JP2003277366A - Benzimidazolone compound, and pigment dispersant comprising the same, pigment disperse composition and colored photosensitive composition - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a benzimidazolone compound easy to synthesize, accomplishing the stable and good dispersion and flow of a pigment without agglomerating it and thus suitable as a pigment dispersant free of deterioration with time, and to provide the pigment dispersant, a pigment dispersed composition and a colored photosensitive composition each containing the above compound. <P>SOLUTION: The benzimidazolone compound is shown by general formula (1) [wherein, X is a single bond, N(R'), N(R')CO, O, OCO, CONH, COO, CO, SO<SB>2</SB>NH, SO<SB>3</SB>or SO<SB>2</SB>; A is an alkylene, arylene or aralkylene group; R is SO<SB>3</SB>H or COOH; R' is H, an alkyl or aryl; and n is an integer of 1-3]. <P>COPYRIGHT: (C)2004,JPO

Description

Detailed Description of the Invention

[0001]

TECHNICAL FIELD The present invention relates to a benzimidazolone compound, a pigment dispersant containing the benzimidazolone compound, a pigment dispersion composition and a colored photosensitive composition, and more specifically, to effectively prevent aggregation of pigments. Pigment dispersant that realizes good dispersion of pigments, containing the pigment dispersant, excellent in pigment dispersibility and fluidity, excellent in coloring power, suitable for a wide range of paints, printing inks, color display boards, etc. Suitable for use in forming a multicolor image on a substrate such as a color proof and for producing a color filter used in a liquid crystal color display, etc. It relates to a colored photosensitive composition that can be used.

[0002]

2. Description of the Related Art Conventionally, pigments have a vivid color tone and high tinting strength and have been widely used in many fields.
Many of these pigments which are practically important are generally fine particles, and a clear color tone and a high tinting strength can be obtained by preventing aggregation of the pigment and making it fine. However, as the pigment is made finer, the dispersion liquid of the pigment often exhibits high viscosity. Therefore, when this pigment dispersion is prepared on an industrial scale, it becomes difficult to take out the pigment dispersion from the disperser, it cannot be transported by a pipeline, and further, gelation occurs during storage. There are problems such as being unusable.

A colored photosensitive composition containing the above pigment is useful as a material for a color filter used in a liquid crystal display or the like, and when a colored filter is produced using the colored photosensitive composition, the quality, A pigment dispersion method, which is excellent in terms of production stability, is widely adopted. In this pigment dispersion method, a coating solution of the colored photosensitive composition is applied on a transparent substrate to provide a colored photosensitive layer, and after pattern exposure, development is performed to form a pixel pattern of the first color,
This is repeated a plurality of times to form pixel patterns of a plurality of colors on the transparent substrate.

However, since a pigment is used as a coloring material here, if the pigment is not sufficiently miniaturized, light is scattered and absorbed by the pigment, and the light transmittance is lowered. Further, there is a problem that the polarization axis is rotated due to light scattering and birefringence due to the pigment, and the contrast of the liquid crystal display device is lowered (1990 7th color optical conference, 512 color display 10. 4 "size TFT-LC
Color filter for D, Ueki, Koseki, Fukunaga, Yamanaka). Therefore, in the colored photosensitive composition, it is necessary to disperse the pigment in a highly finely divided state.

Therefore, it has been conventionally known to use various dispersants in order to obtain a pigment dispersion or a colored photosensitive composition which is excellent in fluidity and dispersibility. The dispersant can be roughly classified into a polymer dispersant and a low molecular compound dispersant. Examples of the polymer dispersant include polyacrylate, sodium maleate olefin copolymer, and terminal carboxyl group-containing polyester (Japanese Patent Publication No. 54-34
No. 009), an acidic group starting from tetrakis (2-hydroxyalkyl) ethylenediamine and /
Alternatively, a polyester having a basic group (Japanese Patent Laid-Open No. 2-24
No. 5231), a macromonomer (oligomer having an ethylenically unsaturated group at the terminal), a monomer having a hydroxyl group, a carboxyl group-containing monomer, and a copolymer other than these monomers (JP-A-8-259876).
No. gazette) is known. Further, as the low-molecular compound dispersant, sorbitan fatty acid ester, polyoxyethylene alkylamine, alkyldiamine, alkanolamine derivative (US Pat. No. 3,536,510) and the like are known. Examples are described in JP-B-5-72943 and JP-A-8-48890.

Similarly, Japanese Patent Publication No. 1-34269 (Japanese Patent Laid-Open No.
-166266), JP-A-10-265697, JP-A-10-46043, JP-A-11-199796, JP-A-11-237754-7, JP-A-2000-23955.
4, various publications such as JP-A 2000-265079 disclose various pigment dispersants. However, all of these pigment dispersants have problems that their synthesis is complicated and their productivity is poor.

On the other hand, a colored photosensitive composition containing a pigment exhibiting a vivid color tone and high tinting strength is useful as an image forming material for producing a color proof, a color filter and the like. When a colored image is formed using the colored photosensitive composition, generally, a coating liquid of the colored photosensitive composition is applied on a substrate to form a layer of the colored photosensitive composition, and then exposure and development are performed. As the developing solution used in this development, an alkaline aqueous solution which has little influence on the environment is often used, and the layer formed by the colored photosensitive composition, that is, the binder in the colored photosensitive composition ( The binder) is required to be soluble in the above alkaline aqueous solution. On the other hand, as the solvent (dispersion medium of the pigment) used for the coating liquid of the colored photosensitive composition, an organic solvent is effective because of easy drying after coating. Therefore, the binder in the colored photosensitive composition has an acidic group, and it is necessary to have a property of being soluble in a suitable organic solvent, in the colored photosensitive composition, the organic pigment, It has such a property and is dispersed in the above binder having an acidic group.

A layer formed of such a colored photosensitive composition is
Generally, it is required to be extremely thin and to have a high coloring density in a thin thickness. Therefore, it is possible to disperse an organic pigment in a highly finely divided state in a binder having an acidic group soluble in an organic solvent. Will be needed.

Japanese Patent Laid-Open No. 2001-172520 discloses that
A pigment dispersant, a pigment composition and a pigment dispersion composed of a specific benzimidazolone pigment derivative are described.
However, in the pigment dispersant described in the above publication, the viscosity is increased at the time of dispersion in a system in which the pigment is made into ultrafine particles for the purpose of increasing the transmittance, which has been found in recent color filter applications.

As described above, at present, a pigment dispersant having excellent dispersibility and fluidity of the pigment, a pigment dispersion composition containing the pigment dispersant, and a colored photosensitive composition have not yet been provided.

