JP2014065834A - Novel azo compound, aqueous solution, ink composition, ink for inkjet recording, inkjet recording method, ink cartridge for inkjet recording and inkjet recorded article - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide an aqueous solution capable of providing an ink having good color tone as a black color ink, high print density, and excellent in suppressing bronze brightness on recording images when using various recorded materials.SOLUTION: There is provided an aqueous solution containing a preservative agent, a specific azo compound or a salt thereof (for example the following compound or a salt thereof) of 1 mass% to 25 mass%.

Description

  The present invention relates to an azo compound, an aqueous solution, an ink composition, an ink for ink jet recording, an ink jet recording method, an ink cartridge for ink jet recording, and an ink jet recorded matter.

The ink jet recording method is rapidly spreading and further developing because of its low material cost, high speed recording, low noise during recording, and easy color recording.
Inkjet recording methods include a continuous method in which droplets are continuously ejected and an on-demand method in which droplets are ejected in accordance with image information signals. There are a method for ejecting droplets, a method for generating bubbles in ink by discharging heat, a method for discharging droplets, a method using ultrasonic waves, and a method for attracting and discharging droplets by electrostatic force. As the ink for ink jet recording, water-based ink, oil-based ink, or solid (melted type) ink is used.

  For the colorant used in such ink for ink jet recording, the solvent has good solubility or dispersibility, high density recording is possible, hue is good, light, heat, environment It is robust against active gases (NOx, oxidizing gases such as ozone, SOx, etc.), has excellent fastness to water and chemicals, and has good fixability to image receiving materials and is difficult to bleed. The ink is required to have excellent storage stability, no toxicity, high purity, and availability at low cost.

In particular, it has a good black hue, is robust to light, humidity, and heat, has a high molar extinction coefficient, excellent storage stability, high text quality in document printing, and reduced bronze gloss. In addition, when printing on an image receiving material having an ink receiving layer containing porous white inorganic pigment particles, an ink composition that is robust against oxidizing gases such as ozone in the environment is strongly desired. ing.
Patent Documents 1 and 2 describe ink compositions containing an azo compound having a specific structure that can solve the above-described problems.

International Publication No. 2012/014954 International Publication No. 2012/014955

  The ink compositions described in Patent Documents 1 and 2 exhibit excellent performance as described above. However, the ink density is improved, and the bronze gloss in recorded images when various recording materials are used. A higher level of performance may be required for suppression.

  An object of the present invention is to provide an aqueous solution capable of providing an ink having a high printing density and excellent in suppressing bronze gloss in a recorded image when various recording materials are used. Also, an ink composition containing the aqueous solution, an ink for ink jet recording, an ink jet recording method using the ink for ink jet recording, an ink cartridge for ink jet recording filled with the ink for ink jet recording, and the ink for ink jet recording are used. The ink-jet recording material formed in this way.

The inventors have improved the solubility of the dye in water, thereby avoiding dye precipitation on the surface of the photographic paper, which causes suppression of bronze gloss, and avoiding loss of dye concentration due to an increase in the proportion of non-aggregates. I thought that the above problem could be solved. As a result of detailed studies, in a diazo compound having a specific structure having a thiophene ring or a thiazole ring substituted with a phenyl group between two azo groups, the phenyl group is meta-positioned to the thiophene ring or thiazole ring. It has been found that the above problems can be solved by substituting the acylamino group and improving the solubility in water.
That is, the said subject is achieved by the following means.

[1]
It contains (a) an antiseptic and (b) at least one azo compound represented by the following general formula (1) or a salt thereof, and the content of (b) is 1% by mass to 25% by mass. Aqueous solution.
General formula (1)

(In General Formula (1), G represents a nitrogen atom or —C (R ₁ ) ═. R ₁ represents a hydrogen atom, a sulfo group, a carboxy group, a substituted or unsubstituted carbamoyl group, or a cyano group. R ₂ represents a monovalent substituent, A represents a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, or a substituted or unsubstituted nitrogen-containing 5-membered or 6-membered heterocyclic group. (The nitrogen-containing 5-membered or 6-membered heterocyclic group may further have a condensed ring structure, and M independently represents a hydrogen atom or a monovalent counter cation.)
[2]
The aqueous solution according to [1], wherein the azo compound represented by the general formula (1) is an azo compound represented by the following general formula (2-1).
General formula (2-1)

(In General Formula (2-1), G ¹ represents a nitrogen atom or —C (CN) ═. A represents a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, or a substituted or unsubstituted group. Represents a nitrogen 5-membered or 6-membered heterocyclic group, and the nitrogen-containing 5-membered or 6-membered heterocyclic group may further have a condensed ring structure, and each M independently represents a hydrogen atom or a monovalent group. Represents the counter cation.)
[3]
The aqueous solution according to [1] or [2], wherein the azo compound represented by the general formula (1) or (2-1) is an azo compound represented by the following general formula (3-1).
Formula (3-1)

