• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    The present invention provides a colored photosensitive composition comprising a colorant (A), a binder polymer (B), a photopolymerizable compound (C), a photopolymerization initiator (D) and a chain transfer agent (E), used to prepare a color filter. In addition, using the colored photosensitive composition, even when the colored photosensitive composition contains a high concentration of a colorant, it is possible to form a color pixel or black matrix having a tapered or forward tapered cross section.
    公开号:KR20020042439A
    申请号:KR1020010073663
    申请日:2001-11-26
    公开日:2002-06-05
    发明作者:다케베가즈오
    申请人:고오사이 아끼오；스미또모 가가꾸 고교 가부시끼가이샤；
    IPC主号:
    专利说明:

    Colored photosensitive composition {COLORED PHOTOSENSITIVE COMPOSITION}
    [9] The present invention relates to colored photosensitive compositions.
    [10] Colored photosensitive compositions, which are photosensitive compositions colored with colorants, are useful as materials for forming color pixels or black matrices that constitute color filters, such as color liquid crystal displays, color solid cameras, and the like. Commonly known compositions comprise a colorant (A), a binder polymer (B), a photopolymerizable compound (C) and a photopolymerization initiator (D).
    [11] In order to produce color pixels and the like with these colored photosensitive compositions, for example, a colored photosensitive composition layer 1 is formed on the substrate 2 (see FIG. 1A), and the layer 1 is formed of a photo-mask ( The light beam 4 is irradiated and exposed through 3) (see FIG. 1B), and then developed. By development, the non-irradiation area 11 which is the area of the colored photosensitive composition layer 1 not irradiated with the light beam 4 is removed, and the irradiation area 12 which is the area irradiated with the light beam is left. Thus, a color pixel or black matrix 5 is formed (see FIG. 1C). Color pixels or black matrices 5 formed in this way are generally cured by heat treatment after development to increase mechanical strength.
    [12] The color pixel or black matrix 5 is preferably thin in thickness and is rectangular (see Fig. 2a) or tapered forward in cross section (see Fig. 2b). In order to form a sufficiently colored color pixel or the like 5 despite its thin thickness, the concentration of the colorant (A) contained in the colored photosensitive composition must be high.
    [13] However, in a conventional colored photosensitive composition, when the concentration of the colorant (A) is increased to form a thin color filter or the like, the resulting color pixel or black matrix 5 tends to become taper in reverse when viewed in cross section. There is (see FIG. 2C).
    [14] The inventors have conducted extensive research to develop colored photosensitive compositions capable of producing color pixels or black matrices having rectangular or forward tapering cross sections even when high concentrations of colorant are included. As a result, the present inventors found that even when the colorant is contained in a high concentration, when the chain transfer agent (E) is added, the obtained color pixel or the like becomes a square or a tapered cross section. Based on these findings, the present invention has been completed.
    [1] 1 is a schematic diagram showing a step of forming a color pixel using a colored photosensitive composition,
    [2] 2 is a schematic diagram showing in cross section the shape of the formed color pixel;
    [3] ※ Explanation of code about main part of drawing ※
    [4] 1: colored photosensitive composition layer 11: non-irradiated area
    [5] 12: irradiation area 2: substrate
    [6] 3: photomask 31: glass substrate
    [7] 32: light shielding layer 33: translucent area
    [8] 4: light beam 5: color pixel or black matrix
    [15] The present invention provides a colored photosensitive composition comprising a colorant (A), a binder polymer (B), a photopolymerizable compound (C), a photopolymerization initiator (D) and a chain transfer agent (E).
    [16] In the colored photosensitive composition of the present invention, the colorant (A) may be an organic colorant or an inorganic colorant. The organic colorant may be a pigment, a dye or a natural colorant. The inorganic colorant may be an inorganic pigment such as a metal oxide, a metal complex salt and an inorganic salt of barium sulfate (present pigment). Among the colorants, organic colorants excellent in heat resistance and colorability, in particular organic pigments, are preferably used.
    [17] Examples of organic pigments include compounds classified as pigments in the Color Index (The Society of Dyers and Clolurists). Specific examples of organic pigments include compounds having the following color index (C.I.) numbers, but organic colorants that may be used in the present invention are not limited to these compounds:
    [18] C.I. Pigment Yellow 1, 3, 12, 13, 14, 15, 16, 17, 20, 24, 31, 53, 83, 86, 93, 94, 109, 110, 117, 125, 128, 137, 138, 139 , 147, 148, 150, 153, 154, 166 and 173;
    [19] C.I. Pigment orange 13, 31, 36, 38, 40, 42, 43, 51, 55, 59, 61, 64,65, 71 and 73;
    [20] C.I. Pigment Red 9, 97, 105, 122, 123, 144, 149, 166, 168, 176, 177, 180, 192, 215, 216, 224, 242, 254, 264 and 265;
    [21] C.I. Pigment blue 15, 15: 3, 15: 4, 15: 6 and 60;
    [22] C.I. Pigment violet 1, 19, 23, 29, 32, 36 and 38;
    [23] C.I. Pigment greens 7 and 36;
    [24] C.I. Pigment brown 23 and 25; And
    [25] C.I. Pigment Black 1 and 7.
    [26] These organic pigments may be used alone or as a mixture of two or more thereof.
    [27] Organic pigments can be treated with rosin, surface treatment with pigment derivatives having acidic or basic groups, bonding treatment on the pigment surface with polymers, particulate treatments such as sulfuric acid microparticles, and organic solvents, water to remove impurities. And so on.
