JP2010043255A - Azo compound, azo pigment, pigment dispersion, colored composition, and inkjet recording ink - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an azo pigment and a pigment dispersion having excellent color characteristics such as coloring power and hue and exhibiting high durability such as light resistance. <P>SOLUTION: The azo pigment represented by formula (1), its tautomer, and salts or hydrates of them are provided. In the formula, G is a hydrogen atom, an aliphatic group, an aryl group, a heterocyclic group, an acyl group, an aliphatic oxycarbonyl group, a carbamoyl group, or a sulfonyl group; R<SB>1</SB>is an amino group, an aliphatic oxy-group, an aliphatic group, an aryl group, or a heterocyclic group; R<SB>2</SB>is a substituent; A is a specific heterocyclic group; m is an integer of 0-5; and n is an integer of 1-4. The formula represents a dimer formed via R<SB>1</SB>, R<SB>2</SB>, A, or G when n=2. The formula represents a trimer formed via R<SB>1</SB>, R<SB>2</SB>, A or G when n=3. The formula represents a tetramer formed via R<SB>1</SB>, R<SB>2</SB>, A or G when n=4. <P>COPYRIGHT: (C)2010,JPO&INPIT

Description

  The present invention relates to a novel nitrogen-containing heterocyclic azo compound, an azo pigment, a pigment dispersion containing the azo pigment, and a colored composition ink jet recording ink.

  In recent years, a material for forming a color image has been mainly used as an image recording material, and specifically, an ink jet recording material, a thermal transfer recording material, an electrophotographic recording material, a transfer halogen. Silver halide photosensitive materials, printing inks, recording pens, and the like are actively used. Further, a color filter is used for recording and reproducing a color image on an image pickup device such as a CCD in a photographing apparatus and on an LCD or PDP in a display. In these color image recording materials and color filters, three primary colors (dyes and pigments) of the so-called additive color mixing method and subtractive color mixing method are used to display or record full color images. In fact, there is no fast-acting dye that has absorption characteristics that can realize the above-mentioned conditions and can withstand various use conditions and environmental conditions, and improvement is strongly desired.

The dyes and pigments used in each of the above applications must have the following properties in common. That is, it has preferable absorption characteristics in terms of color reproducibility, fastness under environmental conditions to be used, for example, light resistance, heat resistance, good resistance to oxidizing gases such as ozone, and the like. In addition, when the dye is a pigment, it is further substantially insoluble in water and organic solvents and has good chemical fastness, and even when used as particles, the preferred absorption characteristics in the molecular dispersion state are impaired. It is also necessary to have properties such as absence. The required characteristics can be controlled by the strength of intermolecular interaction, but it is difficult to achieve both because they are in a trade-off relationship.
In addition, when using the pigment, in addition to having a particle size and a particle shape necessary for expressing the desired transparency, fastness under the environmental conditions used, such as light resistance, heat resistance, Good resistance to oxidative gases such as ozone, and other chemical fastness to organic solvents and sulfurous acid gas. Disperse even fine particles in the medium used, and stable dispersion. , Etc. are also required. In particular, there is a strong demand for pigments that have a good hue, have high coloring power among light, wet heat, and active gases in the environment, and are fast to light.

  In other words, the required performance for pigments is more diverse than dyes that require performance as pigment molecules, and not only the performance as pigment molecules, but also the above requirements as solids (fine particle dispersions) as aggregates of pigment molecules All performance needs to be satisfied. As a result, the group of compounds that can be used as pigments is extremely limited compared to dyes, and even if high-performance dyes are derived into pigments, there are only a few that can satisfy the required performance as fine particle dispersions. It cannot be developed. This is confirmed by the fact that the number of pigments registered in the color index is less than 1/10 of the number of dyes.

  Azo pigments are widely used in printing inks, ink-jet inks, electrophotographic materials and the like because they are excellent in hue and coloring power, which are color characteristics. Of these, the most typically used azo pigments are yellow diarylide pigments and red naphthol azo pigments. Examples of diarylide pigments include C.I. I. Pigment Yellow 12, 13 and 17 and the like. Examples of naphthol azo pigments include C.I. I. Pigment Red 208, 242 and the like. However, these pigments are extremely inferior in fastness, particularly light resistance, and are therefore not suitable for long-term storage of printed matter because the pigment is decomposed and faded when the printed matter is exposed to light.

  In order to improve such defects, azo pigments having improved fastness by increasing the molecular weight or introducing a group having a strong intermolecular interaction are also disclosed (for example, Patent Documents 1 to 3). 3). However, even in the improved pigment, for example, the pigment described in Patent Document 1 has improved light resistance, but is still insufficient. For example, the pigment described in Patent Documents 2 and 3 has a green hue. There was a drawback that coloring power was lowered by taste and color characteristics were inferior.

  Patent Documents 1 to 4 disclose dyes having absorption characteristics excellent in color reproducibility and sufficient fastness. However, the specific compounds described in the patent document have poor fastness even with good hue, poor hue even with good fastness, and are soluble in organic solvents and water. It is easy and the chemical fastness is not enough.

  When expressing a full color using a subtractive color mixing method of three colors of yellow, magenta and cyan, or four colors with black added, if a pigment with only one color is inferior in color fastness, If the balance is changed and a pigment having poor color characteristics is used, the color reproducibility at the time of printing is lowered. Therefore, in order to obtain a printed matter that maintains a high color reproducibility for a long period of time, a pigment and a pigment dispersion having both color characteristics and fastness are desired.

Conventionally, since azo dyes often have various visible light absorptions, they have been used as dyes in various fields. For example, it has come to be used in various fields such as coloring of synthetic resins, printing inks, dyes for sublimation thermal transfer materials, inkjet inks, and color filter dyes. An absorption spectrum is a large performance required for an azo dye as a dye. The hue of the pigment greatly affects the color and texture of an object colored by the pigment, and has a great effect on vision. Therefore, research on the absorption spectrum of dyes has been conducted for a long time.
A conventionally known azo dye having a nitrogen-containing 5-membered ring as an azo component is also disclosed in Patent Document 5. Patent Documents 6 to 8 disclose naphthol-based azo pigments and dyes in which a benzene ring and a naphthalene ring are bonded via an azo group.

WO05 / 52074 pamphlet International Publication No. 00/023525 Pamphlet JP 2008-13472 A JP-T 9-511278 JP 2008-7732 A JP 2004-123866 A Japanese Patent No. 3894726 Japanese Patent No. 2592271

  An object of the present invention is to provide an azo compound, an azo pigment, an azo pigment dispersion, a colored composition, and an ink jet recording which are excellent in color characteristics such as coloring power and hue and excellent in durability such as light resistance and ozone resistance. To provide ink.

  As a result of intensive studies, the present inventors have obtained knowledge that a specific nitrogen-containing heterocyclic azo pigment has a good hue and exhibits good fastness to light, heat and ozone. . Specific means for solving the above problems will be described below.

The azo compound and azo pigment of the present invention are excellent in color characteristics such as high coloring power and hue, and also in durability such as light resistance, ozone resistance and heat resistance.
Furthermore, the pigment dispersion and the inkjet recording ink of the present invention are obtained by dispersing the azo pigment of the present invention in various media, and are excellent in color characteristics, durability, ink liquid stability, and dispersion stability.

It is a figure of the infrared absorption spectrum of specific compound example D-22. It is a figure of the infrared absorption spectrum of specific compound example D-26. It is a figure of the infrared absorption spectrum of specific compound example D-27. It is a figure of the infrared absorption spectrum of specific compound example D-28. It is a figure of the infrared absorption spectrum of specific compound example D-29. It is a figure of the infrared absorption spectrum of specific compound example D-36. It is a figure of the infrared absorption spectrum of specific compound example D-39. It is a figure of the infrared absorption spectrum of specific compound example D-40.

[1]
An azo pigment represented by the following general formula (1), a tautomer thereof, a salt or a hydrate thereof.

(In General Formula (1), G represents a hydrogen atom, an aliphatic group, an aryl group, a heterocyclic group, an acyl group, an aliphatic oxycarbonyl group, a carbamoyl group, an aliphatic sulfonyl group, or an arylsulfonyl group, and R ₁ is represents an amino group, an aliphatic oxy group, an aliphatic group, an aryl group, or a heterocyclic group, _{R 2} represents a substituent, a represents the following general formula (a-1) ~ (a -14), (A- 16) to (A-22) or (A-24) to (A-26)). m represents an integer of 0 to 5, and n represents an integer of 1 to 4. In the case of n = 2, it represents a dimer via R ₁ , R ₂ , A or G. In the case of n = 3, it represents a trimer via R ₁ , R ₂ , A or G. In the case of n = 4, it represents a tetramer via R ₁ , R ₂ , A or G. )

(In the general formulas (A-1) to (A-14), (A-16) to (A-22), (A-24) to (A-26), R _{51 to} R ₅₉ are hydrogen atoms or substituted R ₅₁ and R ₅₂ , R ₅₂ and R ₅₃ , R ₅₃ and R ₅₄ , R ₅₅ and R ₅₆ , R ₅₆ and R ₅₇ , R ₅₅ and R ₅₈ , R ₅₆ and R ₅₈ , R ₅₇ And R ₅₈ , R ₅₅ and R ₅₉ may be bonded to each other to form a 5- to 6-membered ring (* represents a bonding position with the azo group of the general formula (1)).
[2]
The azo pigment represented by the general formula (1) is represented by the following general formula (2-1), the azo pigment according to [1], a tautomer thereof, a salt thereof, or water Japanese products.

(In the general formula (2-1), R ₁ , R ₂ , m, and n are the same as those defined in the general formula (1), and A ₁ represents the following general formulas (A-10) to (A-14). ), (A-16) to (A-22), or (A-24) to (A-26), when n = 2, R ₁ , R ₂ , or A ₁ Represents a dimer, n = 3 represents a trimer via R ₁ , R ₂ , or A ₁ , n = 4 represents a tetramer via R ₁ , R ₂ , or A ₁ Represents the body.)

(Formula (A-10) ~ (A -14), (A-16) ~ (A-22), in (A-24) ~ (A -26), R 55 ~R 59 is formula (1 ) Is the same as defined in)
[3]
The azo pigment represented by the general formula (1) and the general formula (2-1) is represented by the following general formula (2-2), the azo pigment according to [1], and its tautomerism Sex bodies, their salts or hydrates.

(In the general formula (2-2), R ₁ and R ₂ are the same as those defined in the general formula (1), and A ₂ represents the following general formulas (A-13), (A-14), (A -16), (A-18) to (A-22), (A-25), or (A-26), when n = 2, R ₁ , R ₂ , or A ₂ is Represents a dimer via n, if n = 3 represents a trimer via R ₁ , R ₂ , or A _2. If n = 4, it represents via R ₁ , R ₂ , or A ₂ Represents a tetramer.)

(In the general formula (A-13), (A -14), (A-16), (A-18) ~ (A-22), (A-25), (A-26), R 55 ~R ₅₉ is the same as defined in the general formula (1).)
[4]
A pigment dispersion comprising at least one of the azo pigments according to [1] to [3], a tautomer thereof, a salt or a hydrate thereof.
[5]
A coloring composition comprising at least one of the azo pigments according to [1] to [3], a tautomer thereof, a salt or a hydrate thereof.
[6]
Ink for ink jet recording, characterized by using the pigment dispersion described in [4].
[7]
An azo compound represented by the general formula (2-2).

(In General Formula (2-2), G represents a hydrogen atom, an aliphatic group, an aryl group, a heterocyclic group, an acyl group, an aliphatic oxycarbonyl group, a carbamoyl group, an aliphatic sulfonyl group, or an arylsulfonyl group, and R ₁ Represents an amino group, an aliphatic oxy group, an aliphatic group, an aryl group, or a heterocyclic group, R ₂ represents a substituent, A ₂ represents the following general formulas (A-13), (A-14), It represents one of (A-16), (A-18) to (A-22), (A-25), and (A-26), m represents an integer of 0 to 5, and n represents 1 to 4. In the case of n = 2, it represents a dimer through R ₁ , R ₂ , or A _{2. In} the case of n = 3, a trimer through R ₁ , R ₂ , or A ₂ (When n = 4, it represents a tetramer via R ₁ , R ₂ , or A ₂ )

(In the general formula (A-13), (A -14), (A-16), (A-18) ~ (A-22), (A-25), (A-26), R 55 ~R ₅₉ represents a hydrogen atom or a substituent, and adjacent R ₅₁ and R ₅₂ , R ₅₂ and R ₅₃ , R ₅₃ and R ₅₄ , R ₅₅ and R ₅₆ , R ₅₆ and R ₅₇ , R ₅₅ and R ₅₈ , R ₅₆ And R ₅₈ , R ₅₇ and R ₅₈ , R ₅₅ and R ₅₉ may be bonded to each other to form a 5- to 6-membered ring, and * represents a bonding position with the azo group of the general formula (1). )
[8]
The azo compound according to [7], wherein the azo compound represented by the general formula (2-2) is represented by the following general formula (2-3).

(In General Formula (2-3), R ₁ represents an amino group, an aliphatic oxy group, an aliphatic group, an aryl group, or a heterocyclic group, R ₂ represents a substituent, and R ₅₆ and R ₅₈ represent hydrogen. An atom or a substituent is represented, m represents an integer of 0 to 5, and n represents an integer of 1 to 4. R ₅₆ and R ₅₈ may be bonded to each other to form a 5- to 6-membered ring. When n = 2, it represents a dimer via R ₁ , R ₂ , R ₅₆ and R _{58. When} n = 3, a trimer via R ₁ , R ₂ , R ₅₆ and R ₅₈ (When n = 4, it represents a tetramer via R ₁ , R ₂ , R ₅₆ and R ₅₈ ).

First, the aliphatic group, aryl group, heterocyclic group and substituent in the present invention will be described.
In the aliphatic group in the present invention, the aliphatic moiety may be linear, branched or cyclic. Moreover, it may be saturated or unsaturated. Specific examples include an alkyl group, an alkenyl group, a cycloalkyl group, and a cycloalkenyl group. Furthermore, the aliphatic group may be unsubstituted or may have a substituent.

