoms; 1 to 10 carbon atoms or a substituted or unsubstituted [...] be a C20 alkyl. Another one embodiment in the condition, R1 To R7 Hydrogen; methyl; t - view [thil; be or tri methyl thread reel fixed date. The specification of embodiment in the condition, R3 To R5 Is hydrogen are disclosed. The specification of embodiment in the condition, R1 , R2 , R6 And R7 Hydrogen; alkyl of 1 to 10 carbon atoms; 1 to 10 carbon atoms or a substituted or unsubstituted [...] be a C20 alkyl. Another one embodiment in the condition, R1 , R2 , R6 And R7 Hydrogen; methyl; t - view [thil; be or tri methyl thread reel fixed date. The specification of embodiment in the condition, R8 Fluorine; be a fluoroalkyl group or a substituted or unsubstituted. Another one embodiment in the condition, said R8 Fluorine; or a substituted or unsubstituted alkyl C12 implementation being 1 to 10. Another one embodiment in the condition, said R8 Fluorine; 1 to 10 carbon atoms can be alkyl. Another one embodiment in the condition, said R8 Fluorine; can be H or methyl. The specification of embodiment in the condition, said R8 Characterized including the at least one fluorine. The specification of embodiment in the condition, characterized by having said formula 1 is a substituent. Electron-emitting wavelength as the wavelength moves said substituents properties, organic light-emitting blue with a dopant element senses a same high safety device can be achieved. In addition, a process is provided and the other substituents with ether coupling includes a fluorophenyl (Fluorophenyl) said included and enlarging the distance between the rotatable combination a stripe by hydrogen bonding between effective film agglomeration of dopant are disclosed. And the light emitting efficiency with high chromatic purity and the can. The specification of embodiment in the condition, represented by said formula 1 can be represented by formula 2. [Formula 2] In said formula 2, R1 To R8 , And r1 r8 to are the same as defined in said formula 1 for definition. The specification according to one embodiment state, the r8 1 are disclosed. The specification according to one embodiment state, the r8 2 are disclosed. The specification according to one embodiment state, the 3 r8 are disclosed. The specification according to one embodiment state, the 4 r8 are disclosed. The specification according to one embodiment state, the 5 r8 are disclosed. The specification according to one embodiment state, selected from among the compounds of said formula 1 have the following structure in either be a. The method according to one embodiment state number specification number to carry compounds are 1308. bath tank. To carry attainments are representative example described in number but, if necessary, can be substituent number add the outside it will do, substituents can be applied. In addition, based on techniques known to the art, starting material, reagent, reaction conditions and the like can be changing. In said number tank method, R3 To R5 , R8 , And said formula 1 are the same as defined in the definition of the r8 r3 to r5. In said number tank method, R R of the formula 11 And R6 Useful as the definition of R ' R of the formula 12 And R7 The definition of such as disclosed. In said number tank method, X and X ' F halogen element, Cl, Br, I handler, not limited. In addition, the specification of the aforementioned organic electronic element including said compound of said formula 1 is number [...] substrate. The specification of embodiment in the condition, number 1 electrode; said number 1 number 2 opposite electrode having electrode; and said number 1 electrode with said number 2 electrode 1 as organic electronic devices including at least one layer of a solvent, said organic layer including organic electronic element number 1 layer or more of the compounds of said formula 1 is [...] substrate. The specification that the "on" position when any member other members, as well as any other elements member between the two members when joined to another member to if there is a comprises a unit. The specification that the "comprising" when any portion in any configuration elements, particularly the opposite substrate [...] number but without other components further can include other components which means that the other. The specification organic monolayer structure of organic electronic devices may also be used but, 2 at least one layer of organic layer can be laminated multi-layer structure. For example, an organic electronic device of the representative embodiment of the present invention, acts as an organic hole injection layer, hole transport layer, light emitting layer, metal-containing fullerene, like including structure with an may have. However organic electronic devices without limited to the structure of the less number of can be an organic material. The specification according to one embodiment state, said organic light emitting organic electronic devices, organic phosphorescent devices, organic solar cells, organic photoconductor (OPC) and organic transistor can be selected from the group consisting. For example hereinafter in organic light-emitting device 2000. The specification of embodiment in the condition, said organic compound layer is formed and a light emitting layer, said light-emitting layer comprising a compound of said formula 1. The specification of embodiment in the condition, said organic compound layer is formed and a light emitting layer, said light-emitting layer includes a dopant material, said dopant material is comprises compounds of said formula 1. 