(In General Formula (3-1), G ¹ represents a nitrogen atom or —C (CN) ═. X ₁ , X ₂ , X ₃ , X ₄ , and X ₅ are each independently a hydrogen atom, or Represents a monovalent substituent, and each M independently represents a hydrogen atom or a monovalent counter cation.)
[4]
The aqueous solution according to [1] or [2], wherein the azo compound represented by the general formula (1) or (2-1) is an azo compound represented by the following general formula (4-1).
Formula (4-1)

(In General Formula (4-1), G ¹ represents a nitrogen atom or —C (CN) ═. Y ₁ , Y ₂ , Y ₃ , Y ₄ , Y ₅ , Y ₆ , and Y ₇ are each independent. Represents a hydrogen atom or a monovalent substituent, and each M independently represents a hydrogen atom or a monovalent counter cation.)
[5]
The aqueous solution according to [1] or [2], wherein the azo compound represented by the general formula (1) or (2-1) is an azo compound represented by the following general formula (5-1).
General formula (5-1)

(In General Formula (5-1), G ¹ represents a nitrogen atom or —C (CN) ═. Z ₁ , Z ₂ , Z ₃ , and Z ₄ are each independently a hydrogen atom or a monovalent group. Represents a substituent, and each M independently represents a hydrogen atom or a monovalent counter cation.)
[6]
The aqueous solution according to [1], wherein the azo compound represented by the general formula (1) is an azo compound represented by the following general formula (2-2).
General formula (2-2)

(In General Formula (2-2), G ¹ represents a nitrogen atom or —C (CN) ═. R ₁₁ , R ₁₂ , R ₁₃ , and R ₁₄ are each independently a hydrogen atom or a monovalent group. A represents a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, or a substituted or unsubstituted nitrogen-containing 5-membered or 6-membered heterocyclic group. The membered heterocyclic group may further have a condensed ring structure, and each M independently represents a hydrogen atom or a monovalent counter cation.)
[7]
The aqueous solution according to [1] or [6], wherein the azo compound represented by the general formula (1) or (2-2) is an azo compound represented by the following general formula (3-2).
Formula (3-2)

(In General Formula (3-2), G ¹ represents a nitrogen atom or —C (CN) ═. X ₁ , X ₂ , X ₃ , X ₄ , and X ₅ each independently represent a hydrogen atom, or R ₁₁ , R ₁₂ , R ₁₃ , and R ₁₄ each independently represents a hydrogen atom or a monovalent substituent, and M independently represents a hydrogen atom or a monovalent substituent. Represents the counter cation.)
[8]
The aqueous solution according to [1] or [6], wherein the azo compound represented by the general formula (1) or (2-2) is an azo compound represented by the following general formula (4-2).
Formula (4-2)

(In General Formula (4-2), G ¹ represents a nitrogen atom or —C (CN) ═. Y ₁ , Y ₂ , Y ₃ , Y ₄ , Y ₅ , Y ₆ , and Y ₇ are each independently R ₁₁ , R ₁₂ , R ₁₃ , and R ₁₄ each independently represents a hydrogen atom or a monovalent substituent, and M represents each independently a hydrogen atom. Or represents a monovalent counter cation.)
[9]
The aqueous solution according to [1] or [6], wherein the azo compound represented by the general formula (1) or (2-2) is an azo compound represented by the following general formula (5-2).
General formula (5-2)

(In General Formula (5-2), G ¹ represents a nitrogen atom or —C (CN) ═. Z ₁ , Z ₂ , Z ₃ , and Z ₄ are each independently a hydrogen atom or a monovalent group. R ₁₁ , R ₁₂ , R ₁₃ , and R ₁₄ each independently represent a hydrogen atom or a monovalent substituent, and M independently represents a hydrogen atom or a monovalent counter cation. Represents.)
[10]
The general formula (1), (2-1), (2-2), (3-1), (3-2), (4-1), (4-2), (5-1), or The aqueous solution according to any one of [1] to [9], wherein the azo compound represented by (5-2) has three or more ionic hydrophilic groups.
[11]
Furthermore, (c) The aqueous solution of any one of [1]-[10] containing a pH adjuster.
[12]
The aqueous solution according to any one of [1] to [11], which has a pH of 7.0 to 9.0 at 25 ° C.
[13]
An ink composition comprising the aqueous solution according to any one of [1] to [12].
[14]
An ink for ink jet recording containing the aqueous solution according to any one of [1] to [12] or the ink composition according to [13].
[15]
An ink jet recording method for forming a colored image on a recording material using the ink for ink jet recording according to [14].
[16]
An ink cartridge for ink jet recording filled with the ink for ink jet recording according to [14].
[17]
[14] An ink-jet recorded matter in which a colored image is formed on a recording material using the ink for ink-jet recording described in [14].
[18]
An azo compound represented by the following general formula (2-1) or a salt thereof.
General formula (2-1)