The aryl group may be a single ring or a condensed ring. Further, it may be unsubstituted or may have a substituent.
The heterocyclic group has only to have a hetero atom (for example, nitrogen atom, sulfur atom, oxygen atom) in the ring, and the heterocyclic group may be a saturated ring or an unsaturated ring. . Further, it may be a single ring or a condensed ring, and may be unsubstituted or have a substituent.
The acyl group may be an aliphatic carbonyl group, an arylcarbonyl group, a heterocyclic carbonyl group, may have a substituent, and may be substituted. Any group can be used as long as it is a substitutable group among the groups described in the following substituent group. For example, acetyl, propanoyl, benzoyl, 3-pyridinecarbonyl and the like can be mentioned.

  Further, the substituent in the present invention may be any group that can be substituted. For example, an aliphatic group, an aryl group, a heterocyclic group, an acyl group, an acyloxy group, an acylamino group, an aliphatic oxy group, an aryloxy group, a hetero group Ring oxy group, aliphatic oxycarbonyl group, aryloxycarbonyl group, heterocyclic oxycarbonyl group, carbamoyl group, aliphatic sulfonyl group, arylsulfonyl group, heterocyclic sulfonyl group, aliphatic sulfonyloxy group, arylsulfonyloxy group, hetero Ring sulfonyloxy group, sulfamoyl group, aliphatic sulfonamide group, aryl sulfonamide group, heterocyclic sulfonamide group, amino group, aliphatic amino group, arylamino group, heterocyclic amino group, aliphatic oxycarbonylamino group, aryl Oxycarbonylamino group, heterocycle Xoxycarbonylamino group, aliphatic sulfinyl group, arylsulfinyl group, aliphatic thio group, arylthio group, hydroxy group, cyano group, sulfo group, carboxy group, aliphatic oxyamino group, aryloxyamino group, carbamoylamino group, sulfo group Examples include a famoylamino group, a halogen atom, a sulfamoylcarbamoyl group, a carbamoylsulfamoyl group, a dialiphatic oxyphosphinyl group, and a diaryloxyphosphinyl group.

  The azo pigment of the present invention does not contain an ionic hydrophilic group (for example, carboxyl group, sulfo group, phosphono group and quaternary ammonium group) as a substituent from the viewpoint of solubility.

Here, Hammett's substituent constant σp value used in the present specification will be described briefly.
Hammett's rule is a method described in 1935 in order to quantitatively discuss the effect of substituents on the reaction or equilibrium of benzene derivatives. P. A rule of thumb proposed by Hammett, which is widely accepted today. Substituent constants determined by Hammett's rule include a σp value and a σm value, and these values can be found in many general books. A. Dean, “Lange's Handbook of Chemistry”, 12th edition, 1979 (Mc Graw-Hill) and “Chemicals” special edition, 122, 96-103, 1979 (Nankodo). In the present invention, each substituent is limited or explained by Hammett's substituent constant σp, but this means that it is limited to only a substituent having a value known in the literature, which can be found in the above-mentioned book. Needless to say, even if the value is unknown, it includes a substituent that would be included in the range when measured based on Hammett's rule. Although the compound represented by the general formula (1) or (2) of the present invention is not a benzene derivative, the σp value is used as a scale indicating the electronic effect of the substituent regardless of the substitution position. In the present invention, the σp value will be used in this sense.

<Azo pigment>
A pigment is a state in which molecules are firmly bonded to each other by cohesive energy due to strong interaction between dye molecules. In order to create this state, it is described in, for example, Journal of Imaging Society of Japan, Vol. 43, page 10 (2004) that van der Waals force between molecules and hydrogen bonding between molecules are necessary.
In order to increase the van der Waals force between molecules, introduction of an aromatic group, a polar group and / or a hetero atom into the molecule can be considered. Moreover, in order to form an intermolecular hydrogen bond, introduction | transduction of the substituent containing the hydrogen atom couple | bonded with the hetero atom to a molecule | numerator and / or introduction | transduction of an electron-donating ring-setting group etc. can be considered. Further, it is considered preferable that the polarity of the whole molecule is high. For this purpose, for example, a shorter chain group such as an alkyl group is preferred, and a smaller molecular weight / azo group value is preferred.
From these viewpoints, the pigment molecule preferably contains an amide bond, a sulfonamide bond, an ether bond, a sulfone group, an oxycarbonyl group, an imide group, a carbamoylamino group, a hetero ring, a benzene ring and the like.

The azo pigment of the present invention is represented by the following general formula (0).
The compound represented by the general formula (0) can easily form an intermolecular interaction of dye molecules due to its specific structure, has low solubility in water or an organic solvent, and can be an azo pigment.
A pigment is used by being finely dispersed as solid particles such as molecular aggregates in a solvent, unlike a dye used by being dissolved in water or an organic solvent in a molecular dispersion state.
In addition, by having a specific structure represented by the following general formula (0), it exhibits excellent color characteristics such as tinting strength and hue, and also has excellent durability such as light resistance and ozone resistance. Characteristics can be shown.
Next, the pigment represented by the general formula (0) will be described.

An azo pigment represented by the following general formula (0), a tautomer thereof, a salt or a hydrate thereof.

(In the general formula (0), G represents a hydrogen atom, an aliphatic group, an aryl group, a heterocyclic group, an acyl group, an aliphatic oxycarbonyl group, a carbamoyl group, or a sulfonyl group, and R ₁ represents an amino group, An oxy group, an aliphatic group, an aryl group, or a heterocyclic group, R ₂ represents a substituent, A ₀ represents an aromatic 5- or 6-membered heterocyclic group, and m represents an integer of 0 to 5. , N represents an integer of 1 to 4. When n = 2, it represents a dimer via R ₁ , R ₂ , A ₀ or G. When n = 3, R ₁ , R ₂ , A Represents a trimer through ₀ or G. When n = 4, it represents a tetramer through R ₁ , R ₂ , A ₀ or G.)

  The aliphatic group represented by G may have a substituent, may be saturated or unsaturated, and the group that may be substituted is described in the above-mentioned substituent group. Any substituent can be used as long as it is a group that can be substituted. Preferred substituents include a hydroxy group, an aliphatic oxy group, a carbamoyl group, an aliphatic oxycarbonyl group, an aliphatic thio group, an amino group, and an aliphatic amino group. An acylamino group and a carbamoylamino group. The aliphatic group represented by G is preferably an aliphatic group having 1 to 8 carbon atoms in total, more preferably an alkyl group having 1 to 4 carbon atoms in total, such as methyl, ethyl, vinyl, cyclohexyl. , Carbamoylmethyl and the like.

  The aryl group represented by G may be condensed or may have a substituent, and the group that may be substituted is the group described in the above-mentioned substituent group. Any possible group may be used, and preferred substituents include a nitro group, a halogen atom, an aliphatic oxy group, a carbamoyl group, an aliphatic oxycarbonyl group, an aliphatic thio group, an amino group, an aliphatic amino group, and an acylamino group. , A carbamoylamino group. The aryl group represented by G is preferably an aryl group having 6 to 12 carbon atoms, more preferably an aryl group having 6 to 10 carbon atoms, such as phenyl, 4-nitrophenyl, 4-acetylamino. Phenyl, 4-methanesulfonylphenyl and the like.

  The heterocyclic group represented by G may have a substituent, may be saturated or unsaturated, and may be condensed. The group that may be substituted may be any group as long as it is a group that can be substituted with the groups described in the above-mentioned substituent group. Preferred substituents include halogen atoms, hydroxy groups, aliphatic oxy groups, carbamoyl groups, An aliphatic oxycarbonyl group, an aliphatic thio group, an amino group, an aliphatic amino group, an acylamino group, and a carbamoylamino group; The heterocyclic group represented by G is preferably a heterocyclic group bonded with carbon atoms having 2 to 12 carbon atoms in total, more preferably 5 to 6 having 2 to 10 carbon atoms bonded with carbon atoms. It is a membered heterocycle, and examples thereof include 2-tetrahydrofuryl and 2-pyrimidyl.

  The acyl group represented by G may be an aliphatic carbonyl group, an arylcarbonyl group, a heterocyclic carbonyl group, or may have a substituent. The group may be any group as long as it is a group that can be substituted with the groups described in the above-mentioned substituent group. Preferred substituents include a hydroxy group, a halogen atom, an aryl group, an aliphatic oxy group, and a carbamoyl group. An aliphatic oxycarbonyl group, an aliphatic thio group, an amino group, an aliphatic amino group, an acylamino group, and a carbamoylamino group. The acyl group represented by G is preferably an acyl group having 2 to 8 carbon atoms in total, more preferably an acyl group having 2 to 4 carbon atoms in total, such as acetyl, propanoyl, benzoyl, 3-pyridine. Examples include carbonyl and the like.

  The aliphatic oxycarbonyl group represented by G may be saturated or unsaturated, may have a substituent, and may be substituted. In the group described in the section, any group can be used as long as it can be substituted. Preferred substituents include a hydroxy group, an aliphatic oxy group, a carbamoyl group, an aliphatic oxycarbonyl group, an aliphatic thio group, an amino group, and an aliphatic group. An amino group, an acylamino group, and a carbamoylamino group; The aliphatic oxycarbonyl group represented by G is preferably an alkoxycarbonyl group having 2 to 8 carbon atoms in total, more preferably an alkoxycarbonyl group having 2 to 4 carbon atoms in total, such as methoxycarbonyl, ethoxy Examples include carbonyl and (t) -butoxycarbonyl.

The carbamoyl group represented by G may have a substituent. As the group which may be substituted, any group can be used as long as it is a group that can be substituted with the groups described in the above-mentioned substituent group. Preferred examples of the substituent include an aliphatic group, an aryl group, and a heterocyclic group. preferable. The carbamoyl group which may have a substituent represented by G is preferably an unsubstituted carbamoyl group, an alkylcarbamoyl group having 2 to 9 carbon atoms, or a total carbon number of 7 to 11, more preferably none. A substituted carbamoyl group and an alkylcarbamoyl group having 2 to 5 carbon atoms in total, such as N-methylcarbamoyl, N, N-dimethylcarbamoyl, N-phenylcarbamoyl and the like.
The aliphatic sulfonyl group represented by G may be saturated or unsaturated, may have a substituent, and the group which may be substituted includes the above-mentioned substituent group. In the group described in the above, any substituent can be used, and preferred substituents include a hydroxy group, an aryl group, an aliphatic oxy group, a carbamoyl group, an aliphatic oxycarbonyl group, an aliphatic thio group, an amino group, An aliphatic amino group, an acylamino group, and a carbamoylamino group; The aliphatic sulfonyl group represented by G is preferably an alkylsulfonyl group having 1 to 6 carbon atoms in total, more preferably an alkylsulfonyl group having 1 to 4 carbon atoms in total, such as methanesulfonyl. Can be mentioned.
The arylsulfonyl group represented by G may have a substituent, and the group that may be substituted is any group that can be substituted with the groups described in the above-mentioned substituents section. Well, preferred substituents are hydroxy group, aliphatic group, aliphatic oxy group, carbamoyl group, aliphatic oxycarbonyl group, aliphatic thio group, amino group, aliphatic amino group, acylamino group, carbamoylamino group . The arylsulfonyl group represented by G is preferably an arylsulfonyl group having 6 to 10 carbon atoms in total, and examples thereof include benzenesulfonyl.

  G is preferably a hydrogen atom, an aliphatic group, an aryl group or a heterocyclic group, more preferably a hydrogen atom. This is because it is easy to form an intramolecular hydrogen bond or an intramolecular cross-hydrogen bond.

The amino group represented by R ₁ may have a substituent, and the group which may be substituted may be any of the groups described in the above-mentioned substituent group, and may be substituted. Any substituent may be used, and preferred examples of the substituent include an aliphatic group, an aryl group, and a heterocyclic group.
These substituents may further have a substituent, and the substituent is preferably a substituent having an aliphatic group, a hydroxy group, an amide bond, an ether bond, an oxycarbonyl bond, a thioether bond, and the like. A substituent having a bond between a hetero atom and a hydrogen atom is more preferable from the viewpoint of facilitating intermolecular interaction such as intermolecular hydrogen bonding.
As the amino group which may have a substituent represented by R ₁ , an unsubstituted amino group, an alkylamino group having 1 to 10 carbon atoms in total, a dialkylamino group having 2 to 10 carbon atoms in total, An arylamino group having 6 to 13 carbon atoms in total, a heterocyclic amino group which may be saturated or unsaturated having 2 to 12 carbon atoms in total, more preferably an unsubstituted amino group, An alkylamino group having 1 to 8 carbon atoms in total, an arylamino group having 6 to 13 carbon atoms in total, a heterocyclic amino group having 2 to 12 carbon atoms that may be saturated or unsaturated. Yes, for example, methylamino, N, N-dimethylamino, N-phenylamino, N- (2-pyrimidyl) amino and the like.
More preferably, the arylamino group having 6 to 13 carbon atoms which may have a substituent and the saturated or unsaturated group having 2 to 12 total carbon atoms which may have a substituent A heterocyclic amino group which may be

