JP2013129706A - Colored resin composition, color filter, liquid crystal display device, and organic el display - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a colored resin composition that can obtain a color filter excellent in ITO resistance, and the color filter formed by using the colored resin composition, and to provide a liquid crystal display device and an organic EL display device having high quality.SOLUTION: The colored resin composition includes (A) a dye, (B) a solvent, and (C) a binder resin, wherein (A) the dye includes a compound shown by a specific structure.

Description

  The present invention resides in a colored resin composition, a color filter, a liquid crystal display device, and an organic EL display device.

Flat panel displays such as liquid crystal display devices and organic EL display devices are widely used, and color filters are used for these displays.
Taking into account the trend of energy conservation, color filters are required to have higher brightness and higher contrast.
For the color filter, a colored resin composition using a pigment is mainly used. In order to obtain high brightness and high contrast, for example, in Non-Patent Document 1, the particle diameter of pigment particles is set to 1 of the coloration wavelength. Disclosed is a method of finely dispersing to / 2 or less.

However, since the blue pigment has a shorter coloration wavelength than other red and green pigments in particular, further fine dispersion is required in this case, which causes a problem of cost increase and stability after dispersion.
On the other hand, dyes have been developed as colorants.
For example, Patent Document 1 discloses using a triarylmethane derivative as a dye. Patent Documents 2 and 3 disclose that a triarylmethane salt further has a specific structure of an anion.

JP 2008-304766 A JP 2011-132492 A JP 2011-133844 A

Kiyoshi Hashizume, “Color Material Association”, December 1967, p608

However, Patent Documents 1 to 3 improved triarylmethane salts have found that ITO resistance is insufficient. Furthermore, it discovered that light resistance might not be enough.
In addition, ITO tolerance in this invention means the following.
ITO resistance refers to the ability to maintain color characteristics even after ITO is deposited on the pixels.

The index of ITO resistance is represented by ΔE * ab calculated from the spectrum before baking the ITO film and after baking the ITO film-formed substrate at an arbitrary temperature and time.
In view of the above, an object of the present invention is to provide a colored resin composition from which a color filter having good ITO resistance can be obtained.
Another object of the present invention is to provide a color filter formed using the colored resin composition, a high-quality liquid crystal display device, and an organic EL display device.

As a result of intensive studies by the present inventors, it has been found that the above problems can be solved by using a dye having a specific structure, and the present invention has been completed.
That is, this invention contains (A) dye, (B) solvent, and (C) binder resin, and (A) dye is a compound (henceforth "compound (I)") represented by following formula (I). In a colored resin composition, a color filter, a liquid crystal display device, and an organic EL display device.

(In the above formula (I),
[A ⁿ⁻ ] represents an n-valent anion.
n represents an integer of 1 to 4.
R ^{1 to} R ⁴ each independently represents a branched alkyl group having 4 or more carbon atoms in the base chain, which may have a substituent.

R ⁵ and R ⁶ each independently represent a hydrogen atom, an alkyl group which may have a substituent, or an aromatic ring group which may have a substituent.
R ⁷ and R ⁸ each independently represents a hydrogen atom or an arbitrary substituent.
R ⁷ and R ⁸ may be connected to each other to form a ring, and the ring may have a substituent.

Further, the benzene ring and indole ring in the above formula (I) may further have an arbitrary substituent.
In addition, a plurality of cations represented by the following formula (I) _CA in one molecule

May be the same structure or different structures. )

The present invention can provide a colored resin composition from which a color filter having good ITO resistance can be obtained.
The present invention can also provide a color filter formed using the colored resin composition, a high-quality liquid crystal display device, and an organic EL display device.

It is a section schematic diagram showing an example of an organic EL device which has a color filter of the present invention.

Embodiments of the present invention will be described in detail below, but the following description is an example of embodiments of the present invention, and the present invention is not limited to these contents.
In the present invention, “(meth) acryl”, “(meth) acrylate” and the like mean “acryl and / or methacryl”, “acrylate and / or methacrylate” and the like, for example, “(meth) acrylic acid” "Means" acrylic acid and / or methacrylic acid ".

Further, “total solid content” means all components of the colored resin composition of the present invention other than the solvent components described later.
Furthermore, “aromatic ring” means both “aromatic hydrocarbon ring” and “aromatic heterocycle”.
Moreover, terms such as “CI Pigment Green” mean a color index (CI).

The colored resin composition of the present invention contains (A) a dye, (B) a solvent, and (C) a binder resin, and the (A) dye contains the compound (I).
First, the compound (I) in the present invention will be described in detail.
[Compound (I)]

(In the above formula (I),
[A ⁿ⁻ ] represents an n-valent anion.
n represents an integer of 1 to 4.
R ^{1 to} R ⁴ each independently represents a branched alkyl group having 4 or more carbon atoms in the base chain, which may have a substituent.

R ⁵ and R ⁶ each independently represent a hydrogen atom, an alkyl group which may have a substituent, or an aromatic ring group which may have a substituent.
R ⁷ and R ⁸ each independently represents a hydrogen atom or an arbitrary substituent.
R ⁷ and R ⁸ may be connected to each other to form a ring, and the ring may have a substituent.

Further, the benzene ring and indole ring in the above formula (I) may further have an arbitrary substituent.
In addition, a plurality of cations represented by the following formula (I) _CA in one molecule

May be the same structure or different structures. )
[Structural features]
When R ^{1 to} R ⁴ are branched alkyl groups having 4 or more carbon atoms in the base chain, steric hindrance around the nitrogen atom is increased. Thereby, when baking the coating film formed with the colored resin composition, reaction with a compound (I) and peripheral molecules, for example, binder resin, a polymerizable monomer, etc. is suppressed. Therefore, the spectral change due to firing is suppressed. From the above, it is presumed that the pixel formed using the colored resin composition of the present invention has improved ITO resistance.

(For ^R 1 to R ⁴⁾
R ^{1 to} R ⁴ each independently represents a branched alkyl group having 4 or more carbon atoms in the base chain, which may have a substituent.
A group which is a base chain having 4 or more carbon atoms means that at least 4 carbon atoms are connected in a straight chain. For example, taking a butyl group as an example, an n-butyl group is a group that is a base chain having 4 or more carbon atoms, while a sec-butyl group or an iso-butyl group is a group that is a base chain having 3 carbon atoms. In addition, the tert-butyl group is a group that is a base chain having 2 carbon atoms.

  Examples of the branched alkyl group having 4 or more carbon atoms in the base chain include 2-methylbutyl group, 2-ethylbutyl group, 3-methylbutyl group, 2,2-dimethylbutyl group, 2,3-dimethylbutyl group, 2 -Methylpentyl group, 3-methylpentyl group, 4-methylpentyl group, 3,5,5-trimethylpentyl group, 2-ethylhexyl group, 5-methylhexyl group, 2,5-dimethylhexyl group and the like.

The number of carbon atoms in the base chain in R ^{1 to} R ⁴ is usually 4 or more, and usually 14 or less, preferably 10 or less.
The R ¹ to R ⁴ in the branched alkyl group substituent which may be possessed by, for example, those described in the section below [Substituent Group W ^1].

[Substituent Group W ¹ ]
C2-C8 alkenyl group, C1-C8 alkoxy group, C6-C15 aryl group, C2-C9 alkylcarbonyloxy group, C7-C16 arylcarbonyloxy group, carbon C2-C9 alkoxycarbonyl group, C7-C16 aryloxycarbonyl group, carbamoyl group, C2-C9 alkylcarbamoyl group, C7-C16 arylcarbamoyl group, sulfamoyl group, C1-C1 An alkylsulfamoyl group having 8 carbon atoms, an arylsulfamoyl group having 6 to 15 carbon atoms, an alkylcarbonyl group having 2 to 9 carbon atoms, an arylcarbonyl group having 7 to 16 carbon atoms, an alkylsulfonyl group having 1 to 8 carbon atoms, C1-C8 alkylsulfonylamino group, C6-C15 arylsulfonylamino group, Amino group, C1-C8 An alkylamino group formed by bonding an alkyl group, a dialkylamino group formed by bonding an alkyl group having 1 to 4 carbon atoms, an arylamino group having 6 to 15 carbon atoms, an aryl group having 6 to 15 carbon atoms and a carbon number of 1 Arylalkylamino group formed by bonding ~ 4 alkyl, diarylamino group formed by bonding aryl group having 6 to 15 carbon atoms, phenethyl group, hydroxyethyl group, alkylcarbonylamino group having 1 to 8 carbon atoms, carbon An arylcarbonylamino group having 7 to 16 carbon atoms, a dialkylaminoethyl group formed by bonding an alkyl group having 1 to 4 carbon atoms, a trifluoromethyl group, a trialkylsilyl group having 1 to 8 carbon atoms, and an alkyl group having 1 to 8 carbon atoms Alkylthio group, arylthio group having 6 to 15 carbon atoms, hydroxy group, nitro group, cyano group, carboxy group, sulfo group, fluorine atom and chlorine atom Halogen atom and the like.

Examples of the aryl group in the substituent group W ¹ include an aromatic hydrocarbon ring group and an aromatic heterocyclic group.
The aromatic hydrocarbon ring group may be a single ring or a condensed ring, and is not particularly limited as long as the number of carbon atoms forming the ring is 5 to 18, but for example, one free valence Benzene ring, naphthalene ring, anthracene ring, phenanthrene ring, perylene ring, tetracene ring, pyrene ring, benzpyrene ring, chrysene ring, triphenylene ring, acenaphthene ring, fluoranthene ring, fluorene ring and the like.

In addition, the aromatic heterocyclic group may be a single ring or a condensed ring, and is not particularly limited as long as the number of carbon atoms forming the ring is 3 to 10, but for example, one free atom Having a valence, furan ring, benzofuran ring, thiophene ring, benzothiophene ring, pyrrole ring, pyrazole ring, imidazole ring, oxadiazole ring, indole ring, carbazole ring, pyrroloimidazole ring, pyrrolopyrazole ring, pyrrolopyrrole ring, thienopyrrole Ring, thienothiophene ring, furopyrrole ring, furofuran ring, thienofuran ring, benzisoxazole ring, benzisothiazole ring, benzimidazole ring, pyridine ring, pyrazine ring, pyridazine ring, pyrimidine ring, triazine ring, quinoline ring, isoquinoline ring, Synoline ring, quinoxaline ring, phenanthridine ring, Zone imidazole ring, perimidine ring, a quinazoline ring, a quinazolinone ring, groups such as azulene ring.