    [28] Colorant (A) is generally used in an amount of 5-60 mass%, preferably 10-50 mass%, based on the total amount of solids of the colored photosensitive composition. More preferred is an amount of at least 20% by mass, in particular at least 30% by mass. The amount of the organic pigment is preferably 50 mass% or more, more preferably 55 mass% or more, based on the total amount of the colorant (A).
    [29] The binder polymer (B) acts as a dispersion medium for the colorant and gives the colored photosensitive composition layer the properties in which the non-irradiated area 11 is removed by development and the irradiated area 12 is left. The binder polymer (B) is preferably a polymer or copolymer derived from carboxyl group-containing monomers and, preferably, other monomers copolymerizable therewith.
    [30] The carboxyl group-containing monomer may be an unsaturated carboxyl group having one or more carboxyl groups in the molecule, such as, for example, unsaturated monocarboxylic acids and unsaturated dicarboxylic acids. Specific examples thereof include acrylic acid, methacrylic acid, crotonic acid, itaconic acid, maleic acid and fumaric acid. These carboxyl group-containing monomers have carbon-carbon unsaturated bonds and can be used alone or in combination of two or more.
    [31] The binder polymer (B) is more preferably a copolymer derived from a carboxyl group-containing monomer and other monomers copolymerizable therewith. Monomers copolymerizable with such carboxyl group-containing monomers are compounds having a polymerizable carbon-carbon unsaturated bond. Specific examples thereof include aromatic vinyl compounds such as α-methylstyrene and vinyltoluene, methyl (meth) acrylate, ethyl (meth) acrylate, butyl (meth) acrylate and 2-hydroxyethyl (meth) acrylate. , Unsaturated carboxylates such as benzyl (meth) acrylate, unsaturated aminoalkyl carboxylates such as aminoethyl acrylate, unsaturated glycidyl carboxylates such as glycidyl (meth) acrylate, vinyl acetate And vinyl carboxylates such as vinyl propionate, vinyl cyanide compounds such as (meth) acrylonitrile and α-chloroacrylonitrile, 3-methyl-3- (meth) acryloxymethyloxetane, and 3- Unsaturated oxetane carboxylates such as ethyl-3- (meth) acryloxymethyl oxetane, 3-methyl-3- (meth) acryloxyethyl oxetane, and 3-ethyl-3- (meth) acryloxyethyl oxetane Like There. These monomers may also be used alone or in combination of two or more.
    [32] Examples of such copolymers with carboxyl groups include 3-ethyl-3-methacryloxymethyloxetane / benzyl methacrylate / methacrylic acid copolymer, 3-ethyl-3-methacryloxymethyloxetane / benzyl methacryl Latex / methacrylic acid / styrene copolymer, 3-ethyl-3-methacryloxymethyloxetane / methyl methacrylate / methacrylic acid copolymer, 3-ethyl-3-methacryloxymethyloxetane / methyl methacrylate Laterate / methacrylic acid / styrene copolymer, etc. are mentioned.
    [33] The content of the polymerized unit derived from the monomer having a carboxyl group is preferably 5 to 50% by mass, more preferably 10 to 40% by mass based on the total monomers.
    [34] It is preferable that the weight average molecular weight measured by gel permeation chromatography of a binder polymer (B) is 5000-40000, and it is more preferable that it is 10000-30000.
    [35] The binder polymer (B) is generally 5 to 90% by weight, preferably 20 to 70% by weight, based on the total amount of all solid components of the photosensitive composition.
    [36] The photopolymerizable compound (C) is a compound which can be polymerized by the action of an acid or an active radical generated from the photopolymerization initiator (D) by irradiating a light beam. In general, the photopolymerizable compound (C) has a polymerizable carbon-carbon unsaturated bond. It may be a monofunctional monomer as well as a bifunctional or polyfunctional monomer.
    [37] Examples of monofunctional monomers include nonylphenylcarbitol acrylate, 2-hydroxy-3-phenoxypropyl acrylate, 2-ethylhexylcarbitol acrylate, 2-hydroxyethyl acrylate and N-vinylpyrroli Money, etc.
    [38] Examples of difunctional monomers include 1,6-hexanediol di (meth) acrylate, ethylene glycol di (meth) acrylate, neopentyl glycol di (meth) acrylate, triethylene glycol di (meth) acrylate, Bis (acryloyloxyethyl) ether of bisphenol A, 3-methylpentanediol di (meth) acrylate, etc. are mentioned. Examples of other polyfunctional monomers include trimethylolpropane tri (meth) acrylate, pentaerythritol tri (meth) acrylate, pentaerythritol tetra (meth) acrylate, dipentaerythritol penta (meth) acrylate, dipentaerythritol Hexa (meth) acrylate etc. are mentioned.
    [39] These photopolymerizable monomers may be used alone or in combination of two or more. It is preferred that one or more difunctional or other multifunctional monomers are used. The amount of the photopolymerizable compound (C) is generally 0.1 to 70 parts by weight, preferably 1 to 60 parts by weight based on 100 parts by mass of the total amount of the binder polymer (B) and the photopolymerizable compound (C).
    [40] As the photopolymerization initiator (D), mention may be made of an active radical generator which generates active radicals by irradiation of light beams and an acid generator which generates acid by irradiation of light beams. Examples of the active radical generator include acetophenone-based polymerization initiators, benzoin-based polymerization initiators, benzophenone-based polymerization initiators, thioxanthone-based polymerization initiators, triazine-based polymerization initiators and other initiators.