When R ₁ is an arylamino group, the substituent on the aryl group preferably has a substituent at the para position from the bonding position with the amino group, and most preferably has a substituent only at the para position. The substituent may be any group that can be substituted with the group described in the above-mentioned substituent group, and preferably has 1 to 7 carbon atoms in total, more preferably 1 to 4 carbon atoms in total. An aliphatic group which may have a group (for example, methyl, ethyl, allyl, (i) -propyl, (t) -butyl, etc.), 1 to 7 carbon atoms, more preferably 1 to 1 carbon atoms in total. An aliphatic oxy group (for example, methoxy, ethoxy, (i) -propyloxy, allyloxy, etc.) optionally having 4 substituents, a halogen atom (for example, fluorine, chlorine, bromine, etc.), 7, more preferably a carbamoyl group (for example, carbamoyl, N-phenylcarbamoyl, N-methylcarbamoyl, etc.) which may have a substituent having 1 to 4 carbon atoms, more preferably 1 to 7 carbon atoms Is the total carbon field A ureido group (for example, ureido, N-methylureido, N, N-dimethylureido, N-4-pyridylureido, N-phenylureido, etc.) optionally having a substituent of formulas 1-4, nitro group, total Heterocycle condensed with the aryl group having 1 to 7 carbon atoms (for example, imidazolone), hydroxy group, aliphatic thio group optionally having substituents having 1 to 7 carbon atoms (for example, methylthio, ethylthio) , (I) -propylthio, allylthio, (t) -butylthio, etc.), an acylamino group (for example, acetamino) which may have a substituent having 2 to 7 total carbon atoms, more preferably 2 to 4 total carbon atoms , Propionylamino, pivaloylamino, benzoylamino, etc.), an aliphatic group optionally having a substituent having 1 to 7 carbon atoms, more preferably 1 to 4 carbon atoms in total. Cicarbonylamino group (for example, methoxycarbonylamino, propyloxycarbonylamino, etc.), aliphatic oxycarbonyl group which may have a substituent having 1 to 7 total carbon atoms, more preferably 1 to 4 total carbon atoms (For example, methoxycarbonyl, ethoxycarbonyl, etc.), an acyl group which may have a substituent having 2 to 7 carbon atoms in total, more preferably 2 to 4 carbon atoms in total (even an aliphatic carbonyl group, It may be an arylcarbonyl group, a heterocyclic carbonyl group, may have a substituent, and the group which may be substituted is a group described in the above-mentioned substituent group, Any acyl group having 2 to 7 carbon atoms in total, more preferably an acyl group having 2 to 4 carbon atoms in total, such as acetyl, propanoyl, etc. And benzoyl, 3-pyridinecarbonyl and the like. ) And the like.
When the substituent on the aryl group is substituted from the bonding position with the amino group to the para position, since the substituent is at the end of the molecule, intermolecular interaction such as intermolecular hydrogen bonding is likely to occur. Becomes sharper. When the substituent on the aryl group further has a substituent, a substituent having an aliphatic group, a hydroxy group, an amide bond, an ether bond, an oxycarbonyl bond, a thioether bond or the like is preferable, and a bond between a hetero atom and a hydrogen atom Is more preferable from the viewpoint of facilitating intermolecular interaction such as intermolecular hydrogen bonding.
When R ₁ is a heterocyclic amino group, the substituent may be any group that can be substituted with the group described in the above-mentioned substituent group, and preferably the same substituent as in the case of the arylamino group. Groups are preferred. When the substituent on the heterocyclic group further has a substituent, a substituent having an aliphatic group, a hydroxy group, an amide bond, an ether bond, an oxycarbonyl bond, a thioether bond, or the like is preferable. A substituent having a bond is more preferable from the viewpoint of facilitating intermolecular interaction such as intermolecular hydrogen bonding.
More preferred substituents when R ₁ is an arylamino group or a heterocyclic amino group include an aliphatic group, an aliphatic oxy group, a halogen atom, a carbamoyl group, a heterocycle fused with an aryl group, an aliphatic oxy It is a carbonyl group. The substituent is more preferably an aliphatic group having 1 to 4 carbon atoms, an aliphatic oxy group having 1 to 4 carbon atoms, a halogen atom, or a carbamoyl group having 1 to 4 carbon atoms, and still more preferably. Is an aliphatic oxy group having 1 to 4 carbon atoms in total.

The aliphatic oxy group represented by R ₁ may have a substituent, and the substituent is any of the groups described in the above-mentioned substituent group and can be substituted. Of these, preferred substituents are a hydroxy group, an aliphatic oxy group, a carbamoyl group, an aliphatic oxycarbonyl group, an aliphatic thio group, an amino group, an aliphatic amino group, an acylamino group, and a carbamoylamino group. The aliphatic oxy group for R ₁ is preferably an alkoxy group having 1 to 8 carbon atoms, more preferably an alkoxy group having 1 to 4 carbon atoms, and still more preferably 1 to 1 carbon atoms. 2, for example, methoxy, ethoxy, (t) -butoxy, methoxyethoxy, carbamoylmethoxy and the like.
R ₁ is preferably an amino group which may have a substituent.

The aliphatic group represented by R ₁ may have a substituent, and the substituent may be any group as long as it is a group described in the above-mentioned substituent group and can be substituted. Preferred substituents are a hydroxy group, an aliphatic oxy group, a carbamoyl group, an aliphatic oxycarbonyl group, an aliphatic thio group, an aliphatic amino group, an acylamino group, and a carbamoylamino group. The aliphatic group for R ₁ is preferably an alkyl group having 1 to 8 carbon atoms, more preferably an alkyl group having 1 to 4 carbon atoms, such as methyl, ethyl, (s)- Examples include butyl, methoxyethyl, carbamoylmethyl and the like.

The aryl group represented by R ₁ may have a substituent, and preferred substituents include a nitro group, a halogen atom, an aliphatic oxy group, a carbamoyl group, an aliphatic oxycarbonyl group, an aliphatic thio group. A group, an amino group, an aliphatic amino group, an acylamino group, and a carbamoylamino group. As the substituent, any group can be used as long as it is a group described in the above-mentioned substituent group and can be substituted. The aryl group for R ₁ is preferably an aryl group having 6 to 12 carbon atoms in total, more preferably an aryl group having 6 to 10 carbon atoms in total, such as phenyl, 4-methylphenyl, 3- Examples include chlorophenyl.

The heterocyclic group represented by R ₁ may be a saturated heterocyclic ring, an unsaturated heterocyclic group, a condensed ring, or may have a substituent. As the substituent, any group can be used as long as it is a group that can be substituted as described in the above-mentioned substituent group. Preferred substituents include a halogen atom, a hydroxy group, an aliphatic oxy group, an acyl group, and a carbamoyl group. An aliphatic oxycarbonyl group, an aliphatic thio group, an amino group, an aliphatic amino group, an acylamino group, and a carbamoylamino group. The heterocyclic group for R ₁ is preferably a heterocyclic group having 2 to 10 carbon atoms in total, more preferably a 5- to 6-membered non-aromatic group bonded by a nitrogen atom having 2 to 8 carbon atoms in total. Examples of the heterocyclic group include 1-piperidyl, 4-morpholinyl, 1-quinoyl, 2-pyrimidyl, 4-pyridyl, and the like.

R ₁ is preferably an amino group which may have a substituent, an aliphatic oxy group, or a 5- to 6-membered non-aromatic heterocyclic group bonded by a nitrogen atom, more preferably a substituted group. An amino group which may have a group, an aliphatic oxy group, and more preferably an amino group which may have a substituent.

The substituent represented by R ₂ may be any group as long as it is a group that can be substituted with the groups described in the above-mentioned substituent group, and is preferably an aliphatic group, an aryl group, a heterocyclic group, an aliphatic oxycarbonyl group. Group, carboxyl group, optionally substituted carbamoyl group, acylamino group, sulfonamide group, optionally substituted carbamoylamino group, optionally substituted sulfamoyl group, fatty acid An oxy group, an aliphatic thio group, a cyano group, a halogen atom, and a hydroxy group, more preferably an aliphatic oxycarbonyl group, an optionally substituted carbamoyl group, an acylamino group, and a substituent. A carbamoylamino group, an aliphatic oxy group, and a halogen atom which may be present, and most preferably an aliphatic oxy group.
When these substituents further have a substituent, a substituent having an aliphatic group, a hydroxy group, an amide bond, an ether bond, an oxycarbonyl bond, a thioether bond, or the like is preferable, and a substituent having a heteroatom-hydrogen atom bond is preferable. The group is more preferable from the viewpoint of facilitating intermolecular interaction such as intermolecular hydrogen bonding.

The aliphatic group represented by R ₂ may have a substituent, may be saturated or unsaturated, and the group that may be substituted includes the above-mentioned substituent group. Any group can be used as long as it is a substitutable group. The aliphatic group for R ₂ is preferably an alkyl group having 1 to 8 carbon atoms in total, more preferably an alkyl group having 1 to 6 carbon atoms in total, such as methyl, ethyl, i-propyl, cyclohexyl, t-butyl etc. are mentioned.

The aryl group represented by R ₂ may have a substituent, and the group that may be substituted is any group that can be substituted with the groups described in the above-mentioned substituents section. Good. The aryl group for R ₂ is preferably an aryl group having 6 to 12 carbon atoms in total, more preferably an aryl group having 6 to 10 carbon atoms, such as phenyl, 3-methoxyphenyl, 4-carbamoylphenyl. Etc.

The heterocyclic group represented by R ₂ may have a substituent, may be saturated or unsaturated, may be condensed, and may be substituted. Can be any group as long as it is a group that can be substituted with the groups described in the above-mentioned substituent group. The heterocyclic group of R ₂ is preferably a heterocyclic group having 2 to 16 carbon atoms in total, more preferably a 5 to 6-membered heterocyclic group having 2 to 12 carbon atoms, such as 1- Examples include pyrrolidinyl, 4-morpholinyl, 2-pyridyl, 1-pyrrolyl, 1-imidazolyl, 1-benzoimidazolyl and the like.

The aliphatic oxycarbonyl group represented by R ₂ may have a substituent, may be saturated or unsaturated, and the group that may be substituted includes the above-described substituents Any group can be used as long as it is a substitutable group among the groups described in the section. The aliphatic oxycarbonyl group for R ₂ is preferably an alkoxycarbonyl group having 1 to 8 carbon atoms in total, more preferably an alkoxycarbonyl group having 1 to 6 carbon atoms in total, such as methoxycarbonyl or i-propyl. Examples include oxycarbonyl, carbamoylmethoxycarbonyl and the like.

The carbamoyl group represented by R ₂ may have a substituent, and as the group that may be substituted, any group can be used as long as it is a group that can be substituted with the groups described in the above-mentioned substituent group. Of these, an aliphatic group, an aryl group, a heterocyclic group and the like are preferable. The carbamoyl group optionally having a substituent for R ₂ is preferably a carbamoyl group, an alkylcarbamoyl group having 2 to 9 carbon atoms in total, a dialkylcarbamoyl group having 3 to 10 carbon atoms in total, and a total carbon atom number of 7 -13 arylcarbamoyl group, a heterocyclic carbamoyl group having 3 to 12 carbon atoms, more preferably a carbamoyl group, an alkylcarbamoyl group having 2 to 7 carbon atoms, and a dialkylcarbamoyl group having 3 to 6 carbon atoms. Group, an arylcarbamoyl group having 7 to 11 carbon atoms in total, and a heterocyclic carbamoyl group having 3 to 10 carbon atoms in total, such as carbamoyl, methylcarbamoyl, dimethylcarbamoyl, phenylcarbamoyl, 4-pyridinecarbamoyl and the like. .

The acylamino group represented by R ₂ may have a substituent, may be aliphatic, aromatic, heterocyclic, or may be substituted. Can be any group as long as it is a group that can be substituted with the groups described in the above-mentioned substituent group. The acylamino group for R ₂ is preferably an acylamino group having 2 to 12 carbon atoms in total, more preferably an acylamino group having 1 to 8 carbon atoms in total, and still more preferably an alkyl having 1 to 8 carbon atoms in total. Examples of the carbonylamino group include acetylamino, benzoylamino, 2-pyridinecarbonylamino, propanoylamino and the like.

The sulfonamide group represented by R ₂ may have a substituent, may be aliphatic, aromatic, heterocyclic, or may be substituted. As the above, any group can be used as long as it is a group which can be substituted with the groups described in the above-mentioned substituent group. The sulfonamide group of R ₂ is preferably a sulfonamide group having 1 to 12 carbon atoms in total, more preferably a sulfonamide group having 1 to 8 carbon atoms in total, and still more preferably 1 to 1 carbon atoms in total. 8 alkylsulfonamide groups such as methanesulfonamide, benzenesulfonamide, 2-pyridinesulfonamide and the like.

The carbamoylamino group represented by R ₂ may have a substituent, and as the group that may be substituted, any group can be used as long as it is a group that can be substituted with the groups described in the above-mentioned substituents section. Of these, an aliphatic group, an aryl group, a heterocyclic group and the like are preferable. The carbamoylamino group optionally having a substituent for R ₂ is preferably a carbamoylamino group, an alkylcarbamoylamino group having 2 to 9 carbon atoms in total, a dialkylcarbamoylamino group having 3 to 10 carbon atoms in total, An arylcarbamoylamino group having 7 to 13 carbon atoms and a heterocyclic carbamoylamino group having 3 to 12 carbon atoms, more preferably a carbamoylamino group, an alkylcarbamoylamino group having 2 to 7 carbon atoms, and a total carbon A dialkylcarbamoylamino group having 3 to 6 atoms, an arylcarbamoylamino group having 7 to 11 carbon atoms, and a heterocyclic carbamoylamino group having 3 to 10 carbon atoms, such as carbamoylamino, methylcarbamoylamino, N , N-dimethylcarbamoylamino, phenylcarbamoylamino And 4-pyridinecarbamoylamino.

As the sulfamoyl group which may have a substituent represented by R ₂ , the group which may be substituted may be any group as long as it can be substituted with the groups described in the above-mentioned substituent section, An aliphatic group, an aryl group, a heterocyclic group and the like are preferable. The sulfamoyl group optionally having a substituent for R ₂ is preferably a sulfamoyl group, an alkylsulfamoyl group having 1 to 9 carbon atoms in total, a dialkylsulfamoyl group having 2 to 10 carbon atoms in total, An arylsulfamoyl group having 7 to 13 carbon atoms and a heterocyclic sulfamoyl group having 2 to 12 carbon atoms, more preferably a sulfamoyl group, an alkylsulfamoyl group having 1 to 7 carbon atoms, and a total carbon A dialkylsulfamoyl group having 3 to 6 atoms, an arylsulfamoyl group having 6 to 11 carbon atoms, and a heterocyclic sulfamoyl group having 2 to 10 carbon atoms, such as sulfamoyl, methylsulfamoyl, N, N-dimethylsulfamoyl, phenylsulfamoyl, 4-pyridinesulfamoyl and the like can be mentioned.

The aliphatic oxy group represented by R ₂ may have a substituent, may be saturated or unsaturated, and may be substituted. Any group can be used as long as it is a substitutable group. The aliphatic oxy group for R ₂ is preferably an alkoxy group having 1 to 8 carbon atoms in total, more preferably an alkoxy group having 1 to 6 carbon atoms in total, such as methoxy, ethoxy, i-propyloxy, Examples include cyclohexyloxy and methoxyethoxy.

The aliphatic thio group represented by R ₂ may have a substituent, may be saturated or unsaturated, and may be substituted. Any group can be used as long as it is a substitutable group. The aliphatic thio group for R ₂ is preferably an alkylthio group having 1 to 8 carbon atoms, more preferably an alkylthio group having 1 to 6 carbon atoms, such as methylthio, ethylthio, carbamoylmethylthio, t- Examples include butylthio.

The halogen atom represented by R ₂ is preferably a fluorine atom, a chlorine atom, or a bromine atom, and more preferably a chlorine atom.
From the viewpoint of the effect of the present invention, R ₂ is preferably an aliphatic oxy group, an aliphatic oxycarbonyl group, or an optionally substituted carbamoyl group, more preferably an aliphatic oxy group. . In view of the effect of the present invention, m is preferably 0 or 1, and more preferably 0.