(In General Formula (2-1), G ¹ represents a nitrogen atom or —C (CN) ═. A represents a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, or a substituted or unsubstituted group. Represents a nitrogen 5-membered or 6-membered heterocyclic group, and the nitrogen-containing 5-membered or 6-membered heterocyclic group may further have a condensed ring structure, and each M independently represents a hydrogen atom or a monovalent group. Represents the counter cation.)
[19]
The azo compound or a salt thereof according to [18], wherein the general formula (2-1) is represented by the following general formula (3-1).
Formula (3-1)

(In General Formula (3-1), G ¹ represents a nitrogen atom or —C (CN) ═. X ₁ , X ₂ , X ₃ , X ₄ , and X ₅ are each independently a hydrogen atom, or Represents a monovalent substituent, and each M independently represents a hydrogen atom or a monovalent counter cation.)
[20]
The azo compound or a salt thereof according to [18], wherein the general formula (2-1) is represented by the following general formula (4-1).
Formula (4-1)

(In General Formula (4-1), G ¹ represents a nitrogen atom or —C (CN) ═. Y ₁ , Y ₂ , Y ₃ , Y ₄ , Y ₅ , Y ₆ , and Y ₇ are each independent. Represents a hydrogen atom or a monovalent substituent, and each M independently represents a hydrogen atom or a monovalent counter cation.)
[21]
The azo compound or a salt thereof according to [18], wherein the general formula (2-1) is represented by the following general formula (5-1).
General formula (5-1)

(In General Formula (5-1), G ¹ represents a nitrogen atom or —C (CN) ═. Z ₁ , Z ₂ , Z ₃ , and Z ₄ are each independently a hydrogen atom or a monovalent group. Represents a substituent, and each M independently represents a hydrogen atom or a monovalent counter cation.)
[22]
An azo compound represented by the following general formula (2-2) or a salt thereof.
General formula (2-2)

(In General Formula (2-2), G ¹ represents a nitrogen atom or —C (CN) ═. R ₁₁ , R ₁₂ , R ₁₃ , and R ₁₄ are each independently a hydrogen atom or a monovalent group. A represents a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, or a substituted or unsubstituted nitrogen-containing 5-membered or 6-membered heterocyclic group. The membered heterocyclic group may further have a condensed ring structure, and each M independently represents a hydrogen atom or a monovalent counter cation.)
[23]
The azo compound or a salt thereof according to [22], wherein the general formula (2-2) is represented by the following general formula (3-2).
Formula (3-2)

(In General Formula (3-2), G ¹ represents a nitrogen atom or —C (CN) ═. X ₁ , X ₂ , X ₃ , X ₄ , and X ₅ each independently represent a hydrogen atom, or R ₁₁ , R ₁₂ , R ₁₃ , and R ₁₄ each independently represents a hydrogen atom or a monovalent substituent, and M independently represents a hydrogen atom or a monovalent substituent. Represents the counter cation.)
[24]
The azo compound or a salt thereof according to [22], wherein the general formula (2-2) is represented by the following general formula (4-2).
Formula (4-2)

(In General Formula (4-2), G ¹ represents a nitrogen atom or —C (CN) ═. Y ₁ , Y ₂ , Y ₃ , Y ₄ , Y ₅ , Y ₆ , and Y ₇ are each independently R ₁₁ , R ₁₂ , R ₁₃ , and R ₁₄ each independently represents a hydrogen atom or a monovalent substituent, and M represents each independently a hydrogen atom. Or represents a monovalent counter cation.)
[25]
The azo compound or a salt thereof according to [22], wherein the general formula (2-2) is represented by the following general formula (5-2).
General formula (5-2)

(In General Formula (5-2), G ¹ represents a nitrogen atom or —C (CN) ═. Z ₁ , Z ₂ , Z ₃ , and Z ₄ are each independently a hydrogen atom or a monovalent group. R ₁₁ , R ₁₂ , R ₁₃ , and R ₁₄ each independently represent a hydrogen atom or a monovalent substituent, and M independently represents a hydrogen atom or a monovalent counter cation. Represents.)

  According to the present invention, it is possible to provide an ink having a high print density and excellent in suppressing bronze gloss in a recorded image when various recording materials are used.

The present invention is described in detail below.
First, in the present invention, the substituent group A ′, the substituent group J, the ionic hydrophilic group, and Hammett's substituent constant σp value are defined.