    [41] Specific examples of the acetophenone-based polymerization initiators include diethoxyacetophenone, 2-hydroxy-2-methyl-1-phenylpropan-1-one, benzyldimethyl ketal, 2-hydroxy-2-methyl-1- [4 -(2-hydroxyethoxy) phenyl] propan-1-one, 1-hydroxycyclohexylphenyl ketone, 2-methyl-2-morpholino-1- (4-methylthiophenyl) propan-1-one , 2-benzyl-2-dimethylamino-1- (4-morpholinophenyl) butan-1-one and 2-hydroxy-2-methyl-1- [4- (1-methylvinyl) phenyl] propane- Oligomers, such as 1-one, are mentioned.
    [42] Specific examples of the benzoin-based polymerization initiator include benzoin, benzoin methyl ether, benzoin ethyl ether, benzoin isopropyl ether, benzoin isobutyl ether, and the like. Specific examples of the benzophenone-based polymerization initiators include benzophenone, methyl o-benzoylbenzoate, 4-phenylbenzophenone, 4-benzoyl-4'-methyldiphenylsulfide, 3,3 ', 4,4'-tetra ( Tert-butylperoxycarbonyl) benzophenone, 2,4,6-trimethylbenzophenone, and the like.
    [43] Specific examples of thioxanthone type polymerization initiators include 2-isopropyl thioxanthone, 4-isopropyl thioxanthone, 2,4-diethyl thioxanthone, 2,4-dichlorothioxanthone, 1-chloro-4 Propoxy city oxanthone etc. are mentioned.
    [44] Specific examples of the triazine polymerization initiator include 2,4-bis (trichloromethyl) -6- (4-methoxyphenyl) -1,3,5-triazine and 2,4-bis (trichloromethyl)- 6- (4-methoxynaphthyl) -1,3,5-triazine, 2,4-bis (trichloromethyl) -6-piperonyl-1,3,5-triazine, 2,4- Bis (trichloromethyl) -6- (4-methoxystyryl) -1,3,5-triazine, 2,4-bis (trichloromethyl) -6- [2- (5-methylfuran-2 -Yl) ethenyl] -1,3,5-triazine, 2,4-bis (trichloromethyl) -6- [2- (furan-2-yl) ethenyl] -1,3,5-tri Azine, 2,4-bis (trichloromethyl) -6- [2- (4-diethylamino-2-methylphenyl) ethenyl] -1,3,5-triazine, 2,4-bis (trichloro Methyl) -6- [2- (3,4-dimethoxyphenyl) ethenyl] -1,3,5-triazine and the like.
    [45] Examples of active radical generators include 2,4,6-trimethylbenzoyldiphenylphosphine oxide, 2,2'-bis (o-chlorophenyl) -4,4 ', 5,5'-tetraphenyl-1, 2'-biimidazole, 10-butyl-2-chloroacridone, 2-ethylanthraquinone, benzyl, 9,10-phenanthrenequinone, camphorquinone, methyl phenylglyoxylate, titanocene compound and the like Can be.
    [46] Commercially available active radical generators can also be used. Examples thereof include "Irgacure-907" (acetophenone-based polymerization initiator, CIBA-GEIGY), and the like.
    [47] Examples of acid generators include 4-hydroxyphenyldimethylsulfonium p-toluenesulfonate, 4-hydroxyphenyldimethylsulfonium hexafluoroantimonate, 4-acetoxyphenyldimethylsulfonium p-toluenesulfonate, 4-acetoxyphenylmethylbenzylsulfonium hexafluoroantimonate, triphenylsulfonium p-toluenesulfonate, triphenylsulfonium hexafluoroantimonate, diphenyliodonium p-toluenesulfonate and diphenyl Onium salts such as iodonium hexafluoroantimonate; Nitrobenzyl tosylate, benzointosylate and the like.
    [48] Some of the active radical generators are also acid generators. For example, the triazine-based polymerization initiator may act as an acid generator as well as an active radical generator.
    [49] These photopolymerization initiators may each be used alone or in combination of two or more.
    [50] The colored photosensitive composition of the present invention may further comprise a photopolymerization aid. The photopolymerization aid is used in combination with the photopolymerization initiator (D) to accelerate the polymerization of the photopolymerizable compound (C) initiated by the photopolymerization initiator (D). Examples of the photopolymerization aid include amine polymerization aids and alkoxy anthracene polymerization aids.
    [51] Examples of the amine polymerization aid include triethanolamine, methyldiethanolamine, triisopropanolamine, methyl 4-dimethylaminobenzoate, ethyl 4-dimethylaminobenzoate, isoamyl 4-dimethylaminobenzoate, 2-dimethylaminoethyl Benzoate, 2-ethylhexyl 4-dimethylaminobenzoate, N, N-dimethylparatoluidine, 4,4'-bis (dimethylamino) benzophenone (aka Michaelus's ketone), 4,4 ' -Bis (diethylamino) benzophenone, 4, 4'-bis (ethylmethylamino) benzophenone, etc. are mentioned.
    [52] Examples of the alkoxy anthracene-based polymerization assistant include 9,10-dimethoxyanthracene, 2-ethyl-9,10-dimethoxyanthracene, 9,10-diethoxyanthracene, 2-ethyl-9,10-diethoxyanthracene, and the like. Can be mentioned.
    [53] Commercially available photopolymerization auxiliaries may also be used. Examples thereof include "EBA-F" (manufactured by Hodogaya Chemical).