1% by weight to 15% by weight of said dopant includes a semiconductor light emitting layer substance, preferably 1% by weight to 10% by weight, more preferably 1% by weight to 5% by weight having a predetermined wavelength. The specification of embodiment in the condition, said organic compound layer is formed and a light emitting layer, said light-emitting layer includes host materials, comprising the following formula X to said host material. [Formula X] The specification of embodiment in the condition, said Ar1 And Ar2 Is hydrogen; deuterium; a substituted or unsubstituted fluoroalkyl group; substituted or nonsubstituted a substituted aryl group; substituted or unsubstituted [...] be heteroatoms. Another one embodiment in the condition, said Ar1 And Ar2 Is hydrogen; a substituted or unsubstituted alkyl C12 1 to 20; C12 6 60 to a substituted or unsubstituted aryl; a substituted or unsubstituted heterocyclic inhibitors of [...] be C12 2 to 60. Another one embodiment in the condition, said Ar1 And Ar2 With allyl substituted or nonsubstituted is a substituted aryl group; or a substituted or unsubstituted hetero aryl group or heteroaryl with allyl [...] be. Another one embodiment in the condition, said Ar1 And Ar2 6 to 60 carbons of C12 to 60 6 with allyl substituted or unsubstituted aryl; a carbon number of 6 to 60 with allyl oh with reel biting fixed date be substituted or unsubstituted. The specification of embodiment in the condition, said Ar1 And Ar2 Is phenyl; phenyl-; [...]; me [phu; [...]; or can be lung difficulty [thu neel fixed date, phenyl; phenyl-; [...]; me [phu; [...]; or lung difficulty [thu neel crossroad can be substituted or unsubstituted. The specification of embodiment in the condition, said organic compound layer is formed hole injection or a chemical formula and, said hole injection layer or hole transporting layers comprise [...] compounds of said formula 1. The specification of embodiment in the condition, said organic compound layer is formed comprising a metal-containing fullerene or injecting layer, said metal-containing fullerene or [...] comprises compounds of said formula 1. The specification of embodiment in the condition, said organic compound layer is formed comprising electronic interception layer, said compounds of said formula 1 comprises electronic [...]. The specification of embodiment in the condition, said first and second hole injection layer, the hole transport layer. Light-emitting layer, metal-containing fullerene, with an, hole blocking layer or more layers selected from the group consisting 1 2 and electronic blocking results are. The specification of embodiment in the condition, said first and second number 1 electrode; said number 1 number 2 electrode having opposite electrode; said number 1 and light emitting diode and said number 2 light-emitting layer; said light emitting layer between said number 1, 2 at least one layer of organic layers with said number 2 electrode or said light emitting layer, said 2 at least one layer of organic layer comprises at least one of the compounds of said formula 1. The specification of embodiment in the condition, said 2 at least one layer of organic compound layer is formed containing fullerene, with an, electron transport and electron injection from the center of the layer and hole blocking group 2 or more can be selected. The specification of embodiment in the condition, said organic compound layer is formed and more electronic transporting bed 2 layer, at least one of the compounds of said formula 1 comprises alkali metal-containing fullerene at least one layer of said 2. Specifically the specification one embodiment in the condition, said formula 1 may be compounds of the alkali metal-containing fullerene at least one layer of said 2 during 1 layer that is, each 2 at least one layer of reductive dopant can be included. In addition, the specification of embodiment in the condition, said reductive dopant if each 2 at least one layer of said compound, said compound number [...] differing materials can be the same or different each other. The specification of embodiment in the condition, said organic compound layer is formed in addition including organic compounds of said formula 1 amino it will be biting, cover [...] including hole injection or a chemical formula further comprises including compound or a car it will become sleepy and it will raise. Another embodiment in the condition, organic light-emitting device on the substrate anode, 1 at least one layer of organic layer cathodes (normal type) organic light-emitting element be a stacked structure. When electronic [...] organic layer including a compound of said formula 1, said alkyl group further includes n-type dopant can be. Said n-type dopant can be pulled using the known [...] those, such as metals or metal complexes can be. According to one example said formula 1 compound including alkyl group further comprises LiQ can be. Another embodiment in the condition, organic light-emitting device on the substrate cathode, 1 at least one layer of an organic layer and an anode (inverted type) organic light-emitting element can be sequentially reverse structure. For example, the specification also 1 and 2 such as shown in the structure of the organic light emitting device of structure but there is also a textile fabric are not correct. 