METHODS FOR DYEING ULTRA-HIGH MOLECULAR WEIGHT POLYETHYLENE AND DYED ARTICLES MADE BY THE SAME

Dyed articles, such as sutures, and methods for making the same by treating with a supercritical liquid are disclosed. The articles may be made at least partially, if not entirely, from ultra-high molecular weight polyethylene (UHMWPE). The dye may be D&C Violet #2. 1. A method of dyeing an article comprising an ultra-high molecular weight polyethylene (UHMWPE) , comprising contacting the article with a supercritical liquid and D&C Violet #2.2. The method of claim 1 , further comprising applying a pressure from about 3 claim 1 ,600 psi to about 3 claim 1 ,800 psi.3. The method of claim 1 , further comprising applying a temperature from about 110° C. to about 130° C.4. The method of claim 3 , wherein the temperature is maintained for about 90 to about 180 minutes.5. The method of claim 4 , wherein the dyed article has a color contrast of at least about 90%.6. The method of claim 1 , wherein the article is a suture.7. A dyed article made by the process of . This application claims the benefit of U.S. Provisional Application No. 62/275,268, filed on Jan. 6, 2016, the entire contents of which are incorporated by reference herein in entirety.The invention relates to a process for dyeing an article comprising an ultra-high weight polyethylene, with D&C Violet #2. A supercritical liquid is applied to the article with the dye at a specified temperature and pressure to yield the desired dyed article.In a process known in the art, highly oriented ultra-high molecular weight polyethylene fibers are contacted with a dye bath at a temperature of 100-130° C. for 20-60 minutes, with the dye bath consisting of an aqueous dispersion of a finely ground mixture of specific dyes and surfactants whereupon the moulded article is washed and dried. For good dyeing results the fibers are preferably modified by means of a plasma or corona treatment prior to the dyeing operation. An important drawback of the known process is that the dyed fibers, particularly if they are not first modified by ...

COLORED PIGMENT PARTICLES FOR ELECTROPHORETIC DISPLAYS

Electrophoretic displays with an electrophoretic medium having charged pigmented microparticles are disclosed. The microparticles are charged linking molecules polymerized with chromophores of various colors so that microparticles in a variety of colors may be produced. Methods for producing the microparticles and using the microparticles in an electrophoretic display are also disclosed. Such microparticles may be provided separately, or kits may be provided for producing the microparticles. 1. An electrophoretic display comprising:at least one first electrode layer; and 'at least one electrically charged particle disposed in a transparent fluid and capable of moving through the transparent fluid upon application of an electrical field to the transparent fluid, wherein at least one charged particle comprises an alternating copolymer of a chromophore and a charged linker molecule.', 'an electrophoretic medium disposed adjacent at least one first electrode layer, wherein the electrophoretic medium comprises2. The electrophoretic display of claim 1 , further comprising at least one microcapsule having the transparent fluid and at least one charged particle retained therein.3. The electrophoretic display of claim 1 , wherein the charged linker molecule comprises cations selected from a group comprising quaternary ammonium claim 1 , quaternary phosphonium claim 1 , quaternary arsonium claim 1 , quaternary stibonium claim 1 , and ternary sulfonium cations.46-. (canceled)7. The electrophoretic display of claim 1 , wherein the chromophore is a dicarbonyl moiety claim 1 , a diamine moiety claim 1 , a dicarboxylic acid claim 1 , a diacyl halide claim 1 , a dianhydride claim 1 , a diester claim 1 , or a combination thereof.8. The electrophoretic display of claim 1 , wherein:the charged linker molecule comprises at least one of a quaternary ammonium substituent and a quaternary phosphonium substituent;the chromophore is a dicarbonyl moiety, a dicarboxylic acid, a diacyl halide, ...

ANTHRAQUINONE COMPOUND USED FOR COLOR FILTER OF LCD

An anthraquinone compound which is suitable for forming a color filter used for a liquid crystal display device, a composition containing a resin and the anthraquinone compound, an article having a polymer layer formed from the composition and a color filter containing the compound are developed. 2. The compound of claim 1 , wherein n is 2.3. The compound of or claim 1 , wherein Rto Rare independently selected from the group consisting of hydrogen atom or alkyl group having 1 to 8 carbon atoms.6. The method of claim 4 , wherein the mole ratio of the compound (2) with the epoxy compound is from 2/1 to 6/1.7. The method of any of to claim 4 , wherein the epoxy compound is a reaction compound of epihalohydrin with a bisphenol or diol compound selected from the group consisting of bisphenol A claim 4 , bisphenol F claim 4 , 1 claim 4 ,4-butanediol and 1 claim 4 ,6-butanediol.8. A composition comprising the compound of any of to and a resin.9. The composition of claim 8 , further comprising at least one pigment.10. The composition of or further comprising a radiation-sensitive compound.11. The composition of any of to further comprising a solvent.12. An article having a polymer layer formed from the composition of any of to .13. The article of wherein the polymer layer is formed from a negative-type film.14. A color filter comprising the compound of any of to .15. The color filter of claim 14 , further comprising at least one pigment. The present invention relates to an anthraquinone compound which is suitable for forming a color filter used for a liquid crystal display device, a method for synthesis the anthraquinone compound, a composition containing a resin and the anthraquinone compound, an article having a polymer layer formed from the composition and a color filter comprising the anthraquinone compound.Liquid crystal display (LCD) currently dominates the display market because of its excellent performance and small thickness. As a key component of LCD device, ...

NOVEL POLYSULFONATED FLUORESCENCE DYES

The invention relates to compounds of the general formulae (I)-(IV), which are characterized by substituents B comprising one or more sulfonic acid groups and their use as marker groups for the detection of analytes. 2. Compounds of the general formulae (I)-(IV) according to claim 1 , wherein Rand R claim 1 , Rand R claim 1 , Rand Ror/and Rand Rtogether with the atoms to which they are attached claim 1 , form a 5- or 6-membered ring claim 1 , wherein the ring can comprise one or more double bonds or/and one or more substituents preferably selected from the group consisting of halogen claim 1 , CN claim 1 , OH claim 1 , O(alkyl) claim 1 , O(aryl) claim 1 , SH claim 1 , S(alkyl) claim 1 , S(aryl) claim 1 , NH claim 1 , NH(alkyl) claim 1 , NH(aryl) claim 1 , N(alkyl) claim 1 , N(aryl) claim 1 , NO claim 1 , CHO claim 1 , COOH claim 1 , COO(alkyl) claim 1 , COO(aryl) claim 1 , POH claim 1 , SOH and a hydrocarbon group having 1-20 C atoms claim 1 , wherein the hydrocarbon group optionally comprises one or more heteroatoms selected from the group consisting of N claim 1 , O and S or/and one or more substituents preferably selected from the group consisting of halogen claim 1 , CN claim 1 , OH claim 1 , O(alkyl) claim 1 , O(aryl) claim 1 , SH claim 1 , S(alkyl) claim 1 , S(aryl) claim 1 , NH claim 1 , NH(alkyl) claim 1 , NH(aryl) claim 1 , N(alkyl) claim 1 , N(aryl) claim 1 , NO claim 1 , CHO claim 1 , COOH claim 1 , COO(alkyl) claim 1 , COO(aryl) claim 1 , POH claim 1 , and SOH.3. The compounds of the general formulae (I)-(IV) according to claim 1 , wherein at least one 5- or 6-membered ring is substituted with one or more hydrocarbon groups having 1-20 C atoms claim 1 , wherein the hydrocarbon group(s) optionally comprise(s) one or more substituents selected from the group consisting of COOH claim 1 , COO(alkyl) claim 1 , COO(aryl) and SOH.7. The compounds of the general formulae (I)-(IV) according to claim 1 , wherein X═O.8. The compounds of the general formulae (I)-( ...