    [54] The amount of the photopolymerization assistant is 10 mol or less, preferably 0.01 to 5 mol or less, based on 1 mol of the photopolymerization initiator (D). The total amount of the photopolymerization initiator (D) and the photopolymerization assistant is generally 3 to 30 parts by mass, preferably 5 to 25 parts by mass based on 100 parts by mass of the total amount of the binder polymer (B) and the photopolymerizable compound (C).
    [55] The photopolymerization aids may be used alone or in combination of two or more.
    [56] Examples of the chain transfer agent (E) include 2,4-diphenyl-4-methyl-1-pentene, n-dodecyl mercaptan, t-dodecyl mercaptan, n-octyl mercaptan, limonene and the like. The suitable amount of the chain transfer agent (E) is generally 0.5 to 5% by mass based on the total solids amount of the colored photosensitive composition although it depends on the type of colorant, the manufacturing conditions for the color pixels and the like. If the amount is 0.5 mass% or less, a cross section which becomes taper in reverse depending on a coloring agent may arise. It is preferable that the quantity of a chain transfer agent is 1 mass% or more. If the amount exceeds 5 mass%, the sensitivity of the colored photosensitive composition may be lowered.
    [57] The colored photosensitive composition of the present invention may be diluted with solvent (F). Solvents which have conventionally been used in colored photosensitive compositions can be used in the present invention.
    [58] Examples of the solvent include ethylene glycol monoalkyl ethers such as ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monopropyl ether and ethylene glycol monobutyl ether; Diethylene glycol dialkyl ethers such as diethylene glycol dimethyl ether, diethylene glycol diethyl ether, diethylene glycol dipropyl ether, and diethylene glycol dibutyl ether; Ethylene glycol alkyl ether acetates such as methyl cellosolve acetate and ethyl cellosolve acetate; Alkylene glycol alkyl ether acetates such as propylene glycol monomethyl ether acetate, propylene glycol monoethyl ether acetate, propylene glycol monopropyl ether acetate, methoxybutyl acetate and methoxypentyl acetate; Aromatic hydrocarbons such as benzene, toluene and xylene; Ketones such as methyl ethyl ketone, acetone, methyl amyl ketone, methyl isobutyl ketone and cyclonehexanone; Alcohols such as ethanol, propanol, butanol, hexanol, cyclohexanol, ethylene glycol and glycerin; Esters such as ethyl 3-ethoxypropionate and methyl 3-methoxypropionate; Cyclic ester, such as (gamma) -butyrolactone, etc. are mentioned.
    [59] These solvents may each be used alone or in combination of two or more. The amount of solvent used is preferably 50 to 90% by weight, more preferably 60 to 85% by weight based on the total amount of the colored photosensitive composition including the solvent.
    [60] The colored photosensitive composition of the present invention may further comprise an additive (G) if necessary. Examples of the additive include fillers, polymer compounds different from the binder polymer (B), surfactants, adhesion promoters, antioxidants, ultraviolet absorbers, anticoagulants, organic acids, organic amino compounds, and curing agents.
    [61] Specific examples of the filler include glass, silica, alumina and the like.
    [62] Specific examples of the polymer compound different from the binder polymer (B) include polyvinyl alcohol, polyacrylic acid, polyethylene glycol monoalkyl ether, polyfluoroalkyl acrylate, and the like.
    [63] Specific examples of the surfactant include nonionic, cationic and anionic surfactants.
    [64] Specific examples of the adhesion promoter include vinyltrimethoxysilane, vinyltriethoxysilane, vinyltris (2-methoxyethoxy) silane, N- (2-aminoethyl) -3-aminopropylmethyldimethoxysilane, N -(2-aminoethyl) -3-aminopropyltrimethoxysilane, 3-aminopropyltriethoxysilane, 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropylmethyldimethoxysilane, 2- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, 3-chloropropylmethyldimethoxysilane, 3-chloropropyltrimethoxysilane, 3-methacryloxypropyltrimethoxysilane, 3-mercaptopropyl Trimethoxysilane etc. are mentioned.
    [65] Specific examples of the antioxidant include 2,2-thiobis (4-methyl-6-t-butylphenol), 2,6-di-t-butylphenol and the like.
    [66] Specific examples of the ultraviolet absorbent include 2- (3-t-butyl-5-methyl-2-hydroxyphenyl) -5-chlorobenzotriazole, alkoxybenzophenone and the like.
    [67] Specific examples of the anticoagulant include sodium polyacrylate.
    [68] Examples of the organic acid include aliphatic monocarboxylic acids such as formic acid, acetic acid, propionic acid, butyric acid, valeric acid, pivalic acid, caproic acid, diethyl acetic acid, enanthylic acid, and caprylic acid; Oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, brasylic acid, methylmalonic acid, ethylmalonic acid, dimethylmalonic acid, methyl succinic acid, Aliphatic dicarboxylic acids such as tetramethylsuccinic acid, cyclohexanedicarboxylic acid, itaconic acid, citraconic acid, maleic acid, fumaric acid and mesaconic acid; Aliphatic tricarboxylic acids such as tricavalrylic acid, aconitic acid and camphoronic acid; Aromatic monocarboxylic acids such as benzoic acid, toluic acid, cumene acid, hemetic acid and mesitylene acid; Aromatic dicarboxylic acids such as phthalic acid, isophthalic acid and terephthalic acid; Aromatic polycarboxylic acids such as trimellitic acid, trimesic acid, melophanic acid, pyromellitic acid, and the like.