1 also substrate (20) number 1 on electrode (30), a light emitting layer (40) and number 2 electrode (50) sequentially stacked organic light emitting device (10) structure is exemplified in the nanometer range. Said Figure 1 the specification according to one embodiment state organic light-emitting an exemplary structure and, other organic layer contains hollow beads can. Substrate also 2 (20) number 1 on electrode (30), hole injection (60), hole (70), electronic blocking (80), a light emitting layer (40), alkali metal-containing fullerene (90), with an (100) and number 2 electrode (50) sequentially stacked organic light emitting structure of example in the nanometer range. Said Figure 2 the specification state according to an exemplary embodiment of structure and, other organic layer contains hollow beads can. The organic layer 1 compounds of oxidation layer the specification specification an organic light emitting device, including a sugar compound of said formula 1 i.e. number and the number known material technical field [...] 1308. bath method. Said case including a plurality of organic solvent, said organic compound layer is formed can be made of the same material or other. The organic layer 1 specification an organic light emitting device oxidation layer said compound, i.e. a number represented by said formula 1 compounds including [...] sugar and known material number bath 1308. the method technical field. For example, the specification of organic light-emitting device on the substrate electrode number 1, number 2 and number can be the whole electrode layer by depositing high pressure liquid coolant. At this time sputtering method (sputtering) or PVD (physical Vapor Deposition) using a method such as electron beam evaporation (e-a beam evaporation), or conductive metal oxides or alloys thereof anodes deposited metal film on the substrate is formed, on the hole injection layer, hole transport layer, layer is formed on the organic light-emitting layer and electron transport layer including, negative electrode into thereon by depositing a material which can be number bath 1308. In addition such method, organic layer from the anode material on a substrate, an anode material can be organic light emitting pattern on the substrate. In addition, the compounds of the formula 1 number of organic light-emitting morning fair preferably as well as of the whole structure can be formed by solution coating technique. Wherein, solution coating technique the circular spin coating, dip coating, doctor steam turbines, inkjet printing, screen printing, spraying, roll coating will but, only and not limited to these. In addition such method, organic layer from the anode material on a substrate, an anode material deposited organic light-emitting element may also be disclosed (station number patent application disclosure number 2003/012890 call). But, this method number and not the limited to tank. The specification of embodiment in the condition, and said number 1 electrode is an anode, anode are said number 2 are disclosed. Another embodiment in the condition, said number 1 and anode are, anode electrode is said number 2 are disclosed. Said positive electrode material based on organic hole injection layer to a group including the optical cable preferably smooth. The anode material used in the present invention specific examples vanadium, chromium, copper, zinc, flexible or alloys thereof; zinc oxide, indium oxide, indium tin oxide (ITO), indium zinc oxide (IZO) such as metal oxide; ZnO: Al or SnO2 : Combination of metal oxide such as Sb; poly (3 - methyl thiophene), poly [3, 4 - (ethylene - 1, 2 - dioxy) thiophene] (PEDOT), polyaniline conductive polymer such as polypyrrole and is provided to be used, these exclusively are not correct. The whole structure of the optical cable to said anode material for electronic injection hereinafter the workfunction of a preferably small material. Anode material specific examples include magnesium, calcium, sodium, potassium, titanium, indium, yttrium, lithium, gadolinium, aluminum, is, a metal such as tin and zinc or an alloy thereof; or LiF/Al LiO2 /Al multilayer structure material is provided to be used such as, and not limited to only these. The latter [...] said hole injecting electrode, hole injection hole transporting ability to anodes holes in title injector effect, light emitting layer or a light emitting material having excellent hole injection effect, generated in a light emitting layer with an electron injection material or to prevent movement of the excitons release, in addition, a compound preferably thin film forming capability. HOMO (highest occupied molecular orbital) of positive-electrode material in between the peripheral hole of a filler material is preferably al HOMO [...]