Process for Printing Cellulose Containing Textile Fibre Material

The invention relates to a process for printing cellulose textile fibre material or cellulose/polyester mixed textile fibre material, characterised in that the fibre material is treated with a printing paste or printing ink containing a disperse dye of the formula 2. The process according to claim 1 , wherein R-Rin formulas (1)-(4) are C-Calkyl claim 1 , and wherein R-Rin formula (5) are each independently of the other hydrogen claim 1 , halogen claim 1 , C-Calkyl or C-Calkoxy.3. The process according to claim 1 ,{'sub': 4', '2', '6', '7, 'wherein Rin formulas (1)-(4) denotes a radical of the formula —SO—NRR,'}{'sub': 4', '1', '8', '2', '6', '7, 'wherein Rin formula (5) denotes hydrogen, C-Calkyl or a group of the formula —SO—NRR, and'}{'sub': 6', '7', '4, 'claim-ref': {'@idref': 'CLM-00001', 'claim 1'}, 'wherein Rand Rin Rof formulas (1)-(5) are as defined in .'}4. A process according to claim 1 , characterised in that the fibre material is treated with a printing paste or printing ink containing a disperse dye of the formula (1) claim 1 , (2) or (3) claim 1 , wherein Ris a radical of the formula (5) and wherein R-Rin formula (5) are C-Calkyl.5. A process according to claim 4 , wherein Rin formula (5) is —SO—NRR.6. A process according to claim 1 , characterised in that the fibre material is treated with a printing paste or printing ink containing a disperse dye of the formula (1) claim 1 , wherein{'sub': 1', '3', '1', '8, 'R-Rare C-Calkyl,'}{'sub': 4', '2', '6', '7', '6', '7, 'Ris hydrogen or a radical of the formula —SO—NRR, wherein Ris hydrogen and Ris 3-methoxypropyl, and'}{'sub': 5', '1', '3', '1', '8', '4', '2', '6', '7', '6', '7, 'Ris a radical of the formula (5), wherein R-Rare C-Calkyl and Ris hydrogen or a radical of the formula —SO—NRR, wherein Ris hydrogen and Ris 3-methoxypropyl.'}7. The process of claim 1 , characterised in that the fibre material is treated with a printing paste according to the screen printing method.8. The process of claim 1 , ...

Dye dispersion liquid, photosensitive resin composition for color filters, color filter, liquid crystal display device and organic light emitting display device

An object is to provide a photosensitive resin composition for color filters, configured to be able to form a high-luminance color layer with excellent heat resistance and light resistance. Disclosed is a photosensitive resin composition for color filters including the dye dispersion liquid, the dye dispersion liquid including a dye dispersed by a dispersant in a solvent, wherein the dye is a dye having a sulfonic acid group; the dispersant is a graft copolymer having an amine number of 30 mg KOH/g or more and including copolymerizable components that contain a specific monomer having a tertiary amine and a specific polymerizable oligomer; the solvent is a solvent having a solubility of the dye of 0.2 g/100 g solvent or less at 23° C.; and the tertiary amine of the dispersant and the sulfonic acid group of the dye form a micelle.

Reactive Dyes For Contact Lenses

A method for preparing a polymerizable monomer-dye compound is provided in which a monomer, a reactive dye, and base are combined under substantially anhydrous reaction conditions to form the polymerizable monomer-dye compound, wherein the monomer comprises a pendant reactive group that covalently links to the reactive dye to form the monomer-dye compound. 1. A method for preparing a polymerizable monomer-dye compound , comprising:combining a monomer, a reactive dye, and base under substantially anhydrous reaction conditions to form a reaction product comprising the monomer-dye compound, wherein the monomer comprises a pendant reactive group that covalently links to the reactive dye during the reaction to form the polymerizable monomer-dye compound.2. The method of claim 1 , wherein the pendant reactive group is a hydroxyl group claim 1 , an amino group claim 1 , or a sulfhydryl group that forms an ether linkage claim 1 , amino linkage claim 1 , or thioether linkage claim 1 , respectively claim 1 , between the monomer and the dye.3. The method of claim 1 , wherein the monomer is hydroxyethyl methacrylate.4. The method of claim 1 , wherein the monomer is an Si—O-containing monomer.5. The method of claim 1 , wherein the monomer and the reactive dye are in the reaction mixture at a molar ratio of from about 1:1 to about 6:1 claim 1 , respectively.6. The method of claim 1 , wherein the monomer is present in a molar amount that is at least 5 times that of the reactive dye.7. The method of claim 1 , wherein the reactive dye comprises a sulphatoethylsulphonyl group claim 1 , a halotriazine group claim 1 , or a vinyl group claim 1 , that reacts with the pendant reactive group of the monomer to form the covalent linkage between the monomer and the dye.8. The method of claim 1 , wherein the reactive dye is RB19 claim 1 , RB4 or RB69.9. The method of claim 1 , wherein the reactive dye is RB19 at a purity of at least 90%.10. The method of claim 1 , wherein the base is NaOH ...