    [69] Examples of the organic amino compound include n-propylamine, i-propylamine, n-butylamine, i-butylamine, secondary-butylamine, t-butylamine, n-pentylamine, n-hexylamine, n- Heptylamine, n-octylamine, n-nonylamine, n-decylamine, n-undecylamine, n-dodecylamine, cyclohexylamine, 2-methylcyclohexylamine, 3-methylcyclohexylamine, 4- Mono (cyclo) alkylamines such as methylcyclohexylamine; Methylethylamine, diethylamine, methyl-n-propylamine, ethyl-n-propylamine, di-n-propylamine, di-i-propylamine, di-n-butylamine, di-i-butylamine, Di (cyclo) alkyl such as di-tert-butylamine, di-t-butylamine, di-n-pentylamine, di-n-hexylamine, methylcyclohexylamine, ethylcyclohexylamine, dicyclohexylamine Amines; Dimethylethylamine, methyldiethylamine, triethylamine, dimethyl-n-propylamine, diethyl-n-propylamine, methyldi-n-propylamine, ethyldi-n-propylamine, tri-n-propylamine , Tri-i-propylamine, tri-n-butylamine, tri-i-butylamine, tri-tert-butylamine, tri-t-butylamine, tri-n-pentylamine, tri-n-hexylamine Tri (cyclo) alkylamines such as dimethylcyclohexylamine, diethylcyclohexylamine, methyldicyclohexylamine, ethyldicyclohexylamine and tricyclohexylamine; 2-aminoethanol, 3-amino-1-propanol, 1-amino-2-propanol, 4-amino-1-butanol, 5-amino-1-pentanol, 6-amino-1-hexanol, 4-amino Mono (cyclo) alkanolamines such as -1-cyclohexanol; Diethanolamine, di-n-propanolamine, di-i-propanolamine, di-n-butanolamine, di-i-butanolamine, di-n-pentanolamine, di-n-hexanolamine, di- Di (cyclo) alkanolamines such as (4-cyclohexanol) amine; Triethanolamine, tri-n-propanolamine, tri-i-propanolamine, tri-n-butanolamine, tri-i-butanolamine, tri-n-pentanolamine, tri-i-hexanolamine, tri- ( Tri (cyclo) alkanolamines such as 4-cyclohexanol) amine; 3-amino-1,2-propanediol, 2-amino-1,3-propanediol, 4-amino-1,2-butanediol, 4-amino-1,3-butanediol, 4-amino-1,2- Cyclohexanediol, 4-amino-1,3-cyclohexanediol, 3-dimethylamino-1,2-propanediol, 3-diethylamino-1,2-propanediol, 2-dimethylamino-1,3- Amino (cyclo) alkanediols such as propanediol and 2-diethylamino-1,3-propanediol; 1-aminocyclopentanonmethanol, 4-aminocyclopentanonmethanol, 1-aminocyclohexanonemethanol, 4-aminocyclohexanonemethanol, 4-dimethylaminocyclopentanmethanol, 4-diethylaminocyclopentanmethanol, 4 Amino group-containing cycloalkanethanols such as dimethylaminocyclohexanemethanol and 4-diethylaminocyclohexanemethanol; β-alanine, 2-aminobutyric acid, 3-aminobutyric acid, 4-aminobutyric acid, 2-aminoisobutyric acid, 3-aminoisobutyric acid, 2-aminovaleric acid, 5-aminovaleric acid, 6-aminocaproic acid, 1 Aminocarboxylic acids such as aminocyclopropanecarboxylic acid, 1-aminocyclohexanecarboxylic acid, and 4-aminocyclohexanecarboxylic acid; Aniline, o-methylaniline, m-methylaniline, p-methylaniline, p-ethylaniline, pn-propylaniline, pi-propylaniline, pn-butylaniline, pt-butylaniline, 1-naphthylamine, 2- Aromatic amines such as naphthylamine, N, N-dimethylaniline, N, N-diethylaniline and p-methyl-N, N-dimethylaniline; aminobenzyl alcohols such as o-aminobenzyl alcohol, m-aminobenzyl alcohol, p-aminobenzyl alcohol, p-dimethylaminobenzyl alcohol and p-diethylaminobenzyl alcohol; aminophenols such as o-aminophenol, m-aminophenol, p-aminophenol, p-dimethylaminophenol and p-diethylaminophenol; and aminobenzoic acids such as m-aminobenzoic acid, p-aminobenzoic acid, p-dimethylaminobenzoic acid and p-diethylaminobenzoic acid.
    [70] Curing agents are used to increase the mechanical strength of color pixels by curing them by heat treatment after development. Examples of such curing agents include compounds capable of crosslinking with the binder polymer by reaction with carboxyl groups in the binder polymer under heating, which cures color pixels or black matrices by crosslinking of the binder. The curing agent may also be a compound that can self polymerize by heat, which cures the color pixel or black matrix by self-polymerization. As an example of these compounds, an epoxy compound, an oxetane compound, etc. are mentioned.
    [71] Examples of the epoxy compound include bisphenol A epoxy resin, hydrogenated bisphenol A epoxy resin, bisphenol F epoxy resin, hydrogenated bisphenol F epoxy resin, novolac epoxy resin, other aromatic epoxy resin, alicyclic epoxy resin, Epoxy resins such as heterocyclic epoxy resins, glycidyl ester resins, glycidyl amine resins, and epoxidized oils; Brominated derivatives of these epoxy resins; Aliphatic, alicyclic or aromatic epoxy compounds different from the epoxy resin and its brominated derivatives; Epoxidation products of butadiene (co) polymers; Epoxidation products of isoprene (co) polymers; Glycidyl (meth) acrylate (co) polymers; Triglycidyl isocyanurate etc. are mentioned.