The aryl group is a lower alkyl group such as a methyl group or an ethyl group, a lower alkoxy group such as a methoxy group or an ethoxy group, a nitro group, a trifluoromethyl group, a cyano group, a carbamoyl group, a sulfamoyl group, a fluorine atom, or a chlorine atom. May be further substituted as a substituent.
Among them, as R ¹ to R ⁴ substituents which may be alkyl groups have in, preferably an alkoxy group having 1 to 8 carbon atoms, a phenyl group, a tolyl group, an alkylcarbonyloxy group having 2 to 9 carbon atoms, a carbamoyl A group, a sulfamoyl group, an alkylsulfamoyl group having 1 to 8 carbon atoms, a trifluoromethyl group, a cyano group and a fluorine atom.

(About R ⁵ and R ⁶ )
R ⁵ and R ⁶ each independently represent a hydrogen atom, an alkyl group which may have a substituent, or an aromatic ring group which may have a substituent.
Examples of the alkyl group in R ⁵ and R ⁶ include linear, branched or cyclic alkyl groups, and the number of carbon atoms is usually 1 or more, and usually 8 or less, preferably 5 or less. . Specific examples include methyl group, ethyl group, n-propyl group, 2-propyl group, n-butyl group, isobutyl group, tert-butyl group, cyclohexyl group and the like.

Examples of the aromatic ring group for R ⁵ and R ⁶ include an aromatic hydrocarbon ring group and an aromatic heterocyclic group.
The aromatic hydrocarbon ring group may be a single ring or a condensed ring, and is not particularly limited as long as the number of carbon atoms forming the ring is 5 to 18, but for example, one free valence Benzene ring, naphthalene ring, anthracene ring, phenanthrene ring, perylene ring, tetracene ring, pyrene ring, benzpyrene ring, chrysene ring, triphenylene ring, acenaphthene ring, fluoranthene ring, fluorene ring and the like.

  In addition, the aromatic heterocyclic group may be a single ring or a condensed ring, and is not particularly limited as long as the number of carbon atoms forming the ring is 3 to 10, but for example, one free atom Having a valence, furan ring, benzofuran ring, thiophene ring, benzothiophene ring, pyrrole ring, pyrazole ring, imidazole ring, oxadiazole ring, indole ring, carbazole ring, pyrroloimidazole ring, pyrrolopyrazole ring, pyrrolopyrrole ring, thienopyrrole Ring, thienothiophene ring, furopyrrole ring, furofuran ring, thienofuran ring, benzisoxazole ring, benzisothiazole ring, benzimidazole ring, pyridine ring, pyrazine ring, pyridazine ring, pyrimidine ring, triazine ring, quinoline ring, isoquinoline ring, Synoline ring, quinoxaline ring, phenanthridine ring, Zone imidazole ring, perimidine ring, a quinazoline ring, a quinazolinone ring, groups such as azulene ring.

The free valence in the present invention is based on the description in “Organic Chemistry / Biochemical Nomenclature” (Nanedo, published May 20, 1992, translated by Kenzo Hirayama and Kazuo Hirayama, pages 11-12). It is.
Adjacent R ⁵ and R ⁶ may be connected to form a ring, and the ring may have a substituent.

From the viewpoint of chemical stability, R ³ and R ⁴ are preferably each independently a hydrogen atom, a C 1-8 alkyl group which may have a substituent, or a substituent. Good phenyl group.
It has the C1-C8 alkyl group or substituent which may have a substituent more preferably at the point which improves the heat resistance of compound (I) and the heat resistance of the color filter obtained is excellent. It may be a phenyl group.

When R ³ and R ⁴ are an alkyl group having 1 to 8 carbon atoms which may have a substituent, it is presumed that the charges in the cation are dispersed by hyperconjugation and the cation is stabilized.
In addition, when R ⁵ and R ⁶ are phenyl groups that may have a substituent, the conjugated system is extended, so that the charge in the cation is dispersed and the cation is stabilized. As described above, it can be considered that as a result of stabilization of the cation, the heat resistance of the obtained color filter is further improved.
Examples of the substituent that the alkyl group, the aromatic ring group, and the ring formed by connecting to each other in R ⁵ and R ⁶ may have include the following (substituent group W).

(Substituent group W)
Fluorine atom, chlorine atom, alkyl group having 1 to 8 carbon atoms, alkenyl group having 2 to 8 carbon atoms, alkoxyl group having 1 to 8 carbon atoms, phenyl group, mesityl group, tolyl group, naphthyl group, cyano group, acetyloxy Group, an alkylcarbonyloxy group having 2 to 9 carbon atoms, a sulfonic acid amide group, a sulfonealkylamide group having 2 to 9 carbon atoms, an alkylcarbonyl group having 2 to 9 carbon atoms, a phenethyl group, a hydroxyethyl group, an acetylamide group, A dialkylaminoethyl group, a trifluoromethyl group, a trialkylsilyl group having 1 to 8 carbon atoms, a nitro group, and an alkylthio group having 1 to 8 carbon atoms formed by bonding an alkyl group having 1 to 4 carbon atoms.

Among them, as the substituent that the alkyl group, the aromatic ring group, and the ring formed by connecting to each other in R ³ and R ⁴ may have, preferably an alkyl group having 1 to 8 carbon atoms, or 2 to 2 carbon atoms. An alkoxyl group having 8 carbon atoms, a cyano group, an acetyloxy group, an alkyl carboxyl group having 2 to 8 carbon atoms, a sulfonic acid amide group, a sulfone alkylamide group having 2 to 8 carbon atoms, and a fluorine atom.

(About R ⁷ and R ⁸ )
R ⁷ and R ⁸ represent a hydrogen atom or an arbitrary substituent. As this arbitrary substituent, the C1-C8 alkyl group which may have a halogen atom, a substituent, the aromatic ring group which may have a substituent, etc. are mentioned, for example.
In the benzene ring in formula (I), when a bulky group is bonded at the o-position to the carbon atom located at the center of the triarylmethine structure, the planarity of the molecule is inhibited and compound (I) The color purity of the color may be reduced. Accordingly, it is preferable that the o-position does not have a substituent or is substituted with a halogen atom or an alkyl group having 1 to 8 carbon atoms.

In addition, it is preferable that this C1-C8 alkyl group is a C1-C4 alkyl further by the point that steric hindrance is small and the heat resistance of compound (I) improves.
R ⁷ and R ⁸ may be connected to each other to form a ring, and the ring may have a substituent. Examples of the substituent include those described in the above section (Substituent group W).

When R ⁷ and R ⁸ are linked to form a ring, these may be a ring bridged with a heteroatom.
Examples of the structure of the linking moiety of R ⁷ and R ⁸ include the following. The structure of these connecting portions may have a substituent.

(In the above, R ^1b and R ^2b each independently represent a hydrogen atom or an alkyl group.)
R ^1b and R ^2b are preferably a hydrogen atom or a methyl group in terms of (I) the high molecular planarity of _{CA and} the ease with which molecules can associate with each other and high heat resistance.
When the obtained color filter is purple, it is preferable that R ⁷ and R ⁸ are not connected to each other to form a ring from the viewpoint of high luminance.

In addition, when the color filter to be obtained is red, it is preferable that they are connected to each other to form a ring from the viewpoint of high luminance.
In addition, the benzene ring and indole ring in formula (I) may further have an arbitrary substituent. As the substituent that the benzene ring and indole ring in formula (I) may have, a fluorine atom, a chlorine atom, a bromine atom, an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, carbon A C1-C8 alkoxy group, a C1-C10 alkylamino group, etc. are mentioned.

(About n)
n represents an integer of 1 to 4.
It is preferable that n is 1-3 in the point that the solubility with respect to the organic solvent of compound (I) is favorable.
[About ^An- ]
[A ⁿ⁻ ] represents an n-valent anion.

The n-valent anion is not particularly limited as long as the effect of the present invention is not impaired, but disulfonyl is preferred in that it is easy to produce and the anion is stable because the negative charge is delocalized. It is preferably an imide anion.
That is, the compound (I) is preferably a compound represented by the following formula (II) (hereinafter sometimes referred to as “compound (II)”).
[Compound (II)]

(In said formula (II), R < ¹ > -R < ⁸ > is synonymous with the said formula (I) respectively.
R ¹¹ and R ¹² are each independently an optionally substituted alkyl group having 1 to 8 carbon atoms, an optionally substituted alkenyl group having 2 to 6 carbon atoms, or a substituent. The C3-C8 cycloalkyl group which may have is represented.
R ¹¹ and R ¹² may be connected to each other to form a ring, and the ring may have a substituent. )

(About R ¹¹ and R ¹² )
R ¹¹ and R ¹² have an optionally substituted alkyl group having 1 to 8 carbon atoms, an optionally substituted alkenyl group having 2 to 6 carbon atoms, and a substituent. Or a C3-C8 cycloalkyl group.
Examples of the substituent include those described in the above section (Substituent group W).

Among these, in particular, as the substituent of the alkyl group, alkenyl group or cycloalkyl group in R ¹¹ and R ¹² , the anion charge is more delocalized, and the heat resistance of the coloring material is improved. It preferably has a fluorine atom as a substituent.
That is, R ¹¹ and R ¹² are preferably a C 1-8 perfluoroalkyl group in that the anion charge is dispersed and the anion is stabilized.

More specifically, the anion of the compound (II), that is, the anion represented by the following formula (II) _A is preferably a compound represented by the following formula (I ′) _A.