Colored Resin Composition Exhibiting Pleochroism, and Molded Plastics Manufactured Using Same

The present invention relates to a coloring resin composition exhibiting pleochroism comprising 100 parts by weight of a transparent thermoplastic resin (A); 0.01 to 0.03 parts by weight of a dye for coloring a resin (B) which is one selected from the group consisting of an azo-based dye (b1), an anthraquinone-based dye (b2), and a methine dye (b3); and 0.1 to 0.3 parts by weight of a functional black dye (C) obtained by mixing an anthraquinone-based dye (c1) and a perinone-based dye (c2). A resin molded article manufactured by the coloring resin composition exhibiting pleochroism of the present invention is characterized by exhibiting different colors of light according to thicknesses although the resin molded article is irradiated with light sources in a single wavelength. 1. A resin molded article exhibiting pleochrosim wherein light transmitted through the molded article has different exhibited colors depending on the thickness of the molded article so that the molded article satisfies the following Mathematical Formula 1 or Mathematical Formula 2 in case of irradiation with a light source in a single wavelength:{'br': None, 'i': X', 'X', '−X, 'sub': 1', '2, 'Abs(Δ)=||>0.05\u2003\u2003[Mathematical formula 1]'}{'sub': '1', 'X=χ value of a CIE 1931 color space for the resin molded article with a thickness of 1.0 mm and'}{'sub': '2', 'claim-text': {'br': None, 'i': Y', 'Y', '−Y, 'sub': 1', '2, 'Abs(Δ)=||>0.05\u2003\u2003[Mathematical Formula 2]'}, 'X=χ value of a CIE 1931 color space for the resin molded article with a thickness of 1.5 mm,'}{'sub': '1', 'Y=y value of a CIE 1931 color space for the resin molded article with a thickness of 1.0 mm and'}{'sub': '2', 'Y=y value of a CIE 1931 color space for the resin molded article with a thickness of 1.5 mm.'}2. The resin molded article of claim 1 , wherein the resin molded article is prepared by a coloring resin composition comprising:a transparent thermoplastic resin;a dye for coloring a resin (B); anda functional ...

ANTHRAQUINONE COMPOUND USED FOR COLOR FILTER OF LCD

An anthraquinone compound which is suitable for forming a color filter used for a liquid crystal display device, a composition containing a resin and the anthraquinone compound, an article having a polymer layer formed from the composition and a color filter formed from the composition are developed. 2. The compound of claim 1 , wherein Rto Rare selected from the group consisting of alkyl group having 1 to 8 carbon atoms claim 1 , hydrogen atom and -A-(N claim 1 ,N-diallylamide).4. The compound of claim 3 , wherein A is represented by the formula (2).6. The composition of further comprising a radiation-sensitive compound.7. An article having a polymer layer formed from the composition of .8. The article of claim 7 , wherein the polymer layer is a negative-type layer.9. A color filter formed from the composition of .11. The composition of further comprising a radiation-sensitive compound.12. An article having a polymer layer formed from the composition of .13. The article of claim 12 , wherein the polymer layer is a negative-type layer.14. A color filter formed from the composition of . The present invention relates to an anthraquinone compound which is suitable for forming a color filter used for a liquid crystal display device, a method for synthesis the anthraquinone compound, a composition containing a resin and the anthraquinone compound, an article having a polymer layer formed from the composition and a color filter formed from the composition.Liquid crystal display (LCD) currently dominates the display market because of its excellent performance and small thickness. As a key component of LCD device, translucent color filters play the critical role of generating Red/Green/Blue lights by filtering white light from a back sheet. This capacity originates from the Red/Green/Blue colorants comprised in color filter units. Each colorant possesses a characteristic absorbance spectrum and will show one of the three primary colors when illuminated with white visible ...

ANTHRAQUINONIC DERIVATIVES AND THEIR USE AS COLOURING AGENTS

The present invention relates to a compound of formula (I-0) or a salt thereof. The invention further relates to the use of such compound as a colouring agent. The invention also relates to a colouring composition comprising such compound. 116-. (canceled)19. The compound according to claim 17 , wherein Rrepresents a group of formula (II) claim 17 , in which:X is N, and{'sub': a', 'b', '1', '6', '7', '7', '1', '6', '2', '3', '2', '1', '6', '1', '6, 'Rand Rrepresent independently a hydrogen atom, a (C-C)alkyl, a cyclohexyl or a phenyl optionally substituted by at least one radical selected from the group consisting of a halogen atom, —NH(CO)Rwith Rbeing a (C-C)alkyl, —NO, —SOH, —COH, —CN, a (C-C)alkyl optionally substituted by at least one halogen atom, and a tri((C-C)alkyl)ammonium.'}20. The compound according to claim 17 , wherein Rrepresents a group of formula (II′) claim 17 , in which:—X is O, and{'sub': a', '2', '8', '8', '1', '6, 'R′ represents a radical selected from the group consisting of a hydrogen atom and —SO—R, with Rbeing a phenyl substituted by a (C-C)alkyl.'}21. The compound according to claim 17 , wherein Rrepresents a group of formula (II) claim 17 , in which:X is N, and{'sub': a', 'b', '1', '6', '1', '6', '7', '7', '1', '6', '2', '3', '2', '1', '6, 'Rand Rrepresent independently a hydrogen atom, a (C-C) alkyl, a cyclohexyl group or a phenyl group optionally substituted by at least one radical selected from the group consisting of a halogen atom, a (C-C)alkyl optionally substituted by at least one halogen atom, —NH(CO)Rwith Rbeing a (C-C)alkyl, —NO, —SOH, —COH and a tri(C-Calkyl)ammonium.'}22. The compound according to claim 17 , wherein Rand Rrepresent independently a hydrogen atom or —NH.23. The compound according to claim 17 , wherein Ris a (C-C)alkyl claim 17 , a (C-C)alkyl claim 17 , or a methyl group.24. The compound according to claim 17 , wherein Ris a hydrogen atom or —C(O)ORwith Rbeing a hydrogen atom or (C-C)alkyl.25. The compound ...

NOVEL POLYSULFONATED FLUORESCENCE DYES

The invention relates to compounds of the general formulae (I)-(IV), which are characterized by substituents B comprising one or more sulfonic acid groups and their use as marker groups for the detection of analytes. 2. Compounds of the general formulae (I)-(IV) according to claim 1 , wherein Rand R claim 1 , Rand R claim 1 , Rand Ror/and Rand Rtogether with the atoms to which they are attached claim 1 , form a 5- or 6-membered ring claim 1 , wherein the ring can comprise one or more double bonds or/and one or more substituents preferably selected from the group consisting of halogen claim 1 , CN claim 1 , OH claim 1 , O(alkyl) claim 1 , O(aryl) claim 1 , SH claim 1 , S(alkyl) claim 1 , S(aryl) claim 1 , NH claim 1 , NH(alkyl) claim 1 , NH(aryl) claim 1 , N(alkyl) claim 1 , N(aryl) claim 1 , NO claim 1 , CHO claim 1 , COOH claim 1 , COO(alkyl) claim 1 , COO(aryl) claim 1 , POH claim 1 , SOH and a hydrocarbon group having 1-20 C atoms claim 1 , wherein the hydrocarbon group optionally comprises one or more heteroatoms selected from the group consisting of N claim 1 , O and S or/and one or more substituents preferably selected from the group consisting of halogen claim 1 , CN claim 1 , OH claim 1 , O(alkyl) claim 1 , O(aryl) claim 1 , SH claim 1 , S(alkyl) claim 1 , S(aryl) claim 1 , NH claim 1 , NH(alkyl) claim 1 , NH(aryl) claim 1 , N(alkyl) claim 1 , N(aryl) claim 1 , NO claim 1 , CHO claim 1 , COOH claim 1 , COO(alkyl) claim 1 , COO(aryl) claim 1 , POH claim 1 , and SOH.3. The compounds of the general formulae (I)-(IV) according to claim 1 , wherein at least one 5- or 6-membered ring is substituted with one or more hydrocarbon groups having 1-20 C atoms claim 1 , wherein the hydrocarbon group(s) optionally comprise(s) one or more substituents selected from the group consisting of COOH claim 1 , COO(alkyl) claim 1 , COO(aryl) and SOH.7. The compounds of the general formulae (I)-(IV) according to claim 1 , wherein X═O.8. The compounds of the general formulae (I)-( ...