    [72] Examples of the oxetane compound include carbonate bisoxetane, xylene bisoxetane, adipate bisoxetane, terephthalate bisoxetane, cyclohexane dicarboxylic acid bisoxetane and the like.
    [73] The colored photosensitive composition of the present invention may include a compound capable of ring-opening polymerization of an epoxy group in an epoxy compound or an oxetane nucleus in an oxetane compound with a curing agent. Examples of such compounds include polybasic carboxylic acids, polybasic carboxylic anhydrides, acid generators, and the like.
    [74] Examples of the polybasic carboxylic acid include phthalic acid, 3,4-dimethylphthalic acid, isophthalic acid, terephthalic acid, pyromellitic acid, trimellitic acid, 1,4,5,8-naphthalenetetracarboxylic acid, 3,3 Aromatic polybasic carboxylic acids such as', 4,4'-benzophenonetetracarboxylic acid; Aliphatic polybasic carboxylic acids such as succinic acid, glutaric acid, adipic acid, 1,2,3,4-butanetetracarboxylic acid, maleic acid, fumaric acid and itaconic acid; Hexahydrophthalic acid, 3,4-dimethyltetrahydrophthalic acid, hexahydroisophthalic acid, hexahydroterephthalic acid, 1,2,4-cyclopentanetricarboxylic acid, 1,2,4-cyclohexanetricarboxylic acid, cyclopentane Alicyclic polybasic carboxylic acids, such as tetracarboxylic acid and a 1, 2, 4, 5- cyclohexane tetracarboxylic acid, etc. are mentioned.
    [75] Examples of the polybasic carboxylic anhydride include aromatic polybasic carboxylic acids such as phthalic anhydride, pyromellitic anhydride, trimellitic anhydride and 3,3 ', 4,4'-benzophenonetetracarboxylic anhydride. anhydride; Aliphatic polybasic carboxylic anhydrides such as itaconic anhydride, succinic anhydride, citraconic anhydride, dodecenyl succinic anhydride, tricavalyl anhydride, maleic anhydride, 1,2,3,4-butanetetracarboxylic dianhydride ; Hexahydrophthalic anhydride, 3,4-dimethyltetrahydrophthalic anhydride, 1,2,4-cyclopentanetricarboxylic anhydride, 1,2,4-cyclohexanetricarboxylic anhydride, cyclopentanetetracarboxylic anhydride Cycloaliphatic polybasic carboxes such as 1,2,4,5-cyclohexanetetracarboxylic anhydride, 1,2,3,6-tetrahydro-3,6-methanophthalic anhydride, nadic anhydride Acid anhydrides; Ester group containing carboxylic anhydride, such as ethylene glycol bistrimelite anhydride and glycerol tristrimelic anhydride, etc. are mentioned.
    [76] Commercially available products for epoxy resin curing agents can be used as the carboxylic acid anhydride. Examples of such epoxy resin curing agents include "Adeka Hardener EH-700" (trademark, manufactured by Asahi Denka Kogyo KK), "Rikacid HH" (trademark, manufactured by New Japan Chemicals), "MH-700" (trademark, manufactured by New Japan Chemicals, Inc. ), And the like.
    [77] These curing agents may be used alone or in combination of two or more.
    [78] The colored photosensitive composition of the present invention can be prepared by mixing a colorant (A), a binder polymer (B), a photopolymerizable compound (C), a photopolymerization initiator (D) and a chain transfer agent (E) in a solvent (F). have. When it contains an additive (G), a coloring agent (A), a binder polymer (B), a photopolymerizable compound (C), a photoinitiator (D), a chain transfer agent (E), and an additive (G) are a solvent (F). The compositions can be prepared by mixing in place.
    [79] In order to produce a color pixel or black matrix 5 using the colored photosensitive composition of the present invention, for example, a layer 1 of the colored photosensitive composition of the present invention is formed on the substrate 2 (FIG. 1A). The layer 1 is then exposed to light by irradiating the light beam 4 through the photo-mask 3 (see FIG. 1B) and then developed.
    [80] Examples of the substrate 2 include a glass substrate, a silicon wafer, a plastic substrate, and the like. When a silicon wafer or the like is used as the substrate, charge-coupled devices (CCD) or the like may be formed on the surface of the silicon wafer or the like.
    [81] In order to form the colored photosensitive composition layer 1 on the substrate 2, for example, the colored photosensitive composition diluted with a solvent is applied onto the substrate by a spin coating method (spin-coating method), and then the solvent is applied. Evaporate.
    [82] Then, the substrate is irradiated with a light beam 4 to be exposed. Generally, ultraviolet rays such as g-ray (wavelength: 436 nm), i-ray (wavelength: 365 nm) and the like are used as the light beam 4.
    [83] The light beam is irradiated through the light-mask 3. Here, the photo-mask is, for example, a glass substrate 31 having a light shielding layer 32 for covering a light beam on its surface. The light beam 4 is covered by the light shielding layer 32. The region of the glass substrate 31 without the light shielding layer is a translucent region 33 for transmitting the light beam. The colored photosensitive composition layer 2 is exposed according to the pattern of the translucent region 33. The intensity of the light beam to be irradiated is appropriately selected depending on the type and amount of the binder polymer (B), the color and amount of the pigment (A), the type and amount of the photopolymerizable compound (C), the type and amount of the photopolymerization initiator (D), and the like. do.