The aromatic 5- to 6-membered heterocycle represented by A may be condensed or monocyclic, the condensed ring may be a carbocycle, and the condensed ring is a carbocycle. Or a hetero ring, an aromatic ring or a non-aromatic ring, preferably an aromatic 5 to 6 membered ring containing 1 to 3 hetero atoms. The aromatic 5- to 6-membered heterocyclic ring which may be condensed represented by A is preferably 2 to 15 total carbon atoms, more preferably 2 to 12 total carbon atoms, For example, pyridine ring, pyrazine ring, pyrimidine ring, pyridazine ring, triazine ring, pyrrole ring, furan ring, thiophene ring, imidazole ring, pyrazole ring, oxazole ring, thiazole ring, isoxazole ring, isothiazole ring, triazole ring, thiadiazole ring , An oxadiazole ring and the like, and a condensed heterocyclic group of these with a benzene ring derivative and a heterocyclic derivative.
m is preferably 0 to 3, more preferably 0 to 1, and even more preferably 0. n is preferably 1 or 2.

  The azo pigment represented by the general formula (0) is preferably an azo pigment represented by the following general formula (1).

(In General Formula (1), G represents a hydrogen atom, an aliphatic group, an aryl group, a heterocyclic group, an acyl group, an aliphatic oxycarbonyl group, a carbamoyl group, an aliphatic sulfonyl group, or an arylsulfonyl group, and R ₁ represents , An amino group, an aliphatic oxy group, an aliphatic group, an aryl group, or a heterocyclic group, R ₂ represents a substituent, and A represents the following general formulas (A-1) to (A-14), (A -16) to (A-22), and (A-24) to (A-26), m represents an integer of 0 to 5, n represents an integer of 1 to 4, and n = 2. Represents a dimer via R ₁ , R ₂ , A or G. When n = 3, it represents a trimer via R ₁ , R ₂ , A or G. n = 4 The case represents a tetramer via R ₁ , R ₂ , A or G.)

(In the general formulas (A-1) to (A-14), (A-16) to (A-22), (A-24) to (A-26), R _{51 to} R ₅₉ are hydrogen atoms or substituted R ₅₁ and R ₅₂ , R ₅₂ and R ₅₃ , R ₅₃ and R ₅₄ , R ₅₅ and R ₅₆ , R ₅₆ and R ₅₇ , R ₅₅ and R ₅₈ , R ₅₆ and R ₅₈ , R ₅₇ And R ₅₈ , R ₅₅ and R ₅₉ may be bonded to each other to form a 5- to 6-membered ring (* represents a bonding position with the azo group of the general formula (1)).

  The azo pigment represented by the general formula (1) is preferably an azo pigment represented by the following general formula (2).

The amino group represented by R ₁ , the aliphatic oxy group, and the saturated heterocyclic group bonded by a nitrogen atom are the same as those described for R ₁ in the general formula (1).
The substituent represented by R ₂ is preferably the same as that described for R ₂ represented by the general formula (1).

  General formulas (A-1) to (A-14), (A-16) to (A-22), and (A-24) to (A-26) represented by A will be described. The sites represented by the general formulas (A-1) to (A-14), (A-16) to (A-22), (A-24) to (A-26) are preferably total carbon atoms. The number is 2 to 15, and more preferably the total number of carbon atoms is 2 to 12.

The substituent represented by R _{51 to} R ₅₄ may be any group as long as it is a group that can be substituted with the groups described in the above-mentioned substituent group. As a substituent for R _{51 to} R _54, an aliphatic group, an aryl group, a heterocyclic group, an aliphatic oxycarbonyl group, an optionally substituted carbamoyl group, an acylamino group, a sulfonamide group, an aliphatic group An oxy group, an aliphatic thio group, a cyano group, and the like, more preferably an aliphatic group, an aliphatic oxycarbonyl group, an optionally substituted carbamoyl group, an aliphatic oxy group, a cyano group, and the like.

R _{51 to} R ₅₄ are hydrogen atoms, aliphatic groups, aryl groups, heterocyclic groups, aliphatic oxycarbonyl groups, carbamoyl groups which may have a substituent, acylamino groups, sulfonamides in terms of the effects of the present invention. Group, an aliphatic oxy group, an aliphatic thio group, a cyano group, etc., preferably a hydrogen atom, an aliphatic group, an aliphatic oxycarbonyl group, an optionally substituted carbamoyl group, an aliphatic oxy group More preferably, it is a cyano group.

The substituent represented by R ₅₅ may be any group as long as it is a group that can be substituted with the groups described in the above-mentioned substituent group. The substituent for R ₅₅ is preferably an aliphatic group, an aryl group, a heterocyclic group, or the like, more preferably an aliphatic group, an aryl group, or an aromatic 5- to 6-membered heterocyclic group containing a nitrogen atom.

From the viewpoint of the effect of the present invention, R ₅₅ is preferably an aliphatic group, an aryl group, or a heterocyclic group, and an aromatic group containing an aromatic group, aryl group, or aromatic group containing a nitrogen atom adjacent to the binding site with the nitrogen atom. The group is more preferably a 5- to 6-membered heterocyclic group, and more preferably an aromatic 5- to 6-membered heterocyclic group containing a nitrogen atom adjacent to the binding site with the nitrogen atom. _R55 is an aromatic 5- to 6-membered heterocyclic group containing a nitrogen atom adjacent to the binding site with the nitrogen atom, so that not only the intermolecular interaction of the dye molecule but also the intramolecular interaction is firmly formed. It becomes easy to do. This makes it easy to construct a pigment having a stable molecular arrangement, which is preferable in terms of showing good hue and high fastness (light resistance, gas, heat, water, etc.).

In terms of the effects of the present invention, the aliphatic group preferable as R ₅₅ may have a substituent, may be saturated or unsaturated, and may be substituted. Any group can be used as long as it is a group that can be substituted with the groups described in the section of the substituent. The aliphatic group for R ₅₅ is preferably an alkyl group having 1 to 8 carbon atoms in total, more preferably an alkyl group having 1 to 6 carbon atoms in total, such as methyl, ethyl, i-propyl, cyclohexyl, Examples include t-butyl, methoxyethyl and the like.
In terms of the effects of the present invention, the aromatic 5- to 6-membered heterocyclic group containing a nitrogen atom, which is preferable as R ₅₅ , may have a substituent. Any substituent can be used as long as it is a group that can be substituted with the groups described in the substituting group. Preferred substituents include a hydroxy group, an aliphatic oxy group, a carbamoyl group, an aliphatic oxycarbonyl group, an aliphatic thio group, an amino group. Group, aliphatic amino group, acylamino group, carbamoylamino group, which may be a saturated hetero ring, an unsaturated hetero ring, or a condensed hetero ring, preferably a total carbon atom It is an aromatic 5- to 6-membered heterocyclic group containing a nitrogen atom at the position adjacent to the bonding site with the azo group of 2 to 12, more preferably an aromatic containing a nitrogen atom having 2 to 10 carbon atoms in total. It is a 5-6 membered heterocyclic group. For example, 2-thiazolyl, 2-benzothiazolyl, 2-oxazolyl, 2-benzoxazolyl, 2-pyridyl, 2-pyrazinyl, 3-pyridazinyl, 2-pyrimidinyl, 4-pyrimidinyl, 2-imidazolyl, 2-benzimidazolyl, 2-triazinyl and the like can be mentioned, and these heterocyclic groups may have a tautomeric structure together with a substituent.

In view of the effects of the present invention, the aryl group preferable as R ₅₅ may have a substituent, and the group which may be substituted may be substituted with the group described in the above-mentioned substituent group. As long as it is a group, preferred substituents include a hydroxy group, a nitro group, an aliphatic oxy group, a carbamoyl group, an aliphatic oxycarbonyl group, an aliphatic thio group, an amino group, an aliphatic amino group, an acylamino group, It is a carbamoylamino group. The aryl group for R ₅₅ is preferably an aryl group having 6 to 12 carbon atoms in total, more preferably an aryl group having 6 to 10 carbon atoms in total, such as phenyl, 3-methoxyphenyl, 4-carbamoylphenyl. The phenyl group is preferable.
As the substituent represented by R _{55 to} R ₅₇ and R ₅₉ , any group can be used as long as it is a group that can be substituted with the groups described in the above-mentioned substituent group. As a substituent for R _{55 to} R ₅₇ and R _59, an aliphatic group, an aryl group, a heterocyclic group, an aliphatic oxycarbonyl group, an optionally substituted carbamoyl group, an acylamino group, and a sulfonamide group An aliphatic oxy group, an aliphatic thio group, a cyano group, and the like, more preferably an aliphatic group, an aliphatic oxy group, an aliphatic thio group, a cyano group, and the like.

In view of the effect of the present invention, R _{55 to} R ₅₇ and R ₅₉ are aliphatic groups, aryl groups, heterocyclic groups, aliphatic oxycarbonyl groups, carbamoyl groups optionally having substituents, acylamino groups, sulfones. An amide group, aliphatic oxy group, aliphatic thio group, cyano group and the like are preferable, and an aliphatic group, aliphatic oxy group, aliphatic thio group, and cyano group are more preferable.

The substituent represented by R ₅₈ may be any group as long as it is a group that can be substituted with the groups described in the above-mentioned substituent group. In view of the effect of the present invention, R ₅₈ is preferably a heterocyclic group or an electron-withdrawing group having Hammett's substituent constant σp value of 0.2 or more, and σp value of 0.3 or more. It is preferably an attractive group. The upper limit is 1.0 or less electron withdrawing group.

Specific examples of R ₅₈ which is an electron-attracting group having a σp value of 0.2 or more include acyl group, acyloxy group, carbamoyl group, alkyloxycarbonyl group, aryloxycarbonyl group, cyano group, nitro group, dialkylphosphonic group Group, diarylphosphono group, diarylphosphinyl group, alkylsulfinyl group, arylsulfinyl group, alkylsulfonyl group, arylsulfonyl group, sulfonyloxy group, acylthio group, sulfamoyl group, thiocyanate group, thiocarbonyl group, alkyl halide Groups, halogenated alkoxy groups, halogenated aryloxy groups, halogenated alkylamino groups, halogenated alkylthio groups, aryl groups substituted with other electron-withdrawing groups having a σp value of 0.2 or more, heterocyclic groups, Halogen atom, azo group, or selenasia Include the over door group.
From the viewpoint of the effect of the present invention, R ₅₈ is preferably the following (Y-1) to (Y-13), and a 6-membered ring described below is used in order to make it easy to take an intramolecular hydrogen bond structure. More preferably, it is any one of (Y-1) to (Y-6), and any one of the following (Y-1), (Y-3), (Y-4), and (Y-6). The case is more preferable, and the case of (Y-1) or (Y-4) below is particularly preferable. * In the general formulas (Y-1) to (Y-13) represents a bonding site with the N atom of the pyrazole ring. Y _{1 to} Y ₁₁ represent a hydrogen atom or a substituent. G ₁₁ in (Y-13) represents a nonmetallic atom group that can form a 5- to 6-membered heterocycle, and the heterocycle represented by G ₁₁ has a substituent even if it is unsubstituted. The heterocycle may be monocyclic or condensed. Formulas (Y-1) to (Y-13) may have tautomeric structures together with substituents.

The substituent represented by Y _{1 to} Y ₁₁ may be any group as long as it is a group that can be substituted with the groups described in the above-mentioned substituent group. As the substituent for Y _{1 to} Y _11, an aliphatic group, an aryl group, a heterocyclic group, an aliphatic oxycarbonyl group, an optionally substituted carbamoyl group, an acylamino group, a sulfonamide group, an aliphatic group An oxy group, an aliphatic thio group, a cyano group, and the like, more preferably an aliphatic group, an aliphatic oxy group, an aliphatic thio group, a cyano group, and the like. Two adjacent substituents in Y _{1 to} Y ₁₁ may form a 5- to 6-membered ring.
Y ₁ to Y ₁₁ are hydrogen atoms, aliphatic groups, aryl groups, heterocyclic groups, aliphatic oxycarbonyl groups, carbamoyl groups optionally having substituents, acylamino groups, sulfonamides in terms of the effects of the present invention. Group, an aliphatic oxy group, an aliphatic thio group, a cyano group, etc., preferably a hydrogen atom, an aliphatic group, an aliphatic oxycarbonyl group, an optionally substituted carbamoyl group, an aliphatic oxy group More preferably, it is a cyano group.
In view of the effect of the present invention, A is preferably a 5-membered heterocycle from the viewpoint of hue, more preferably a nitrogen-containing or sulfur-containing 5-membered heterocycle, and it contains 2 or more heteroatoms. More preferably, it is a 5-membered heterocycle.
A is preferably any one of (A-10) to (A-14), (A-16) to (A-22), and (A-24) to (A-26).

In terms of the effects of the present invention, the pigment represented by the general formula (1) is an amino group, an aliphatic oxy group, or a nitrogen atom in which G is a hydrogen atom and R ₁ may have a substituent. When m is 0 or 1 and m is 1, R ₂ may have an aliphatic oxy group, an aliphatic oxycarbonyl group, or a substituent. A carbamoyl group, wherein A is any one of (A-10) to (A-14), (A-16) to (A-22), (A-24) to (A-26), The case where n is 1 or 2 is preferable,
G is a hydrogen atom, R ₁ is an optionally substituted amino group, an aliphatic oxy group, m is 0 or 1, and R ₂ is an aliphatic oxy group, , A is any one of (A-13), (A-14), (A-16), (A-18) to (A-22), (A-25), and (A-26). N is more preferably 1 or 2, G is a hydrogen atom, R ₁ is an amino group which may have a substituent, m is 0, and A is (A-16), (A-22), or (A-26), wherein n is 1 or 2 is more preferred, G is a hydrogen atom, and R ₁ is a substituent. Most preferably, it is an amino group which may have, m is 0, A is (A-16) and n is 1 or 2.

  In terms of the effects of the present invention, the azo pigment represented by the general formula (0) and the general formula (1) is preferably an azo pigment represented by the following general formula (2-1).

  Hereinafter, the azo pigment represented by the general formula (2-1), its tautomer, salt or hydrate thereof will be described in detail.

(In the general formula (2-1), R ₁ , R ₂ , m, and n are the same as those defined in the general formula (1), and A ₁ represents the following general formulas (A-10) to (A-14). ), (A-16) to (A-22), or (A-24) to (A-26), when n = 2, R ₁ , R ₂ , or A ₁ Represents a dimer, n = 3 represents a trimer via R ₁ , R ₂ , or A ₁ , n = 4 represents a tetramer via R ₁ , R ₂ , or A ₁ Represents the body.)