COLOR MATERIAL DISPERSION LIQUID FOR COLOR FILTER, COLOR RESIN COMPOSITION FOR COLOR FILTER, COLOR MATERIAL, COLOR FILTER, LIQUID CRYSTAL DISPLAY DEVICE, AND LIGHT-EMITTING DISPLAY DEVICE

Disclosed is a color material dispersion liquid for a color filter, the dispersion liquid being capable of forming a high-luminance coating film with excellent light resistance; a color resin composition for a color filter, the composition being capable of forming a high-luminance coating film with excellent light resistance; a color material that has, while it can form a high-luminance coating film, excellent light resistance; a high-contrast, high-luminance color filter; a liquid crystal display device including the color filter; and a light-emitting display device including the color filter. The color material dispersion liquid for a color filter, includes: (A) a color material, (B) a dispersant and (C) a solvent, wherein the color material (A) contains a cerium lake color material of an acid dye. 1. A color material dispersion liquid for a color filter , comprising: (A) a color material , (B) a dispersant and (C) a solvent , wherein the color material (A) contains a cerium lake color material of an acid dye.2. The color material dispersion liquid for a color filter according to claim 1 , wherein the acid dye in the cerium lake color material of the acid dye claim 1 , is a rhodamine-based acid dye.5. A color resin composition for a color filter claim 1 , comprising the color material dispersion liquid for a color filter defined by and (D) a binder component.6. A color material comprising a cerium lake color material of an acid dye claim 1 , wherein the acid dye is one or more kinds selected from the group consisting of a rhodamine-based acid dye claim 1 , a fluorescein-based acid dye claim 1 , an anthraquinone-based acid dye claim 1 , an indigo-based acid dye and a triarylmethane-based acid dye.7. A color filter comprising at least a transparent substrate and color layers disposed on the substrate claim 1 , wherein at least one of the color layers contains a cerium lake color material of an acid dye.8. A liquid crystal display device comprising the color filter ...

Processo, composição absorvente de luz e compostos diácidos.

"PROCESSO, COMPOSIçãO ABSORVENTE DE LUZ E COMPOSTOS, DIáCIDOS". A presente invenção relata um processo que compreende reagir em um solvente, na presença de uma base: a) pelo menos um monómero diácido compreendendo cerca de 1 a 100% em mol de pelo menos 1 monómero absorvente de luz tendo um máximo de absorção de luz entre cerca de 300 nm de 1.200 nm e de 99 a 0% em mol de um mon de um monómero não absorvente de luz que não absorve luz significante em comprimentos de onda acima de 300nm ou tem um máximo de absorção de luz abaixo de 300 nm, com b) um composto orgânico da Fórmula (II): X-B-X~ 1~em que B é um radical orgânico bivalente, para formar uma composição polimérica absorvente de luz tendo a Fórmula (I) em que B é como definido acima; n- é pelo menos 2 e A compreenden o resíduo de um monómero de ácido, compreendendo cerca de 1a 100% em mol de pelo menos um monómero, absorvente de luz tendo um máximo de absorção de luz entre cerca de 300 nm e cerca de 1000 nm e que a porção remasnescente de A compreende o resíduo de um monómero não absorvente de luz que não absorve luz significante em comprimentos de onda acima de 300 nm ou tem uma absorção de luz máxima abaixo de 300 nm.

Method for preparing light-absorbing polymeric compositions

The present invention recites a method comprising reacting in a solvent in the presence of a base a) at least one diacidic monomer comprising about 1 to 100 mole % of at least one light-absorbing monomer having a light absorption maximum between about 300 nm and about 1200 nm and 99-0 mole % of a non-light absorbing monomer which does not absorb significant light at wavelengths above 300 nm or has a light absorption maximum below 300 nm, with b) an organic compound of the Formula (II): X-B-X1 wherein B is a divalent organic radical to form a light-absorbing polymeric composition having Formula (I) wherein B is a defined above; n is at least 2 and A comprises the residue of a diacidic monomer comprising about 1 to 100 mole % of at least one light-absorbing monomer having a light absorption maximum between about 300 nm and about 1000 nm and wherein the remaining portion of A comprises the residue of a non-light absorbing monomer which does not absorb significant light at wavelengths above 300 nm or has a light absorption maximum below 300 nm.

DYED THERMOPLASTIC RESIN COMPOSITIONS FOR LASER WELDING, COLORING THEREFOR FROM MIXTURES OF ANTHRACHINONE AND MONOAZO COMPLEX DYES AND THE MOLDED PRODUCT THEREOF

Thermoplastic resin compositions are described in which amine salts of anthraquinone dyes and monoazo complex dyes are added. These compositions show superior performance in laser welding applications.

具有带有深光泽效果的半透明聚碳酸酯组合物成型体的led照明元件

本发明涉及具有半透明成型体的LED照明元件，所述成型体由基于聚碳酸酯的模塑料制成，包含着色剂混合物、炭黑、散射添加剂和任选的白色颜料，如将其例如用作具有日间/夜间设计的遮盖物。通过与一个或多个RGB‑LED组合，可以在夜间设计中实现令人惊讶的色彩效果，而日间设计中存在灰色或黑色的成型体的深光泽效果。

Laser welded body of laser light transmitting member containing alkaline earth metal salt of anthraquinone acid dye

A laser-welded article comprises: a laser-transmissible workpiece made from a laser-transmissible colored resin composition including at least a thermoplastic resin and an alkaline earth metal salt of an anthraquinone-type acidic dye represented by the following chemical formulae (1) and/or (2) and a laser-absorptive workpiece putting the laser-transmissible workpiece together, wherein the workpieces are welded at the put position thereof by irradiated laser towards the laser-transmissible workpiece that transmits therethrough and is absorbed into the laser-absorptive workpiece.