[0011]

SUMMARY OF THE INVENTION It is an object of the present invention to solve the above-mentioned problems of the prior art and achieve the following objects. That is, an object of the present invention is to provide a benzimidazolone compound which can be easily synthesized and is suitable for a pigment dispersant. It is another object of the present invention to provide a pigment dispersant which does not aggregate the pigment, realizes stable and good dispersibility and fluidity of the pigment, and does not deteriorate with time. Further, the present invention contains the pigment dispersant to disperse the pigment,
It is an object of the present invention to provide a pigment dispersion composition which is excellent in fluidity and the like, has high coloring power, is excellent in alkali developability, and can be suitably used in a wide range of paints, printing inks, color display boards and the like. The present invention also includes a color filter containing the pigment dispersion composition, which has a high coloring power, is excellent in alkali developability, and is used for forming a multicolor image on a substrate such as a color proof and for a liquid crystal color display. An object of the present invention is to provide a colored photosensitive composition that can be suitably used for the production of

[0012]

[Means for Solving the Problems] Means for solving the above problems are as follows. That is, the present invention is <1> a benzimidazolone compound represented by the following general formula (1).

[0013]

[Chemical 2]

[In the general formula (1), X is a single bond, -N
(R ')-, -N (R') CO-, -O-, -OCO
-, - CONH -, - CO 2 -, - CO -, - SO 2 NH
-, - SO ₃ - or -SO ₂ - shows a. A is alkylene,
An arylene or aralkylene group is shown, which may have a substituent and may be interrupted by a divalent linking group. R represents SO ₃ H or CO ₂ H, and R ′ represents a hydrogen atom or an alkyl or aryl group which may have a substituent. n shows the integer of 1-3. ]

<2> A pigment dispersant containing the benzimidazolone compound of the above <1>.

<3> A pigment dispersion composition comprising the pigment dispersant of the above <2> and a pigment dispersed in an organic solvent.

<4> Further, a polymer having a basic group is dispersed in an organic solvent <3>
It is the described pigment dispersion composition.

<5> The pigment dispersion composition according to the above <3> or <4>, further containing a binder polymer having an acidic group.

<6> The pigment dispersion composition according to <5> above,
A colored photosensitive composition comprising a polyfunctional monomer having two or more ethylenically unsaturated double bonds and a photopolymerization initiator.

[0020]

BEST MODE FOR CARRYING OUT THE INVENTION The present invention will be described in detail below. << Benzimidazolone Compound >> The benzimidazolone compound of the present invention is characterized by being represented by the following general formula (1). Since the benzimidazolone compound of the present invention can be synthesized by a simple process, it has excellent productivity. Examples of the use of the benzimidazolone compound of the present invention include pigment dispersants, colorants, reaction agents for pigmentation, pharmaceuticals, intermediates such as agricultural chemicals, pH adjusters, etc., and are particularly suitable as pigment dispersants. Can be used.

[0021]

[Chemical 3]

[In the general formula (1), X is a single bond, -N
(R ')-, -N (R') CO-, -O-, -OCO
-, - CONH -, - CO 2 -, - CO -, - SO 2 NH
-, - SO ₃ - or -SO ₂ - shows a. A is alkylene,
An arylene or aralkylene group is shown, which may have a substituent and may be interrupted by a divalent linking group. R represents SO ₃ H or CO ₂ H, and R ′ represents a hydrogen atom or an alkyl or aryl group which may have a substituent. n shows the integer of 1-3. ]

In the general formula (1), X is a single bond, -N.
(R ')-, -N (R') CO-, -O-, -OCO
-, -CONH-, -CO₂-, -CO-, -SO₂NH
-, -SO ₃-Or-SO₂-Indicates -N (R ')
-, -N (R ') CO-, -O-, and -OCO- are particularly preferable.
Good In addition, -N (R ')-, -N (R') CO-
Of the groups represented by R ', the alkyl group has 1 carbon atom.
~ 24 alkyl groups are preferred, specifically methyl
Group, ethyl group, n-propyl group, i-propyl group, n-
Butyl group, i-butyl group, sec-butyl group, tert
-Butyl group, pentyl group, hexyl group, heptyl group, n
-Octyl group, 2-ethylhexyl group, t-octyl group
Group, nonyl group, decyl group, dodecyl group, tridecyl group,
Tetradecyl group, pentadecyl group, n-hexadecyl group
Group, 2-hexyldecyl group, heptadecyl group, octadecyl group
Syl, nonadecyl, icosyl, henicosyl, do
Examples include cosyl group, tricosyl group, tetracosyl group
It Examples of the aryl group include a phenyl group and a naphthyl group.
You can These alkyl groups or aryl groups have a substituent
It may have a substituent.
Examples include lucoxy group and halogen atoms such as chlorine atom.
It As the alkyl and aryl groups having a substituent,
2-methoxyethyl group, 3-methoxyphenyl group, 3,
4-dichlorophenyl group etc. are mentioned. Indicated by R '
Among these groups, a hydrogen atom and a methyl group are particularly preferable.
Group, ethyl group, butyl group, and hexyl group.

In the general formula (1), A is alkylene or aryl.
A len or aralkylene group, which has a substituent
Optionally, an oxygen atom, a nitrogen atom, a sulfur atom, and
Interrupted by divalent linking groups such as esters, amides, etc.
Good. Specifically, methylene, ethylene, propylene
Hexane, tetramethylene, pentamethylene, hexamethylene
N, octamethylene, -C₂H_FourOC₂H_Four-, -C_FiveH_Ten
CONHC₃H₆-, Phenylene, naphthalene diyl, a
Ntracenediyl, toluylene, dimethoxyphenyle
Amine, chlorophenylene, pyridinediyl, -CH₂C₆H
_Four-, -CH₂C₆H_FourCH₂-, Etc. are particularly preferred.
Specifically, methylene, ethylene, tetramethylene, penta
Methylene, hexamethylene, octamethylene, -C_FiveH
_TenCONHC₃H ₆-, Phenylene, toluylene, chloro
Phenylene, -CH₂C₆H_FourCH₂-Is mentioned.

R represents SO ₃ H or CO ₂ H, both of which are preferred groups. n is an integer of 1 to 3, and n may be 1 to 3 from the viewpoint of dispersion performance, but 1 or 2 is preferable from the viewpoint of easy introduction of the group.

Specific examples of the benzimidazolone compounds represented by the general formula (1) (compounds (1) to (15)) are shown below, but the invention is not limited thereto.

[0027]

[Chemical 4]

The benzimidazolone compound represented by the above general formula (1) of the present invention can be synthesized by an azo coupling reaction between a known 5-acetoacetylaminobenzimidazolone compound and a corresponding aniline derivative. . Below, the synthetic example of the benzimidazolone compound represented by the said General formula (1) is shown.

-Synthesis of Compound (13) -4.2 parts of 5-nitroisophthalic acid, potassium carbonate 6.1
And dimethylacetamide (20 parts) were heated to 100 ° C., and 5.4 parts of 1,3-propanesartone were slowly added with stirring. The stirring was continued for 3 hours, then poured into 200 parts of acetonitrile, and the stirring was continued for another hour.
The obtained crystals were filtered, washed with water and dried to obtain 5-nitroisophthalic acid bis- (3-sulfopropyl) ester. The obtained 5-nitroisophthalic acid bis- (3-sulfopropyl) ester was reduced to 3.4
Parts, ammonium chloride 0.4 parts, isopropyl alcohol 60 parts, and water 30 parts with heating under reflux for 3 hours. After hot filtration, 100 parts of acetonitrile was added to this solution, and the mixture was further stirred at room temperature for 1 hour. The obtained crystals are filtered,
After washing with water and drying, 9.0 parts of 5-aminoisophthalic acid bis- (3-sulfopropyl) ester was obtained.