(In said formula (II-1) _A , n and n 'represent the integer of 1-8 each independently.)
n and n 'are an integer of 1-8, Preferably it is an integer of 1-4.
n and n ′ may be the same or different.
Specific examples of the sulfonylimide anion when n and n ′ are the same include bis (trifluoromethanesulfone) imide, bis (pentafluorobutanesulfone) imide and the like.

Specific examples of the sulfonylimide anion when n and n ′ are different include pentafluoroethanesulfone trifluoromethanesulfonimide, trifluoromethanesulfone heptafluoropropanesulfonimide, fluorobutanesulfone trifluoromethanesulfonimide, and the like.
Among these, bis (pentafluoromethanesulfone) imide, where n = n ′ = 1, is particularly preferable because the anion is most stabilized.

On the other hand, R ¹¹ and R ¹² may be connected to each other to form a ring.
In the case of forming a ring, the group formed by connecting R ²¹ and R ²² is particularly preferably a fluoroalkylene group having 2 to 12 carbon atoms.
That is, the anion represented by the following formula (II) _A is preferably an anion represented by the following formula (II-2) _A.

(In the above formula (II-2) _A , n ″ represents an integer of 2 to 12.)
n ″ is preferably 2 to 8 and more preferably 3 in terms of good heat resistance.
The smaller the number of n ″, the smaller the effect of steric repulsion and the stronger the interaction. That is, it is presumed that the smaller the n ″, the greater the interaction between the anion and the cation, the more counterion is stabilized, and the heat resistance of the dye is improved.
The compound represented by the formula (I) are, for example, from R ¹ to R ^6, stretched a linker, may form a like a dimer or trimer.

[Molecular weight]
The molecular weight of the compound (I) in the present invention is usually 800 or more, preferably 950 or more, and usually 5000 or less.
It is preferable that it is within the above-mentioned range in terms of good solubility in a solvent and easy production.

[Synthesis method]
The compound represented by the formula (I) can be synthesized, for example, according to the method described in International Publication No. 2009/107734.
Although the preferable specific example of the compound represented by Formula (I) in this invention is shown below, this invention is not limited to these.
[Specific Examples of Compound (I)]

(Content)
In the colored resin composition of the present invention, the compound (I) in the total solid content is preferably 0.01% by weight or more, more preferably 0.1% by weight or more, particularly preferably 1% by weight or more, and preferably It is contained in a proportion of not more than 50% by weight, more preferably not more than 40% by weight, particularly preferably not more than 30% by weight.

It is preferable for it to be less than or equal to the above upper limit because the curability of the coating film is unlikely to decrease and the film strength is sufficient. Moreover, since it is sufficient for coloring power to be more than the said minimum, since the chromaticity of a desired density | concentration is easy to be obtained and it is hard to become thick, it is preferable.
In the colored resin composition of this invention, only 1 type of compound (I) may be contained as (A) dye, and 2 or more types may be contained.

Furthermore, 1 type (s) or 2 or more types of other dyes other than compound (I) may be contained. The content of all (A) dyes in the colored resin composition is preferably 0.1% by weight or more, or preferably 30% by weight or less in the colored resin composition.
In addition, in the colored resin composition of this invention, it is preferable that content of compound (I) is 30 weight% or more in solid content of all the (A) dyes.

[(B) Solvent]
The solvent (B) contained in the colored resin composition of the present invention has a function of adjusting the viscosity by dissolving or dispersing each component contained in the colored resin composition.
The solvent (B) may be any solvent as long as it can dissolve or disperse each component constituting the colored resin composition, and a solvent having a boiling point in the range of 100 to 200 ° C. is preferably selected. More preferably, it has a boiling point of 120-170 ° C.

Examples of such solvents include the following.
Ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monopropyl ether, ethylene glycol monobutyl ether, propylene glycol monomethyl ether, propylene glycol-mono t-butyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, methoxymethylpentanol, propylene Glycol monoalkyl ethers such as glycol monoethyl ether, dipropylene glycol monoethyl ether, dipropylene glycol monomethyl ether, 3-methyl-3-methoxybutanol, tripropylene glycol monomethyl ether;

Glycol dialkyl ethers such as ethylene glycol dimethyl ether, ethylene glycol diethyl ether, diethylene glycol dimethyl ether, diethylene glycol diethyl ether, diethylene glycol dipropyl ether, diethylene glycol dibutyl ether;
Ethylene glycol monomethyl ether acetate, ethylene glycol monoethyl ether acetate, propylene glycol monomethyl ether acetate, propylene glycol monoethyl ether acetate, propylene glycol monopropyl ether acetate, methoxybutyl acetate, 3-methoxybutyl acetate, methoxypentyl acetate, diethylene glycol monoethyl Glycol alkyl ether acetates such as ether acetate, diethylene glycol monobutyl ether acetate, dipropylene glycol monomethyl ether acetate, 3-methyl-3-methoxybutyl acetate;

Ethers such as diethyl ether, dipropyl ether, diisopropyl ether, diamyl ether, ethyl isobutyl ether, dihexyl ether;
Ketones such as acetone, methyl ethyl ketone, methyl amyl ketone, methyl isopropyl ketone, methyl isoamyl ketone, diisopropyl ketone, diisobutyl ketone, methyl isobutyl ketone, cyclohexanone, ethyl amyl ketone, methyl butyl ketone, methyl hexyl ketone, methyl nonyl ketone;
Mono- or polyhydric alcohols such as ethanol, propanol, butanol, hexanol, cyclohexanol, ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, glycerin;
aliphatic hydrocarbons such as n-pentane, n-octane, diisobutylene, n-hexane, hexene, isoprene, dipentene, dodecane;
Cycloaliphatic hydrocarbons such as cyclohexane, methylcyclohexane, methylcyclohexene, bicyclohexyl;

Aromatic hydrocarbons such as benzene, toluene, xylene, cumene;
Amyl formate, ethyl formate, ethyl acetate, butyl acetate, propyl acetate, amyl acetate, methyl isobutyrate, ethylene glycol acetate, ethyl propionate, propyl propionate, butyl butyrate, isobutyl butyrate, methyl isobutyrate, ethyl Caprylate, butyl stearate, ethyl benzoate, methyl 3-ethoxypropionate, ethyl 3-ethoxypropionate, methyl 3-methoxypropionate, ethyl 3-methoxypropionate, propyl 3-methoxypropionate, 3-methoxypropionic acid Linear or cyclic esters such as butyl, γ-butyrolactone;
Alkoxycarboxylic acids such as 3-methoxypropionic acid and 3-ethoxypropionic acid;
Halogenated hydrocarbons such as butyl chloride and amyl chloride;
Ether ketones such as methoxymethylpentanone;
Nitriles such as acetonitrile and benzonitrile:

Commercially available solvents corresponding to the above include mineral spirit, Barsol # 2, Apco # 18 Solvent, Apco thinner, Soal Solvent No. 1 and no. 2, Solvesso # 150, Shell TS28 Solvent, carbitol, ethyl carbitol, butyl carbitol, methyl cellosolve, ethyl cellosolve, ethyl cellosolve acetate, methyl cellosolve acetate, diglyme (all trade names) and the like.
These solvents may be used alone or in combination of two or more.

Of these solvents, glycol monoalkyl ethers are preferred from the viewpoint of the solubility of the dye (A) in the present invention. Among these, propylene glycol monomethyl ether is particularly preferable from the viewpoint of solubility of various components in the colored resin composition.
In addition, for example, in the case of containing a pigment (F) described later as an optional component, the balance of coatability, surface tension, etc. is good, and from the viewpoint that the solubility of the constituent components in the colored resin composition is relatively high, It is more preferable to use a mixture of glycol alkyl ether acetates. In addition, in colored resin compositions containing pigments, glycol monoalkyl ethers are highly polar and tend to aggregate the pigment, which may reduce storage stability, such as increasing the viscosity of the colored resin composition. For this reason, it is preferable that the amount of the glycol monoalkyl ether used is not excessively large, and the proportion of the glycol monoalkyl ether in the solvent (B) is preferably 5 to 50% by weight, more preferably 5 to 30% by weight. .

  Further, from the viewpoint of suitability for a slit coat method corresponding to a recent large substrate or the like, it is also preferable to use a solvent having a boiling point of 150 ° C. or higher. In this case, the content of such a high boiling point solvent is preferably 3 to 50% by weight, more preferably 5 to 40% by weight, and particularly preferably 5 to 30% by weight based on the total amount of the solvent (B). If the amount of the high boiling point solvent is too small, for example, a dye component may precipitate and solidify at the tip of the slit nozzle to cause foreign matter defects, and if it is too large, the drying speed of the composition will be slowed down. There is a concern that the filter manufacturing process may cause problems such as tact defects in the vacuum drying process and pin marks of prebaking.

The solvent having a boiling point of 150 ° C. or higher may be glycol alkyl ether acetates or glycol alkyl ethers. In this case, a solvent having a boiling point of 150 ° C. or higher may not be included separately. .
The colored resin composition of the present invention may be used for color filter production by the ink jet method, but in color filter production by the ink jet method, the ink emitted from the nozzle is very small, from several to several tens pL, There is a tendency for the solvent to evaporate and the ink to concentrate and dry before landing on the periphery of the nozzle opening or in the pixel bank. In order to avoid this, it is preferable that the solvent has a high boiling point. Specifically, it is preferable that the solvent (B) contains a solvent having a boiling point of 180 ° C. or higher. In particular, it is preferable to contain a solvent having a boiling point of 200 ° C. or higher, particularly 220 ° C. or higher. Moreover, it is preferable that the high boiling point solvent whose boiling point is 180 degreeC or more is 50 weight% or more in (B) solvent. When the ratio of such a high boiling point solvent is less than 50% by weight, the effect of preventing evaporation of the solvent from the ink droplets may not be sufficiently exhibited.

  In the colored resin composition of the present invention, the content of the (B) solvent is not particularly limited, but the upper limit is usually 99% by weight. When the content of the (B) solvent in the composition exceeds 99% by weight, the concentration of each component excluding the (B) solvent becomes too small and may be inappropriate for forming a coating film. . On the other hand, the lower limit of the content of the solvent (B) is usually 75% by weight, preferably 80% by weight, and more preferably 82% by weight in consideration of viscosity suitable for coating.