Polychromatic Resin Composition and Molded Articles Employing same

본 발명은 투명 열가소성 수지(A) 100 중량부; 아조계열(Azo) 염료(b1), 안트라퀴논계열(Anthraquinone) 염료(b2), 및 메틴계열(Methine) 염료(b3)로 이루어진 군에서 선택된 1종의 수지 착색용 염료(B) 0.01 내지 0.03 중량부; 및 안트라퀴논 계열 염료(c1) 및 페리논 계열 염료(c2)를 혼합하여 이루어진 기능성 블랙 염료(C) 0.1 내지 0.3 중량부;를 포함하는 다색성 발현 착색용 수지 조성물에 관한 것이다. 본 발명의 다색성 발현 착색용 수지 조성물로 제조된 수지 성형품은 동일한 파장의 광원을 조사하여도 두께에 따라 발현되는 빛의 색상이 상이한 것을 특징으로 한다. The present invention relates to a transparent thermoplastic resin composition comprising 100 parts by weight of a transparent thermoplastic resin (A) (B) a resin dyeing dye (B) selected from the group consisting of azo azo dyes (b1), anthraquinone dyes (b2), and methine dyes (b3) part; And 0.1 to 0.3 parts by weight of a functional black dye (C) obtained by mixing an anthraquinone-based dye (c1) and a perinone-based dye (c2). The resin molded article produced from the resin composition for coloring with a pleochroism of the present invention is characterized in that the color of light emitted according to its thickness is different even when a light source of the same wavelength is irradiated.

Laser welded material of laser beam permeable member containing alkaline earth metal salt of anthraquinone acid dye

레이저 용착체는 하기 화학식 (1) 및/또는 (2)로 표시되는 안트라퀴논계 산성 염료의 알칼리 토금속염 및 열가소성 수지를 적어도 함유하는 레이저 광투과성 착색 수지조성물에 의해서 형성된 레이저 광투과성 부재와, 이것에 접촉하고 있는 레이저광 흡수성 부재가, 상기 레이저광 투과성 부재에 조사되어 이것을 투과하여 상기 레이저광 흡수성 부재에 흡수된 레이저광에 의해서, 상기 접촉하고 있는 부위에서 레이저 용착되어 있다: The laser weld body is a laser light transmitting member formed of a laser light transmitting colored resin composition containing at least an alkaline earth metal salt of an anthraquinone acid dye represented by the following formulas (1) and / or (2) and a thermoplastic resin, and this The laser light absorbing member in contact with the laser beam is irradiated to the laser light transmissive member and laser-welded at the contacting site by the laser light absorbed by the laser light absorbing member and transmitted therethrough: . . 안트라퀴논계 산성 염료의 알칼리 토금속염, 열가소성 수지, 레이저 용착체 Alkaline earth metal salts of anthraquinone acid dyes, thermoplastic resins, laser welders

Anthraquinone quencher dyes, their methods of preparation and use

The invention provides novel anthraquinone compositions that are useful as broad-spectrum quenchers of fluorescence and provides methods for making and using them. The anthraquinone quenchers can be conjugated to a variety of biologically relevant compounds, including lipids, nucleic acids, polypeptides, and more specifically antigens, steroids, vitamins, drugs, haptens, metabolites, toxins, environmental pollutants, amino acids, peptides, proteins, nucleotides, oligonucleotides, polynucleotides, carbohydrates, and their analogs. The invention also provides kits comprising, in one or more containers, at least one anthraquinone quencher dye composition of the present invention, and instructions for using that composition.

Di-alpha amino anthraquinone compositions

The invention provides novel anthraquinone compositions that are useful as broad-spectrum quenchers of fluorescence and provides methods for making and using them. The anthraquinone quenchers can be conjugated to a variety of biologically relevant compounds, including lipids, nucleic acids, polypeptides, and more specifically antigens, steroids, vitamins, drugs, haptens, metabolites, toxins, environmental pollutants, amino acids, peptides, proteins, nucleotides, oligonucleotides, polynucleotides, carbohydrates, and their analogs. The invention also provides kits comprising, in one or more containers, at least one anthraquinone quencher dye composition of the present invention, and instructions for using that composition.

Method of dyeing textiles made from natural or synthetic polyamide fibres

Photosensitive resin coloring composition for color filter, color filter formed therefrom, new anthraquinone compound and preparing method thereof

칼라 필터 착색층의 형성 재료인, 수지 및 색소를 함유하여 이루어지는 칼라 필터용 감광성 수지 착색 조성물은, 그 색소가 퀴니자린 골격에 있어서, 5, 6, 7 및 8위치의 1∼3개 또한 6 및 7위치의 적어도 하나가 제2급 아미노기이고, 또한 5, 6, 7 및 8위치의 나머지 위치가 수소 원자, 할로겐 원자, 치환되어 있어도 좋은 알콕시기, 치환되어 있어도 좋은 페녹시기, 치환되어 있어도 좋은 알킬티오기 및 치환되어 있어도 좋은 페닐티오기로 이루어진 군에서 선택된 적어도 1종인 퀴니자린 화합물 (A), 안트라퀴논 골격에 있어서, 1, 2, 3 및 4위치의 1∼3개가 제2급 아미노기, 치환되어 있어도 좋은 알콕시기, 치환되어 있어도 좋은 페녹시기, 치환되어 있어도 좋은 알킬티오기 및 치환되어 있어도 좋은 페닐티오기로 이루어진 군에서 선택된 적어도 1종이며, 또한 1, 2, 3 및 4위치의 잔기가 수소 원자, 할로겐 원자인 안트라퀴논 화합물 (B) 및 하기의 As for the photosensitive resin coloring composition for color filters which consists of resin and a pigment | dye which is a formation material of a color filter colored layer, the pigment | dye is 1-3 pieces of 5, 6, 7, and 8 positions in a quinizarine skeleton, and 6 and At least one of position 7 is a secondary amino group, and the remaining positions at positions 5, 6, 7, and 8 are hydrogen atoms, halogen atoms, optionally substituted alkoxy groups, optionally substituted phenoxy groups, and optionally substituted alkyls. In the at least one quinizaline compound (A) and anthraquinone skeleton selected from the group consisting of a thio group and a phenylthio group which may be substituted, 1 to 3 in 1, 2, 3 and 4 positions are secondary amino groups and substituted. At least one selected from the group consisting of an alkoxy group which may be substituted, a phenoxy group which may be substituted, an alkylthio group which may be substituted, and a phenylthio group which may be substituted, and 1, 2, Anthraquinone compound (B), wherein the residues at the 3 and 4 positions are a hydrogen atom, a halogen atom, and the following [화학식 1] [Formula 1] (단, 식 중에서 M은 2가 또는 리간드를 갖고 있는 4가 금속이다)에 의해 표시된 프탈로시아닌 골격의 벤젠핵 16개의 치환이 가능한 위치 중에서 1∼8개가 치환되어 있어도 좋은 알콕시기 및/또는 치환되어 있어도 좋은 페녹시기로 치환되어 있어도 되며, 또한 나머지 위치가 할로겐 원자인 프탈로시아인 화합물 (C)로 이루어진 (A)∼(C)군 중에서, (C)군(상기 화학식 1에 있어서, 치환되어 있어도 좋은 알콕시기 및/또는 치환되어 있어도 좋은 페녹시기가 2, 3, 6, 7, 10, 11, 14 및 15위치에 1∼8개 치환되어 이루어진 것으로 한정됨) 단독 또는 (A)+(B)군, (A)+(C)군, (B)+(C ...