5-aminoisophthalic acid bis-
After dissolving 9.0 parts of (3-sulfopropyl) ester in 100 parts of water, 1.3 parts of sodium nitrite is added and dissolved under ice cooling. This aqueous solution was added dropwise to a previously prepared mixture of 5.8 parts of concentrated hydrochloric acid and 50 parts of ice under ice cooling, and the mixture was stirred for 10 minutes,
A diazonium salt solution was prepared.

Next, to 50 parts of water, sodium hydroxide 2.
3 parts and 4.4 parts of 5-acetoacetylaminobenzimidazolone are added and dissolved, and the diazonium salt solution prepared above is slowly added while stirring under ice cooling. After stirring for 1 hour, 100 parts of acetonitrile was added and stirred for 1 day, and the obtained crystals were filtered and washed with acetonitrile. The crystals obtained here were dissolved in 20 parts of water to prepare an ion exchange resin (Amberlite IR-12).
00 (plus)) (100 parts) and the mixture was stirred at room temperature for 3 hours. After removing the ion exchange resin by filtration, 200 parts of acetonitrile was added to the aqueous solution, and the mixture was stirred at room temperature for 1 hour.
After the obtained crystals were washed with acetonitrile and dried. Grinding in a mortar gave 7.0 parts of compound (13) as a yellow powder.

1H-NMR (DMSO-d6); 13.
21 (s, 1H), 10.85 (s, 1H), 10.7
0 (s, 1H), 10.61 (s, 1H), 8.32
(S, 2H), 8.16 (s, 1H), 7.60 (s, 1
H), 7.03 (d, 1H), 6.90 (d, 1H),
4.40 (t, 2H), 2.64 (m, 2H), 2.29
(S, 3H), 2.06 (t, 2H)

-Synthesis of Compound (1) -In the synthesis of Compound (13), 3-nitrobenzoic acid is used instead of 5-nitroisophthalic acid, and 5-bromopentanesulfone is used instead of 1,3-propanesartone. Compound (1) was obtained in the same manner as in the synthesis of compound (13) except that an acid was used.

-Synthesis of Compound (8) -In the synthesis of Compound (13), 4-nitrophenol was used in place of 5-nitroisophthalic acid, and 5-chlorocarbonylpentano was used in place of 1,3-propanesartone. Compound (8) was obtained in the same manner as in the synthesis of compound (13) except that ic acid was used.

-Synthesis of Compound (10) -In the same manner as in the synthesis of Compound (13) except that 1,2-dihydroxy-4-nitrobenzene was used instead of 5-nitroisophthalic acid in the synthesis of Compound (13). ,
Compound (10) was obtained.

-Synthesis of Compound (12) -In the synthesis of Compound (13), 1,3-dihydroxy-4-nitrobenzene was used in place of 5-nitroisophthalic acid, and 6-in place of 1,3-propanesartone. Compound (12) was obtained in the same manner as in the synthesis of compound (13) except that -bromohexanoic acid was used.

<< Pigment Dispersant >> The pigment dispersant of the present invention contains a benzimidazolone compound represented by the above general formula (1) (hereinafter sometimes referred to as “imidazolone compound of the present invention”). Other components appropriately selected are contained as needed. Since the pigment dispersant of the present invention contains the benzimidazolone compound of the present invention, the pigment is not aggregated, stability of the pigment, good dispersibility and fluidity are realized, and there is no deterioration with time. Furthermore, when the pigment dispersant of the present invention is used, even in a system where ultrafine particles are formed, the viscosity does not increase during dispersion. The content of the benzimidazolone compound of the present invention in the pigment dispersant is 50 to 100% by mass.
Is preferable and 70-100 mass% is more preferable. When the content is less than 50% by mass, the viscosity of the pigment dispersion may increase.

(Other Components) The pigment dispersant of the present invention comprises
It may contain only the imidazolone compound of the present invention, or may further contain other components appropriately selected as necessary. Examples of the other components include known dispersants, and specifically, nonanoamide, decane amide, dodecane amide, N-dodecyl hexadecane amide, N-octadecyl propioamide, N, N-dimethyldodecane amide and N, Amide compounds such as N-dihexylacetamide, diethylamine, diheptylamine, dibutylhexadecylamine, N, N, N ′, N ′
Amine compounds such as tetramethylmethanamine, triethylamine, tributylamine and trioctylamine, monoethanolamine, diethanolamine, triethanolamine, N, N, N ′, N ′-(tetrahydroxyethyl) -1,2-diamino Ethane, N, N,
N'-tri (hydroxyethyl) -1,2-diaminoethane, N, N, N ', N'-tetra (hydroxyethylpolyoxyethylene) -1,2-diaminoethane, 1,
4-bis (2-hydroxyethyl) piperazine and 1
Examples thereof include amines having a hydroxy group such as-(2-hydroxyethyl) piperadisi, and compounds such as pecotamide, isonipecotamide, and nicotinic acid amide.
These may be commercially available products or those synthesized as appropriate, and examples of the commercially available products include Shigenox-105 (trade name, manufactured by Hakkol Chemical Co.).

The content of the above-mentioned other components in the pigment dispersant is preferably 1 to 90% by mass, and 1 to 7% by mass.
0 mass% is more preferable. If the content is less than 1% by mass, the viscosity increase of the pigment dispersion composition may not be suppressed, and if it exceeds 90% by mass, the performance as a pigment dispersant may not be sufficiently exhibited.

The pigment dispersant of the present invention may further contain an amine compound represented by the following general formula (2) or (3).

[0041]

[Chemical 5]

In the above general formula (2), R^{twenty one}And R^{twenty two}
Is a hydrogen atom or an optionally substituted alkyl group.
Represents a killed group or an aralkyl group, which are bound to each other.
Combined to form a 5- to 6-membered saturated ring containing a nitrogen atom
Good. This saturated ring further includes an oxygen atom, a sulfur atom and
It may contain 1 to 3 atoms selected from nitrogen atoms.
Yes. R^{twenty three}Contains an alkylene group or an ether bond
Represents an alkylene group. X ²Is -CON (Y^{twenty one})
(Y^{twenty two}), -OCON (Y^{twenty one}) (Y^{twenty two}), -N (Y^{twenty three})
CO (Y^{twenty four}), Or -N (Y^{twenty three}) CON (Y^{twenty one})
(Y^{twenty two}) Represents. Y^{twenty one}, Y ^{twenty two}, Y^{twenty three}And Y^{twenty four}Is hydrogen
An atom or an alkyl group which may have a substituent, ara
It represents a alkyl group or an aryl group.

[0043]

[Chemical 6]

In the above general formula (3), R ³¹ , R ³² , R
³⁶ and R ³⁷ represent a hydrogen atom, or an optionally substituted alkyl group or aralkyl group, which are bonded to each other to form a 5-membered to 6-membered saturated ring containing a nitrogen atom. Good. The saturated ring may further contain 1 to 3 atoms selected from oxygen atom, sulfur atom and nitrogen atom. R ³³ and R ³⁵ represent an alkylene group or an alkylene group having an ether bond. Z ³ is −
^{CON (Y 31) -, -} OCON (Y 31) - or N (Y
³² ) CON (Y ³³ ) −. Y ³¹ , Y ³² and Y ³³
Is synonymous with Y ²¹ , Y ²² and Y ²³ in the above general formula (2) in this order.