(Substituent group A ′)
C1-C12 linear or branched alkyl group, C7-C18 linear or branched aralkyl group, C2-C12 linear or branched alkenyl group, C2-C12 linear Or a branched alkynyl group, a C3-C12 cycloalkyl group, a C3-C12 cycloalkenyl group (for example, methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, sec-butyl) , T-butyl, 2-ethylhexyl, 2-methylsulfonylethyl, 3-phenoxypropyl, trifluoromethyl, cyclopentyl), halogen atom (for example, chlorine atom, bromine atom), aryl group (for example, phenyl, 4-t- Butylphenyl, 2,4-di-t-amylphenyl), heterocyclic groups (eg imidazolyl, pyrazolyl, triazolyl, 2-furyl, 2-thiol) Nyl, 2-pyrimidinyl, 2-benzothiazolyl), cyano group, hydroxyl group, nitro group, carboxy group, amino group, alkyloxy group (for example, methoxy, ethoxy, 2-methoxyethoxy, 2-methylsulfonylethoxy), aryloxy Groups (for example, phenoxy, 2-methylphenoxy, 4-t-butylphenoxy, 3-nitrophenoxy, 3-t-butyloxycarbonylphenoxy, 3-methoxycarbonylphenyloxy, acylamino groups (for example, acetamide, benzamide, 4- (3-t-butyl-4-hydroxyphenoxy) butanamide), alkylamino groups (eg methylamino, butylamino, diethylamino, methylbutylamino), arylamino groups (eg phenylamino, 2-chloroanilino) Ureido group (for example, phenylureido, methylureido, N, N-dibutylureido), sulfamoylamino group (for example, N, N-dipropylsulfamoylamino), alkylthio group (for example, methylthio, octylthio, 2- Phenoxyethylthio), arylthio groups (eg phenylthio, 2-butoxy-5-t-octylphenylthio, 2-carboxyphenylthio), alkyloxycarbonylamino groups (eg methoxycarbonylamino), alkylsulfonylamino groups and aryls A sulfonylamino group (eg, methylsulfonylamino, phenylsulfonylamino, p-toluenesulfonylamino), a carbamoyl group (eg, N-ethylcarbamoyl, N, N-dibutylcarbamoyl), a sulfamoyl group (eg, For example, N-ethylsulfamoyl, N, N-dipropylsulfamoyl, N-phenylsulfamoyl), sulfonyl group (for example, methylsulfonyl, octylsulfonyl, phenylsulfonyl, p-toluenesulfonyl), alkyloxycarbonyl group (For example, methoxycarbonyl, butyloxycarbonyl), heterocyclic oxy group (for example, 1-phenyltetrazol-5-oxy, 2-tetrahydropyranyloxy), azo group (for example, phenylazo, 4-methoxyphenylazo, 4- Pivaloylaminophenylazo, 2-hydroxy-4-propanoylphenylazo), acyloxy group (for example, acetoxy), carbamoyloxy group (for example, N-methylcarbamoyloxy, N-phenylcarbamoyloxy), silyloxy group For example, trimethylsilyloxy, dibutylmethylsilyloxy), aryloxycarbonylamino group (for example, phenoxycarbonylamino), imide group (for example, N-succinimide, N-phthalimide), heterocyclic thio group (for example, 2-benzothiazolyl) Ruthio, 2,4-di-phenoxy-1,3,5-triazole-6-thio, 2-pyridylthio), sulfinyl group (eg 3-phenoxypropylsulfinyl), phosphonyl group (eg phenoxyphosphonyl, octyloxy) Phosphonyl, phenylphosphonyl), aryloxycarbonyl group (for example, phenoxycarbonyl), acyl group (for example, acetyl, 3-phenylpropanoyl, benzoyl), ionic hydrophilic group (carboxyl group, sulfo group, etc.) Be These substituents may be further substituted, and examples of the further substituent include groups selected from the substituent group A ′ described above.

(Substituent group J)
For example, halogen atom, alkyl group, aralkyl group, alkenyl group, alkynyl group, aryl group, heterocyclic group, cyano group, hydroxyl group, nitro group, alkoxy group, aryloxy group, silyloxy group, heterocyclic oxy group, acyloxy group , Carbamoyloxy group, alkoxycarbonyloxy group, aryloxycarbonyloxy group, amino group, acylamino group, aminocarbonylamino group, alkoxycarbonylamino group, aryloxycarbonylamino group, sulfamoylamino group, alkyl or arylsulfonylamino group , Mercapto group, alkylthio group, arylthio group, heterocyclic thio group, sulfamoyl group, alkyl or arylsulfinyl group, alkyl or arylsulfonyl group, acyl group, aryloxycarboni Examples include groups, alkoxycarbonyl groups, carbamoyl groups, aryl or heterocyclic azo groups, imide groups, phosphino groups, phosphinyl groups, phosphinyloxy groups, phosphinylamino groups, silyl groups, and ionic hydrophilic groups. . These substituents may be further substituted, and examples of the further substituent include a group selected from the substituent group J described above.