[(C) Binder resin]
(C) What preferable binder resin changes with the hardening means of a colored resin composition.
When the colored resin composition of the present invention is a photopolymerizable resin composition, examples of the (C) binder resin include JP-A-7-2072111, JP-A-8-259876, and JP-A-10-300922. The polymer compounds described in JP-A-11-140144, JP-A-11-174224, JP-A-2000-56118, JP-A-2003-233179, and the like can be used. However, among them, the following resins (C-1) to (C-5) are preferable.

(C-1): With respect to a copolymer of an epoxy group-containing (meth) acrylate and another radical polymerizable monomer, an unsaturated monobasic acid is added to at least a part of the epoxy group of the copolymer. Resin to be added, or an alkali-soluble resin (hereinafter referred to as “resin (C-1)”) obtained by adding a polybasic acid anhydride to at least a part of the hydroxyl group generated by the addition reaction. .)
(C-2): Carboxyl group-containing linear alkali-soluble resin (C-2) (hereinafter sometimes referred to as “resin (C-2)”)
(C-3): a resin obtained by adding an epoxy group-containing unsaturated compound to the carboxyl group portion of the resin (C-2) (hereinafter sometimes referred to as “resin (C-3)”).
(C-4): (Meth) acrylic resin (hereinafter sometimes referred to as “resin (C-4)”)
(C-5): Epoxy acrylate resin having a carboxyl group (hereinafter sometimes referred to as “resin (C-5)”)
Of these, the resin (C-1) is particularly preferable, and the resin will be described below.

The resins (C-2) to (C-5) may be anything as long as they are dissolved in an alkaline developer and are soluble to the extent that the desired development processing is performed. It is the same as that described as the same item of 2009-025813 gazette. The preferred embodiment is also the same.
(C-1): With respect to a copolymer of an epoxy group-containing (meth) acrylate and another radical polymerizable monomer, an unsaturated monobasic acid is added to at least a part of the epoxy group of the copolymer. As one of particularly preferable resins of the alkali-soluble resin resin (C-1) obtained by adding a polybasic acid anhydride to at least a part of the hydroxyl group generated by the addition reaction, or an epoxy group, Unsaturated in 10 to 100 mol% of the epoxy group of the copolymer with respect to the copolymer of 5 to 90 mol% of (meth) acrylate and 10 to 95 mol% of other radical polymerizable monomer Examples thereof include a resin obtained by adding a monobasic acid, or an alkali-soluble resin obtained by adding a polybasic acid anhydride to 10 to 100 mol% of a hydroxyl group generated by the addition reaction.

  Examples of the epoxy group-containing (meth) acrylate include glycidyl (meth) acrylate, 3,4-epoxybutyl (meth) acrylate, (3,4-epoxycyclohexyl) methyl (meth) acrylate, and 4-hydroxybutyl (meth) acrylate. ) Acrylate glycidyl ether and the like. Of these, glycidyl (meth) acrylate is preferred. These epoxy group-containing (meth) acrylates may be used alone or in combination of two or more.

  The other radical polymerizable monomer copolymerized with the epoxy group-containing (meth) acrylate is not particularly limited as long as the effects of the present invention are not impaired. For example, vinyl aromatics, dienes, (meth) Examples include acrylic acid esters, (meth) acrylic acid amides, vinyl compounds, unsaturated dicarboxylic acid diesters, monomaleimides, and the like, and in particular, mono (meth) having a structure represented by the following formula (7) Acrylate is preferred.

  The repeating unit derived from the mono (meth) acrylate having the structure represented by the following formula (7) contains 5 to 90 mol% among the repeating units derived from “other radical polymerizable monomers”. The content is preferably 10 to 70 mol%, more preferably 15 to 50 mol%.

In the above formula (7), R ⁸⁹ represents a hydrogen atom or a methyl group, and R ⁹⁰ represents a structure represented by the following formula (8).

The formula ^{(8), R} 91 ~R ⁹⁸ independently represents a hydrogen atom or an alkyl group having 1 to 3 carbon atoms. R ⁹⁶ and R ⁹⁸ may be connected to each other to form a ring.
The ring formed by connecting R ⁹⁶ and R ⁹⁸ is preferably an aliphatic ring, may be saturated or unsaturated, and preferably has 5 to 6 carbon atoms.
Among them, among the structures represented by the formula (8), those represented by the following structural formulas (8a), (8b), or (8c) are particularly preferable.

In addition, the mono (meth) acrylate which has a structure represented by the said Formula (8) may be used individually by 1 type, and may use 2 or more types together.
As "other radical polymerizable monomers" other than the mono (meth) acrylate having the structure represented by the formula (8), the heat resistance and strength excellent in the colored resin composition can be improved. , Styrene, (n-butyl) (meth) acrylate, tert-butyl (meth) acrylate, cyclohexyl (meth) acrylate, isobornyl (meth) acrylate, adamantyl (meth) acrylate, benzyl (meth) acrylate , (Meth) acrylic acid-2-hydroxyethyl, N-phenylmaleimide, N-cyclohexylmaleimide.

The content of the repeating unit derived from at least one selected from the above monomer group is preferably 1 to 70 mol%, more preferably 3 to 50 mol%.
A known solution polymerization method is applied to the copolymerization reaction between the epoxy group-containing (meth) acrylate and the other radical polymerizable monomer.
In the present invention, as a copolymer of the epoxy group-containing (meth) acrylate and the other radical polymerizable monomer, 5 to 90 mol% of repeating units derived from the epoxy group-containing (meth) acrylate, and others Is preferably composed of 10 to 95 mol% of repeating units derived from the radically polymerizable monomer, more preferably composed of 20 to 80 mol% of the former and 80 to 20 mol% of the latter. What consists of 70 mol% and the latter 70-30 mol% is especially preferable.

Within the above range, the addition amount of the polymerizable component and alkali-soluble component described later is sufficient, and the heat resistance and the strength of the film are sufficient, which is preferable.
The epoxy group portion of the epoxy group-containing copolymer synthesized as described above is reacted with an unsaturated monobasic acid (polymerizable component) and a polybasic acid anhydride (alkali-soluble component).
Here, as an unsaturated monobasic acid added to an epoxy group, a well-known thing can be used, For example, unsaturated carboxylic acid which has an ethylenically unsaturated double bond is mentioned.

  Specific examples include (meth) acrylic acid, crotonic acid, o-, m-, p-vinylbenzoic acid, α-position substituted with a haloalkyl group, an alkoxyl group, a halogen atom, a nitro group, or a cyano group. And monocarboxylic acids such as (meth) acrylic acid. Of these, (meth) acrylic acid is preferred. These may be used alone or in combination of two or more.

By adding such components, polymerizability can be imparted to the binder resin used in the present invention.
These unsaturated monobasic acids are usually added to 10 to 100 mol% of the epoxy group of the copolymer, preferably 30 to 100 mol%, more preferably 50 to 100 mol%. It is preferable for it to be within the above range because the colored resin composition has excellent temporal stability. In addition, a well-known method is employable as a method of adding unsaturated monobasic acid to the epoxy group of a copolymer.

Furthermore, a well-known thing can be used as a polybasic acid anhydride added to the hydroxyl group produced when an unsaturated monobasic acid is added to the epoxy group of a copolymer.
For example, dibasic acid anhydrides such as maleic anhydride, succinic anhydride, itaconic anhydride, phthalic anhydride, tetrahydrophthalic anhydride, hexahydrophthalic anhydride, chlorendic anhydride; trimellitic anhydride, pyromellitic anhydride, benzophenone Examples thereof include anhydrides of three or more bases such as tetracarboxylic acid anhydride and biphenyltetracarboxylic acid anhydride. Of these, succinic anhydride and tetrahydrophthalic anhydride are preferred. These polybasic acid anhydrides may be used individually by 1 type, and may use 2 or more types together.

By adding such a component, alkali solubility can be imparted to the binder resin used in the present invention.
These polybasic acid anhydrides are usually added to 10 to 100 mol% of the hydroxyl group generated by adding an unsaturated monobasic acid to the epoxy group of the copolymer, preferably 20 to 90 mol. %, More preferably 30 to 80 mol%.

Within the above range, the remaining film ratio and solubility during development are sufficient, which is preferable.
In addition, a well-known method is employable as a method of adding a polybasic acid anhydride to the said hydroxyl group.
Furthermore, in order to improve photosensitivity, after adding the above-mentioned polybasic acid anhydride, glycidyl (meth) acrylate or a glycidyl ether compound having a polymerizable unsaturated group is added to a part of the generated carboxyl group. May be. Such a resin structure is described in, for example, Japanese Patent Application Laid-Open Nos. 8-297366 and 2001-89533.

The polystyrene-reduced weight average molecular weight (Mw) of the above-described binder resin (C-1) measured by GPC (gel permeation chromatography) is preferably 3000 to 100,000, and particularly preferably 5000 to 50000. Within the above range, heat resistance, film strength, and solubility in a developer are preferable.
Moreover, as a standard of molecular weight distribution, the ratio of weight average molecular weight (Mw) / number average molecular weight (Mn) is preferably 2.0 to 5.0.

In addition, the acid value of binder resin (C-1) is 10-200 mg-KOH / g normally, Preferably it is 15-150 mg-KOH / g, More preferably, it is 25-100 mg-KOH / g. If the acid value is too low, the solubility in the developer may be reduced. Conversely, if it is too high, film roughening may occur.
Content of (C) binder resin in a colored resin composition is 0.1 to 80 weight% normally in a total solid, Preferably it is 1 to 60 weight%.
Within the above range, the adhesion to the substrate is good, the permeability of the developer to the exposed area is moderate, and the surface smoothness and sensitivity of the pixels are good.