Preferable examples of the amine compound represented by the above general formula (2) or (3) include bis (2- (1-morpholino) ethyl) terephthalamide.

The pigment dispersant of the present invention may contain various surfactants, and the presence of the surfactant is effective for improving dispersion stability. Examples of the surfactant include an alkylnaphthalene sulfonate, an anionic surfactant represented by a phosphoric acid ester salt, a cationic surfactant represented by an amine salt, an aminocarboxylic acid, and a betaine type. Examples include amphoteric surfactants.

(Dispersion) Next, the dispersion of the pigment by the pigment dispersant of the present invention will be described. When the pigment dispersant of the present invention is used, the pigment dispersant is adsorbed on the surface of pigment particles. At this time, the nitrogen atom in the pigment dispersant is adsorbed on the surface of the pigment particle. The pigment particles are in a state of being covered with the imidazolone compound of the present invention. Since the imidazolone compound of the present invention is adsorbed on the surface of each pigment particle, the pigment particles are not adsorbed and aggregated with each other, and remain in a finely divided state, and are uniformly dispersed by the imidazolone compound of the present invention. , It becomes easy to flow.

When an ordinary pigment dispersant is used in the colored photosensitive composition, the acidic group in the binder polymer having an acidic group and the nitrogen atom in the pigment dispersant contained in the colored photosensitive composition are contained. Often forms a salt or binds with a strong intermolecular force, but in the case of the pigment dispersant of the present invention containing the imidazolone compound of the present invention, it has a pigment mother nucleus. Therefore, since the affinity with the pigment is higher, such behavior can be suppressed, while the stability after dispersion can be improved and the effect of improving dispersibility by the nitrogen atom can be enhanced. Further, according to the imidazolone compound of the present invention, when the organic pigment is dispersed, there is no thickening,
The dispersibility of the organic pigment is good, and particularly the dispersibility in an acidic organic pigment is good.

Dispersion with the pigment dispersant of the present invention means that the pigment particles that are generally present in the state of secondary particles are loosened to the state of primary particles to prevent reaggregation. The pigment dispersant of the present invention has an adsorption site on the pigment, and in order to prevent re-aggregation after the pigment is dispersed in the form of primary particles, coexistence of a binder having an acidic group causes steric repulsion. It is possible to impart sex. Dispersion of the pigment by the pigment dispersant of the present invention is effectively achieved by directly mixing the pigment dispersant and the pigment, and it is preferable to carry out in the state where there are as few particles as the dispersible other than the pigment as much as possible. When the pigment is dispersed in such a state, the pigment dispersant of the present invention is instantly adsorbed around the pigment particles, the pigment particles are well dispersed and flow well, and the pigment particles are aggregated. Is effectively suppressed. On the other hand, when the pigment is dispersed in the presence of particles that can be dispersed in addition to the pigment particles, the pigment dispersant of the present invention does not adsorb onto the surface of the intended pigment particles, but onto other particle surfaces, The pigment dispersion effect of the pigment dispersant may be impaired. Therefore, for example, in the case of producing a light-sensitive material or the like, in order to include the pigment in the light-sensitive material or the like in a state in which the pigment is well dispersed,
It is preferable to mix the pigment and the pigment dispersant of the present invention at an early stage and to add a binder polymer having an acidic group before or during the dispersion, which is slow when preparing a coating solution for a photosensitive layer or the like. It is not preferable to add and mix the pigment dispersant of the present invention at that time.

The pigment dispersant of the present invention can be suitably used for dispersing known pigments, and can be particularly preferably used for the pigment dispersion composition and the colored photosensitive composition of the present invention described later.

<< Pigment Dispersion Composition >> The pigment dispersion of the present invention comprises at least the pigment dispersant of the present invention and a pigment.
It is dispersed in an organic solvent, and preferably, a polymer having a basic group and / or a binder polymer having an acidic group is dispersed.

The content of the pigment dispersant in the pigment dispersion composition is usually 0.1 to 100 parts by mass, preferably 1 to 20 parts by mass, relative to 100 parts by mass of the pigment. If the content is less than 1 part by mass, the viscosity of the pigment dispersion composition may increase, and if it exceeds 20 parts by mass, it becomes difficult to adjust the chromaticity when producing a color filter or the like. Sometimes.

(Pigment) Examples of the pigment include organic pigments. As the organic pigment, for example, yellow pigment, orange pigment, red pigment, violet pigment, blue pigment,
Examples include green pigments, brown pigments, black pigments, and the like.

Examples of the yellow pigment include C.I. I.
Pigment Yellow 20, C.I. I. Pigment Yellow 24, C.I. I. Pigment Yellow 12, C.I. I pigment yellow 17, C.I. I. Pigment Yellow 83,
C. I. Pigment Yellow 86, C.I. I. Pigment Yellow 93, C.I. I. Pigment Yellow 109,
C. I. Pigment Yellow 110, C.I. I. Pigment Yellow 117, C.I. I. Pigment Yellow 12
5, C.I. I. Pigment Yellow 137, C.I. I. Pigment Yellow 138, C.I. I. Pigment Yellow 1
39, C.I. I. Pigment Yellow 185, C.I. I. Pigment Yellow 147, C.I. I. Pigment Yellow 148, C.I. I pigment yellow 153, C.I. I. Pigment Yellow, C.I. I. Pigment Yellow 15
4, C.I. I. Pigment Yellow 166, C.I. I. Pigment Yellow 168, C.I. I. Pigment Yellow 1
85 and the like.

Examples of the orange pigment include C.I.
I. Pigment Orange 36, C.I. I. Pigment Orange 43, C.I. I. Pigment Orange 51, C.I. I.
Pigment Orange 55, C.I. I. Pigment Orange 59, C.I. I. Pigment Orange 61, C.I. I. Pigment Orange 71, and the like.

Examples of the red pigment include C.I. I.
Pigment Red 9, C.I. I. Pigment Red 97,
C. I. Pigment Red 122, C.I. I. Pigment Red 123, C.I. I. Pigment Red 149, C.I.
I. Pigment Red 168, C.I. I. Pigment Red 177, C.I. I. Pigment Red 180, C.I. I.
Pigment Red 192, C.I. I. Pigment Red 2
15, C.I. I. Pigment Red 216, C.I. I. Pigment Red 217, C.I. I. Pigment Red 22
0, C.I. I. Pigment Red 223, C.I. I. Pigment Red 224, C.I. I. Pigment Red 226,
C. I. Pigment Red 227, C.I. I. Pigment Red 228, C.I. I. Pigment Red 240, C.I.
I. Pigment Red 48: 1, C.I. I. Pigment Red 209, C.I. I. Pigment Red 146, C.I.
I. Pigment Red 11, C.I. I. Pigment Red 81, C.I. I. Pigment Red 213, C.I. I. Pigment Red 272, C.I. I. Pigment Red 27
0, C.I. I. Pigment Red 255, C.I. I. Pigment Red 264, C.I. I. Pigment Red 254,
Etc.