(Formula (A-10) ~ (A -14), (A-16) ~ (A-22), in (A-24) ~ (A -26), R 55 ~R 59 is formula (1 ) Is the same as defined in)

In general formula (2-1), the preferable ranges of R ₁ , R ₂ , m, n, and R _{55 to} R ₅₉ are also the same as those in general formula (1).
In terms of the effect of the present invention, in the pigment represented by the general formula (2-1), R ₁ is an amino group or an aliphatic oxy group which may have a substituent, and m is 0 or 1. And when m is 1, R ₂ is an aliphatic oxy group, an aliphatic oxycarbonyl group, an optionally substituted carbamoyl group, and A ₁ is (A-13), (A-16), (A-18), (A-19), (A-21), (A-22), (A-25), (A-26), and R ₅₈ When there is an acyl group, a carbamoyl group, an alkyloxycarbonyl group, a cyano group, an alkylsulfonyl group, a sulfamoyl group, (Y-1) to (Y-13), and n is 1 or 2 If preferred, an amino group which may R ₁ is substituted, a m is 0 or 1, m If 1, _{R 2} is an aliphatic oxy group, an aliphatic oxycarbonyl group, a carbamoyl group which may have a substituent group, _{A 1} is, (A-13), ( A-16), (A-22), (A-26), and when R ₅₈ is present, any of carbamoyl group, alkyloxycarbonyl group, cyano group, (Y-1) to (Y-6) More preferably, n is 1 or 2, R ₁ is an amino group which may have a substituent, m is 0, and A ₁ is (A-13), When any of (A-16), (A-22), and (A-26) is R ₅₈ , a carbamoyl group, an alkyloxycarbonyl group, a cyano group, (Y-1), (Y- 4) to be either (Y-6), more preferably when n is 1 or 2, _{R 1} is location A an amino group which may have a group, a m is 0, _{A 1} is, (A-16), be either _(A-22), if there is _{R 58} is Particularly preferred is a carbamoyl group, an alkyloxycarbonyl group, or a cyano group. Further, R ₅₆ of (A-16) is most preferably R ₅₉ .

  In terms of the effects of the present invention, the azo pigment represented by the general formula (0), the general formula (1), and the general formula (2-1) is an azo pigment represented by the following general formula (2-2). Preferably there is.

  Hereinafter, the azo pigment represented by the general formula (2-2), its tautomer, salt or hydrate thereof will be described in detail.

(In the general formula (2-2) _are the same as those defined in R _1, R 2, m, n is the general formula (1) and the general formula (2-1), _{A 2} is represented by the following general formula (A -13), (A-14), (A-16) to (A-22), (A-25), or (A-26), when n = 2, R ₁ , R ₂ or a dimer through A _{2. When} n = 3, it represents R ₁ , R ₂ , or a trimer through A _{2. When} n = 4, R ₁ , R ₂ , or it represents a tetramer formed through _{a 2.)}

(Formula (A-13), (A -14), (A-16) ~ (A-22), (A-25), (A-26) _in, R 55 _{to R 59} of the general formula (2 The same as defined in -1).)

In general formula (2-2), the preferable ranges of R ₁ , R ₂ , m, n, and R _{55 to} R ₅₉ are also the same as in general formula (2-1).
In terms of the effect of the present invention, the pigment represented by the general formula (0), the general formula (1), and the general formula (2-1) has a “total carbon number / number of azo groups” of 40 or less. Is more preferable, and is 30 or less. In terms of the effects of the present invention, the pigment represented by the general formula (0), the general formula (1), and the general formula (2-1) preferably has a “molecular weight / number of azo groups” of 700 or less. . The pigment represented by the general formula (0), the general formula (1) and the general formula (2-1) is not substituted with an ionic substituent such as a sulfo group or a carboxyl group in terms of the effect of the present invention. Is preferred.

The present invention includes in its scope tautomers of the azo pigments represented by general formula (0), general formula (1), general formula (2-1), and general formula (2-2).
General formula (0), general formula (1), general formula (2-1), and general formula (2-2) are in the form of an extreme structural formula among several tautomers that can be taken in terms of chemical structure. Although shown, tautomers other than the described structure may be used, or a mixture containing a plurality of tautomers may be used.
For example, the pigment represented by the general formula (0) may be an azo-hydrazone tautomer represented by the following general formula (1 ′).
The present invention includes in its scope a compound represented by the following general formula (1 ′), which is a tautomer of the azo pigment represented by the general formula (0).

In general formula (1 ′), R ₁ , R ₂ , A, m, and n are the same as those defined in general formula (1). In general formula (1 ′), G ′ is a group corresponding to G defined in general formula (1). When n = 2, it represents a dimer via R ₁ , R ₂ , A or G ′. When n = 3, it represents a trimer via R ₁ , R ₂ , A or G ′. When n = 4, it represents a tetramer through R ₁ , R ₂ , A or G ′.

  Among the azo pigments represented by the general formula (1), the general formula (2-1), and the general formula (2-2), examples of the preferable general formula of the azo pigment as described above include the following general formula (3 -1) to azo pigments represented by formula (3-4). The pigment represented by the general formula (1) is preferably an azo pigment represented by the following general formula (3-1) or general formula (3-4). However, even if A is a compound that cannot be represented by these general formulas (3-1) to (3-4), such as (A-16), (A-22), and (A-26), , Hue, light fastness and the like are preferable from the viewpoint of the effects of the present invention.

  Hereinafter, the azo pigments represented by the general formulas (3-1) to (3-4), tautomers thereof, salts or hydrates thereof will be described in detail.

(In general formula (3-1) to general formula (3-4), R ₁ , R ₂ , m, and n are general formula (0), general formula (1), general formula (2-1), and general formula. X is the same as defined in Formula (2-2), X represents a carbon atom or a nitrogen atom, and Ax and Bx are (A-1) to (A-) defined in A of Formula (1). 14), (A-16) to (A-22), and (A-24) to (A-26) are applicable, Yx together with the nitrogen atom and carbon atom in the general formula (1) R ₂₃ represents a corresponding heterocyclic group defined by R _55. R ₂₃ is a corresponding substituent among the substituents R ₅₁ , R ₅₄ , R _57, R _{58 and the} like defined in the general formula (1). R ′ ₁ represents a substituent corresponding to a group obtained by removing —NH— from the amino group of R ₁ defined by the general formula (1). )

Many tautomers can be considered in the azo pigments represented by the general formulas (0), (1), (2-1), (2-2), and (3-1) to (3-4). .
In the present invention, the azo pigment represented by the general formula (1) preferably has a substituent that forms an intramolecular hydrogen bond or an intramolecular cross-hydrogen bond. It is more preferable to have at least one substituent that forms an intramolecular hydrogen bond, and it is particularly preferable to have a substituent that forms at least one intramolecular cross-hydrogen bond.

As a factor that this structure is preferable, as shown by the general formulas (3-1) to (3-4), when R ₁ in the general formula (1) is an amino group, an intramolecular hydrogen bond is more easily formed. Structure is preferable.
As a result, the planarity of the molecule is improved, the intramolecular / intermolecular interaction is further improved, and the crystallinity of the azo pigment represented by the general formula (3-1) to the general formula (3-4) is increased ( It is more preferable because it is easy to form a higher order structure), and the required performance as a pigment is greatly improved in light fastness, heat stability, wet heat stability, water resistance, gas resistance and / or solvent resistance. An example.
Also from this viewpoint, the pigments represented by the general formulas (0), (1), (2-1), and (2-2) are pigments represented by (3-1) to (3-4). It is preferable that the pigment is represented by formulas (3-2) and (3-4). However, it is also preferable from the viewpoint of the effect of the present invention that R ₅₈ deviating from this structure is a cyano group. Since these molecules are compact, the molecules are likely to have a planar structure, the intramolecular / intermolecular interaction is improved, and the crystallinity of the azo pigment is increased (higher order structures are easily formed). It is considered that the light fastness, heat stability, wet heat stability, water resistance, gas resistance and / or solvent resistance, which are required performance as a pigment, are greatly improved.

<Azo compound>
The present invention also relates to an azo compound represented by the general formula (2-2), a tautomer thereof, a salt or a hydrate thereof.

(In General Formula (2-2), G represents a hydrogen atom, an aliphatic group, an aryl group, a heterocyclic group, an acyl group, an aliphatic oxycarbonyl group, a carbamoyl group, an aliphatic sulfonyl group, or an arylsulfonyl group, and R ₁ Represents an amino group, an aliphatic oxy group, an aliphatic group, an aryl group, or a heterocyclic group, R ₂ represents a substituent, A ₂ represents the following general formulas (A-13), (A-14), It represents one of (A-16), (A-18) to (A-22), (A-25), and (A-26), m represents an integer of 0 to 5, and n represents 1 to 4. In the case of n = 2, it represents a dimer through R ₁ , R ₂ , or A _{2. In} the case of n = 3, a trimer through R ₁ , R ₂ , or A ₂ (When n = 4, it represents a tetramer via R ₁ , R ₂ , or A ₂ )

(In the general formula (A-13), (A -14), (A-16), (A-18) ~ (A-22), (A-25), (A-26), R 55 ~R ₅₉ represents a hydrogen atom or a substituent, and adjacent R ₅₅ and R ₅₆ , R ₅₆ and R ₅₇ , R ₅₅ and R ₅₈ , R ₅₆ and R ₅₈ , R ₅₇ and R ₅₈ , R ₅₅ and R ₅₉ are bonded to each other. And a 5- to 6-membered ring may be formed. * Represents a bonding position with the azo group of the general formula (1).

  The azo compound represented by the general formula (2-2) is preferably an azo compound of the following general formula (2-3), a tautomer thereof, a salt or a hydrate thereof.

(In General Formula (2-3), R ₁ represents an amino group, an aliphatic oxy group, an aliphatic group, an aryl group, or a heterocyclic group, R ₂ represents a substituent, and R ₅₆ and R ₅₈ represent hydrogen. An atom or a substituent is represented, m represents an integer of 0 to 5, and n represents an integer of 1 to 4. R ₅₆ and R ₅₈ may be bonded to each other to form a 5- to 6-membered ring. When n = 2, it represents a dimer via R ₁ , R ₂ , R ₅₆ and R _{58. When} n = 3, a trimer via R ₁ , R ₂ , R ₅₆ and R ₅₈ (When n = 4, it represents a tetramer via R ₁ , R ₂ , R ₅₆ and R ₅₈ ).

The salts and hydrates of the azo compounds represented by the general formula (2-2) and the general formula (2-3) of the present invention and their tautomerism include the salts and hydrates of the azo pigments of the present invention and their The same thing as tautomerism can be mentioned.
The novel azo compound of the present invention is useful as an azo pigment.

  Specific examples of the azo pigments and azo compounds represented by the general formula (0), general formula (1), and general formula (2) are shown below. The azo pigments used in the present invention and the azo pigments of the present invention are as follows. The compounds are not limited to the following examples. The structures of the following specific examples are shown in the form of an ultimate structural formula among several tautomers that can be taken in terms of chemical structure, but may be tautomeric structures other than those described. Needless to say.

  The pigment represented by general formula (0), general formula (1), and general formula (2-1) to general formula (2-3) of the present invention has a chemical structural formula of general formula (0), general formula (1) and general formula (2-1) to general formula (2-3) or a tautomer thereof may be used, and any crystal form pigment also called polymorph may be used.

  Crystal polymorphs refer to the same chemical composition but different arrangement of building blocks (molecules or ions) in the crystal. The crystal structure determines the chemical and physical properties, and each polymorph can be distinguished by its rheology, color, and other color characteristics. Different polymorphs can also be confirmed by X-Ray Diffraction (powder X-ray diffraction measurement result) or X-Ray Analysis (X-ray crystal structure analysis result).

When a crystal polymorph exists in the pigment represented by the general formula (0), general formula (1) and general formula (2-1) to general formula (2-3) of the present invention, which polymorph is In addition, a mixture of two or more polymorphs may be used, but it is preferable that the main component is a single crystal form. That is, it is preferable that the crystalline polymorph is not mixed, and the content of the azo pigment having a single crystal type is 70% to 100%, preferably 80% to 100%, more preferably 90% with respect to the entire azo pigment. -100%, more preferably 95% -100, particularly preferably 100%. By using an azo pigment having a single crystal form as a main component, the regularity of the dye molecule arrangement is improved, the intramolecular / intermolecular interaction is strengthened, and a higher-order three-dimensional network is easily formed. . As a result, it is preferable in terms of performance required for pigments such as improvement of hue, light fastness, heat fastness, humidity fastness, oxidizing gas fastness and solvent resistance.
The mixing ratio of crystal polymorphs in azo pigments is based on solid physicochemical measurements such as single crystal X-ray crystal structure analysis, powder X-ray diffraction (XRD), crystal micrograph (TEM), IR (KBr method), etc. I can confirm.

  The tautomerism and / or crystal polymorphism described above can be controlled by the production conditions during the coupling reaction.

  In the present invention, the azo pigment represented by the general formula (0), the general formula (1), and the general formula (2-1) to the general formula (2-3) has an acid group. A part or all of them may be of a salt type, and a salt type pigment and a free acid type pigment may be mixed. Examples of the salt type include salts of alkali metals such as Na, Li and K, ammonium salts optionally substituted with an alkyl group or hydroxyalkyl group, and organic amine salts. Examples of organic amines include lower alkyl amines, hydroxy-substituted lower alkyl amines, carboxy-substituted lower alkyl amines, and polyamines having 2 to 10 alkyleneimine units having 2 to 4 carbon atoms. In the case of these salt types, the type is not limited to one type, and a plurality of types may be mixed.

  Further, in the structure of the pigment used in the present invention, when a plurality of acid groups are contained in one molecule, the plurality of acid groups may be salt type or acid type and may be different from each other.

  In the present invention, the azo pigments represented by the general formula (0), general formula (1), and general formula (2-1) to general formula (2-3) are hydrates containing water molecules in the crystal. It may be.

  Next, an example of a method for producing the azo pigment represented by the general formula (0) will be described. For example, a heterocyclic amine represented by the following general formula (4) is diazonium with non-aqueous acidity, a coupling reaction is performed with a compound represented by the following general formula (5) in an acidic state, and post-treatment by a conventional method is performed. It can carry out and can manufacture the azo pigment represented by General formula (6) of this invention. The azo pigment represented by the general formula (0) can be produced by using the heterocyclic amine corresponding to A of the general formula (1) instead of the general formula (4) and performing the same operation.