  More specifically, examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom.

  Examples of the alkyl group include linear, branched, and cyclic substituted or unsubstituted alkyl groups, and include cycloalkyl groups, bicycloalkyl groups, and tricyclo structures having many ring structures. An alkyl group (for example, an alkyl group of an alkoxy group or an alkylthio group) in a substituent described below also represents such an alkyl group. Specifically, the alkyl group is preferably an alkyl group having 1 to 30 carbon atoms, for example, methyl group, ethyl group, n-propyl group, i-propyl group, t-butyl group, n-octyl group, eicosyl. Group, 2-chloroethyl group, 2-cyanoethyl group, 2-ethylhexyl group and the like, and the cycloalkyl group is preferably a substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms such as cyclohexyl group, A cyclopentyl group, 4-n-dodecylcyclohexyl group and the like. The bicycloalkyl group is preferably a substituted or unsubstituted bicycloalkyl group having 5 to 30 carbon atoms, that is, a bicycloalkane having 5 to 30 carbon atoms. Monovalent groups from which one hydrogen atom has been removed, for example, bicyclo [1,2,2] heptan-2-yl group, bicycl [2,2,2] octan-3-yl group.

  Examples of the aralkyl group include a substituted or unsubstituted aralkyl group, and the substituted or unsubstituted aralkyl group is preferably an aralkyl group having 7 to 30 carbon atoms. For example, a benzyl group and a 2-phenethyl group can be mentioned.

  Examples of the alkenyl group include linear, branched, and cyclic substituted or unsubstituted alkenyl groups, and include cycloalkenyl groups and bicycloalkenyl groups. Specifically, the alkenyl group is preferably a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, such as a vinyl group, an allyl group, a prenyl group, a geranyl group, an oleyl group, and the like. Is preferably a substituted or unsubstituted cycloalkenyl group having 3 to 30 carbon atoms, that is, a monovalent group obtained by removing one hydrogen atom of a cycloalkene having 3 to 30 carbon atoms, such as 2-cyclopentene-1 -Yl group, 2-cyclohexen-1-yl group and the like, and as the bicycloalkenyl group, a substituted or unsubstituted bicycloalkenyl group, preferably a substituted or unsubstituted bicycloalkenyl group having 5 to 30 carbon atoms, That is, a monovalent group obtained by removing one hydrogen atom of a bicycloalkene having one double bond, for example, bicyclo [2 2,1] hept-2-en-1-yl group, a bicyclo [2,2,2] oct-2-en-4-yl group and the like.

  The alkynyl group is preferably a substituted or unsubstituted alkynyl group having 2 to 30 carbon atoms such as an ethynyl group, a propargyl group, and a trimethylsilylethynyl group.

  The aryl group is preferably a substituted or unsubstituted aryl group having 6 to 30 carbon atoms, such as a phenyl group, a p-tolyl group, a naphthyl group, an m-chlorophenyl group, an o-hexadecanoylaminophenyl group, and the like. Can be mentioned.

  The heterocyclic group is preferably a monovalent group obtained by removing one hydrogen atom from a 5- or 6-membered substituted or unsubstituted aromatic or non-aromatic heterocyclic compound, and more preferably a carbon number. Examples thereof include 3 to 30 5- or 6-membered aromatic heterocyclic groups such as 2-furyl group, 2-thienyl group, 2-pyrimidinyl group, and 2-benzothiazolyl group.

  The alkoxy group is preferably a substituted or unsubstituted alkoxy group having 1 to 30 carbon atoms, such as a methoxy group, an ethoxy group, an isopropoxy group, a t-butoxy group, an n-octyloxy group, or a 2-methoxyethoxy group. Etc.

  The aryloxy group is preferably a substituted or unsubstituted aryloxy group having 6 to 30 carbon atoms, such as a phenoxy group, 2-methylphenoxy group, 4-t-butylphenoxy group, 3-nitrophenoxy group, 2 -Tetradecanoylaminophenoxy group etc. are mentioned.

  Preferred examples of the silyloxy group include substituted or unsubstituted silyloxy groups having 0 to 20 carbon atoms such as a trimethylsilyloxy group and a diphenylmethylsilyloxy group.

  Preferred examples of the heterocyclic oxy group include substituted or unsubstituted heterocyclic oxy groups having 2 to 30 carbon atoms, such as a 1-phenyltetrazole-5-oxy group and a 2-tetrahydropyranyloxy group.