[(D) Polymerizable monomer]
The colored resin composition of the present invention preferably contains (D) a polymerizable monomer.
(D) The polymerizable monomer is not particularly limited as long as it is a polymerizable low-molecular compound, but it may be an addition-polymerizable compound having at least one ethylenic double bond (hereinafter referred to as “ethylenic compound”). Is preferred).
The ethylenic compound is a compound having an ethylenic double bond that undergoes addition polymerization and cures by the action of a photopolymerization initiation component described later when the colored resin composition of the present invention is irradiated with actinic rays. In addition, the (D) polymerizable monomer in this invention means the concept opposite to what is called a polymeric substance, and also includes a dimer, a trimer, and an oligomer other than a monomer in a narrow sense.

  (D) Examples of the ethylenic compound in the polymerizable monomer include unsaturated carboxylic acids such as (meth) acrylic acid; esters of monohydroxy compounds and unsaturated carboxylic acids; aliphatic polyhydroxy compounds and unsaturated carboxylic acids; Esters of aromatic polyhydroxy compounds and unsaturated carboxylic acids; Esterification of unsaturated carboxylic acids with polyvalent carboxylic acids and polyhydric hydroxy compounds such as aliphatic polyhydroxy compounds and aromatic polyhydroxy compounds described above An ester obtained by the reaction; an ethylenic compound having a urethane skeleton obtained by reacting a polyisocyanate compound and a (meth) acryloyl group-containing hydroxy compound;

Esters of aliphatic polyhydroxy compounds and unsaturated carboxylic acids include ethylene glycol di (meth) acrylate, triethylene glycol di (meth) acrylate, trimethylolpropane tri (meth) acrylate, trimethylolethane tri (meth) acrylate , Pentaerythritol di (meth) acrylate, pentaerythritol tri (meth) acrylate, pentaerythritol tetra (meth) acrylate, dipentaerythritol tetra (meth) acrylate, dipentaerythritol penta (meth) acrylate, dipentaerythritol hexa (meth) Examples include (meth) acrylic acid esters such as acrylate and glycerol (meth) acrylate. In addition, the (meth) acrylic acid portion of these (meth) acrylic acid esters is replaced with an itaconic acid portion, a crotonic acid portion replaced with a crotonic acid portion, or a maleic acid ester replaced with a maleic acid portion, etc. Is mentioned.

Examples of the ester of an aromatic polyhydroxy compound and an unsaturated carboxylic acid include hydroquinone di (meth) acrylate, resorcin di (meth) acrylate, pyrogallol tri (meth) acrylate, and the like.
The ester obtained by the esterification reaction of an unsaturated carboxylic acid with a polyvalent carboxylic acid and a polyvalent hydroxy compound may be a single substance or a mixture. Representative examples are condensates of (meth) acrylic acid, phthalic acid, and ethylene glycol; condensates of (meth) acrylic acid, maleic acid, and diethylene glycol; condensation of (meth) acrylic acid, terephthalic acid, and pentaerythritol A condensate of (meth) acrylic acid, adipic acid, butanediol, and glycerin.

  Examples of the ethylenic compound having a urethane skeleton obtained by reacting a polyisocyanate compound and a (meth) acryloyl group-containing hydroxy compound include aliphatic diisocyanates such as hexamethylene diisocyanate and trimethylhexamethylene diisocyanate; alicyclic rings such as cyclohexane diisocyanate and isophorone diisocyanate. Formula diisocyanates; aromatic diisocyanates such as tolylene diisocyanate and diphenylmethane diisocyanate, and (meth) acryloyl such as 2-hydroxyethyl (meth) acrylate and 3-hydroxy [1,1,1-tri (meth) acryloyloxymethyl] propane A reaction product with a group-containing hydroxy compound is exemplified.

In addition, examples of the ethylenic compound used in the present invention include (meth) acrylamides such as ethylene bis (meth) acrylamide; allyl esters such as diallyl phthalate; vinyl group-containing compounds such as divinyl phthalate. .
Among these, esters of aliphatic polyhydroxy compounds and unsaturated carboxylic acids are preferred, pentaerythritol or (meth) acrylic acid esters of dipentaerythritol are more preferred, and dipentaerythritol hexa (meth) acrylate is particularly preferred.

  The ethylenic compound may be a monomer having an acid value. The monomer having an acid value is, for example, an ester of an aliphatic polyhydroxy compound and an unsaturated carboxylic acid, and a non-aromatic carboxylic acid anhydride is reacted with an unreacted hydroxyl group of the aliphatic polyhydroxy compound. A polyfunctional monomer having a group is preferable, and in this ester, the aliphatic polyhydroxy compound is pentaerythritol and / or dipentaerythritol.

These monomers may be used alone, but since it is difficult to obtain a single compound in production, a mixture of two or more kinds may be used.
Moreover, you may use together the polyfunctional monomer which does not have an acid group, and the polyfunctional monomer which has an acid group as (D) polymeric monomer as needed.
A preferable acid value of the polyfunctional monomer having an acid group is 0.1 to 40 mg-KOH / g, and particularly preferably 5 to 30 mg-KOH / g.

When it is within the above range, the development and dissolution characteristics are hardly deteriorated, and the production and handling are easy. Furthermore, it is preferable because the photopolymerization performance is hardly lowered and the curability such as the surface smoothness of the pixel is good.
In the present invention, a more preferred polyfunctional monomer having an acid group is, for example, a mixture containing succinic acid ester of dipentaerythritol hexaacrylate, dipentaerythritol pentaacrylate, dipentaerythritol pentaacrylate as a main component. It is also possible to use this polyfunctional monomer in combination with another polyfunctional monomer.

In the colored resin composition of the present invention, the content of the polymerizable monomer (D) is usually 1% by weight or more, preferably 5% by weight or more, more preferably 10% by weight or more in the total solid content. Further, it is usually 80% by weight or less, preferably 70% by weight or less, more preferably 50% by weight or less, and particularly preferably 40% by weight or less.
The ratio of the (D) polymerizable monomer to the (A) dye is usually 1% by weight or more, preferably 5% by weight or more, more preferably 10% by weight or more, and particularly preferably 20% by weight or more. Moreover, it is 200 weight% or less normally, Preferably it is 100 weight% or less, More preferably, it is 80 weight% or less.

  Within the above range, photocuring is appropriate, poor adhesion during development is difficult to place, the cross-section after development is difficult to reverse taper, and further, peeling phenomenon and omission failure due to lower solubility are difficult to place. preferable.

[(E) Photopolymerization initiation component and / or thermal polymerization initiation component]
The colored resin composition of the present invention preferably contains (E) a photopolymerization initiation component and / or a thermal polymerization initiation component for the purpose of curing the coating film. However, the curing method may be other than those using these initiators.
In particular, when the colored resin composition of the present invention includes a resin having an ethylenic double bond as the component (C), or includes an ethylenic compound as the component (D), it directly absorbs light, or It is preferable to contain a photopolymerization initiating component that has a function of generating a polymerization active radical and / or a thermal polymerization initiating component that generates a polymerization active radical by heat. In the present invention, the component (E) as a photopolymerization initiation component refers to a photopolymerization initiator (hereinafter also referred to as “(E1) component”), a polymerization accelerator (hereinafter, optionally referred to as “(E2) component”). ")" And a sensitizing dye (hereinafter also referred to as "(E3) component").

[(E) Photopolymerization initiation component]
The (E) photopolymerization initiating component in the present invention is usually a mixture of (E1) a photopolymerization initiator and, if necessary, (E2) a polymerization accelerator and (E3) an additive such as a sensitizing dye. And is a component having a function of generating a polymerization active radical by directly absorbing light or being photosensitized to cause a decomposition reaction or a hydrogen abstraction reaction.

  Examples of (E1) photopolymerization initiator constituting the photopolymerization initiating component include titanocene derivatives described in JP-A Nos. 59-152396 and 61-151197, etc .; JP-A-10-300922 Hexaarylbiimidazole derivatives described in JP-A-11-174224, JP-A-2000-56118, etc .; halomethylated oxadiazole derivatives described in JP-A-10-39503, etc., halomethyl-s -Radical activators such as triazine derivatives, N-aryl-α-amino acids such as N-phenylglycine, N-aryl-α-amino acid salts, N-aryl-α-amino acid esters, α-aminoalkylphenone derivatives And oxime ester derivatives described in JP-A No. 2000-80068 and the like.

Specific examples include photopolymerization initiators described in International Publication No. 2009/107734 pamphlet and the like.
Among these photopolymerization initiators, α-aminoalkylphenone derivatives, oxime ester derivatives, biimidazole derivatives, acetophenone derivatives, and thioxanthone derivatives are more preferable.

  The oxime ester derivatives include 1,2-octanedione, 1- [4- (phenylthio) phenyl]-, 2- (o-benzoyloxime), ethanone, 1- [9-ethyl-6- ( 2-methylbenzoyl) -9H-carbazol-3-yl], 1- (o-acetyloxime), and a compound represented by the following formula (XI).

(In formula (XI), R ¹⁰¹ represents a hydrogen atom, an alkyl group having 1 to 20 carbon atoms, an alkenyl group having 2 to 25 carbon atoms, a heteroaryl group having 3 to 20 carbon atoms, or a heteroaryl group having 4 to 25 carbon atoms. An alkyl group, each of which may have a substituent, or R ¹⁰¹ may be bonded to X or Z to form a ring;
R ¹⁰² represents an alkanoyl group having 2 to 20 carbon atoms, an alkenoyl group having 3 to 25 carbon atoms, a cycloalkanoyl group having 4 to 8 carbon atoms, an aryloyl group having 7 to 20 carbon atoms, or an alkoxycarbonyl group having 2 to 10 carbon atoms. , An aryloxycarbonyl group having 7 to 20 carbon atoms, a heteroaryl group having 2 to 20 carbon atoms, a heteroaryloyl group having 3 to 20 carbon atoms, or an alkylaminocarbonyl group having 2 to 20 carbon atoms, It may have a substituent.
X represents a divalent aromatic hydrocarbon ring group and / or an aromatic hetero group formed by condensation of two or more rings which may have a substituent.