    [84] It develops after exposure. To develop, for example, the exposed colored photosensitive composition layer is immersed in a developing solution. As an example of a developing solution, the aqueous solution of alkaline compounds, such as sodium carbonate, sodium hydroxide, potassium hydroxide, potassium carbonate, tetramethylammonium hydroxide, is mentioned.
    [85] By development, the non-irradiation region 11, which is the colored photosensitive composition layer region not irradiated with the light beam, is removed, and the irradiation region 22, which is the region irradiated with the light beam, remains, so that the color pixel or the black matrix 5 is removed. Configure.
    [86] In general, after development, the product can be washed with water and dried to obtain the desired color filter or black matrix 5.
    [87] After drying, heat treatment may be performed. By this heat treatment, the formed color pixels and the like are cured to increase the mechanical strength. Since the mechanical strength of the color pixel or black matrix is further improved by the heat treatment, it is preferable to use a colored photosensitive composition comprising a curing agent. The heat treatment temperature is generally at least 180 ° C, preferably about 200 ° C to 250 ° C.
    [88] The color pixel or black matrix 5 obtained by this method has a thickness of, for example, 1 µm to 3 µm. If the thickness is 2 탆 or less, or 1.8 탆 or less, the cross section is rectangular or tapering forward, so that any transparent conductive film formed on the color pixel, such as in indium-tin complex oxide (ITO), hardly cracks, The width W 1 of the upper surface is less than or equal to the width W 2 of the lower surface (ie, the substrate surface) of the color pixel (see FIG. 2A) (see FIG. 2B).
    [89] To obtain a color filter by forming color pixels of another color or black matrix, the above process is repeated while changing the color of the colorant (A). In this way, color pixels or black matrices of each color can be formed.
    [90] Using the colored photosensitive composition of the present invention, even when the colored photosensitive composition contains a high concentration of colorant, it is possible to form a color pixel or black matrix having a tapered or tapering cross section forward.
    [91] The present invention will be described in more detail with reference to the following examples, which should not be construed as limiting the scope of the invention.
    [92] Example
    [93] A colored photosensitive composition having the composition shown in Table 1 was applied by spin-coating on the surface of a glass substrate ("# 7059", manufactured by Corning Glass Works). Drying at 100 ° C. for 3 minutes gave a colored photosensitive composition layer 1. After cooling, i-rays (wavelength: 365 nm) were irradiated onto the colored photosensitive composition layer 1 formed through the photo-mask 3. An ultrahigh pressure mercury lamp was used as an i-ray light source. The intensity of the radiation was 150 mJ / cm 2 . The photo-masks used are linear pixels with line widths of 3 μm, 4 μm, 5 μm, 6 μm, 7 μm, 8 μm, 9 μm, 10 μm, 20 μm, 30 μm, 40 μm, 50 μm and 100 μm It was a photo-mask for simultaneous formation.
    [94] Then, the substrate was immersed in a developing solution (an aqueous solution containing 0.05% potassium hydroxide and 0.2% by weight sodium butylnaphthalenesulfonate, respectively) and developed, washed with purified water, heated at 230 ° C. for 20 minutes, and The color pixel 5 was obtained.
    [95] The green-colored pixel 5 had a tapering cross section forward and 1.6 mu m thick. The minimum value of the line width of the color pixel formed in desired shape (resolution) was 20 micrometers.
    [96] Quantity (parts by mass) Pigment (A) Binder polymer (B) Photopolymerizable compound (C) Photopolymerization initiator (D) Photopolymerization adjuvant Chain transfer agent (E) Solvent (F) Additive (G)CI pigment green 36C.I. pigment yellow 150 methacrylic acid / benzyl methacrylate copolymer (ratio: ratio of methacrylic acid unit / benzyl methacrylate unit is 0.30 / 0.60, the weight average molecular weight is 35,000) Dipentaerythritol hexaacrylate ("KAYARAD DPHA", manufactured by Nippon Kayaku) "Irgacure-907" (manufactured by Ciba-Geigy) "EAB-F" (manufactured by Hodogaya Chemicals) 2,4-diphenyl-4-methyl-1- Pentene Propylene Glycol Monomethyl Ether Acetate Pigment Dispersant4.952.285.005.001.200.400.6080.001.17
    [97] Example 2
    [98] 5.00 parts by mass of 3-ethyl-3-methacryloxymethyloxetane / benzyl methacrylate / methacrylic acid copolymer (weight average molecular weight was 53,000) The procedure of Example 1 was repeated except that the ratio of 3-ethyl-3-methacryloxymethyloxetane units / benzyl methacrylate / methacrylic acid units was 0.10 / 0.50 / 0.30 in terms of concentration ratio). The green-colored color pixel 5 was formed.
    [99] The green-colored pixels had a tapering cross section forward, 1.6 μm thick and 20 μm in resolution.
    [100] Example 3
    [101] The procedure of Example 1 was repeated to form green-colored color pixels, except that the amount of chain transfer agent was changed to 1.00 parts by mass.
    [102] The green-colored pixel had a tapering cross section forward, 1.6 mu m thick, and 100 mu m resolution.
    [103] Comparative Example 1
    [104] The procedure of Example 1 was repeated to form green-colored color pixels, except that the colored photosensitive composition was prepared without a chain transfer agent.
    [105] The green-colored pixel had a tapered cross section, with a thickness of 1.6 μm and a resolution of 7 μm.
    [106] Comparative Example 2
    [107] The procedure of Example 1 was repeated to form green-colored color pixels, except that 0.60 parts by mass of p-methoxyphenol was used instead of the chain transfer agent.