  The acyloxy group is preferably a formyloxy group, a substituted or unsubstituted alkylcarbonyloxy group having 2 to 30 carbon atoms, a substituted or unsubstituted arylcarbonyloxy group having 6 to 30 carbon atoms, such as an acetyloxy group, Examples include a pivaloyloxy group, a stearoyloxy group, a benzoyloxy group, and a p-methoxyphenylcarbonyloxy group.

  The carbamoyloxy group is preferably a substituted or unsubstituted carbamoyloxy group having 1 to 30 carbon atoms, such as N, N-dimethylcarbamoyloxy group, N, N-diethylcarbamoyloxy group, morpholinocarbonyloxy group, N , N-di-n-octylaminocarbonyloxy group, Nn-octylcarbamoyloxy group and the like.

  The alkoxycarbonyloxy group is preferably a substituted or unsubstituted alkoxycarbonyloxy group having 2 to 30 carbon atoms, such as a methoxycarbonyloxy group, an ethoxycarbonyloxy group, a t-butoxycarbonyloxy group, or an n-octylcarbonyloxy group. Etc.

  The aryloxycarbonyloxy group is preferably a substituted or unsubstituted aryloxycarbonyloxy group having 7 to 30 carbon atoms, such as phenoxycarbonyloxy group, p-methoxyphenoxycarbonyloxy group, pn-hexadecyloxy. Examples include phenoxycarbonyloxy group.

  The amino group includes an alkylamino group, an arylamino group, and a heterocyclic amino group, preferably an amino group, a substituted or unsubstituted alkylamino group having 1 to 30 carbon atoms, a substituted or unsubstituted group having 6 to 30 carbon atoms. Examples of the substituted anilino group include a methylamino group, a dimethylamino group, an anilino group, an N-methyl-anilino group, a diphenylamino group, and a triazinylamino group.

  The acylamino group is preferably a formylamino group, a substituted or unsubstituted alkylcarbonylamino group having 1 to 30 carbon atoms, a substituted or unsubstituted arylcarbonylamino group having 6 to 30 carbon atoms, such as an acetylamino group, Examples include pivaloylamino group, lauroylamino group, benzoylamino group, 3,4,5-tri-n-octyloxyphenylcarbonylamino group, and the like.

  The aminocarbonylamino group is preferably a substituted or unsubstituted aminocarbonylamino group having 1 to 30 carbon atoms, such as a carbamoylamino group, N, N-dimethylaminocarbonylamino group, or N, N-diethylaminocarbonylamino group. And a morpholinocarbonylamino group.

  The alkoxycarbonylamino group is preferably a substituted or unsubstituted alkoxycarbonylamino group having 2 to 30 carbon atoms, such as methoxycarbonylamino group, ethoxycarbonylamino group, t-butoxycarbonylamino group, n-octadecyloxycarbonylamino. Group, N-methyl-methoxycarbonylamino group and the like.

  The aryloxycarbonylamino group is preferably a substituted or unsubstituted aryloxycarbonylamino group having 7 to 30 carbon atoms, such as phenoxycarbonylamino group, p-chlorophenoxycarbonylamino group, mn-octyloxyphenoxy. Examples thereof include a carbonylamino group.

  The sulfamoylamino group is preferably a substituted or unsubstituted sulfamoylamino group having 0 to 30 carbon atoms, such as a sulfamoylamino group, N, N-dimethylaminosulfonylamino group, Nn- Examples include octylaminosulfonylamino group.

The alkyl or arylsulfonylamino group is preferably a substituted or unsubstituted alkylsulfonylamino group having 1 to 30 carbon atoms, a substituted or unsubstituted arylsulfonylamino group having 6 to 30 carbon atoms, such as a methylsulfonylamino group. Butylsulfonylamino group, phenylsulfonylamino group, 2,3,5-trichlorophenylsulfonylamino group, p-methylphenylsulfonylamino group, and the like.
Preferred examples of the alkylthio group include substituted or unsubstituted alkylthio groups having 1 to 30 carbon atoms, such as a methylthio group, an ethylthio group, and an n-hexadecylthio group.

  Preferred examples of the arylthio group include substituted or unsubstituted arylthio groups having 6 to 30 carbon atoms such as a phenylthio group, a p-chlorophenylthio group, and an m-methoxyphenylthio group.

  Preferred examples of the heterocyclic thio group include substituted or unsubstituted heterocyclic thio groups having 2 to 30 carbon atoms, such as a 2-benzothiazolylthio group and a 1-phenyltetrazol-5-ylthio group.

  The sulfamoyl group is preferably a substituted or unsubstituted sulfamoyl group having 0 to 30 carbon atoms, such as N-ethylsulfamoyl group, N- (3-dodecyloxypropyl) sulfamoyl group, N, N-dimethylsulfuryl group. Examples include a famoyl group, an N-acetylsulfamoyl group, an N-benzoylsulfamoyl group, and an N- (N′-phenylcarbamoyl) sulfamoyl group.