. Specific examples include metal porphyrin (porphyrin) hole injection material, thiophene oligomer, arylamine-based organic, organic-based process the nitrile [heyk it buys oh character tree phenyl [leyn, quinacridone (quinacridone) based organic, organic-perylene (perylene), polyaniline and polythiophene-based conductive polymer is provided to be used and anthraquinone, these exclusively are not correct. From hole to hole to receive said light-emitting layer hole transport [...] hole injection layer, hole transport title either as an anode or hole injection layer receives from hole transporting light emitting layer stores material converted into large hole on an suitable material. Specific examples arylamine-based organic, conductive polymer, and conjugated portion portion is provided to be used for the polymerization of the block copolymer are shown, these exclusively are not correct. Said light-emitting layer is connected with an electronic [...] hole injection from are injected past of prolonging the life and efficiency by preventing layer and improve, if necessary publicly known for forming bit lines are produced with the aid of suitable electronic [...] can be between light emitting layer. Title and the electrons from said organic layer organic light emitting materials that emit light of visible region by combining each transport receives as a material which can be, for good quantum efficiency preferably fluorescent or phosphorescent material. Specific examples 8 - hydroxy quinoline - aluminum complex (Alq3 ); Carbazole compounds; dimerization (dimerized styryl) styryl compounds; BAlq; 10 - hydroxy benzo quinoline - metal compound; benzoxazole, benzthiazole and benzimidazole-based compound; poly (p - phenylene vinylene) (PPV) blended with polymer; spiro (spiro) compound; polyfluorenes, base [pu is provided to be used, these exclusively are not correct. Said light-emitting layer host material and dopants can be material. Host material etc. condensation aromatic cyclic derivative or heterocyclic-containing compound. Specifically condensation aromatic cyclic derivatives include anthracene derivatives, pyrene derivatives, naphthalene derivatives, pentacene derivatives, phenanthrene compound, fluoranthene compound at sea, heterocyclic containing compounds include compounds, dibenzo furan derivatives, ladder furan compounds, pyrimidine derivatives is provided to be used, is not limited. Said dopant materials include aromatic amine derivatives, [su reel amine compounds, boron complex, fluoranthene compound, metal complex etc.. Specifically aromatic amine derivatives include substituted or unsubstituted having a condensation aromatic cyclic derivatives as the biting amino it will raise, the biting amino it will raise with pyrene, anthracene, cleaning compound, such as peripheral [...] which, styryl amine compounds include substituted or nonsubstituted substituted in biting amine has been substituted compound of at least 1 biting vinyl giga, aryl group, silyl group, alkyl, 1 or 2 substituents at the at least one selected from the group consisting of cycloalkyl and biting amino crossroad is substituted with substituted or nonsubstituted. Specifically styryl amine, styryl diamine, styryl tree amine, styryl tetra amine is provided to be used, is not limited. In addition, metal complexes the iridium complexes, platinum complex is provided to be used, is not limited. Said alkyl group receives electrons from the light-emitting layer with an electron transport layer receives electrons from the cathode to transporting electrons title as consisting of a material which can be moving a good injection, greater mobility for electrons suitable material. Specific examples of 8 - hydroxyquinoline Al complexes; Alq3 Including complex; organic radical compound; hydroxy Petioles - metal complex is provided to be used, these exclusively are not correct. As used electron transport layer according to a conventional technique can be use with any desired materials. In particular, examples of suitable cathode material is formed on the aluminum layer or sliver layer with conventional material that followed. Specifically cesium, barium, calcium, ytterbium and samarium and, in each case aluminum layer or sliver layer 369. Said electronic [...] electrode electrons from the latter, and capable of transporting electrons, cathode electron injector effect, light emitting layer or a light emitting material has excellent injector effect, preventing to hole injection layer produced generated in a light emitting layer, in addition, a compound preferably thin film forming capability. Specifically fluorenone, do not sprout the [khwi roh die methane, die lung roh [khwi rice field, profound pyrans, oxazole, oxadiazole, triazole, imidazole, vinyl [leyn the tetra car luck thread it buys, five [ley neel it was burnt pregabalin methane, magnetron inside [thu like their derivatives, metal complex compound and nitrogenous 5 membered ring derivatives is provided to be used, is not limited. Said metal complex