Centrifugal separator

Dye dispersion, photosensitive resin composition for color filter, color filter, liquid crystal display device, and organoluminescent display device

도막 형성 시에 색 불균일이나 이물 석출이 발생하지 않고, 용매에의 재용해성, 알칼리 현상성이 우수하고, 또한, 내열성 및 내광성이 우수하고, 고휘도의 착색층을 형성할 수 있는 컬러 필터용 감광성 수지 조성물을 제공한다. (A)염료가, (B)분산제가 의해, (C)용매에 분산되어 이루어지는 염료 분산액이며, (A)염료가 술폰산기를 갖는 염료이며, (B)분산제가 3급 아민을 갖는 특정한 단량체와, 특정한 중합성 올리고머를 공중합 성분으로서 함유하고, 아민가(b)가 30mgKOH/g 이상인 그래프트 공중합체이며, (C)용매가 23℃에서의 (A)염료의 용해도가 0.2(g/100g 용매) 이하인 용매이며, (B)분산제가 갖는 3급 아민과 (A)염료의 술폰산기가 미셀을 형성하고 있는 염료 분산액 및 당해 염료 분산액을 사용한 컬러 필터용 감광성 수지 조성물이다. A photosensitive resin for a color filter capable of forming a coloring layer having high heat resistance and light fastness and excellent in re-solubility in a solvent, alkaline developability, and color heterogeneity and foreign matter precipitation at the time of forming a coating film Lt; / RTI > (A) a dye in which (A) a dye is dispersed in (B) a dispersant, (C) a solvent, (A) the dye is a dye having a sulfonic acid group, (B) the dispersant comprises a specific monomer having a tertiary amine, Wherein the graft copolymer (A) contains a specific polymerizable oligomer as a copolymerization component and has an amine value (b) of 30 mgKOH / g or more, and the solvent is a solvent having a solubility of the dye (A) , And (B) a dye dispersion in which sulfonic acid groups of a tertiary amine and (A) dye possessed by a dispersant form micelles, and a photosensitive resin composition for a color filter using the dye dispersion.

Anthraquinone compound, liquid crystal composition, cell and display device employing the same

하나 이상의 액정 화합물 및 하나 이상의 하기 화학식 1 로 표시되는 안트라퀴논 화합물을 함유하는 액정 조성물이 개시되었다: A liquid crystal composition containing at least one liquid crystal compound and at least one anthraquinone compound represented by Formula 1 is disclosed: [화학식 1] [Formula 1] (식 중, R 2 내지 R 8 은 각각 독립적으로 수소 또는 치환기를 나타내고; Het 는 황 또는 산소이고; B 1 및 B 2 는 각각 독립적으로, 임의로 치환된 아릴렌, 헤테로아릴렌, 시클로알칸-디일 또는 시클로 알켄-디일을 나타내고; C 1 은 임의로 치환된 알킬, 시클로알킬, 알콕시, 알콕시카르보닐 또는 아실옥시이고; p, q 및 r 은 각각 0 내지 5 의 수를 나타내고, n 은 3 ≤(p+r) ×n ≤10 을 만족시키는 1 내지 3 의 수이고; {(B 1 ) p -(Q 1 ) q -(B 2 ) r } 이 복수로 존재하는 경우에는, 상기는 동일 또는 상이할 수 있다). Wherein R 2 to R 8 each independently represent hydrogen or a substituent; Het is sulfur or oxygen; B 1 and B 2 are each independently an optionally substituted arylene, heteroarylene, cycloalkane-diyl Or cyclo alkene-diyl; C 1 is optionally substituted alkyl, cycloalkyl, alkoxy, alkoxycarbonyl or acyloxy; p, q and r each represent a number from 0 to 5 and n is 3 ≦ (p + r) x is a number from 1 to 3 that satisfies 10; {(B 1 ) p- (Q 1 ) q- (B 2 ) r } In the case where there are a plurality of these, the above may be the same or different).

Anthraquinone compound and colored resin molding composition using the same

Lightfast colorant and lightfast ink composition comprising the same

본 발명은 내광성 착색제 및 이를 포함하는 내광성 잉크 조성물에 관한 것이다. 본 내광성 착색제는 신나메이트 유도체와 착색제를 공유결합을 통하여 결합시켜서 얻어진 것으로서, 이를 이용하여 제조된 잉크 조성물은 내광성 뿐만 아니라 보존 안정성도 개선될 수 있다. The present invention relates to a light resistant colorant and a light resistant ink composition comprising the same. The light-resistant colorant is obtained by combining a cinnamate derivative and a colorant through a covalent bond, and the ink composition prepared using the same may improve not only light resistance but also storage stability.

Color filter and liquid crystal display device having the same

인접하여 배치된 다른 분광특성을 갖는 복수의 착색층을 구비한 컬러필터. 복수의 착색층 중 적어도 하나의 착색층은 폴리머 사슬에 화학적으로 결합한 염료를 함유한다. A color filter having a plurality of colored layers having different spectral characteristics disposed adjacent to each other. At least one colored layer of the plurality of colored layers contains a dye chemically bonded to the polymer chain. 컬러필터, 착색층, 폴리머 사슬, 염료, 액정표시장치 Color filter, colored layer, polymer chain, dye, liquid crystal display device

Polymeric hair dyes

所公开的为阳离子低聚染料，其包含：包含重复单元(1a)或(1b)的低分子量多胺，其中至少90％多胺分子选自四胺、五胺及六胺；和R为阳离子染料的残基，其共价键结至多胺的氮原子，任选通过连接基；或氢；其中多胺重复单元(1a)及(1b)包含至少一个阳离子染料残基；及n为从3-12的数。该染料特征在于其色调深度及其良好的耐洗坚牢度性质，举例而言，例如耐光、耐洗发剂及耐摩擦坚牢度。

Dyeing of polyamide fiber

(57)【要約】本公報は電子出願前の出願データであるた め要約のデータは記録されません。

Anthraquinone dye-containing material, composition including the same, camera including the same, and associated methods

A (meth)acrylate ester includes a (meth)acrylate moiety having an ester oxygen, an anthraquinone moiety having a transmittance spectrum producing blue light, and a linking group covalently bound to the ester oxygen and to a ring of the anthraquinone moiety, the linking group including, as a first component: phenyl, naphthyl, a linear alkyl group having from 1 to about 6 carbons, a branched alkyl group having from 3 to about 6 carbons, a cycloalkyl group having from about 3 to about 20 carbons, or a substituted aromatic group.

Anthraquinone dye-containing material, composition including the same, camera including the same, and associated methods

A (meth)acrylate ester includes a (meth)acrylate moiety having an ester oxygen, an anthraquinone moiety having a transmittance spectrum producing blue light, and a linking group covalently bound to the ester oxygen and to a ring of the anthraquinone moiety, the linking group including, as a first component: phenyl, naphthyl, a linear alkyl group having from 1 to about 6 carbons, a branched alkyl group having from 3 to about 6 carbons, a cycloalkyl group having from about 3 to about 20 carbons, or a substituted aromatic group.