  The alkyl or arylsulfinyl group is preferably a substituted or unsubstituted alkylsulfinyl group having 1 to 30 carbon atoms, a substituted or unsubstituted arylsulfinyl group having 6 to 30 carbon atoms, such as a methylsulfinyl group, an ethylsulfinyl group, phenyl. Examples thereof include a sulfinyl group and a p-methylphenylsulfinyl group.

  The alkyl or arylsulfonyl group is preferably a substituted or unsubstituted alkylsulfonyl group having 1 to 30 carbon atoms, a substituted or unsubstituted arylsulfonyl group having 6 to 30 carbon atoms, such as a methylsulfonyl group, an ethylsulfonyl group, or a phenyl group. A sulfonyl group, p-methylphenylsulfonyl group, etc. are mentioned.

  The acyl group is preferably a formyl group, a substituted or unsubstituted alkylcarbonyl group having 2 to 30 carbon atoms, a substituted or unsubstituted arylcarbonyl group having 7 to 30 carbon atoms, a substituted or unsubstituted group having 2 to 30 carbon atoms. Heterocyclic carbonyl groups bonded to carbonyl groups at substituted carbon atoms, such as acetyl, pivaloyl, 2-chloroacetyl, stearoyl, benzoyl, pn-octyloxyphenylcarbonyl, 2-pyridyl Examples thereof include a carbonyl group and a 2-furylcarbonyl group.

  The aryloxycarbonyl group is preferably a substituted or unsubstituted aryloxycarbonyl group having 7 to 30 carbon atoms, such as phenoxycarbonyl group, o-chlorophenoxycarbonyl group, m-nitrophenoxycarbonyl group, pt- A butylphenoxycarbonyl group etc. are mentioned.

  The alkoxycarbonyl group is preferably a substituted or unsubstituted alkoxycarbonyl group having 2 to 30 carbon atoms, such as a methoxycarbonyl group, an ethoxycarbonyl group, a t-butoxycarbonyl group, and an n-octadecyloxycarbonyl group.

  The carbamoyl group is preferably a substituted or unsubstituted carbamoyl group having 1 to 30 carbon atoms, such as a carbamoyl group, an N-methylcarbamoyl group, an N, N-dimethylcarbamoyl group, or an N, N-di-n-octyl group. Examples thereof include a carbamoyl group and an N- (methylsulfonyl) carbamoyl group.

  The aryl or heterocyclic azo group is preferably a substituted or unsubstituted arylazo group having 6 to 30 carbon atoms, a substituted or unsubstituted heterocyclic azo group having 3 to 30 carbon atoms, such as phenylazo, p-chlorophenylazo, 5-ethylthio-1,3,4-thiadiazol-2-ylazo and the like.

  Preferred examples of the imide group include an N-succinimide group and an N-phthalimide group.

  The phosphino group is preferably a substituted or unsubstituted phosphino group having 0 to 30 carbon atoms, such as a dimethylphosphino group, a diphenylphosphino group, a methylphenoxyphosphino group, and the like.

  The phosphinyl group is preferably a substituted or unsubstituted phosphinyl group having 0 to 30 carbon atoms, such as a phosphinyl group, a dioctyloxyphosphinyl group, a diethoxyphosphinyl group, and the like.

  Preferred examples of the phosphinyloxy group include substituted or unsubstituted phosphinyloxy groups having 0 to 30 carbon atoms such as a diphenoxyphosphinyloxy group and a dioctyloxyphosphinyloxy group.

  The phosphinylamino group is preferably a substituted or unsubstituted phosphinylamino group having 0 to 30 carbon atoms, such as a dimethoxyphosphinylamino group or a dimethylaminophosphinylamino group.

  Preferred examples of the silyl group include substituted or unsubstituted silyl groups having 0 to 30 carbon atoms such as a trimethylsilyl group, a t-butyldimethylsilyl group, and a phenyldimethylsilyl group.

(Ionic hydrophilic group)
A sulfo group, a carboxyl group, a thiocarboxyl group, a sulfino group, a phosphono group, a dihydroxyphosphino group and the like can be mentioned. Particularly preferred are a sulfo group and a carboxyl group. The carboxyl group, phosphono group and sulfo group may be in the form of a salt. Examples of counter cations that form a salt include ammonium ion, alkali metal ion (eg, lithium ion, sodium ion, potassium ion) and organic. Cation (eg, tetramethylammonium ion, tetramethylguanidinium ion, tetramethylphosphonium) is included, lithium salt, sodium salt, potassium salt, ammonium salt is preferable, lithium salt or mixed salt containing lithium salt as a main component Are more preferred, and lithium salts are most preferred.