Examples of the violet pigment include, for example,
C. I. Pigment violet 19, C.I. I. Pigment Violet 23, C.I. I. Pigment Violet 29, C.I. I. Pigment Violet 30, C.I.
I. Pigment Violet 37, C.I. I. PIMEND violet 40, C.I. I. Pigment Violet 5
0, etc.

Examples of the blue pigment include C.I. I.
Pigment Blue 15, C.I. I. Pigment Blue 1
5: 6, C.I. I. Pigment Blue 22, C, I.I. Pigment Blue 60, C.I. I. Pigment Blue 64 and the like.

Examples of the green pigment include C.I. I.
Pigment Green 7, C.I. I. Pigment Green 3
6, etc. are mentioned. Examples of the brown pigment include C.I. I. Pigment Brown 23, C.I. I. Pigment Brown 25, C.I. I. Pigment Brown 26,
Etc. Examples of the black pigment include C.I.
I. Pigment Black 7 and the like.

These pigments may be used alone or in combination of two or more. In the present invention, among these, pigments having an acidic group such as Pigment Yellow 138, Pigment Yellow 139, Pigment Yellow 185 and Pigment Yellow 83 are preferable,
Pigment Yellow 138, Pigment Yellow 13
9, Pigment Yellow 185, Pigment Red 25
4, Pigment Green 36, Pigment Blue 15 and the like are particularly preferable.

The content of the above pigment in the above pigment dispersion composition is usually 1 to 50% by mass, preferably 5 to 30% by mass. If the content is less than 5% by mass, the coloring power may not be sufficient, and if it exceeds 30% by mass, the viscosity of the pigment dispersion composition may increase.

(Organic Solvent) The above organic solvent is not particularly limited and may be appropriately selected from known ones, for example, ethylene glycol monomethyl ether,
(Poly) alkylene glycol monoalkyl ethers such as ethylene glycol monoethyl ether, propylene glycol monomethyl ether, propylene glycol monoethyl ether, diethylene glycol monomethyl ether, ethylene glycol monoethyl ether and acetic acid esters thereof; ethyl acetate, n-propyl acetate , I-propyl acetate, n-butyl acetate, i-acetic acid
Acetates such as butyl; aromatic hydrocarbons such as benzene, toluene, xylene; ketones such as methyl ethyl ketone, acetone, methyl isobutyl ketone, cyclohexanone; ethanol, propanol, butanol, hexanol, cyclohexanol, ethylene glycol, diethylene glycol, Examples thereof include alcohols such as glycerin. These may be used alone or in combination of two or more. Among these, alkylene glycol monoalkyl ethers, acetic acid esters thereof, acetic acid esters, methyl ethyl ketone, and the like are preferable.

The content of the organic solvent in the pigment dispersion composition is usually 10 to 1000 parts by mass, preferably 20 to 800 parts by mass, relative to 100 parts by mass of the pigment. When the content is less than 10 parts by mass,
The viscosity of the pigment dispersion composition may increase to 1000
If it exceeds the mass part, it may be difficult to secure a space during storage.

(Polymer Having Basic Group) The polymer having a basic group in the present invention is a polymer having, for example, a group having nitrogen as a basic group. Specific examples of the basic group include primary amines, secondary amines, tertiary amines, anilines, guanidines, nitrogen-containing cyclic compounds, and the like, and more specifically, amino. Group, methylamino group, dimethylamino group, ethylamino group, diethylamino group, butylamino group, dibutylamino group, hexylamino group, octylamino group, N-
Methyl-N-octylamino group, degenerate product of amino group and dicyclohexylcarbodiimide, degenerate product of amino group and diisopropylcarbodiimide, pyridinyl group, pyrrolidino group, piperidino group, morpholino group, diazabicycloundecene-derived functionality Groups, and the like.

The above-mentioned polymer having a basic group is a monomer having the above-mentioned basic group alone, or radical polymerization of the above-mentioned monomer having a basic group and another monomer,
It is a homopolymer or copolymer obtained by polycondensation or conversion of a functional group of a polymer having no basic group.

More specifically, JP-A-10-33994
9, JP-A-2000-234007, JP-A-2001-31
The compounds described in 885, polyethyleneimine, polyallylamine, amide amine salt of polyester acid, and the like can be mentioned.

Among these, amine-containing polymers are preferable as the polymer having a basic group in the present invention. The polymer containing the amine may be a homopolymer of a monomer having an amino group or a copolymer with another monomer. Further, these modified products may be used and are not particularly limited as long as at least an amino group is present as a repeating unit in the polymer.

As the above-mentioned monomer having an amino group,
Vinylamine, allylamine, N, N-dimethylaminoethyl (meth) acrylate, N, N-dimethylaminopropyl (meth) acrylate, 1- (N, N-dimethylamino) -1,1-dimethylmethyl (meth) acrylate, N, N-dimethylaminohexyl (meth) acrylate, N, N-diethylaminoethyl (meth) acrylate, N, N-diisopropylaminoethyl (meth)
Acrylate, N, N-di-n-butylaminoethyl (meth) acrylate, N, N-di-i-butylaminoethyl (meth) acrylate, morpholinoethyl (meth) acrylate, piperidinoethyl (meth) acrylate, 1-pyrroli Dinoethyl (meth) acrylate,
N, N-methyl-2-pyrrolidylaminoethyl (meth)
Acrylate and N, N-methylphenylaminoethyl (meth) acrylate (above (meth) acrylates); dimethyl (meth) acrylamide, diethyl (meth) acrylamide, diisopropyl (meth) acrylamide, di-n-butyl (meth) acrylamide. , The-
i-Butyl (meth) acrylamide, morpholino (meth) acrylamide, piperidino (meth) acrylamide, N-methyl-2-pyrrolidyl (meth) acrylamide and N, N-methylphenyl (meth) acrylamide (above (meth) acrylamides) 2- (N, N-
Dimethylamino) ethyl (meth) acrylamide, 2-
(N, N-diethylamino) ethyl (meth) acrylamide, 3- (N, N-diethylamino) propyl (meth) acrylamide, 3- (N, N-dimethylamino)
Propyl (meth) acrylamide, 1- (N, N-dimethylamino) -1,1-dimethylmethyl (meth) acrylamide and 6- (N, N-diethylamino) hexyl (meth) acrylamide (above aminoalkyl (meth) acrylamide) ); And vinylpyridine. Among these, N, N-dimethylaminopropyl (meth) acrylate, 3- (N, N-diethylamino) propyl (meth) acrylamide, 6-
(N, N-diethylamino) hexyl (meth) acrylamide, 1-pyrrolidinoethyl (meth) acrylate,
Allylamine is preferred.