compound as 8 - hydroxy [...] lithium, bis (8 - hydroxy [...]) zinc, bis (8 - hydroxy [...]) copper, bis (8 - hydroxy [...]) manganese, tris (8 - hydroxy [...]) aluminum, tris (2 - methyl - 8 - hydroxy [...]) aluminum, tris (8 - hydroxy [...]) gallium, bis (10 - hydroxy benzo [...]) beryllium, bis (10 - hydroxy benzo [...]) zinc, bis (2 - methyl - 8 - [...]) gallium chloro, bis (2 - methyl - 8 - [...]) gallium (o - cresol toe), bis (2 - methyl - 8 - [...]) (1 - naphthol toe) aluminum, bis (2 - methyl - 8 - [...]) (2 - naphthol toe) gallium is provided to be used, is not limited. Said stopping layer electron and hole [...] cathode arrival, generally hole with implantation layer can be formed otherwise identical conditions. Specifically oxadiazole derivatives or triazole derivatives, phenanthroline derivatives, BCP, aluminum complex (aluminum complex) is provided to be used, is not limited. The specification according to materials used in the first and second formed at each-emitting, backlit or be a two-sided light emitting type. The specification of embodiment in the condition, said formula 1 compound in addition organic solar cells can be included in the organic or organic transistor. The specification according to compounds are organic phosphorescent devices, organic solar cells, organic photoreceptor, including organic electronic devices such as organic light emitting organic transistor even acting principle can be applied to change. Hereinafter, the specification specifically account for example in the embodiment detailed the on-sensors other. However, the shape can be a variety of different specification according to in the embodiment are, in the embodiment discussed below are limited to the range of the specification does not interpreted. The specification with average knowledge in the embodiment of art are to the specification to more fully describe which ball number are disclosed. [In the embodiment] <Synthesis example 1> 1) synthesis of compounds 1 a-a [Compound 1 a-a] Nitrogen atmosphere triethylamine (Triethylamine) 500 ml round bottom cap to ball 20. 7 ml to 120 ml acetonitrile (Acetonitrile) mixing the reflux stirring-gate. Pentafluorophenol herein (Pentafluorophenol) (5. 00g, 27. 2mmol), p - fluoro nitrobenzene (p a-fluoronitrobenzene) (4. 02g, 28. 5mmol) entire solution dropwise to 240 ml of acetonitrile (Acetonitrile) was kiln 1 over time. After that initial setup time-gate 13 contain reflux conditions. Then, after solvent temperature is decreased down to the normal temperature is concentrated at a reduced pressure, column chromatography on silica gel the remainder through chemical 1 a-a (7. 63g, yield: 92%) number was a high pressure liquid coolant. MS [M + H]+ =306 2) synthesis of compounds 1 a-b [Compound 1 a-b] 500 ml round bottom cap to compound 1 a-a (7. 40g, 24. 2mmol), iron (Iron) (6. 77g, 121. 2 mmmol), aluminum chloride (ammonium chloride) (2. 59g, 48. 5mmol) a THF 120 ml, EtOH 120 ml, H2O 40 ml same reflux conditions-gate cutting with agitation. 2 hours after 2000 light (celite) is divided into two temperature 80 °C filter, washing of a filter cake to 50 °C was 150 ml methanol. Organic solvent in vacuum interposed between the frame number after a stand-alone, saturated NaHCO 3 aqueous solution until pH 8 with respect to the neutralizing. 3 times 100 ml ethyl acetate (ethyl acetate) to same (brine) to extract over knife of wash me. Magnesium sulfate anhydride which can be organic solution thus obtained after filtering a cream or said compound 1 a-b (6. 34g, yield: 95%) number was a high pressure liquid coolant. MS [M + H]+ =276 3) synthesis of compounds 1 a-c [Compound 1 a-c] Nitrogen atmosphere 500 ml round bottom cap to compound 1 a-b (6. 00g, 21. 8mmol), bromobenzene (Bromobenzene) (3. 42g, 21. 8mmol), tris (d it cuts it is a quality and the acetone which is burnt) [...] (0) (Tris (dibenzylideneacetone) dipalladium (0)) (0. 30g, 0. 3mmol), 2, 2 '- bis ([...]) - 1, 1' - bi-naphthalene (2, 2 '- Bis (diphenylphosphino) - 1, 1' - binaphthalene) (0. 41g, 0. 7mmol) and sodium (sodium tert-a butoxide) [...] t - (2. 51g, 26. 2mmol) after melting is toluene 180 ml, reflux conditions stirring time-gate 8. The end point of the reaction at ambient temperature after cooling, and dichloro methane and water pressure are extracted using toluene in a stand-alone number which can be silica gel after the solvent was vacuum distilling a crude magnesium sulfate anhydride. Then, dichloro methane and hexane (n a-hexane) to give compound 1 a-c using recrystallization and filter (6. 51 g, yield: 85%) number was a high pressure liquid coolant. MS [M + H]+ =352 4) synthesis of compound 1 [Compound 1] 500 ml round bottom cap to ball with d [pu fur [leyn 1, 6 - (1, 6 a-Dibromopyrene) (3. 10g, 8. 6mmol), compound 1 a-c (6. 35g, 18. 1mmol), sodium (sodium tert-a butoxide) [...] t - (1. 99g, 20. 7mmol) placed in a 200 ml of xylene (xylene) with agitation and heating reflux conditions have been. Return conditions herein a bis (tree - t - [...]) palladium (0) (palladium (0) bis (tri-a tertbutylphosphine)) (0. 04 g, 0. 