Fluid and stable dispersions of anionic dyestuffs

The present invention concerns new fluid and stable dispersions of anionic dyestuffs, containing (a) dispersed anionic dyestuff with a maximum particle size of 5μ, (b) a dispersing agent which comprises (i) a combination of at least two different anion-active dispersing agents or (ii) a combination of an anion-active dispersing agent and at least one wetting agent or (iii) a combination of at least two different anion-active dispersing agents and at least one wetting agent, (c) optionally further auxiliaries and (d) water, As well as a process for their production and their application to dyeing and printing of organic material, in particular fibre material of natural and synthetic polyamide.

Patent FR2229807A1

Photo-electrophoretic copying using sensitised pigment - of alpha-acyl-amino-anthraquinone type

A spectrally sensitised anthraquinone pigment (I) with at least one, pref. 2 acylamino gp(s). in the alpha-position is used in a photoelectrophoretic copying process involving exposure of a suspension of a pigment, which is light-sensitive in an electric field, in an insulating liquid to an electric field between 2 electrodes and selectively to actinic light at the same time, so that a pigment image is formed on at least one of the electrodes by transfer of pigment particles. Used for single and multi-colour copying. (I) gives good results and extends the range of pigments suitable for this process.

Patent FR2028928A7

Process for the dyeing of nitrogen-containing fibre material

Process for dyeing polyester fibers

Process for dyeing synthetic polyamides

Novel dyes, their preparation process and uses

New solutions for hair dyeing and new compounds that can be used in these solutions

Process for the production of a new dye of the anthraquinone series.

Dispersion dyes of (1,4)-diamino-anthraquinone series - contg. (2)-carboxylic ester or amide substituents, for synthetic fibres

The dispersion dyes are of formula (I): (in which Z is -OR1 or -NR3R4. R is opt. substd. alkyl or cycloalkyl or H. R1 is opt.substd. alkyl, cycloalkyl, aralkyl or phenyl. R2 is -NHR3R4 or OX. X is as R1. R3 and R4 are H or opt.substd.alkyl, or together form a 5- or 6-memembered ring). (I) are used for dyeing or printing synthetic fibres, esp. polyesters and cellulose acetate, in greenish-blue shades, and for spin-dyeing of synthetic fibres. They give strong shades with good general fastness, reserve on wool and cotton, and heat resistance. In an example, 1-amino 4-brom anthraquinone 2-carboxylic acid n-propyl ester is reacted at 135 degrees C with ethyl p-aminobenzoate in the presence of K acetate and CuCl to give a dispersion dye which colours polyester fibres in greenish-blue shades.

Substantive dyes of the anthraquinone series, their manufacturing process and applications

Device for rewinding freshly spun artificial silk

Process for the production of vat dyes

Prepn of anthraquinone dyes for synthetic textiles

Anthraquinone dyes are produced by the reaction of an anthraquinone compound (I) with an amine (II) and the eliminations of HW. Esp. for the dyeing of aromatic polyesters in fast blue shades. The dyes posses good affinity. Also for cellulose esters such as cellulose triacetate. In (II) Z is -O- or -N(R1)- where R1 is lower alkyl. R is alkyl, alkenyl or cycloalkyl or a group of the formula -N(R2)R3 where R2 and R3 are alkyl or together with the N atom form a heterocyclic residue.

New anthraquinone dyes and their preparation

PROCESS FOR PREPARING ANTHRAQUINONE COMPOUNDS

1,4-Diaminoanthraquinones of the formula I are prepared by (A) reacting the compound of the formula II with amines of the formula HN-R4R5 (B), subsequent halogenation (C) and condensation with amines of the formula HN-R6R7 (D), the reaction from A to D or from B to D being carried out in one operation without isolation of the intermediate stages. The compounds prepared are useful dyes or dye intermediates.

New anthraquinone dyes insoluble in water

New anthraquinone dyes for polyester fibers

Unissou dyes of the anthraquinone series, their manufacturing process and applications

Isopropyl 1-amino-4-m-toluidinoanthraquinone-2- carboxylate, cyan composition for sublimation transfer record and cyan composition for color toner containing it

ABSTRACT OF THE DISCLOSURE Disclosed are a novel compound represented by the formula

Soluble dyes of the anthraquinone series and their preparation process

Colorants for vat

ANTHRAQUINONIC DYES

L'invention concerne l'industrie des matières colorantes. Elle a pour objet des colorants anthraquinoniques hydrosolubles de formule : The invention relates to the dyestuff industry. It relates to water-soluble anthraquinone dyes of formula:

Acid anthraquinone dyes and their preparation

Orange-violet-blue anthraquinone dyes - derived from N:N-disubstd sulphamic acid halides, for natural and synthetic fibres esp polyamides

The novel anthraquinone dyes, free from water solubilising acid groups, but however, being very sol. in aqs. media are of formula (I): (where AQ is an anthraquinone residue opt. carrying one or more non-ionic substituents such as halogen, alkyl, nitro, cyano, carboxyalkyl, carboxamide, hydroxy, alkoxy, acyloxy, thioalkyl, thiaryl, amino, alkylamino, arylamino, acylamino or arylsulphonylamino; x is a bridge -O-, -S-, -NH- or -CO N-; R is opt. branched alkyl, or aralkyl, the alkyl chain in both cases being opt. interrupted by one or more hetero atoms; R1 and R2 are the same or different lower alkyl groups; n = 1 or 2). (I) are useful as orange-rose-violet and blue dyes for natural and synthetic fibres, esp. natural and synthetic polyamides which are dyed fast shades, esp. to light. (I) may be used for printing textiles either directly or by transfer.

Anthraquinone dyestuffs for polyester - dyeing

Anthraquinone dyestuffs of formula: in which X is hydroxy or amino, R is hydroxy, alkoxy, mercapto- or alkyl mercapto- groups, Z is a phenylene or naphthalene radical, which may be further substituted, and the rings A and B may be substituted, may be prepared by reacting an anthraquinone, in the presence of an acid catalyst, with a compound of formula HZR, (Z and R as defined above). The dyestuffs e.g. 1-amino-2-(4'-hydroxybenzyl)-anthraquinone and 1-hydroxy-2-(4'-hydroxybenzyl) anthraquinone, are useful for colouring synthetic textiles e.g. polyester fibres.