As the above-mentioned other monomer copolymerizable with the above-mentioned monomer having an amino group, there are aromatic vinyl compounds (eg, styrene, α-methylstyrene, vinyltoluene); (meth) acrylic acid alkyl ester (eg, methyl). (Meth) acrylate, ethyl (meth) acrylate, n-butyl (meth) acrylate, i-butyl (meth) acrylate; (meth) acrylic acid alkylaryl ester (for example, benzyl (meth) acrylate, glycidyl (meth) acrylate) ); Carboxylic acid vinyl ester (for example, vinyl acetate, vinyl propionate); vinyl cyanide (for example, (meth) acrylonitrile, α-chloroacrylonitrile); aliphatic conjugated diene (for example, 1,3-butadiene, isoprene) The end meta Cryloylated polymethylmethacrylate (trade name: AA-6, manufactured by Toagosei Co., Ltd.) and the like can also be mentioned, and more than one of these can be used.
Among these, styrene, n-butyl (meth) acrylate, benzyl (meth) acrylate, and methacryloyl-terminated polymethylmethacrylate (AA-6) are preferable.

When the above-mentioned other monomer is used, the repeating unit derived from this monomer is contained in the range of 1 to 99% by mass of all the repeating units, and the repeating unit derived from the monomer having an amino group is contained in all the repeating units. 1 to 9
It is preferably contained in the range of 9% by mass (particularly 5 to 50% by mass). Specific examples of the copolymer of the above-mentioned monomer having an amino group and another monomer include dimethylaminoethyl acrylate / methyl methacrylate copolymer,
3- (N, N-dimethylamino) propyl methacrylamide / benzyl methacrylate / AA-6 copolymer,
Examples thereof include N, N-dimethylaminopropyl methacrylate / butyl methacrylate / AA-6 copolymer.

The weight average molecular weight (Mw) of the above-mentioned polymer having a basic group is preferably in the range of 2,000 to 100,000, particularly preferably in the range of 3,000 to 20,000. The weight average molecular weight is a polystyrene equivalent weight average molecular weight measured by gel permeation chromatography (carrier: tetrahydrofuran).

The content of the polymer having a basic group in the pigment dispersion composition of the present invention is 0.1 to 30.
Mass% is preferable, and 1 to 20 mass% is more preferable. If the content is less than 1% by mass, the viscosity may increase during dispersion, and if it exceeds 30% by mass, the binder polymer having an acidic group may increase the viscosity.

(Binder Polymer Having Acidic Group) The pigment dispersion composition of the present invention preferably contains a binder polymer having an acidic group. The binder polymer having an acidic group is capable of imparting both properties of dispersion stability of the pigment and alkali developability when used as a colored photosensitive composition. For example, (meth) acrylic acid and Examples thereof include copolymers with (meth) acrylic acid esters, styrene / maleic anhydride copolymers, and reaction products of styrene / maleic anhydride copolymers with alcohols. These may be used alone or in combination of two or more. Among these, excellent in pigment dispersibility, when used as a colored photosensitive composition, polyfunctional monomer, excellent compatibility with the photopolymerization initiator, alkali developer solubility, organic solvent solubility, strength, softening Those having an appropriate temperature and the like are preferable, and specifically, a copolymer of (meth) acrylic acid and (meth) acrylic acid ester is preferable.

The weight average molecular weight of the binder polymer having an acidic group is preferably 5,000 to 200,000. If the weight average molecular weight is less than 5,000, there may be a problem in forming a coating film when used as a colored photosensitive composition, and if it exceeds 200,000, the viscosity of the colored photosensitive composition increases. Sometimes.

The content of the binder polymer having an acidic group in the pigment dispersion composition is usually 10 to 200 parts by mass, preferably 20 to 150 parts by mass with respect to 100 parts by mass of the pigment. The above content is 1
If it is less than 0 parts by mass, the steric repulsion effect may not be obtained, and if it exceeds 200 parts by mass, the viscosity of the dispersion may increase.

The pigment dispersion composition of the present invention can be prepared, for example, by the following method. 1) A method in which a composition obtained by previously mixing the pigment and the pigment dispersant is added to and dispersed in the organic solvent (or vehicle) 2) The organic solvent (or vehicle) is mixed with the pigment and the above Method in which pigment dispersant is added separately to disperse 3) Method in which the above pigment and the above pigment dispersant are separately dispersed in the above organic solvent (or vehicle) in advance, and the resulting dispersion is mixed (in this case, The pigment dispersant may be dispersed only in the organic solvent) 4) A method of dispersing the pigment in the organic solvent (or vehicle) and then adding the pigment dispersant to the obtained dispersion.

The vehicle means a portion of a medium in which the pigment is dispersed when the coating material is in a liquid state, and is a component (binder) which is in a liquid state and binds with the pigment to harden the coating film. And a component for dissolving and diluting (the above organic solvent).

The disperser used to disperse the pigment is not particularly limited, and examples thereof include known dispersers such as a kneader, roll mill, attritor, super mill, dissolver, homomixer and sand mill.

To form a colored image using the pigment dispersion composition, for example, a coating liquid containing the pigment dispersion composition is applied on a support and dried to form a layer of the pigment dispersion composition.
Alternatively, a layer of this pigment dispersion composition formed on a temporary support is transferred onto a support, and a layer of a known positive or negative photosensitive resin composition is formed thereon, exposed and developed. ,
Then, it can be carried out by a method of removing the unexposed layer of the photosensitive resin composition and the layer of the pigment dispersion composition in the same region.

<< Colored Photosensitive Composition >> The colored photosensitive composition contains at least the pigment dispersion composition and a photosensitive composition.

(Photosensitive Composition) Examples of the photosensitive composition include the photosensitive compositions described in JP-A-3-282404, and specifically, a negative type diazo resin and Examples thereof include a photosensitive composition containing a binder, a photopolymerizable composition, a photosensitive composition containing an azide compound and a binder, and a cinnamic acid type photosensitive composition. As the photosensitive composition, those developable with an alkaline aqueous solution and those developable with an organic solvent are known, but those developable with an alkaline aqueous solution in terms of pollution prevention, labor safety, etc. preferable.

-Photopolymerizable Composition- In the invention, the photopolymerizable composition is particularly preferable among the above-mentioned photosensitive compositions. The photopolymerizable composition contains at least a binder polymer having an acidic group, a polyfunctional monomer having two or more ethylenically unsaturated double bonds, and a photopolymerization initiator.

--Binder Polymer Having Acidic Group--
-The binder polymer having an acidic group contained in the photopolymerizable composition is a binder polymer having an acidic group suitably contained in the pigment dispersion composition of the present invention.

The content of the binder polymer having an acidic group in the colored photosensitive composition is about 20 to 80% by mass based on the total solid content. If the content is less than 20% by mass, problems may occur in forming the coating film, and if it exceeds 80% by mass, the ability of other materials may be difficult to be exhibited.

--Polyfunctional Monomer Having Two or More Ethylenically Unsaturated Double Bonds-- Examples of the polyfunctional monomer having two or more ethylenically unsaturated double bonds include those described in JP-A-60-258539.
Known (meth) acrylic acid ester, urethane (meth) acrylate, (meth)
Acrylic acid amides, allyl compounds, vinyl esters and the like can be mentioned. These may be used alone,
You may use 2 or more types together. Among these, (meta)
Acrylic acid esters are preferred.