1mmol) dropwise 20 ml xylene (xylene) 30 minutes stirring for 1 to 8 that are incorporated into a time chains. After cooling the end point of the reaction, ethyl acetate (ethyl acetate) and xylene (xylene) number after recrystallization using a stand-alone, compounds 1 through sublimation positive number (3. 0g, yield 39%) number was a high pressure liquid coolant. MS [M + H]+ =902 <Synthesis example 2> 1) synthesis of compound 2 a-a [Compound 2 a-a] Nitrogen atmosphere 250 ml 3 - fluoro phenol bottom cap to ball round (3 a-fluorophenol) (5. 00g, 44. 6mmol), 1 - fluoro - 2 - nitrobenzene (1 a-fluoro-a 2 non-nitrobenzene) (5. 34g, 46. 8mmol), cesium carbonate (cesium carbonate) (15. 26g, 46. 8mmol) DMF 150 ml 1 in a time-gate 110 °C stirring for 1 to 3. After this, lowers the temperature down to the normal temperature using ethyl acetate (ethyl acetate) (brine) to extract the knife of H2O to wash me. Magnesium sulfate anhydride which can be organic solution thus obtained after filtering a cream or said compound 2 a-a (9. 36g, yield: 90%) number was a high pressure liquid coolant. MS [M + H]+ =234 2) synthesis of compound 2 a-b [Compound 2 a-b] 1L 2 provided a rounded bottom cap to compound (9. 00g, 38. 6mmol), iron (Iron) (10. 78g, 193. 0 mmmol), ammonium chloride (ammonium chloride) (4. 13g, 77. 2mmol) a THF 180 ml, EtOH 180 ml, H2O 60 ml same reflux conditions-gate cutting with agitation. 2 hours after 2000 light (celite) is divided into two temperature 80 °C filter, washing of a filter cake was 50 °C to 200 ml methanol. Organic solvent in vacuum interposed between the frame number after a stand-alone, saturated NaHCO 3 aqueous solution until pH 8 with respect to the neutralizing. 3 times 150 ml ethyl acetate (ethyl acetate) to same knife of wash (brine) to extract over me. Magnesium sulfate anhydride which can be organic solution thus obtained after filtering a cream or said compound 2 a-b (7. 29g, yield: 93%) number was a high pressure liquid coolant. MS [M + H]+ =204 3) synthesis of compound 2 a-c [Compound 2 a-c] Nitrogen atmosphere 500 ml round bottom cap to compound 2 a-b (7. 00g, 34. 4mmol), bromobenzene (Bromobenzene) (5. 41g, 34. 4mmol), tris (d it cuts it is a quality and the acetone which is burnt) [...] (0) (Tris (dibenzylideneacetone) dipalladium (0)) (0. 47g, 0. 5mmol), 2, 2 '- bis ([...]) - 1, 1' - bi-naphthalene (2, 2 '- Bis (diphenylphosphino) - 1, 1' - binaphthalene) (0. 64g, 1. 0mmol) and sodium (sodium tert-a butoxide) [...] t - (3. 97g, 41. 3mmol) after melting is toluene 250 ml, reflux conditions stirring time-gate 8. The end point of the reaction at ambient temperature after cooling, and dichloro methane and water pressure are extracted using toluene in a stand-alone number which can be silica gel after the solvent was vacuum distilling a crude magnesium sulfate anhydride. Then, dichloro methane and hexane (n-a hexane) pt and filter using the compounds 2 a-c (8. 37 g, yield: 87%) number was a high pressure liquid coolant. MS [M + H] +=280 4) synthesis of compound 2 [Compound 2] 500 ml round bottom cap to ball with d [pu fur [leyn 1, 6 - (1, 6 a-Dibromopyrene) (5. 00g, 13. 9mmol), compounds 2 a-c (8. 15g, 29. 2mmol), sodium t - [...] (sodium tert-a butoxide) (3. 20g, 33. 3mmol) placed in a 300 ml of xylene (xylene) with agitation and heating reflux conditions have been. Return conditions herein a bis (tree - t - [...]) palladium (0) (palladium (0) bis (tri-a tertbutylphosphine)) (0. 07 g, 0. 1mmol) 30 ml xylene (xylene) 30 minutes stirring for 1 to the base of a dropwise incorporated into 8 time chains. After cooling the end point of the reaction, ethyl acetate (ethyl acetate) and xylene (xylene) number after recrystallization using a stand-alone, positive number sublimation through compound 2 (3. 8g, yield 36%) number was a high pressure liquid coolant. MS [M + H]+ =758 <Synthesis example 3> 1) synthesis of compound 3 a-a [Compound 3 a-a] 2, 4, 6 - trifluoro nitrogen atmosphere 250 ml round bottom cap to ball phenol (2, 4, 6 a-trifluorophenol) (4. 00g, 27. 0mmol), 1 - fluoro - 3 - nitrobenzene (1 a-fluoro-a 3 a-nitrobenzene) (4. 00g, 28. 4mmol), cesium carbonate (cesium carbonate) (9. 24g, 28. 4mmol) DMF 120 ml for 1 to 1 in a time-gate 110 °C stirring. After this, lowers the temperature down to the normal temperature using ethyl acetate (ethyl acetate) (brine) to extract the knife of H2O to wash me. Magnesium sulfate anhydride which can be organic solution thus obtained after filtering a cream or said compound 3 a-a (6. 18g, yield: 85%) number was a high pressure liquid coolant. MS [M + H]+ =270 2) synthesis of compound 3 a-b [Compound 3 a-b] 500 ml round bottom cap to compound 3 a-a (6. 00g, 22. 3mmol), iron (Iron) (6. 22g, 111. 4 mmmol), ammonium chloride (ammonium chloride) (2. 38g, 44. 6mmol) THF 110 ml a, EtOH 110 ml, H2O 38 ml same reflux conditions-gate cutting with agitation. 3 hours after 2000 light (celite) is divided into two temperature 80 °C filter, washing of a filter cake to 50 °C was 150 ml methanol. Organic solvent in vacuum interposed between the frame number after a stand-alone, saturated NaHCO 3 aqueous solution until pH 8 with respect to the neutralizing. 