Z represents an aromatic ring group which may have a substituent. )
Of the compounds represented by the formula (XI), compounds in which X is a carbazole ring which may have a substituent are preferable. Specifically, compounds represented by the following formula (XII) Among them, the compound represented by the following formula (XIII) is particularly preferable.

(Wherein R ¹⁰¹ , R ¹⁰² and Z have the same meanings as in formula (XI), R ^103.
To R ¹⁰⁹ is a hydrogen atom or an arbitrary substituent independently. )

(In the formula, R ^101a represents an alkyl group having 1 to 3 carbon atoms or a group represented by the following formula (XIIIa).

(Wherein R ¹⁰³ and R ¹⁰⁴ each independently represent a hydrogen atom, a phenyl group or an N-acetyl-N-acetoxyamino group.
* Represents a binding site. )
R ^102a represents an alkanoyl group having 2 to 4 carbon atoms, and X ^a represents a 3,6-carbazolyl group in which the nitrogen atom may be substituted with an alkyl group having 1 to 4 carbon atoms. Za represents ^a phenyl group which may be substituted with an alkyl group or a naphthyl group which may be substituted with a morpholino group. )

In addition, benzoin alkyl ethers, anthraquinone derivatives; acetophenone derivatives such as 2-methyl- (4′-methylthiophenyl) -2-morpholino-1-propanone, 2-ethylthioxanthone, 2,4-diethylthioxanthone, etc. Examples also include thioxanthone derivatives, benzoate derivatives, acridine derivatives, phenazine derivatives, anthrone derivatives and the like.
Among these photopolymerization initiators, α-aminoalkylphenone derivatives, thioxanthone derivatives, and oxime ester derivatives are more preferable. In particular, oxime ester derivatives are preferable.

Examples of the (E2) polymerization accelerator used as necessary include N, N-dialkylaminobenzoic acid alkyl esters such as N, N-dimethylaminobenzoic acid ethyl ester; 2-mercaptobenzothiazole, 2-mercapto Examples thereof include mercapto compounds having a heterocyclic ring such as benzoxazole and 2-mercaptobenzimidazole; mercapto compounds such as aliphatic polyfunctional mercapto compounds.
Each of these (E1) photopolymerization initiator and (E2) polymerization accelerator may be used alone or in combination of two or more.

Further, (E3) sensitizing dye is used for the purpose of increasing the sensitivity as required. As the sensitizing dye, an appropriate one is used according to the wavelength of the image exposure light source. For example, xanthene dyes described in JP-A-4-221958 and JP-A-4-219756; No. 239703, JP-A-5-289335, etc. Coumarin dyes having a heterocyclic ring; JP-A-3-239703, JP-A-5-289335, etc .; 3-ketocoumarin dyes; Pyrromethene dyes described in JP-A-6-19240, etc .; JP-A-47-2528, JP-A-54-155292, JP-B-45-37377, JP-A-48-
84183, JP 52-112681, JP 58-15503, JP 60-88005, JP 59-56403, JP 2-69, JP 57-168088, Examples thereof include dyes having a dialkylaminobenzene skeleton described in JP-A-5-107761, JP-A-5-210240, JP-A-4-288818, and the like.

(E3) A sensitizing dye may also be used alone or in combination of two or more.
In the colored resin composition of the present invention, the content of these (E) photopolymerization initiating components is usually 0.1% by weight or more, preferably 0.2% by weight or more, more preferably 0.8% by weight in the total solid content. It is 5% by weight or more, usually 40% by weight or less, preferably 30% by weight or less, and more preferably 20% by weight or less.

Within the above range, the sensitivity to the exposure light beam is good, the solubility of the unexposed part in the development station is good, and it is preferable in that it is difficult to induce poor development.
[(E) Thermal polymerization starting component]
Specific examples of the (E) thermal polymerization initiating component that may be contained in the colored resin composition of the present invention include azo compounds, organic peroxides, and hydrogen peroxide. Of these, azo compounds are preferably used. More specifically, for example, a thermal polymerization initiating component described in International Publication No. 2009/107734 can be used.
These thermal polymerization initiating components may be used alone or in combination of two or more.

[Other optional ingredients]
In addition to the above components, the colored resin composition of the present invention comprises a surfactant, an organic carboxylic acid and / or an organic carboxylic acid anhydride, a thermosetting compound, a plasticizer, a thermal polymerization inhibitor, a storage stabilizer, a surface It may contain a protective agent, an adhesion improver, a development improver, and the like. Moreover, when it contains the below-mentioned (F) pigment, you may contain a dispersing agent and a dispersing aid. As these optional components, for example, various compounds described in JP-A-2007-113000 can be used.

[(F) Pigment]
The colored resin composition of the present invention may contain (F) a pigment within a range not impairing the effects of the present invention for the purpose of improving the heat resistance of the obtained color filter.
(F) As a pigment, for example, when forming a pixel of a color filter, pigments of various colors such as blue and purple can be used. Examples of the chemical structure include organic pigments such as phthalocyanine, quinacridone, benzimidazolone, dioxazine, indanthrene, and perylene. In addition, various inorganic pigments can be used. Hereinafter, specific examples of usable pigments are indicated by pigment numbers.

  Examples of blue pigments include C.I. I. Pigment Blue 1, 1: 2, 9, 14, 15, 15: 1, 15: 2, 15: 3, 15: 4, 15: 6, 16, 17, 19, 25, 27, 28, 29, 33, 35, 36, 56, 56: 1, 60, 61, 61: 1, 62, 63, 66, 67, 68, 71, 72, 73, 74, 75, 76, 78, 79 and the like.

Among these, a blue copper phthalocyanine pigment is preferable, and examples of the copper phthalocyanine pigment include C.I. I. Pigment Blue 15, 15: 1, 15: 2, 15: 3, 15: 4, 15: 6 and the like are preferable, and C.I. I. Pigment Blue 15: 6.
For this reason, when the colored resin composition of this invention contains a blue pigment, it is 80 weight% or more with respect to the total content of a blue pigment, Especially 90 weight% or more, Especially 95-100 weight% is C.I. I. Pigment Blue 15: 6 is preferable.

Examples of purple pigments include C.I. I. Pigment Violet 1, 1: 1, 2, 2: 2, 3, 3: 1, 3: 3, 5, 5: 1, 14, 15, 16, 19, 23, 25, 27, 29, 31, 32, 37, 39, 42, 44, 47, 49, 50 and the like.
Among these, a purple dioxazine pigment is preferable, and as the dioxazine pigment, C.I. I. Pigment Violet 19 and 23 are preferable, and C.I. I. Pigment Violet 23.

For this reason, when the colored resin composition of this invention contains a purple pigment, it is 80 weight% or more with respect to the total content of a purple pigment, Especially 90 weight% or more, Especially 95-100 weight% is C.I. I. Pigment Violet 23 is preferable.
These may be used alone or in a combination of two or more in any combination and ratio.

The (F) pigment used in the colored resin composition of the present invention preferably has a small average primary particle diameter from the viewpoint of forming a high-contrast pixel. Specifically, the average primary particle diameter is 40 nm or less. Is preferable, and it is more preferable that it is 35 nm or less.
Particularly for the blue copper phthalocyanine pigment, the average primary particle size is preferably 40 nm or less, more preferably 35 nm or less, and still more preferably 20 to 30 nm.

Moreover, about a dioxazine pigment, an average primary particle diameter becomes like this. Preferably it is 40 nm or less, More preferably, it is 25-35 nm. From the viewpoint that the pigment is less likely to aggregate in the colored resin composition, it is preferable that the average primary particle size is not too small.
Here, the average primary particle size of the (F) pigment is a value measured and calculated by the following method.

  First, (F) a pigment is ultrasonically dispersed in chloroform, dropped onto a collodion film-attached mesh, dried, and a primary particle image of the pigment is obtained by observation with a transmission electron microscope (TEM). From this image, the particle size of each pigment particle is determined for a plurality of (usually about 200 to 300) pigment particles, with the diameter corresponding to the area circle converted to the diameter of a circle having the same area.

Using the obtained primary particle size value, the number average value is calculated according to the following formula to obtain the average particle size.
The particle diameter of each pigment _{particle: X 1, X 2, X} 3, X 4, ····, X i, ······ X m

{Blending amount}
In the present invention, when the pigment (F) is contained, the content of the pigment in the colored resin composition is usually 80% by weight or less, preferably 50% by weight or less in the total solid content.
Moreover, content with respect to 100 weight part of said (A) dye is 2000 weight part or less normally, Preferably it is 1000 weight part or less.
Within the above-mentioned range, it is preferable in that the heat resistance of the obtained pixel is likely to be better without greatly affecting the transmittance of the compound (I).

[Dispersant]
When the colored resin composition of the present invention contains (F) a pigment, it is preferable to further contain a dispersant.
The dispersant in the present invention is not particularly limited as long as the pigment is dispersed and can maintain stability.

  For example, cationic, anionic, nonionic or amphoteric dispersants can be used, but polymer dispersants are preferred. Specific examples include block copolymers, polyurethanes, polyesters, alkylammonium salts or phosphate esters of polymer copolymers, and cationic comb graft polymers. Of these dispersants, block copolymers, polyurethanes, and cationic comb graft polymers are preferred. In particular, a block copolymer is preferable, and among these, a block copolymer composed of an A block having solvophilicity and a B block having a functional group containing a nitrogen atom is preferable.

Specifically, the B block having a nitrogen atom-containing functional group includes a unit structure having a quaternary ammonium base and / or an amino group in the side chain, while the solvophilic A block includes a quaternary ammonium. Examples include a unit structure having no base and amino group.
The B block constituting the acrylic block copolymer has a unit structure having a quaternary ammonium base and / or an amino group, and has a pigment adsorption function.

Further, when the B block has a quaternary ammonium base, the quaternary ammonium base may be directly bonded to the main chain, but may be bonded to the main chain via a divalent linking group. Good.
Examples of such block copolymers include those described in JP-A-2009-025813.