(In the formula, R ₅₆ and R ₅₈ have the same meaning as defined in the general formula (1).)

(In the formula, R ₁ , R ₂ and m are as defined in the general formula (1).)
The reaction scheme is shown below.

(In the formula, G, R _{1 to} R ₂ , R ₅₅ , R ₅₆ , R ₅₈ , n and m have the same meanings as defined in general formula (0), general formula (1) and general formula (2)). )

Heterocycle corresponding to the amino form of the above general formulas (4) and (A-1) to (A-14), (A-16) to (A-22), (A-24) to (A-26) Although some amines can be obtained as commercial products, they can be generally produced by a known and commonly used method, for example, the method described in Japanese Patent No. 4022271. Although the heterocyclic coupler represented by the general formula (5) can be obtained as a commercial product, it can be produced by the method described in JP-A-2008-13472 and a method analogous thereto. The diazoniumation reaction of the heterocyclic amine represented by the above reaction scheme is carried out at a temperature of 15 ° C. or less with a reagent such as sodium nitrite, nitrosylsulfuric acid, isoamyl nitrite in an acidic solvent such as sulfuric acid, phosphoric acid, and acetic acid. The reaction can be carried out for about 6 minutes to 6 minutes. The coupling reaction is carried out by reacting the diazonium salt obtained by the above-described method with the compound represented by the general formula (5) at 40 ° C. or less, preferably 25 ° C. or less for about 10 minutes to 12 hours. Can do.
General formula (0), General formula (1), General formula (2), General formula (2-1)-When general formula (2-3) n is 2 or more, the synthesis method is general formula (4). Alternatively, in R _{1 to} R ₂ , R ₅₅ , R ₅₆ , R _{58 and the} like of the general formula (5), a raw material into which a divalent, trivalent, or tetravalent substituent that can be substituted is introduced is synthesized, and the same as the above scheme Can be synthesized.
In some cases, crystals are precipitated in this way, but in general, water or an alcohol solvent is added to the reaction solution to precipitate the crystals, and the crystals can be collected by filtration. it can. In addition, an alcohol solvent, water or the like can be added to the reaction solution to precipitate crystals, and the precipitated crystals can be collected by filtration. The crystals collected by filtration can be washed and dried as necessary to obtain an azo pigment represented by the general formula (1).

  Although the compound represented by the general formula (0), the general formula (1), and the general formula (2-1) to the general formula (2-3) is obtained as a crude azo pigment (crude) by the above production method. When used as the pigment of the present invention, it is desirable to perform post-treatment. Examples of post-treatment methods include solvent salt milling, salt milling, dry milling, solvent milling, pigment particle control step by grinding treatment such as acid pasting, solvent heating treatment, resin, surfactant and dispersant. The surface treatment process by etc. is mentioned.

The compounds represented by general formula (0), general formula (1) and general formula (2-1) to general formula (2-3) of the present invention are subjected to solvent heat treatment and / or solvent salt milling as post-treatment. It is preferable.
Examples of the solvent used in the solvent heat treatment include water, aromatic hydrocarbon solvents such as toluene and xylene, halogenated hydrocarbon solvents such as chlorobenzene and o-dichlorobenzene, and alcohols such as isopropanol and isobutanol. Examples thereof include solvents, polar aprotic organic solvents such as N, N-dimethylformamide, N, N-dimethylacetamide, N-methyl-2-pyrrolidone, glacial acetic acid, pyridine, and mixtures thereof. An inorganic or organic acid or base may be further added to the solvents mentioned above. The temperature of the solvent heat treatment varies depending on the desired primary particle size of the pigment, but is preferably 40 to 150 ° C, more preferably 60 to 100 ° C. The treatment time is preferably 30 minutes to 24 hours.
As solvent salt milling, for example, a crude azo pigment, an inorganic salt, and an organic solvent that does not dissolve the crude azo pigment are charged into a kneader and kneaded and ground therein. As the inorganic salt, a water-soluble inorganic salt can be preferably used. For example, an inorganic salt such as sodium chloride, potassium chloride, sodium sulfate is preferably used. Moreover, it is more preferable to use an inorganic salt having an average particle size of 0.5 to 50 μm. The amount of the inorganic salt used is preferably 3 to 20 times by mass, more preferably 5 to 15 times by mass with respect to the crude azo pigment. As the organic solvent, a water-soluble organic solvent can be suitably used, and the solvent easily evaporates due to a temperature rise during kneading, so that a high boiling point solvent is preferable from the viewpoint of safety. Examples of such organic solvents include diethylene glycol, glycerin, ethylene glycol, propylene glycol, liquid polyethylene glycol, liquid polypropylene glycol, 2- (methoxymethoxy) ethanol, 2-butoxyethanol, 2- (isopentyloxy) ethanol, 2- (hexyloxy) ethanol, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol monobutyl ether, triethylene glycol, triethylene glycol monomethyl ether, 1-methoxy-2-propanol, 1-ethoxy-2-propanol, diethylene glycol Propylene glycol, dipropylene glycol monomethyl ether, dipropylene glycol monomethyl ether, dipropylene Glycol or mixtures thereof. The amount of the water-soluble organic solvent used is preferably 0.1 to 5 times by mass with respect to the crude azo pigment. The kneading temperature is preferably 20 to 130 ° C, particularly preferably 40 to 110 ° C. As a kneader, for example, a kneader or a mix muller can be used.

[Pigment dispersion (1)]
The pigment dispersion of the present invention comprises an azo pigment represented by the general formula (0), the general formula (1), and the general formula (2-1) to the general formula (2-3), a tautomer, a salt thereof, or the like. It contains at least one hydrate. Thereby, it can be set as the pigment dispersion excellent in chromatic characteristics, durability, and dispersion stability.

  The pigment dispersion of the present invention may be aqueous or non-aqueous, but is preferably an aqueous pigment dispersion. As the aqueous liquid in which the pigment is dispersed in the aqueous pigment dispersion of the present invention, a mixture containing water as a main component and optionally adding a hydrophilic organic solvent can be used.

  Examples of the hydrophilic organic solvent include methanol, ethanol, propanol, isopropanol, butanol, isobutanol, sec-butanol, t-butanol, pentanol, hexanol, cyclohexanol, benzyl alcohol and other alcohols, ethylene glycol, diethylene glycol Polyhydric alcohols such as triethylene glycol, polyethylene glycol, propylene glycol, dipropylene glycol, polypropylene glycol, butylene glycol, hexanediol, pentanediol, glycerin, hexanetriol, thiodiglycol, ethylene glycol monomethyl ether, ethylene glycol mono Ethyl ether, ethylene glycol butyl ether, diethylene glycol mono Chill ether, diethylene glycol monobutyl ether, propylene glycol monomethyl ether, propylene glycol monobutyl ether, dipropylene glycol monomethyl ether, triethylene glycol monomethyl ether, ethylene glycol diacetate, ethylene glycol monomethyl ether acetate triethylene glycol monoethyl ether, ethylene glycol monophenyl ether Glycol derivatives such as ethanolamine, diethanolamine, triethanolamine, N-methyldiethanolamine, N-ethyldiethanolamine, morpholine, N-ethylmorpholine, ethylenediamine, diethylenetriamine, triethylenetetramine, polyethyleneimine, tetramethylpropylenediamine Such as amine, formamide, N, N-dimethylformamide, N, N-dimethylacetamide, dimethyl sulfoxide, sulfolane, 2-pyrrolidone, N-methyl-2-pyrrolidone, N-vinyl-2-pyrrolidone, 2-oxazolidone, 1 , 3-dimethyl-2-imidazolidinone, acetonitrile, acetone and the like.

  Further, the aqueous pigment dispersion of the present invention may contain an aqueous resin. Examples of the aqueous resin include a water-soluble resin that dissolves in water, a water-dispersible resin that disperses in water, a colloidal dispersion resin, or a mixture thereof. Specific examples of the aqueous resin include acrylic, styrene-acrylic, polyester, polyamide, polyurethane, and fluorine resins.

  When the aqueous pigment dispersion in the present invention contains an aqueous resin, the content is not particularly limited. For example, it can be 0 to 100% by mass with respect to the pigment.

  Further, surfactants and dispersants may be used to improve pigment dispersion and image quality. Examples of the surfactant include anionic, nonionic, cationic, and zwitterionic surfactants. Any surfactant may be used, but anionic or nonionic surfactants may be used. It is preferable to use it.

  When the aqueous pigment dispersion in the present invention contains a surfactant, the content is not particularly limited. For example, it can be 0 to 100% by mass with respect to the pigment.

  Examples of the anionic surfactant include fatty acid salts, alkyl sulfate esters, alkylbenzene sulfonates, alkyl naphthalene sulfonates, dialkyl sulfosuccinates, alkyl diaryl ether disulfonates, alkyl phosphates, and polyoxyethylene alkyls. Examples thereof include ether sulfate, polyoxyethylene alkylaryl ether sulfate, naphthalenesulfonic acid formalin condensate, polyoxyethylene alkyl phosphate ester salt, glycerol borate fatty acid ester, polyoxyethylene glycerol fatty acid ester and the like.

  Nonionic surfactants include, for example, polyoxyethylene alkyl ether, polyoxyethylene alkyl aryl ether, polyoxyethylene oxypropylene block copolymer, sorbitan fatty acid ester, polyoxyethylene sorbitan fatty acid ester, polyoxyethylene sorbitol fatty acid ester, glycerin fatty acid Examples include esters, polyoxyethylene fatty acid esters, polyoxyethylene alkylamines, fluorine-based and silicon-based.

  In the non-aqueous pigment dispersion of the present invention, the pigments represented by the general formula (0), the general formula (1), and the general formula (2-1) to the general formula (2-3) are dispersed in a non-aqueous vehicle. It will be. Resins used in non-aqueous vehicles are, for example, petroleum resins, casein, shellac, rosin modified maleic resin, rosin modified phenolic resin, nitrocellulose, cellulose acetate butyrate, cyclized rubber, chlorinated rubber, oxidized rubber, hydrochloric acid rubber , Phenolic resin, alkyd resin, polyester resin, unsaturated polyester resin, amino resin, epoxy resin, vinyl resin, vinyl chloride, vinyl chloride-vinyl acetate copolymer, acrylic resin, methacrylic resin, polyurethane resin, silicone resin, fluorine resin , Drying oil, synthetic drying oil, styrene / maleic acid resin, styrene / acrylic resin, polyamide resin, polyimide resin, benzoguanamine resin, melamine resin, urea resin chlorinated polypropylene, butyral resin, vinylidene chloride resin and the like. A photocurable resin may be used as the non-aqueous vehicle.

  Examples of the solvent used in the non-aqueous vehicle include aromatic solvents such as toluene, xylene, and methoxybenzene, and acetates such as ethyl acetate, butyl acetate, propylene glycol monomethyl ether acetate, and propylene glycol monoethyl ether acetate. Solvents, propionate solvents such as ethoxyethyl propionate, alcohol solvents such as methanol and ethanol, ether solvents such as butyl cellosolve, propylene glycol monomethyl ether, diethylene glycol ethyl ether, diethylene glycol dimethyl ether, methyl ethyl ketone, methyl isobutyl ketone, cyclohexanone, etc. Ketone solvents, aliphatic hydrocarbon solvents such as hexane, N, N-dimethylformamide, γ-butyrolactam, N Methyl-2-pyrrolidone, aniline, nitrogen compound-based solvent such as pyridine, a lactone-based solvents such as γ- butyrolactone, carbamic acid esters such as a mixture of 48:52 of methyl carbamate and ethyl carbamate acid.

  In the present invention, the volume average particle diameter of the pigment is preferably 10 nm or more and 250 nm or less. The volume average particle diameter of the pigment particles refers to the particle diameter of the pigment itself or the particle diameter to which the additive has adhered when an additive such as a dispersant is attached to the pigment. In the present invention, a Nanotrac UPA particle size analyzer (UPA-EX150; manufactured by Nikkiso Co., Ltd.) was used as a measuring device for the volume average particle diameter of the pigment. The measurement was performed according to a predetermined measuring method by putting 3 ml of the pigment dispersion in a measuring cell. As parameters to be input at the time of measurement, ink viscosity was used as the viscosity, and pigment density was used as the density of the dispersed particles.

  A more preferable volume average particle diameter is 20 nm or more and 250 nm or less, and further preferably 30 nm or more and 230 nm or less. When the number average particle size of the particles in the pigment dispersion is less than 20 nm, there are cases where the storage stability cannot be ensured, whereas when it exceeds 250 nm, the optical density may be lowered.

  The concentration of the pigment contained in the pigment dispersion of the present invention is preferably in the range of 1 to 35% by mass, and more preferably in the range of 2 to 25% by mass. If the density is less than 1% by mass, sufficient image density may not be obtained when the pigment dispersion is used alone as the ink. If the concentration exceeds 35% by mass, the dispersion stability may decrease.

  The pigment dispersion of the present invention can be obtained by dispersing the above azo pigment and an aqueous or non-aqueous medium using a dispersing device. Dispersing devices include simple stirrer, impeller stirring method, in-line stirring method, mill method (for example, colloid mill, ball mill, sand mill, bead mill, attritor, roll mill, jet mill, paint shaker, agitator mill, etc.), ultrasonic method Further, a high-pressure emulsification dispersion system (high-pressure homogenizer; specific commercially available devices such as gorin homogenizer, microfluidizer, DeBEE2000, etc.) can be used.

  Applications of the azo pigments of the present invention include image recording materials for forming images, particularly color images. Specifically, the ink-jet recording materials described in detail below, thermal recording materials, Pressure recording material, recording material using an electrophotographic method, transfer type silver halide photosensitive material, printing ink, recording pen, etc., preferably an ink jet recording material, a thermal recording material, a recording material using an electrophotographic method, More preferred are ink jet recording materials.

  The present invention can also be applied to a solid-state image pickup device such as a CCD, a color filter for recording / reproducing a color image used in a display such as an LCD or PDP, and a dyeing solution for dyeing various fibers.

  The azo pigment of the present invention is used by adjusting physical properties such as solvent resistance, dispersibility, and heat mobility suitable for the application with a substituent. Further, the azo pigment of the present invention can be used in an emulsified and dispersed state and further in a solid dispersed state depending on the system used.