3 times 100 ml ethyl acetate (ethyl acetate) to same (brine) to extract over knife of wash me. Magnesium sulfate anhydride which can be organic solution thus obtained after filtering a cream or said compound 3 a-b (5. 01g, yield: 94%) number was a high pressure liquid coolant. MS [M + H]+ =240 3) synthesis of compound 3 a-c [Compound 3 a-c] Nitrogen atmosphere 500 ml round bottom cap to compound 3 a-b (5. 00g, 20. 9mmol), 1 - bromo - 4 - (t - [...]) benzene (1 a-bromo-a 4 - (tert-a butyl) benzene) (4. 45g, 20. 9mmol), tris (d it cuts it is a quality and the acetone which is burnt) [...] (0) (Tris (dibenzylideneacetone) dipalladium (0)) (0. 29g, 0. 3mmol), 2, 2 '- bis ([...]) - 1, 1' - bi-naphthalene (2, 2 '- Bis (diphenylphosphino) - 1, 1' - binaphthalene) (0. 39g, 0. 6mmol) and sodium (sodium tert-a butoxide) [...] t - (2. 41g, 25. 1mmol) after melting is toluene 180 ml, reflux conditions stirring time-gate 6. The end point of the reaction at ambient temperature after cooling, and dichloro methane and water pressure are extracted using toluene in a stand-alone number which can be silica gel after the solvent was vacuum distilling a crude magnesium sulfate anhydride. Then, dichloro methane and hexane (n a-hexane) to give compound 3 a-c using recrystallization and filter (6. 52 g, yield: 84%) number was a high pressure liquid coolant. MS [M + H]+ =372 4) synthesis of compound 3 [Compound 3] 500 ml round bottom cap to ball with d [pu fur [leyn 1, 6 - (1, 6 a-Dibromopyrene) (3. 00g, 8. 3mmol), compound 3 a-c (6. 50g, 17. 5mmol), sodium (sodium tert-a butoxide) [...] t - (1. 92g, 20. 0mmol) placed in a 200 ml of xylene (xylene) with agitation and heating reflux conditions have been. Return conditions herein a bis (tree - t - [...]) palladium (0) (palladium (0) bis (tri-a tertbutylphosphine)) (0. 04 g, 0. 1mmol) dropwise a 20 ml xylene (xylene) 30 minutes stirring for 1 to 10 time that are incorporated into chains. After cooling the end point of the reaction, ethyl acetate (ethyl acetate) and xylene (xylene) number after recrystallization using a stand-alone, positive number sublimation through compound 3 (3. 3g, yield: 42%) number was a high pressure liquid coolant. MS [M + H]+ =942 <In the embodiment 1> Glass substrate coated with a thin film coating has a thickness of 1,400 Å ITO (Indium Tin Oxide) is executed to his cleaning which melts a number cells in distilled water. At this time, cells include Fischer yarn number (Fischer Co.) O2 article number, number 2 (Filter) mixed with distilled water (Millipore Co.) include Miller gun [e company to exhaust as well as a filter article in distilled water. A 30 minutes 10 minutes after washing the reservoir 2 to ultrasonic ITO periodical repetition of abortion. After the end of the cleaning distilled water, isopropyl alcohol, acetone, and dried by washing after been conveyed to plasma cleaner for an ultrasonic number of methanol. In addition, oxygen plasma into said 5 minutes after cleaning the substrate using vacuum deposition with respect to the brush. The ITO transparent electrode over prepared to process each 650 Å oh character tree phenyl [leyn [HI provided A] nitrile and hexafluoropropylene (hexaazatriphenylene; HAT), percent hole-injecting layer has a thickness of 50 Å by thermal vacuum deposition sequentially. [HI provided A] Hole thereon is selectively a 600 Å after vacuum deposition thickness [HT provided A] electronic obstruction layer has a thickness of 50 Å is selectively [HT provided B] was a thermal vacuum deposition. [HT provided A] [HT provided B] Then consisting of 4 wt % dopant [compound 1] to a thickness of 200 Å on a host [BH-a A] was vacuum deposition. [Compound 1] [BH-a A] Then, electron transport layer and electron injection layer has a thickness of 360 Å [compound 2 - 1] to a 1:1 ratio of a thickness of 5 Å thermal vacuum deposition followed was vacuum deposition. [ET provided A] A thickness of said sequentially on a magnesium silver ratio of 10:1 with an 220 Å, 1000 Å formed aluminum cathode evaporation method, high pressure liquid coolant organic light emitting his number. <In the embodiment 2> In said in the embodiment 1, the number 1 in the embodiment 1 and a dopant material in the range of 0.1 [...] compounds instead of compound 2 the same organic light-emitting element method number was high pressure liquid coolant. <In the embodiment 3> In said in the embodiment 1, the number 1 in the range of 0.1 in the embodiment 1 and a dopant material compounds instead of compound 3 [...] organic light-emitting element number was the same method high pressure liquid coolant. <Comparison example 1> In said in the embodiment 1, a number in the range of 0.1 and 1 BD provided A dopant material compounds instead the same method in the embodiment 1 [...] organic light-emitting element number was high pressure liquid coolant. <Comparison example 2> In said in the embodiment 1, a number in the range of 0.1 and 1 dopant material compounds instead of the same method in the embodiment 1 BD provided B [...] the organic light-emitting element number was high pressure liquid coolant. The blue light emission number it became work 10 mA/cm2 When the current density of 1 shown applied to measure the performance of semiconductor decreases. [Compound 2] [compound 3] [BD provided A] [BD provided B] [Formula 1] of the present invention can be found in table 1 as said compound when used as dopant in the emissive layer of organic light-emitting high chromatic purity and significant rise in the succinic acid were able to confirm that the effect. 