Moreover, the colored resin composition of the present invention may contain a dispersant other than those described above. Examples of other dispersants include those described in JP-A-2006-343648, for example.
When the colored resin composition of the present invention contains (F) a pigment, the content of the dispersant in the total solid content is 2 to 1000% by weight, particularly 5 to 500% by weight of the total content of (F) pigment. %, Particularly 10 to 250% by weight.
Within the above range, it is preferable in that good pigment dispersibility can be ensured without affecting the heat resistance of the compound (I), and the pigment dispersion stability becomes better.

[Dispersion aid]
The colored resin composition of the present invention may contain a dispersion aid. The dispersion aid here may be a pigment derivative. Examples of the pigment derivative include JP-A Nos. 2001-220520, 2001-271004, 2002-179976, and 2007-. Various compounds described in Japanese Patent Application Publication No. 113000 and Japanese Patent Application Publication No. 2007-186681 can be used.

  The content of the dispersion aid in the colored resin composition of the present invention is usually 0.1% by weight or more, usually 30% by weight or less, preferably 20% by weight or less, based on the total solid content of the pigment. Preferably it is 10 weight% or less, More preferably, it is 5 weight% or less. By controlling the addition amount within the above range, it is preferable in that the effect as a dispersion aid is exhibited and the dispersibility and dispersion stability are better.

[Dispersion resin]
The colored resin composition of the present invention may contain a part or all of the resin selected from the (C) binder resin or other binder resins as the following dispersion resin.
Specifically, in [Preparation Method of Colored Resin Composition], which will be described later, by adding (C) binder resin together with the components such as the above-mentioned dispersant, the (C) binder resin is combined with the dispersant. It contributes to the dispersion stability of the pigment (F) by a synergistic effect. As a result, the amount of dispersant added may be reduced, which is preferable. Further, it is preferable because the developability is improved, the undissolved matter does not remain in the non-pixel portion of the substrate, and the adhesion of the pixel to the substrate is improved.
Thus, the (C) binder resin used in the dispersion treatment step may be referred to as a dispersion resin. The dispersion resin is preferably used in an amount of about 0 to 200% by weight, more preferably about 10 to 100% by weight, based on the total amount of the pigment in the colored resin composition.

[Preparation Method of Colored Resin Composition]
In the present invention, the colored resin composition can be prepared by an appropriate method. For example, the (A) dye and the (C) binder resin containing the compound (I), the (B) solvent, and as necessary. It can prepare by mixing with the arbitrary component used.

  In addition, as a preparation method in the case of containing (F) a pigment, in the solvent containing (F) pigment, in the presence of a dispersing agent and a dispersing aid to be added if necessary, (C) a binder resin may be used. A pigment dispersion liquid is prepared by mixing and dispersing together with the parts, for example, using a paint shaker, sand grinder, ball mill, roll mill, stone mill, jet mill, homogenizer, and the like. In the pigment dispersion, (A) dye containing compound (I), (C) binder resin, (D) polymerizable monomer, (E) photopolymerization initiating component and / or thermal polymerization initiating component, if necessary, The method of preparing by adding etc. and mixing can be mentioned.

[Application of colored resin composition]
The colored resin composition of the present invention is usually in a state where all the constituent components are dissolved or dispersed in a solvent. Such a colored resin composition is supplied onto a substrate to form components such as a color filter, a liquid crystal display device, and an organic EL display device.
Hereinafter, as an application example of the colored resin composition of the present invention, an application as a pixel of a color filter, a liquid crystal display device (panel) and an organic EL display device using them will be described.

<Color filter>
The color filter of the present invention has a pixel formed from the colored resin composition of the present invention.
The method for forming the color filter of the present invention will be described below.
The pixel of the color filter can be formed by various methods. Here, although the case where it forms by the photolithographic method using a photopolymerizable colored resin composition is demonstrated to an example, a manufacturing method is not limited to this.

  First, on the surface of the substrate, if necessary, a black matrix is formed so as to partition a portion for forming pixels, and after applying the colored resin composition of the present invention on this substrate, pre-baking is performed. The solvent is evaporated to form a coating film. Then, after exposing this coating film through a photomask, developing with an alkali developer, dissolving and removing the unexposed portion of the coating film, and then post-baking, each of red, green, and blue A color filter can be manufactured by forming a pixel pattern.

The substrate used for forming the pixels is not particularly limited as long as it is transparent and has an appropriate strength. For example, polyester resin, polyolefin resin, polycarbonate resin, acrylic resin, thermoplastic resin Examples thereof include a sheet made, an epoxy resin, a thermosetting resin, and various glasses.
In addition, these substrates may be appropriately subjected to pretreatment as desired, such as thin film formation treatment with a silane coupling agent or urethane resin, surface treatment such as corona discharge treatment or ozone treatment, if desired.

When applying the colored resin composition to the substrate, a spinner method, a wire bar method, a flow coating method, a slit and spin method, a die coating method, a roll coating method, a spray coating method, and the like can be given. Of these, the slit and spin method and the die coating method are preferable.
The thickness of the coating film is usually 0.2 to 20 μm, preferably 0.5 to 10 μm, particularly preferably 0.8 to 5.0 μm as the film thickness after drying.

Within the above range, it is preferable in that the gap can be easily adjusted in the pattern development or liquid crystal cell forming step, and a desired color can be easily expressed.
As the radiation used in the exposure, for example, visible light, ultraviolet light, far ultraviolet light, electron beam, X-ray or the like can be used, and radiation having a wavelength in the range of 190 to 450 nm is preferable.

  The light source used for image exposure for using radiation having a wavelength of 190 to 450 nm is not particularly limited. Lamp light sources such as medium pressure mercury lamp, low pressure mercury lamp, carbon arc, fluorescent lamp; laser light sources such as argon ion laser, YAG laser, excimer laser, nitrogen laser, helium cadmium laser, semiconductor laser, and the like. An optical filter can also be used when used by irradiating light of a specific wavelength.

Exposure of radiation, 10~10,000J / ^{m 2} is preferred.
Examples of the alkaline developer include sodium hydroxide, potassium hydroxide, lithium hydroxide, sodium carbonate, potassium carbonate, sodium hydrogen carbonate, potassium hydrogen carbonate, sodium silicate, potassium silicate, sodium metasilicate, sodium phosphate, Inorganic alkaline compounds such as potassium phosphate, sodium hydrogen phosphate, potassium hydrogen phosphate, sodium dihydrogen phosphate, potassium dihydrogen phosphate, ammonium hydroxide; mono-di- or tri-ethanolamine, mono-di-, or tri -Methylamine, mono-, di-, or tri-ethylamine, mono-, or di-isopropylamine, n-butylamine, mono-, di-, or tri-isopropanolamine, ethyleneimine, ethylenediimine, tetramethylammonium Hydroxide (TMAH) Aqueous solution of an organic alkaline compound choline are preferred.

An appropriate amount of a water-soluble organic solvent such as isopropyl alcohol, benzyl alcohol, ethyl cellosolve, butyl cellosolve, phenyl cellosolve, propylene glycol, diacetone alcohol, or the like can be added to the alkali developer. In addition, it is usually washed with water after alkali development.
As the development processing method, any method such as an immersion development method, a spray development method, a brush development method, and an ultrasonic development method can be used. The development conditions are preferably 5 to 300 seconds at room temperature (23 ° C.).

There are no particular restrictions on the conditions of the development processing, but the development temperature is usually 10 ° C. or higher, especially 15 ° C. or higher, more preferably 20 ° C. or higher, and usually 50 ° C. or lower, especially 45 ° C. or lower, further 40 ° C. or lower. Is preferred.
The developing method can be any one of immersion developing method, spray developing method, brush developing method, ultrasonic developing method and the like.

When the color filter thus produced is used in a liquid crystal display device, a transparent electrode such as ITO is formed on the image as it is and used as a part of a component such as a color display or a liquid crystal display device. Although used, in order to improve surface smoothness and durability, a top coat layer such as polyamide or polyimide can be provided on the image as necessary. Further, in some applications such as a planar alignment type drive system (IPS mode), the transparent electrode may not be formed. In the vertical alignment type driving method (MVA mode), ribs may be formed. Further, a column structure (photo spacer) by a photolithography method may be formed instead of the bead dispersion type spacer.

<Liquid crystal display device>
The liquid crystal display device of the present invention uses the above-described color filter of the present invention. There is no restriction | limiting in particular about the model and structure of the liquid crystal display device of this invention, It can assemble according to a conventional method using the color filter of this invention.
For example, the liquid crystal display device of the present invention can be formed by the method described in “Liquid Crystal Device Handbook” (Nikkan Kogyo Shimbun, September 29, 1989, Japan Society for the Promotion of Science 142nd Committee).

<Organic EL display device>
When producing an organic EL display device having the color filter of the present invention, for example, as shown in FIG. 1, on a blue color filter in which pixels 20 are formed on a transparent support substrate 10 by the colored resin composition of the present invention. A multicolor organic EL element is manufactured by laminating the organic light-emitting body 500 through the organic protective layer 30 and the inorganic oxide film 40.

  As a method for laminating the organic light emitter 500, a transparent anode 50, a hole injection layer 51, a hole transport layer 52, a light emitting layer 53, an electron injection layer 54, and a cathode 55 are sequentially formed on the upper surface of the color filter. For example, a method of adhering the organic light-emitting body 500 formed on another substrate onto the inorganic oxide film 40 can be used. The organic EL element 100 manufactured as described above can be applied to both a passive drive type organic EL display device and an active drive type organic EL display device.

Next, although a synthesis example, an Example, and a comparative example are given and this invention is demonstrated more concretely, this invention is not limited to a following example, unless the summary is exceeded.
[Synthesis of dyes]
(Synthesis Example 1: Synthesis of Dye 1)

  4,4′-dichlorobenzophenone (manufactured by Tokyo Chemical Industry Co., Ltd., 5.02 g), toluene (100 mL), di (2-ethylhexyl) amine (manufactured by Tokyo Chemical Industry Co., Ltd., 19.3 g), sodium t-butoxy ( Tokyo Chemical Industry Co., Ltd., 7.68 g), palladium acetate (Wako Pure Chemical Industries, Ltd., 0.54 g), tri-t-butylphosphine (Wako Pure Chemical Industries, Ltd., 1.00 g). The mixture was stirred with heating for 9 hours. After allowing to cool to room temperature, distilled water was added, followed by filtration using celite. After extraction with toluene, the extract was washed with saturated brine. The extract was dried over anhydrous sodium sulfate, concentrated under reduced pressure, and purified by silica gel column chromatography (hexane / ethyl acetate = 15/1) to give Compound C1 (6.20 g).