[Coloring composition]
The colored composition of the present invention means a colored composition containing at least one azo pigment of the present invention. The coloring composition of the present invention can contain a medium, but when a solvent is used as the medium, it is particularly suitable as an ink for inkjet recording. The coloring composition of the present invention can be produced by using a lipophilic medium or an aqueous medium as a medium and dispersing the azo pigment of the present invention in the medium. Preferably, an aqueous medium is used. The coloring composition of the present invention includes an ink composition excluding a medium. The coloring composition of the present invention may contain other additives as necessary within a range that does not impair the effects of the present invention. Other additives include, for example, anti-drying agents (wetting agents), anti-fading agents, emulsion stabilizers, penetration enhancers, ultraviolet absorbers, preservatives, anti-fungal agents, pH adjusters, surface tension adjusters, Known additives (described in JP-A No. 2003-306623) such as a foaming agent, a viscosity modifier, a dispersant, a dispersion stabilizer, a rust inhibitor, and a chelating agent can be used. These various additives are directly added to the ink liquid in the case of water-soluble ink. In the case of oil-soluble ink, it is common to add to the dispersion after preparation of the azo pigment dispersion, but it may be added to the oil phase or water phase at the time of preparation.

[Ink for inkjet recording]
Next, the ink for inkjet recording of the present invention will be described.
The pigment dispersion described above is used for the inkjet recording ink of the present invention (hereinafter sometimes referred to as “ink”). Preferably, it is prepared by mixing a water-soluble solvent, water and the like. However, if there is no particular problem, the pigment dispersion of the present invention may be used as it is.

  The content ratio of the pigment dispersion in the ink of the present invention is preferably in the range of 1 to 100% by mass in consideration of the hue, color density, saturation, transparency and the like of the image formed on the recording medium. The range of mass% is particularly preferable, and the range of 3 to 10 mass% is most preferable among them.

  The pigment of the present invention is preferably contained in an amount of 0.1 to 20 parts by mass, more preferably 0.2 to 10 parts by mass in 100 parts by mass of the ink of the present invention. It is more preferable to contain 10 parts by mass. Further, in the ink of the present invention, other pigments may be used in combination with the pigment of the present invention. When two or more kinds of pigments are used in combination, the total content of the pigments is preferably within the above range.

  The ink of the present invention can be used not only for monochromatic image formation but also for full color image formation. In order to form a full color image, a magenta color ink, a cyan color ink, and a yellow color ink can be used, and a black color ink may be further used to adjust the color tone.

  Furthermore, in the ink of the present invention, other pigments can be used simultaneously in addition to the azo pigment of the present invention. Examples of yellow pigments that can be applied include C.I. I. P. Y. 74, C.I. I. P. Y. 128, C.I. I. P. Y. 155, C.I. I. P. Y. 213, and magenta pigments that can be applied include C.I. I. P. V. 19, C.I. I. P. R. 122, and examples of applicable cyan pigments include C.I. I. P. B. 15: 3, C.I. I. P. B. 15: 4 can be mentioned, and apart from these, any one can be used. Applicable black materials include disazo, trisazo, and tetraazo pigments, as well as carbon black dispersions.

  As the water-soluble solvent used in the ink jet recording ink of the present invention, polyhydric alcohols, polyhydric alcohol derivatives, nitrogen-containing solvents, alcohols, sulfur-containing solvents and the like are used. Specific examples of polyhydric alcohols include ethylene glycol, diethylene glycol, propylene glycol, butylene glycol, triethylene glycol, 1,5-pentanediol, 1,2,6-hexanetriol, and glycerin.

  Examples of the polyhydric alcohol derivative include ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monobutyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol monobutyl ether, propylene glycol monobutyl ether, dipropylene glycol monobutyl ether, diglycerin. And ethylene oxide adducts.

  Examples of the nitrogen-containing solvent include pyrrolidone, N-methyl-2-pyrrolidone, cyclohexyl pyrrolidone, and triethanolamine. Examples of alcohols include alcohols such as ethanol, isopropyl alcohol, butyl alcohol, and benzyl alcohol. Examples of the solvent include thiodiethanol, thiodiglycerol, sulfolane, dimethyl sulfoxide and the like. In addition, propylene carbonate, ethylene carbonate, or the like can be used.

  The water-soluble solvent used in the present invention may be used alone or in combination of two or more. The content of the water-soluble solvent is 1% by mass or more and 60% by mass or less, preferably 5% by mass or more and 40% by mass or less of the entire ink. When the amount of the water-soluble solvent in the ink is less than 1% by mass, a sufficient optical density may not be obtained. Conversely, when the amount is more than 60% by mass, the viscosity of the liquid increases. In some cases, the ejection characteristics of the ink liquid become unstable.

Preferred physical properties of the ink for ink jet recording of the present invention are as follows.
The surface tension of the ink is preferably 20 mN / m or more and 60 mN / m or less. More preferably, it is 20 mN or more and 45 mN / m or less, More preferably, it is 25 mN / m or more and 35 mN / m or less. If the surface tension is less than 20 mN / m, liquid may overflow on the nozzle surface of the recording head, and printing may not be performed normally. On the other hand, if it exceeds 60 mN / m, the permeability to the recording medium after printing may be slow, and the drying time may be slow.
The surface tension was measured under the environment of 23 ° C. and 55% RH using a Wilhelmy surface tension meter as described above.

The viscosity of the ink is preferably from 1.2 mPa · s to 8.0 mPa · s, more preferably from 1.5 mPa · s to less than 6.0 mPa · s, still more preferably from 1.8 mPa · s to 4. It is less than 5 mPa · s. When the viscosity is greater than 8.0 mPa · s, the dischargeability may be reduced. On the other hand, when it is smaller than 1.2 mPa · s, the long-term jetting property may deteriorate.
The viscosity (including those described later) was measured using a rotational viscometer Rheomat 115 (manufactured by Contraves) at 23 ° C. and a shear rate of 1400 s-1.

  In addition to the components described above, water is added to the ink in the range of the above-described preferable surface tension and viscosity. The amount of water added is not particularly limited, but is preferably 10% by mass to 99% by mass, and more preferably 30% by mass to 80% by mass with respect to the entire ink.

  Furthermore, if necessary, for the purpose of controlling properties such as ejection improvement, cellulose derivatives such as polyethyleneimine, polyamines, polyvinylpyrrolidone, polyethylene glycol, ethylcellulose, carboxymethylcellulose, polysaccharides and derivatives thereof, other water-soluble polymers, acrylics Polymer emulsion, polyurethane emulsion, polymer emulsion such as hydrophilic latex, hydrophilic polymer gel, cyclodextrin, macrocyclic amines, dendrimers, crown ethers, urea and its derivatives, acetamide, silicone surfactant, fluorine-based A surfactant or the like can be used.

In order to adjust conductivity and pH, compounds of alkali metals such as potassium hydroxide, sodium hydroxide, lithium hydroxide, ammonium hydroxide, triethanolamine, diethanolamine, ethanolamine, 2-amino-2-methyl Nitrogen-containing compounds such as -1-propanol, alkaline earth metal compounds such as calcium hydroxide, acids such as sulfuric acid, hydrochloric acid and nitric acid, strong acid and weak alkali salts such as ammonium sulfate, and the like can be used.
In addition, a pH buffer, an antioxidant, a fungicide, a viscosity modifier, a conductive agent, an ultraviolet absorber, and the like can be added as necessary.

  EXAMPLES The present invention will be specifically described below based on examples, but the present invention is not limited to these examples. In the following examples, “%” and “parts” represent “% by mass” and “parts by mass” unless otherwise specified, and the molecular weight indicates the weight average molecular weight.

[Synthesis Example 1]
Synthesis of Specific Compound Example D-22 Specific Compound Example D-22 was synthesized by the following route.

1.0 g of the compound (1) was dissolved in 10 ml of phosphoric acid (Wako Pure Chemical Industries, Ltd .; reagent special purity 85%, the same applies hereinafter). This solution was ice-cooled and kept at -5 to 0 ° C., 0.55 g of sodium nitrite was added and stirred for 1 hour to obtain a diazonium salt solution. Separately, 20 ml of NMP (N-methylpyrrolidone) was added to 1.60 g of compound (0), and the above diazonium salt solution was added at 8 ° C. or lower with stirring. Upon completion of the addition, the ice bath was removed and the mixture was further stirred for 3 hours. 50 ml of methanol was added to the reaction solution and stirred for 30 minutes. The precipitated crystals were filtered off and washed with 30 ml of methanol. The crystals were added to 100 ml of water without drying, and a solution of 0.5 g of sodium bicarbonate dissolved in 30 ml of water was added, followed by stirring at 20 to 25 ° C. for 30 minutes. The precipitated crystals were separated by filtration, and further thoroughly washed with water. The obtained crystals were added to 20 ml of NMP and 10 ml of water without drying, and heated and stirred at 100 ° C. for 30 minutes. The mixture was stirred at room temperature for 30 minutes, and the precipitated crystals were filtered and washed with 20 ml of NMP / water = 2/1 and 20 ml of water. The obtained crystals were dried to obtain 1.8 g of the compound D-22 of the present invention. Yield 72%.
FIG. 1 shows an infrared absorption chart.
[Synthesis Example 2]
Synthesis of Specific Compound Example D-28 Specific Compound Example D-28 was synthesized by the following route.

1.0 g of compound (2) was dissolved in 10 ml of phosphoric acid. This solution was ice-cooled and kept at −5 to 0 ° C., 0.54 g of sodium nitrite was added and stirred for 1 hour to obtain a diazonium salt solution. Separately, 20 ml of NMP (N-methylpyrrolidone) was added to 1.60 g of compound (3), and the above diazonium salt solution was added at 8 ° C. or lower with stirring. Upon completion of the addition, the ice bath was removed and the mixture was further stirred for 1 hour. 40 ml of methanol was added to the reaction solution, and the mixture was stirred for 30 minutes. The precipitated crystals were separated by filtration and washed with 30 ml of methanol. The crystals were added to 100 ml of water without drying and stirred at 20-25 ° C. for 30 minutes. The precipitated crystals were separated by filtration, and further thoroughly washed with water. The obtained crystals were added to 20 ml of NMP and 10 ml of water without drying, and heated and stirred at 100 ° C. for 30 minutes. The mixture was stirred at room temperature for 30 minutes, and the precipitated crystals were filtered and washed with 20 ml of NMP / water = 2/1 and 20 ml of water. The obtained crystals were dried to obtain 2.0 g of the compound D-28 of the present invention. Yield 80%.
FIG. 2 shows an infrared absorption chart.
Other compounds were synthesized in the same manner as in the specific compound example 2. Infrared absorption charts of the synthesized compounds are shown in FIGS.

〔Example〕
[Synthesis Example 1 of Comparative Compound]
Synthesis of Comparative Compound 4 Comparative compound 4 was synthesized by the following route.

  Water (15 ml) and concentrated hydrochloric acid (2.2 ml) were added to 2.1 g of the compound (a), and the mixture was stirred at -2 ° C to 2 ° C. To this solution, a solution of 0.72 g of sodium nitrite dissolved in 5 ml of water was added dropwise over 10 minutes to obtain a diazonium salt solution. Separately, 10 ml of DMAc was added to 2.50 g of compound (b), and the above diazonium salt solution was added at 5 ° C. to 10 ° C. with stirring. Upon completion of the addition, the ice bath was removed and the mixture was further stirred for 2 hours. The precipitated crystals were separated by filtration and washed with 50 ml of water. The obtained crystal was recrystallized with 50 ml of methanol, cooled to 25 ° C., and the precipitated crystal was separated by filtration. The obtained crystal was dried to obtain 2.4 g of Comparative Compound 4. Yield 51.8%.

[Synthesis Example 2 of Comparative Compound]
Synthesis of Comparative Compound 5 Comparative compound 5 was synthesized by the following route.

  To 1.9 g of compound (d), 15 ml of water and 2.2 ml of concentrated hydrochloric acid were added and stirred at -2 ° C to 2 ° C. To this solution, a solution of 0.72 g of sodium nitrite dissolved in 5 ml of water was added dropwise over 10 minutes to obtain a diazonium salt solution. Separately, 40 g of water and 2 g of sodium carbonate were added to 2.6 g of compound (b), and the above diazonium salt solution was added at 5 ° C. to 10 ° C. with stirring. Upon completion of the addition, the ice bath was removed and the mixture was further stirred for 2 hours. The reaction solution was added to 200 ml of saturated saline. The precipitated crystals were separated by filtration, washed with 30 ml of saturated brine and dried. The obtained crystals were heated with 100 ml of methanol, and insoluble matters were filtered. The solution was purified by Sephadex column chromatography, the water / methanol solution was concentrated, the precipitated crystals were filtered off, washed with methanol, and 1.7 g of Comparative Compound 5 was obtained. Yield 35.4%.

[Comparative Compound 6]
Compounds described in Japanese Patent No. 3894726

[Example 1]
Specific compound example D-22 pigment 2.5 parts, sodium oleate 0.5 part, glycerin 5 parts and water 42 parts are mixed, and each 100 parts of zirconia beads having a diameter of 0.1 mm are used with a planetary ball mill. Dispersion was performed at 300 rpm for 6 hours. After the completion of dispersion, zirconia beads were separated to obtain pigment dispersion 1.

[Example 2]
Methacrylic acid-methacrylic acid ester represented by Dispersant Solution 10 described on page 22 of International Publication No. WO2006 / 064193 as a polymer dispersant, 5 parts of pigment (D-22) synthesized in Example 1 25.5 parts of an aqueous copolymer solution and 19.5 parts of water were mixed, and dispersion was performed at 300 rpm for 6 hours using a planetary ball mill together with 100 parts of zirconia beads having a diameter of 0.1 mm. After the completion of dispersion, zirconia beads were separated to obtain pigment dispersion 2.

[Comparative Example 1]
In place of the pigment of Example 1, C.I. I. A red comparative pigment dispersion 1 was obtained in the same manner as in Example 1 except that CI Pigment Red 254 (B-CF manufactured by Ciba Specialty) was used.
[Comparative Example 2]
Instead of the pigment (D-22) used in Example 1, C.I. I. A yellow comparative pigment dispersion 2 was obtained in the same manner as in Example 1 except that CI Pigment Yellow 74 (Iralite YELLOW GO manufactured by Ciba Specialty) was used.