10, 11: organic light emitting device 20: substrate 30: number 1 electrode 40: light emitting layer 50: number 2 electrode 60: hole injection layer 70: hole 80: electronic blocking 90: alkali metal-containing fullerene 100: with an An embodiment of the present invention relates to a compound represented by a chemical formula 1 and an organic electronic device including the same. In the chemical formula 1, R1 to R7 are the same as or different from and are individually and independently hydrogen; heavy hydrogen; a halogen group; a nitrile group; a nitro group; a hydroxy group; a carbonyl group; an ester group; an imide; an amide group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted alkenyl group; a substituted or unsubstituted silyl group; a substituted or unsubstituted boron group; a substituted or unsubstituted phosphine oxide group; a substituted or unsubstituted amine group; a substituted or unsubstituted arylamine group; a substituted or unsubstituted aryl group; or a substituted or unsubstituted heteroaryl group. The compound enables the organic electronic device to obtain high efficiency and high color purity. COPYRIGHT KIPO 2017 A compound having a formula 1: [formula 1] In said formula 1, R1 To R7 Hereinafter and R2 represent same or different, are independently hydrogen; deuterium; for halogen; nitrile group; nitro; hydroxy; neel carbonate; ester; for imide; amide group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted fluoroalkyl group; a substituted or unsubstituted cycloalkyl; substituted or nonsubstituted substituted between the light-emitting; a substituted or unsubstituted silyl group; a substituted or unsubstituted to boron; substituted or unsubstituted phosphine [...]; substituted or a substituted or unsubstituted amine group; a substituted or unsubstituted [...]; substituted or nonsubstituted a substituted aryl group; or a substituted or unsubstituted heteroaryl and R, R8 Fluorine; or a substituted or unsubstituted alkyl group, R8 Wherein at least one of the fluorine, the r1 integer number of 1 to 4, 1 to 5 and r2 is an integer, the integer number of 1 to 4 r3, r4 is positive numbers of 1 to 2, 1 to 2 r5 is integer number of, the positive numbers of 1 to 4 r6, the r7 integer number of 1 to 5, the positive numbers of 1 to 5 r8, r1 is 2 or more, a plurality of R1 Or on each other and hereinafter, r2 is 2 or more, a plurality of R2 Or on each other and hereinafter, r3 is 2 or more, a plurality of R3 R2 represent same or different hereinafter and, r4 is 2 or more, a plurality of R4 On which aids to hereinafter, r5 is 2 or more, a plurality of R5 Or on each other and hereinafter, r6 is 2 or more, a plurality of R6 Or on each other and hereinafter, r7 is 2 or more, a plurality of R7 Or on each other and hereinafter, r8 is 2 or more, a plurality of R8 As each other or different hereinafter disclosed. According to Claim 1, said formula 1 compound represented by formula 2: [formula 2] In said formula 2, R1 To R8 , And r1 r8 to are the same as defined in said formula 1 for definition. According to Claim 1, said formula 1 is a compound selected from a compound having a cost: Number 1 electrode; said number 1 number 2 opposite electrode having electrode; and said number 1 electrode with said number 2 electrode 1 as organic electronic devices including at least one layer of a solvent, said organic layer according to claim 1 including at least one layer is 1 to 3 compound is either anti an organic electronic device. According to Claim 4, a light emitting layer and said organic compound layer is formed, said compound including said light emitting layer is an organic electronic device. According to Claim 4, said organic compound layer is formed and a light emitting layer, said light-emitting layer includes a dopant material, the compound including said dopant material is an organic electronic device. According to Claim 4, comprising said organic compound layer is formed with an or electronic transporting bed, said said compound including metal-containing fullerene or [...] is an organic electronic device. According to Claim 4, said organic compound layer is formed as the hole and electronic blocking interception layer, said hole including said compound is [...] electronic blocking an organic electronic device. According to Claim 4, said light emitting layer organic electronic devices, hole injection, hole. Electron injection, alkali metal-containing fullerene, electronic blocking and hole blocking layer or 2 further including at least one layer selected from the group consisting 1 is an organic electronic device. Dopant @ 10 mA/cm2 V Cd/A CIE-a x CIE-a y In the embodiment 1 Compound 1 3. 87 5. 53 0. 137 0. 098 In the embodiment 2 Compound 2 3. 85 5. 61 0. 137 0. 108 In the embodiment 3 Compound 3 3. 90 5. 68 0. 136 0. 104 Comparison example 1 BD-a A 3. 91 4. 83 0. 141 0. 140 Comparison example 2 BD-a B 3. 94 4. 80 0. 139 0. 119