The content of the polyfunctional monomer having an ethylenically unsaturated double bond in the colored photosensitive composition is preferably 10 to 60% by mass based on the total solid content. If the content is less than 10% by mass, the curing power at the time of exposure may be insufficient, and if it exceeds 60% by mass, the ability of other materials may be difficult to be exhibited.

--Photopolymerization Initiator-- As the above photopolymerization initiator, the wavelength is about 300 to 500 n.
It is preferable to use at least one compound having a molecular extinction coefficient of at least about 50 in m, and examples of such a compound include, for example, JP-A-2-48664, JP-A-1-152449, and JP-A-1-152449. 2-153
Aromatic ketones, lophine dimers, benzoin, benzoin ethers, polyhalogens, and the like, as described in Japanese Patent No. 353,353 are cited. These may be used alone or in combination of two or more.
Among these, 4,4'-bis (diethylamino) benzophenone and 2- (o-chlorophenyl) -4,5-
A combination of diphenylimidazole dimers, and 4
-[P-N, N-di (ethoxycarbonylmethyl)-
2,6-di (trichloromethyl) -s-triazine] is preferred.

The content of the photopolymerization initiator in the colored photosensitive composition is preferably 0.2 to 10% by mass based on the total solid content of the colored photosensitive composition. If the content is less than 0.2% by mass, the exposure sensitivity may be lowered, and if it exceeds 10% by mass, the exposure sensitivity may be too high (control becomes difficult).

The colored photosensitive composition can be prepared, for example, by mixing the pigment dispersion composition and the photosensitive composition according to appropriately selected conditions and techniques.

The formation of a colored image using the above colored photosensitive composition can be basically performed by the following steps (1) to (3). (1) After preparing the pigment dispersion composition, the step of preparing the colored photosensitive composition using the same (2) The obtained colored photosensitive composition is applied onto a substrate and dried, or A step of transferring a layer formed by coating on another temporary support and drying it to a substrate to form a layer of the colored photosensitive composition (3) Layer of the colored photosensitive composition formed on the substrate Of exposing and developing a pattern to form a pattern

The color filter used for a liquid crystal display or the like can be manufactured by repeating the steps (2) and (3) and combining the patterns of the second and subsequent colors. A method of manufacturing a color filter by a transfer method is described in, for example, Japanese Patent Application Laid-Open No. 4-208940, Japanese Patent Application Laid-Open No. 5-72724, Japanese Patent Application Laid-Open No. 5-80503, and Japanese Patent Application Laid-Open No. 5-173320.

A transparent material such as a glass plate or a transparent plastic plate is generally used as the substrate. In order to improve the adhesion between the substrate and the colored photosensitive composition, various commercially available silane coupling agents or the like are added to the colored photosensitive composition, or the substrate is subjected to a coupling treatment in advance. You may stay.

The coating solution of the colored photosensitive composition can be applied to the substrate by using a known coating means such as a spin coater, a roll coater, a bar coater or a curtain coater.

As a method of transferring the layer of the colored photosensitive composition formed on the temporary support to the substrate, a method of using a heat roll laminator under normal pressure or reduced pressure is preferably exemplified.

Examples of the developing solution used in the above development include alkali metal or alkaline earth metal hydroxides or carbonates, hydrogen carbonates, asimonia water, quaternary ammonium salt aqueous solutions, and the like. To be These may be used alone or in combination of two or more. Among these, sodium carbonate aqueous solution is particularly preferable.

[0096]

EXAMPLES Examples of the present invention will be described below, but the present invention is not limited to these examples.

Example 1 A red pigment dispersion composition having the following composition was prepared. -C. I. Pigment Red 254 6.4 g-Compound (1) 0.5 g-Disparlon DA-725 0.6 g (polymer having basic group; Kusumoto Kasei Co., Ltd.)-Methacrylic acid / benzyl methacrylate copolymer 15. 8 g (molar ratio 28/72, weight average molecular weight: 30,000, 40% 1-methoxy-2-propyl acetate solution) 1-methoxy-2-propyl acetate 57.2 g

The red pigment composition having the above composition was dispersed in a motor mill M-50 (manufactured by Eiger) using zirconia beads having a diameter of 0.65 mm at a peripheral speed of 9 m / s for 9 hours,
A red pigment dispersion composition was prepared.

The following evaluations were carried out on the obtained pigment dispersion composition. (1) Viscosity measurement: The viscosity of the obtained pigment dispersion composition was measured at 30 ° C. using a RE80 viscometer manufactured by Toki Sangyo Co., Ltd. Viscosity measurements were performed on samples immediately after pigment dispersion and after the pigment dispersion composition was stored at room temperature and 40 ° C. for 7 days. The results are shown in Table 1.

(2) Contrast measurement: The obtained pigment dispersion composition was applied on a glass substrate to a thickness of 5 μm to prepare a sample. This sample was placed between two polarizing plates, the amount of transmitted light when the polarization axes were parallel and perpendicular, and the ratio was defined as the contrast ("199
Year 0 7th Color Optical Conference, 512 color display 1
0.4 size TFT-LCD color filter, Ueki, Koseki, Fukunaga, Yamanaka ”. ). The results are shown in Table 1.
Shown in.

[Embodiment 2] In the first embodiment, C.I. I.
Pigment Red 254 is C.I. I. A yellow pigment dispersion composition was prepared in the same manner as in Example 1 except that Pigment Yellow 138 was used, and the same evaluation as in Example 1 was performed.

[Third Embodiment] In the first embodiment, the C.I. I.
Pigment Red 254 is C.I. I. A green pigment dispersion composition was prepared in the same manner as in Example 1 except that the pigment green 36 was used, and the same evaluation as in Example 1 was performed.

[Embodiment 4] In the first embodiment, C.I. I.
Pigment Red 254, C.I. I. A blue pigment dispersion composition was prepared in the same manner as in Example 1 except that Pigment Blue 15: 6 was used, and the same evaluation as in Example 1 was performed.

Example 5 A red pigment dispersion composition was prepared in the same manner as in Example 1 except that 0.5 g of the compound (1) was replaced by 0.5 g of the compound (9). Then, the same evaluation as in Example 1 was performed.

Example 6 A red pigment dispersion composition was prepared in the same manner as in Example 1 except that 0.5 g of the compound (1) was replaced by 0.6 g of the compound (10). Then, the same evaluation as in Example 1 was performed.

Example 7 A red pigment dispersion composition was prepared in the same manner as in Example 1 except that 0.5 g of the compound (1) was replaced by 0.7 g of the compound (13). Then, the same evaluation as in Example 1 was performed.

[Example 8] A yellow pigment dispersion composition was prepared in the same manner as in Example 2 except that 0.5 g of the compound (1) in Example 2 was replaced with 0.5 g of the compound (8). Then, the same evaluation as in Example 2 was performed.

[Example 9] A green pigment dispersion composition was prepared in the same manner as in Example 3 except that 0.5 g of the compound (1) was replaced by 0.6 g of the compound (12). Then, the same evaluation as in Example 3 was performed.

[Example 10] A blue pigment dispersion composition was prepared in the same manner as in Example 4 except that 0.5 g of the compound (1) in Example 4 was replaced with 0.5 g of the compound (6). Then, the same evaluation as in Example 4 was performed.