    [108] The green-colored pixel had a tapered cross section, with a thickness of 1.6 μm and a resolution of 7 μm.
    [109] Using the colored photosensitive composition of the present invention, even when the colored photosensitive composition contains a high concentration of colorant, it is possible to form a color pixel or black matrix having a square or forward tapering cross section.
    权利要求:
    Claims (9)
    [1" claim-type="Currently amended] A colored photosensitive composition comprising a colorant (A), a binder polymer (B), a photopolymerizable compound (C), a photopolymerization initiator (D) and a chain transfer agent (E).
    [2" claim-type="Currently amended] The method of claim 1,
    Colored photosensitive composition, characterized in that the amount of the chain transfer agent (E) is 0.5 to 5% by mass based on the total amount of solids of the colored photosensitive composition.
    [3" claim-type="Currently amended] The method of claim 1,
    The colored photosensitive composition, characterized in that the amount of the coloring agent (A) is 5 to 60% by mass based on the total amount of solids of the colored photosensitive composition.
    [4" claim-type="Currently amended] The method of claim 2,
    The colored photosensitive composition, characterized in that the amount of the coloring agent (A) is 5 to 60% by mass based on the total amount of solids of the colored photosensitive composition.
    [5" claim-type="Currently amended] The method of claim 2,
    The binder photopolymer (B) is a colored photosensitive composition, characterized in that the copolymer derived from a carboxyl group-containing monomer and other monomers copolymerizable therewith.
    [6" claim-type="Currently amended] The method of claim 1,
    Colored photosensitive composition, characterized in that the composition further comprises a photopolymerization aid.
    [7" claim-type="Currently amended] The method of claim 1,
    Colored photosensitive composition, characterized in that the composition further comprises a solvent (F).
    [8" claim-type="Currently amended] Forming a colored photosensitive composition layer according to claim 1 on a substrate; Filter manufacturing method.
    [9" claim-type="Currently amended] The method of claim 8,
    And the thickness of the color pixel or black matrix is 3 μm or less.
    类似技术:
    公开号 | 公开日 | 专利标题
    KR100518992B1|2005-10-06|Radiation Sensitive Composition
    JP6409936B2|2018-10-24|Colored photosensitive composition, black photo spacer, color filter, and liquid crystal display device
    KR100423220B1|2005-01-15|Radiation Sensitive Composition
    KR100820610B1|2008-04-10|Photosensitive composition, photosensitive colored compositions, color filters, and liquid crystal displays
    JP5109903B2|2012-12-26|Radiation-sensitive composition for forming colored layer, color filter, and liquid crystal display device
    TWI518450B|2016-01-21|Color filter for low temperature applications
    JP4788485B2|2011-10-05|Colored photosensitive resin composition
    JP4635935B2|2011-02-23|Radiation-sensitive composition for forming colored layer, color filter, and color liquid crystal display element
    JP4595374B2|2010-12-08|Black photosensitive resin composition
    KR102111300B1|2020-05-15|Coloring photosensitive composition, cured film, pattern forming method, infrared blocking filter with light shielding film, solid-state imaging element, image display device and infrared sensor
    KR101047703B1|2011-07-08|colored photosensitive resin composition and color filter
    KR101784247B1|2017-11-06|Polymerizable composition, cured film, color filter, method of producing color filter and solid-state image sensor
    TWI444767B|2014-07-11|Radiation sensitive composition for forming a colored layer, color filter and color liquid crystal display device
    CN103135350B|2015-07-15|Photosensitive resin composition for color filter and color filter including the same
    KR101128171B1|2012-03-26|A colored photosensitive resin composition
    JP4998906B2|2012-08-15|Colored photosensitive resin composition, color filter produced using the same, and liquid crystal display device
    KR101243547B1|2013-03-20|Colored Photosensitive Resin Composition
    KR101152447B1|2012-06-01|Polymers, Radiation Sensitive Compositions for Color Filters, Color Filters and Color Liquid Crystal Display Device or Panel
    JP2003277673A|2003-10-02|Pigment-dispersing agent, pigment dispersed composition, colored coating composition and color filter
    JP6091831B2|2017-03-08|Colored photosensitive resin composition
    KR101901459B1|2018-09-21|Colored curable resin composition
    KR20110068861A|2011-06-22|Coloring composition, color filter and color liquid crystal display device
    TWI419905B|2013-12-21|Black-colored photosensitive resin composition, black matrix prepared by using thereof and color filter comprising the black matrix
    JP4631808B2|2011-02-23|Colored photosensitive resin composition
    JP5905939B2|2016-04-20|Alkali-soluble resin, photosensitive resin composition, color filter and method for producing the same, and liquid crystal display device
    同族专利:
    公开号 | 公开日
    US20020094485A1|2002-07-18|
    TW553958B|2003-09-21|
    US6641961B2|2003-11-04|
    JP2002167404A|2002-06-11|
    KR100863794B1|2008-10-16|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    2000-11-29|Priority to JP2000362826A
    2000-11-29|Priority to JPJP-P-2000-00362826
    2001-11-26|Application filed by 고오사이 아끼오, 스미또모 가가꾸 고교 가부시끼가이샤
    2002-06-05|Publication of KR20020042439A
    2008-10-16|Application granted
    2008-10-16|Publication of KR100863794B1
    优先权:
    申请号 | 申请日 | 专利标题
    JP2000362826A|JP2002167404A|2000-11-29|2000-11-29|Colored photosensitive composition|
    JPJP-P-2000-00362826|2000-11-29|
    [返回顶部]