Patent FR2070876A1

Process for the production of arylaminated aminoanthraquinones

Anthraquinone dye and its preparation

6/7-HALOGENO-ANTHRAQUINONIC COMPOUNDS, THEIR PREPARATION PROCESS AND THEIR APPLICATION

Nouveaux composés 6/7-halogéno-anthraquinoniques et leur mélanges. Les composés répondent à la formule : New 6/7-halogeno-anthraquinone compounds and their mixtures. The compounds correspond to the formula:

NEW COLORANTS FOR CELLULOSIC TEXTILE MATERIALS, THEIR OBTAINING AND THEIR APPLICATIONS

Synthetic linear polyesters coloring process

Process for dyeing and printing fibrous substances

New anthraquinone dyes

Process for modifying the properties of objects molded from aromatic polyesters

New nitro pigment dyes and their production process

Production of anthraquinone series coloring matter

Acid anthraquinone dyes and process for their preparation

New anthraquinone dyes

NEW ANTHRAQUINONIC COLORANTS AND THEIR PREPARATION

Arylaminoanthraquinones

Arylaminoanthraquinones Abstract of the Disclosure An arylaminoanthraquinone of the formula (I) in which one X, in the 5- or 8-position, denote either the radical of the formula or a hydrogen atom, the other X denote hydrogen atoms, alkoxy groups with 1-4 C atoms, aryloxy, arylmercapto or acylamino groups, one Y denotes a nitro group and the other denotes a hydrogen atom, one or two Z which are not adjacent to the nitro group denote chlorine atoms and the remaining Z denote hydrogen atoms, and the Q denote hydrogen or halogen atoms which is useful for colouring high-molecular material. - 1a -

New acylated tetraminoanthraquinones and their preparation and use process

New Acid Anthraquinone Dyes and Their Preparation

Basic anthraquinone dyes, their manufacturing process and applications

Synthetic linear polyesters coloring process

New vat dyes and their production process

Process for dyeing and printing synthetic fibers with tetra-alpha-substituted anthraquinone derivatives

Fuller dyes of the anthraquinone series and their preparation

New anthraquinone series dyes

Process for the preparation of anthraquinone dyes

New anthraquinone dyes

Anthraquinone dyes

Bulk coloring of synthetic polyesters

Phenylamino-anthraquinone compounds containing sulfamyl groups

ANTHRAKHINON DYES

ÐÎÑÑÈÉÑÊÀß ÔÅÄÅÐÀÖÈß (19) RU (51) ÌÏÊ 7 (11) 2004 131 534 (13) A C 09 B 1/32, 1/514 ÔÅÄÅÐÀËÜÍÀß ÑËÓÆÁÀ ÏÎ ÈÍÒÅËËÅÊÒÓÀËÜÍÎÉ ÑÎÁÑÒÂÅÍÍÎÑÒÈ, ÏÀÒÅÍÒÀÌ È ÒÎÂÀÐÍÛÌ ÇÍÀÊÀÌ (12) ÇÀßÂÊÀ ÍÀ ÈÇÎÁÐÅÒÅÍÈÅ (21), (22) Çà âêà: 2004131534/04, 13.03.2003 (71) Çà âèòåëü(è): ÖÈÁÀ ÑÏÅØÈÀËÒÈ ÊÅÌÈÊÝËÇ ÕÎËÄÈÍà ÈÍÊ. (CH) (30) Ïðèîðèòåò: 22.03.2002 EP 02405226.8 (43) Äàòà ïóáëèêàöèè çà âêè: 10.07.2005 Áþë. ¹ 19 (85) Äàòà ïåðåâîäà çà âêè PCT íà íàöèîíàëüíóþ ôàçó: 22.10.2004 (74) Ïàòåíòíûé ïîâåðåííûé: Âåñåëèöêà Èðèíà Àëåêñàíäðîâíà (86) Çà âêà PCT: EP 03/02616 (13.03.2003) Àäðåñ äë ïåðåïèñêè: 101000, Ìîñêâà, Ì.Çëàòîóñòèíñêèé ïåð., ä.10, êâ.15, "ÅÂÐÎÌÀÐÊÏÀÒ", È.À.Âåñåëèöêîé (54) ÀÍÒÐÀÕÈÍÎÍÎÂÛÅ ÊÐÀÑÈÒÅËÈ Ôîðìóëà èçîáðåòåíè R U , A 2 0 0 4 1 3 1 5 3 4 A 1. Ñîåäèíåíèå ôîðìóëû I â êîòîðîé R1 îáîçíà÷àåò ðàäèêàë ôîðìóëû II , R2 îáîçíà÷àåò -NH2 èëè ðàäèêàë ôîðìóëû II, R3 è R4 êàæäûé íåçàâèñèìî äðóã îò äðóãà îáîçíà÷àåò âîäîðîäíûé àòîì, ãèäðîêñèë, -NH2 èëè ðàäèêàë ôîðìóëû II, R5 îáîçíà÷àåò àòîì âîäîðîäà èëè ãàëîãåíà èëè -X-(CH2)n-Y, ãäå Õ îáîçíà÷àåò ïð ìóþ ñâ çü, -Î- èëè -S-, Y îáîçíà÷àåò -ÎÍ èëè -OSO3H, à n îáîçíà÷àåò ÷èñëî îò 0 äî 6 ïðè óñëîâèè, ÷òî ïî ìåíüøåé ìåðå îäèí èç ðàäèêàëîâ R3, R4 è R5 íå îáîçíà÷àåò âîäîðîäíûé àòîì. 2. Ñîåäèíåíèå ôîðìóëû I ïî ï.1, â êîòîðîé R1 îáîçíà÷àåò ðàäèêàë ôîðìóëû II, â Ñòðàíèöà: 1 RU 2 0 0 4 1 3 1 5 3 4 (87) Ïóáëèêàöè PCT: WO 03/080734 (02.10.2003) R U (72) Àâòîð(û): Óðñ ËÀÓÊ (CH), Ïàòðèê ÍÎÂÀÊ (DE) êîòîðîé Õ îáîçíà÷àåò ïð ìóþ ñâ çü, à n îáîçíà÷àåò ÷èñëî 2. 3. Ñîåäèíåíèå ôîðìóëû I ëèáî ïî ï.1 èëè 2, â êîòîðîé R1 îáîçíà÷àåò ðàäèêàë ôîðìóëû II, â êîòîðîé Y îáîçíà÷àåò -ÎÍ. 4. Ñîåäèíåíèå ôîðìóëû I ïî ï.1, â êîòîðîé R1 îáîçíà÷àåò ðàäèêàë ôîðìóëû II, â êîòîðîé Õ îáîçíà÷àåò ïð ìóþ ñâ çü, n îáîçíà÷àåò ÷èñëî 2, à Y îáîçíà÷àåò -ÎÍ. 5. Ñîåäèíåíèå ôîðìóëû I ïî ï.1, â êîòîðîé R3 è R4 îáîçíà÷àþò âîäîðîäíûé àòîì èëè ãèäðîêñèë. 6. Ñîåäèíåíèå ôîðìóëû I ïî ï.1, â êîòîðîé R5 îáîçíà÷àåò àòîì âîäîðîäà èëè õëîðà èëè -S-(CH2)2-OH. 7. Ñîåäèíåíèå ôîðìóëû I ïî ï.1 â ñîîòâåòñòâèè ñ ëþáîé îäíîé ...

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Patent FR2357531B1