Comparative Example 1 A red pigment dispersion composition was prepared in the same manner as in Example 1 except that the compound (1) was replaced with 0.8 g of the following comparative compound. The same evaluation was performed.

[0111]

[Chemical 7]

[Comparative Example 2] In Comparative Example 1, C.I. I.
Pigment Red 254 is C.I. I. A yellow pigment dispersion composition was prepared in the same manner as in Comparative Example 1 except that Pigment Yellow 138 was used, and the same evaluation as in Comparative Example 1 was performed.

[Comparative Example 3] In Comparative Example 1, C.I. I.
Pigment Red 254 is C.I. I. A green pigment dispersion composition was prepared in the same manner as in Comparative Example 1 except that the pigment green 36 was used, and the same evaluation as in Comparative Example 1 was performed.

[Comparative Example 4] In Comparative Example 1, C.I. I.
Pigment Red 254, C.I. I. A blue pigment dispersion composition was prepared in the same manner as in Comparative Example 1 except that Pigment Blue 15: 6 was used, and the same evaluation as in Comparative Example 1 was performed.

Example 11 The following compositions were mixed to prepare a colored photosensitive composition for producing a color filter. -Red pigment dispersion composition of Example 1 34.8 g-Methacrylic acid / benzyl methacrylate copolymer 9.0 g (molar ratio 28/72, weight average molecular weight 30,000, 30% 1-methoxy-2-propyl acetate solution) ) -Pentaerythritol tetraacrylate 5.2 g 4- [p-N, N-di (ethoxycarbonylmethyl)]-2,6-di (trichloromethyl) -5-triazine 0.2 g-Hydroquinone monomethyl ether 0.01 g・ 1-Methoxy-2-propyl acetate 62 g

The above mixing was carried out by a motor mill M50 (manufactured by Eiger) using zirconia beads having a diameter of 0.65 mm at a peripheral speed of 9 m / s for 9 hours. Regarding the obtained colored photosensitive composition for producing a color filter, Example 1
The viscosity was measured in the same manner as in 1. to prepare a color filter as described below, and the contrast was measured in the same manner as in Example 1. The results are shown in Table 1.

That is, the above colored photosensitive composition for producing a color filter was applied onto a glass substrate using a spin coater and dried at 100 ° C. for 2 minutes to form a film having a thickness of about 2 μm. Next, under a nitrogen stream, it was exposed with an ultra-high pressure mercury lamp and then developed with a 1% sodium carbonate aqueous solution. The contrast of the obtained color filter was measured in the same manner as in Example 1.

[Example 12] A colored photosensitive composition was prepared in the same manner as in Example 11 except that the red pigment dispersion composition of Example 1 was replaced with the yellow pigment dispersion composition of Example 2. The product was prepared and evaluated in the same manner as in Example 11.

[Example 13] A colored photosensitive material was prepared in the same manner as in Example 11 except that the red pigment dispersion composition of Example 1 was replaced with the green pigment dispersion composition of Example 3. A composition was prepared and evaluated in the same manner as in Example 11.

[Example 14] Colored photosensitive material was prepared in the same manner as in Example 11 except that the red pigment dispersion composition of Example 1 was replaced with the blue pigment dispersion composition of Example 4. A composition was prepared and evaluated in the same manner as in Example 11.

[0121]

[Table 1]

From the results shown in Table 1, the pigment dispersion composition of the present invention containing the benzimidazolone compound represented by the general formula (1) and the colored photosensitive composition using the same have low viscosity and high viscosity. It is clear that contrast is obtained. It is speculated that the high contrast is obtained because the pigment particles are dispersed in a finely divided state. On the other hand, in the case of the pigment dispersion composition of Comparative Example, the viscosity was high and the dispersion could not be performed.

[0123]

According to the present invention, simple synthesis is possible,
A benzimidazolone compound suitable for a pigment dispersant can be provided. Moreover, according to the present invention, stable and good dispersibility and fluidity of the pigment are realized without aggregating the pigment,
It is possible to provide a pigment dispersant that does not deteriorate with time. Furthermore, according to the present invention, the pigment is excellent in dispersibility, fluidity, etc., has high coloring power, is also excellent in alkali developability, and can be suitably used in a wide range of paints, printing inks, color display boards, etc. A dispersion composition can be provided. Further, according to the present invention, it has a high coloring power, is excellent in alkali developability, and is suitably used for forming a multicolor image on a substrate such as a color proof and for manufacturing a color filter used for a liquid crystal color display and the like. A colored photosensitive composition to be obtained can be provided.

Front page continuation (51) Int.Cl. ⁷ Identification code FI theme code (reference) C09B 67/20 C09B 67/20 L 67/46 67/46 B G02B 5/20 101 G02B 5/20 101 5/22 5 / 22 G03F 7/004 505 G03F 7/004 505 (72) Inventor Sachiko Arai, 200, Onakasato, Fujinomiya-shi, Shizuoka Prefecture Fuji Photo Fuji Co., Ltd. (72) Inventor, Eri Komori 200, Onakasato, Fujinomiya-shi, Shizuoka Fuji Photo F-terms in film Co., Ltd. (reference) 2H025 AA00 AB09 AB13 AC01 AD01 BC42 CC13 CC20 2H048 BA02 BA45 BA47 BB02 BB42 CA04 CA14 CA19 CA21 4J002 BG012 BG022 BG071 BG131 BH012 BJ001 CM011 EN016 EN056 EU116 PA65 PA6922 PA83 PA88 PB25 PB39 PB40 PC02 PC08 QA23 RA04 RA07 RA10 SA21 SA78 TA03 TA04 UA01 VA01 WA01 4J026 AA17 AA43 AA45 AA47 AA50 AA54 AA60 AA76 AB07 AB38 AC18 AC23 AC26 AC33 BA12 BA19 BA27 BA36 BA29 DB06 DB11 BA39 BA39 BA39 BA39 BA39

Claims (6)

[Claims] 1. A benzimidazolone compound represented by the following general formula (1). [Chemical 1] [In general formula (1), X is a single bond, -N (R ')-, -N.
(R ') CO-, -O-, -OCO-, -CONH-,
_{-CO 2 -, - CO -,} - SO 2 NH -, - SO 3 - or -SO ₂ - shows a. A represents an alkylene, arylene or aralkylene group, which may have a substituent and may be interrupted by a divalent linking group. R is SO ₃
H or CO ₂ H is shown, and R ′ is a hydrogen atom or an optionally substituted alkyl or aryl group. n
Represents an integer of 1 to 3. ] 2. A pigment dispersant containing the benzimidazolone compound according to claim 1. 3. A pigment dispersion composition comprising the pigment dispersant according to claim 2 and a pigment dispersed in an organic solvent. 4. The pigment dispersion composition according to claim 3, which further comprises a polymer having a basic group dispersed in an organic solvent. 5. The pigment dispersion composition according to claim 3 or 4, further comprising a binder polymer having an acidic group. 6. A colored photosensitive composition comprising the pigment dispersion composition according to claim 5, a polyfunctional monomer having two or more ethylenically unsaturated double bonds, and a photopolymerization initiator. object.