  Phosphorus oxychloride (manufactured by Wako Pure Chemical Industries, 1.74 g) was added to a mixture of compound C1 (3.00 g), compound D (manufactured by Tokyo Chemical Industry Co., Ltd., 0.94 g) and toluene (15 mL), and 7 Heated to reflux for hours. After cooling to room temperature, water was added and the mixture was extracted with chloroform, and the organic layer was washed with water and saturated brine. Purification by silica gel column chromatography (chloroform / methanol 100/0 to 30/1 to 10/1) gave Compound E1 (3.3 g).

A mixture of Compound E1 (0.71 g), Compound F (manufactured by Tokyo Chemical Industry Co., Ltd., 0.28 g) and methanol (15 mL) was heated and stirred at an external temperature of 50 ° C. for 1.5 hours. The solvent was distilled off, and the resulting crude product was dissolved in chloroform and washed twice with water. Further, the organic layer was extracted twice with an aqueous solution in which Compound F was dissolved, and the solvent was distilled off to obtain Dye 1 (0.82 g).
(Reference Synthesis Example 1: Synthesis of comparative dye)

  Compound B0 (Tokyo Chemical Industry Co., Ltd., 138 g) was dissolved in N, N-dimethylformamide (520 mL), cooled in an ice bath, and t-butoxypotassium (115 g) was added little by little. Further, an N, N-dimethylformamide (180 mL) solution of Compound A (manufactured by Tokyo Chemical Industry Co., Ltd., 37.0 g) was added dropwise over 30 minutes with cooling in an ice bath, and the mixture was stirred at 50 ° C. for 3 hours. Water and toluene were added, the organic layer was separated, and the organic layer was washed with water. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. Purification by silica gel column chromatography (hexane / ethyl acetate 15/1 to 10/1) gave Compound C0 (63.6 g).

  To a mixture of Compound C0 (24.0 g), Compound D (manufactured by Tokyo Chemical Industry Co., Ltd., 11.1 g) and toluene (130 mL), phosphorus oxychloride (manufactured by Wako Pure Chemical Industries, Ltd., 7.3 mL) is added, and 5 Heated to reflux for hours. After cooling to room temperature, water was added, extracted with chloroform, and the organic layer was washed 3 times with saturated brine. The extract was dried over anhydrous sodium sulfate, concentrated under reduced pressure, and purified by silica gel column chromatography (chloroform / methanol = 12/1) to obtain Compound E0 (34.8 g).

  Compound E0 (34.0 g), C.I. I. A mixture of Acid Blue 80 (17.1 g) and methanol (100 mL) was stirred at 50 ° C., and after confirming that it was dissolved, the mixture was concentrated under reduced pressure, washed with water / methanol = 3/1, and the comparative dye (42 0.6 g) was obtained.

(Reference Synthesis Example 2: Synthesis of Resin A)
145 parts by weight of propylene glycol monomethyl ether acetate was stirred while purging with nitrogen, and the temperature was raised to 120 ° C. Here, 5.2 parts by weight of styrene, 132 parts by weight of glycidyl methacrylate, and 4.4 parts by weight of monoacrylate FA-513M (manufactured by Hitachi Chemical Co., Ltd.) having a tricyclodecane skeleton were added dropwise, and 2.2′-azobis-2 -8.47 weight part of methylbutyronitrile was dripped over 3 hours, and also it stirred at 90 degreeC for 2 hours. Next, the inside of the reaction vessel was changed to air substitution, 1.1 parts by weight of trisdimethylaminomethylphenol and 0.19 parts by weight of hydroquinone were added to 67.0 parts by weight of acrylic acid, and the reaction was continued at 100 ° C. for 12 hours. Thereafter, 15.2 parts by weight of tetrahydrophthalic anhydride (THPA) and 0.2 parts by weight of triethylamine were added and reacted at 100 ° C. for 3.5 hours. The weight average molecular weight Mw measured by GPC of the resin A thus obtained was about 9000 and the acid value was 25 mg-KOH / g.

(Reference Synthesis Example 3: Synthesis of Resin B)
“NC3000H” (epoxy equivalent 288, softening point 69 ° C.) (manufactured by Nippon Kayaku Co., Ltd.) 400 parts by weight, acrylic acid 102 parts by weight, p-methoxyphenol 0.3 part by weight, triphenylphosphine 5 parts by weight The reaction vessel was charged with 264 parts by weight of monomethyl ether acetate and stirred at 95 ° C. until the acid value became 3 mg-KOH / g or less. It took 9 hours for the acid value to reach the target (acid value 2.2 mg-KOH / g). Next, 151 parts by weight of tetrahydrophthalic anhydride was further added and reacted at 95 ° C. for 4 hours.
Resin B having a weight average molecular weight (Mw) of 3900 in terms of polystyrene measured by g-KOH / g and GPC was obtained.

[Preparation of colored resin composition]
The dye 1 obtained in Synthesis Example 1, the comparative dye obtained in Reference Synthesis Example 1, and the resins A and B obtained in Reference Synthesis Examples 2 and 3 have the compositions described in Table 1 below. Other components were mixed to prepare a colored resin composition.
In addition, the numerical value of Table 1 represents the weight part of each component to add.

In mixing, the components were stirred for 1 hour or more until they were sufficiently mixed, and finally filtered through a 5 μm piece filter to remove foreign matters.
Dye 1 was used for the colored resin composition used in Example 1, and a comparative dye was used for the colored resin composition used in Comparative Example 1.

The numerical values in Tables 1 and 2 both represent parts by weight of each component to be added.
Each compound in Tables 1 and 2 is as follows.
PGMEA: Propylene glycol monomethyl ether acetate PGME: Propylene glycol monomethyl ether

[Production of colored resin film and evaluation of ITO resistance and light resistance]
Each colored resin composition prepared in the above [Preparation of colored resin composition] was applied onto a glass substrate cut into 5 cm square by spin coating so that the y value after drying was 0.120, and the pressure was reduced. After drying, it was pre-baked on a hot plate at 80 ° C. for 3 minutes. Thereafter, the entire surface was exposed at an exposure amount of 60 mJ / cm ^{2 and} then baked at 230 ° C. for 30 minutes in a clean oven. Spectral transmittance was measured with a spectrophotometer U-3310 (manufactured by Hitachi, Ltd.) (transmission spectrum 1).

Subsequently, using a load lock sputtering apparatus CFS-4EP-LL (manufactured by Shibaura Mechatronics), room temperature DC sputtering was performed so that the ITO film thickness would be 1300 mm in an atmosphere with an oxygen flow rate of 0.8 sccm and an argon flow rate of 30 sccm. Carried out. The sputtered substrate was baked in a clean oven at 230 ° C. for 130 minutes. The transmission spectrum of the baked substrate was measured with a spectrophotometer U-3310 (manufactured by Hitachi, Ltd.) (transmission spectrum 2). The color difference ΔE * ab, which is ITO resistant, was calculated from the transmission spectra 1 and 2, and the evaluation results are summarized in Table 2.

As shown in Table 2, pixels formed using the colored resin composition of the present invention are excellent in ITO resistance.
From this, the color filter which has the pixel formed using the colored resin composition of this invention, and the liquid crystal display device and organic electroluminescence display which have this color filter are high quality.

DESCRIPTION OF SYMBOLS 100 Organic EL element 20 Pixel 30 Organic protective layer 40 Inorganic oxide film 500 Organic light-emitting body 51 Hole injection layer 54 Electron injection layer

Claims (9)

(A) a dye, (B) a solvent and (C) a binder resin,
(A) A colored resin composition, wherein the dye contains a compound represented by the following formula (I).

(In the above formula (I),
[A ⁿ⁻ ] represents an n-valent anion.
n represents an integer of 1 to 4.
R ^{1 to} R ⁴ each independently represents a branched alkyl group having 4 or more carbon atoms in the base chain, which may have a substituent.
R ⁵ and R ⁶ each independently represent a hydrogen atom, an alkyl group which may have a substituent, or an aromatic ring group which may have a substituent.
R ⁷ and R ⁸ each independently represents a hydrogen atom or an arbitrary substituent.
R ⁷ and R ⁸ may be connected to each other to form a ring, and the ring may have a substituent.
Further, the benzene ring and indole ring in the above formula (I) may further have an arbitrary substituent.
In addition, a plurality of cations represented by the following formula (I) _CA in one molecule

May be the same structure or different structures. )   The colored resin composition according to claim 1, wherein the n-valent anion is an n-valent disulfonylimide anion. The colored resin composition according to claim 1 or 2, wherein the compound represented by the formula (I) is a compound represented by the following formula (II).

(In said formula (II), R < ¹ > -R < ⁸ > is synonymous with the said formula (I) respectively.
R ¹¹ and R ¹² are each independently an optionally substituted alkyl group having 1 to 8 carbon atoms, an optionally substituted alkenyl group having 2 to 6 carbon atoms, or a substituent. The C3-C8 cycloalkyl group which may have is represented.
R ¹¹ and R ¹² may be connected to each other to form a ring, and the ring may have a substituent. ) The colored resin composition according to claim 3, wherein at least one of R ¹¹ and R ¹² is a group containing a fluorine atom.   The colored resin composition according to claim 1, further comprising (D) a polymerizable monomer.   The colored resin composition according to any one of claims 1 to 5, further comprising (E) a photopolymerization initiation component and / or a thermal polymerization initiation component.   It has a pixel formed using the colored resin composition as described in any one of Claims 1-6, The color filter characterized by the above-mentioned.   A liquid crystal display device comprising the color filter according to claim 7. An organic EL display device comprising the color filter according to claim 7.

Images