[Comparative Example 3]
Instead of the pigment (D-22) used in Example 1, C.I. I. A yellow comparative pigment dispersion 3 was obtained in the same manner as in Example 1 except that CI Pigment Yellow 155 (INKJET YELLOW 4G VP2532 manufactured by Clariant) was used.
[Comparative Example 4]
A red comparative pigment dispersion 4 was obtained in the same manner as in Example 1 except that the comparative compound 4 was used instead of the pigment (D-22) used in Example 1.

[Comparative Example 5]
A red comparative pigment dispersion 5 was obtained in the same manner as in Example 1 except that the comparative compound 5 was used instead of the pigment (D-22) used in Example 1.
[Comparative Example 6]
A red comparative pigment dispersion 6 was obtained in the same manner as in Example 1 except that the comparative compound 6 was used instead of the pigment (D-22) used in Example 1.

(Evaluation)
<Dispersion stability>
The volume average particle size of each pigment dispersion obtained above was measured by a conventional method using a dynamic light scattering particle size measuring device (Nikkiso Microtrack UPA150). The volume average particle diameter measured 2 hours after preparing the pigment dispersion and the volume average particle diameter after storage at 70 ° C for 2 days are both 230 nm or less (good), either of which is 230 nm or more X (defect). The results are shown in Table 1.
<Evaluation of coloring power>
Each pigment dispersion obtained above was designated as No. No. 3 bar coater was applied to a photo mat paper <pigment only> manufactured by Seiko Epson Corporation. The image density of the obtained coated material was measured using a reflection densitometer (X-Rite 938 manufactured by X-Rite), and the result is shown in Table 1 as “coloring power (OD: Optical Density)”.
<Light resistance evaluation>
The coated product having an image density of 1.0 used for evaluating the coloring power was irradiated with xenon light (170000 lux .; in the presence of a cut filter of 325 nm or less) for 14 days using a fade meter, and the image density before and after the xenon irradiation was measured as the reflection density. It was measured using a meter and evaluated as a dye residual ratio [(post-irradiation density / pre-irradiation density) × 100%]. The results are shown in Table 1.

[Examples 3 to 11]
Pigment dispersions 3 to 11 were prepared in the same manner except that the specific compound example D-22 of Example 1 was changed as shown in Table 1, and the same evaluation was performed.

Example 101
The polymer dispersant represented by Dispersant 10 described on page 22 of International Publication No. WO06 / 064193 was neutralized with an aqueous potassium hydroxide solution. In 75 parts by mass of the resulting aqueous dispersant solution (solid content concentration 20%), 30 parts by mass of the synthetic azo pigment (D-22) and 95 parts by mass of ion-exchanged water are added and mixed with a disper stirring blade.・ Roughly disperse. 600 parts by mass of zirconia beads were added to the mixed and roughly dispersed liquid, and this was dispersed with a disperser (sand grinder mill) for 4 hours, and then separated into beads and a dispersion. While stirring the resulting mixture, 2 parts by mass of polyethylene glycol diglycidyl ether was slowly added at 25 ° C., and the mixture was stirred at 50 ° C. for 6 hours. Furthermore, impurities were removed using an ultrafiltration membrane having a fractional molecular number of 300K, and this was attached to a filter having a pore size of 5 μm (acetylcellulose membrane, outer diameter: 25 mm, manufactured by Fuji Film Co., Ltd.). By filtering with a syringe and removing coarse particles, a pigment dispersion 101 (particle size 80 nm: measured using Nanotrac 150 (UPA-EX150) manufactured by Nikkiso Co., Ltd.) having a solid content concentration of 10% was obtained.

[Comparative Example 101]
A comparison was made in the same manner as in Example 101 except that a red pigment (CI Pigment Red 254 (B-CF manufactured by Ciba Specialty)) was used instead of the azo pigment (D-22) used in Example 101. A pigment dispersion 101 was obtained.

Example 102
5% by mass of the pigment dispersion 101 obtained in Example 101, 10% by mass of glycerin, 5% by mass of 2-pyrrolidone, 2% by mass of 1,2-hexanediol, 2% by mass of triethylene glycol monobutyl ether, Each component was added so that it might become 0.5 mass% of propylene glycol, and 75.5 mass% of ion-exchange water, and the obtained liquid mixture was filtered with a 1 μm pore size filter (acetylcellulose membrane, outer diameter: 25 mm, Fujifilm Corporation). The pigment ink liquid 5 of the present invention shown in Table 2 was obtained by filtering through a syringe with a capacity of 20 ml equipped with a) and removing coarse particles.

[Comparative Example 102]
A comparative pigment ink liquid 5 was obtained in the same manner as in Example 102 except that the comparative pigment dispersion 101 obtained in Comparative Example 101 was used instead of the pigment dispersion 101 obtained in Example 101.

  In Table 2, “Ejection stability”, “Light fastness”, “Heat fastness”, “Ozone fastness”, “Metal gloss”, and “Ink liquid stability” are the same for each ink. ) Installed in a magenta ink cartridge of an ink jet printer PX-V630 manufactured by the company, PX-V630 pigment ink liquid was used for the other color inks, and the image receiving sheet was a photographic paper <glossy> manufactured by Seiko Epson Corporation. In addition, the recommended mode is printed on photographic paper Krispia <High Gloss> made by Seiko Epson Co., Ltd., and a monochrome image pattern and green, red, and gray image patterns with density changes in a staircase pattern are printed. And image robustness were evaluated. Evaluations other than metallic luster were performed in a single color.

  The following evaluation was performed on the inkjet inks of Example 102 (pigment ink liquid 5) and Comparative Example (comparative pigment ink liquid 5). The results are shown in Table 2.

(Evaluation experiment)
1) About discharge stability, after setting a cartridge in a printer and confirming the protrusion of the ink from all the nozzles, 20 sheets of A4 were output and evaluated according to the following criteria.
A: No printing disturbance from the start to the end of printing B: Output with a printing disorder occurs C: There is a printing disturbance from the start to the end of printing

2) For image storage stability, the following evaluation was performed using a print sample.
[1] Light fastness is measured by measuring the image density Ci immediately after printing with X-rite 310, then irradiating the image with xenon light (100,000 lux) for 14 days using a weather meter manufactured by Atlas, and then again image density Cf Was measured to obtain an image residual ratio Cf / Ci × 100.
The image afterimage rate is evaluated at three points of reflection density of 1, 1.5, and 2. A is the case when the image remaining rate is 80% or more at any density, and B is the case when the point is less than 80%. When the concentration was less than 80%, C was designated.

[2] For heat fastness, the density before and after storing the print sample for 7 days under the condition of 80 ° C. and 60% RH was measured with X-rite 310, and the image residual ratio was determined and evaluated. The image afterimage rate is evaluated at three points of reflection density of 1, 1.5 and 2, and A is the case where the image remaining rate is 95% or more at any density, and B is the case where the point is less than 95%. The case where the concentration was less than 95% was defined as C.

[3] For ozone resistance (ozone fastness), the sample was left in a box where the ozone gas concentration was set to 5 ppm (25 ° C; 50%) for 14 days. -Measured using a Photographic Densitometer 310) manufactured by Rite and evaluated as an image residual ratio. The reflection density was measured at three points of 1, 1.5 and 2.0. The ozone gas concentration in the box was set using an ozone gas monitor (model: OZG-EM-01) manufactured by APPLICS.
The evaluation was made in three stages, with A as the case where the image remaining ratio was 80% or higher at any density, and B when 1 or 2 points were less than 80%, and C when less than 70% at all densities.

3) Presence or absence of occurrence of metallic luster: The yellow, green and red solid print portions were visually observed and evaluated with reflected light.
The case where the metallic luster was not visible was evaluated as “◯”, and the case where the metallic luster was visible was evaluated as “x”.

4) Ink liquid stability: After aging the pigment ink liquids of Examples and Comparative Examples at 60 ° C. for 10 days, the evaluation was made with “◯” indicating no change in the particle diameter in the pigment ink liquid and “X” indicating that the particle diameter was changed. did. The results are shown in Table 2 below.

From the results in Table 2, it was found that the pigment ink liquid using the pigment of the present invention was excellent in ejection properties and weather resistance, suppressed the occurrence of metallic luster, and excellent in pigment ink liquid stability.
As is apparent from the results in Table 2, it can be seen that the system using the ink liquid of the present invention is excellent in all performance. In particular, light fastness and ink liquid stability are superior to the comparative example.

Example 103
The pigment ink liquid prepared in Example 102 was printed on Fujifilm's inkjet paper photo glossy paper “Painting” with PX-V630 manufactured by Epson Corporation, and the same as in Example 8. When similar evaluations were made, similar results were obtained.
As is clear from the results in Tables 1 and 2, Pigment Dispersions 1 to 8 and Pigment Ink Liquid 5 using the pigment of the present invention are excellent in color tone and exhibit high coloring power and light resistance.
Therefore, the pigment dispersion using the pigment of the present invention can be suitably used, for example, for printing ink such as inkjet.

Claims (8)

An azo pigment represented by the following general formula (1), a tautomer thereof, a salt or a hydrate thereof.

(In General Formula (1), G represents a hydrogen atom, an aliphatic group, an aryl group, a heterocyclic group, an acyl group, an aliphatic oxycarbonyl group, a carbamoyl group, an aliphatic sulfonyl group, or an arylsulfonyl group, and R ₁ is represents an amino group, an aliphatic oxy group, an aliphatic group, an aryl group, or a heterocyclic group, _{R 2} represents a substituent, a represents the following general formula (a-1) ~ (a -14), (A- 16) to (A-22) and (A-24) to (A-26), m represents an integer of 0 to 5, n represents an integer of 1 to 4, and n = 2. The case represents a dimer via R ₁ , R ₂ , A or G. The case where n = 3 represents the trimer via R ₁ , R ₂ , A or G. The case where n = 4 Represents a tetramer via R ₁ , R ₂ , A or G.)

(In the general formulas (A-1) to (A-14), (A-16) to (A-22), (A-24) to (A-26), R _{51 to} R ₅₉ are hydrogen atoms or substituted R ₅₁ and R ₅₂ , R ₅₂ and R ₅₃ , R ₅₃ and R ₅₄ , R ₅₅ and R ₅₆ , R ₅₆ and R ₅₇ , R ₅₅ and R ₅₈ , R ₅₆ and R ₅₈ , R ₅₇ And R ₅₈ , R ₅₅ and R ₅₉ may be bonded to each other to form a 5- to 6-membered ring (* represents a bonding position with the azo group of the general formula (1)). The azo pigment represented by the general formula (1) is represented by the following general formula (2-1), the azo pigment according to claim 1, a tautomer thereof, a salt thereof, or water. Japanese products.

(In the general formula (2-1), R ₁ , R ₂ , m, and n are the same as those defined in the general formula (1), and A ₁ represents the following general formulas (A-10) to (A-14). ), (A-16) to (A-22), or (A-24) to (A-26), when n = 2, R ₁ , R ₂ , or A ₁ Represents a dimer, n = 3 represents a trimer via R ₁ , R ₂ , or A ₁ , n = 4 represents a tetramer via R ₁ , R ₂ , or A ₁ Represents the body.)

(Formula (A-10) ~ (A -14), (A-16) ~ (A-22), in (A-24) ~ (A -26), R 55 ~R 59 is formula (1 ) Is the same as defined in) 2. The azo pigment according to claim 1, wherein the azo pigment represented by the general formula (1) and the general formula (2-1) is represented by the following general formula (2-2): Sex bodies, their salts or hydrates.

(In the general formula (2-2), R ₁ and R ₂ are the same as those defined in the general formula (1), and A ₂ represents the following general formulas (A-13), (A-14), (A -16), (A-18) to (A-22), (A-25), or (A-26), when n = 2, R ₁ , R ₂ , or A ₂ is Represents a dimer via n, if n = 3 represents a trimer via R ₁ , R ₂ , or A _2. If n = 4, it represents via R ₁ , R ₂ , or A ₂ Represents a tetramer.)

(In the general formula (A-13), (A -14), (A-16), (A-18) ~ (A-22), (A-25), (A-26), R 55 ~R ₅₉ is the same as defined in the general formula (1).)   A pigment dispersion comprising at least one of the azo pigments according to claims 1 to 3, tautomers thereof, salts or hydrates thereof.   A coloring composition comprising at least one of the azo pigments according to claims 1 to 3, tautomers thereof, salts or hydrates thereof.   An ink for inkjet recording, wherein the pigment dispersion according to claim 4 is used. An azo compound represented by the general formula (2-2).

(In General Formula (2-2), G represents a hydrogen atom, an aliphatic group, an aryl group, a heterocyclic group, an acyl group, an aliphatic oxycarbonyl group, a carbamoyl group, an aliphatic sulfonyl group, or an arylsulfonyl group, and R ₁ Represents an amino group, an aliphatic oxy group, an aliphatic group, an aryl group, or a heterocyclic group, R ₂ represents a substituent, A ₂ represents the following general formulas (A-13), (A-14), It represents one of (A-16), (A-18) to (A-22), (A-25), and (A-26), m represents an integer of 0 to 5, and n represents 1 to 4. In the case of n = 2, it represents a dimer through R ₁ , R ₂ , or A _{2. In} the case of n = 3, a trimer through R ₁ , R ₂ , or A ₂ (When n = 4, it represents a tetramer via R ₁ , R ₂ , or A ₂ )

(In the general formula (A-13), (A -14), (A-16), (A-18) ~ (A-22), (A-25), (A-26), R 55 ~R ₅₉ represents a hydrogen atom or a substituent, adjacent R ₅₅ and R ₅₆ , R ₅₆ and R ₅₇ , R ₅₆ and R ₅₈ may be bonded to each other to form a 5- to 6-membered ring. (Represents the bonding position with the azo group of formula (1).) The azo compound according to claim 7, wherein the azo compound represented by the general formula (2-2) is represented by the following general formula (2-3).

(In General Formula (2-3), R ₁ represents an amino group, an aliphatic oxy group, an aliphatic group, an aryl group, or a heterocyclic group, R ₂ represents a substituent, and R ₅₆ and R ₅₈ represent hydrogen. represents an atom or a substituent, m represents an integer of 0 to 5, n is may combine to form a 5- to 7-membered ring with each other _{.R 56} and _{R 58} represents an integer of 1 to 4 .n = for ₂ to R _1, R _{2, R 56} and the case of .n = 3 representing a dimer formed through _{R 58, R 1, R 2} , 3 dimer formed through _{R 56} and _{R 58} (If n = 4, it represents a tetramer via R ₁ , R ₂ , R ₅₆ and R _58. )

Images