The counter cation (monovalent counter cation) of the ionic hydrophilic group contained in the azo compound of the present invention preferably contains lithium ions as a main component. The counter cations may not be all lithium ions, but the lithium ion concentration in each of the ink compositions is preferably 50% by mass or more, more preferably based on the total counter cations in each ink composition. Is 75% by mass or more, more preferably 80% by mass, and particularly preferably 95% by mass or more.
Under such conditions, hydrogen ions, alkali metal ions (for example, sodium ions, potassium ions), alkaline earth metal ions (for example, magnesium ions, calcium ions, etc.), quaternary ammonium ions, quaternary phosphoniums Ions, sulfonium ions, and the like can be included as counter cations.

About the kind and ratio of the counter cation of the colorant, “New Experimental Chemistry Course 9” edited by the Chemical Society of Japan
Analytical Chemistry "(1977 Maruzen) and the Chemical Society of Japan" 4th edition Experimental Chemistry Course 15 Analysis "(1991 Maruzen) describes various theories about analytical methods and elements, so refer to them for analysis. The method can be selected, analyzed and quantified, among which it is easy to determine by an analytical method such as ion chromatography, atomic absorption, inductively coupled plasma emission spectrometry (ICP).
As a method for obtaining the colorant of the present invention in which the counter cation contains lithium ions, any method may be used. For example, (1) a method of converting a counter cation from another cation to lithium ions using an ion exchange resin, (2) a method of acid precipitation or salting out from a system containing lithium ions, and (3) a counter cation of lithium ions A method of forming a colorant using a raw material and a synthetic intermediate, and (4) a method of introducing an ionic hydrophilic group by functional group conversion of each colorant using a reactive agent whose counter cation is a lithium ion (5) A compound in which the counter cation of the ionic hydrophilic group in the colorant is a silver ion is synthesized, and this is reacted with a lithium halide solution to remove the precipitated silver halide. The method of making it.

The ionic hydrophilic group in each colorant may be any as long as it is an ionic dissociation group. Preferred ionic hydrophilic groups include a sulfo group (may be a salt), a carboxyl group (may be a salt), a hydroxyl group (may be a salt), a phosphono group (may be a salt), a quaternary ammonium group, and an acylsulfamoyl group. (May be a salt), a sulfonylcarbamoyl group (may be a salt), a sulfonylsulfamoyl group (may be a salt), and the like.
A sulfo group, a carboxyl group, or a hydroxyl group (including salts thereof) is preferable. When the ionic hydrophilic group is a salt, a preferable counter cation is lithium or a mixed salt of an alkali metal (for example, sodium, potassium), ammonium, and an organic cation (for example, pyridinium, tetramethylammonium, guanidinium) based on lithium. Among them, lithium or an alkali metal mixed salt containing lithium as a main component is preferable, and a lithium salt of a sulfo group and a lithium salt of a carboxy group are particularly preferable.

(Hammett's substituent constant σp value)
Hammett's substituent constant σp value used in this specification will be described.
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 concerning this invention is not a benzene derivative, (sigma) p value is used as a scale which shows the electronic effect of a substituent irrespective of a substitution position. In the present invention, the σp value will be used in this sense.

  In the present invention, when the compound is a salt, the salt is dissociated into ions in the aqueous solution and the ink composition, but it is expressed as “contains a salt” for convenience.

<Aqueous solution>
The aqueous solution of the present invention contains (a) a preservative and (b) at least one azo compound represented by the general formula (1) or a salt thereof, and the content of (b) is 1% by mass to 25% by mass.

[(A) Preservative]
In the aqueous solution, generation of insoluble matter due to decay may be a problem. In order to prevent this, a preservative is added to the aqueous solution of the present invention.
Various preservatives that can be used in the present invention can be used.
Examples of the preservative include inorganic preservatives (such as silver ion-containing substances) and salts containing heavy metal ions. Organic preservatives include quaternary ammonium salts (tetrabutylammonium chloride, cetylpyridinium chloride, benzyltrimethylammonium chloride, etc.), phenol derivatives (phenol, cresol, butylphenol, xylenol, bisphenol, etc.), phenoxyether derivatives (phenoxyethanol) Etc.), heterocyclic compounds (benzotriazole, proxel, 1,2-benzisothiazolin-3-one, etc.), acid amides, carbamic acid, carbamates, amidine / guanidine, pyridines (sodium pyridinethione- 1-oxide, etc.), diazines, triazines, pyrrole / imidazoles, oxazoles / oxazines, thiazoles / thiadiazines, thioureas, thiosemicarbazides , Dithiocarbamates, sulfides, sulfoxides, sulfones, sulfamides, antibiotics (penicillin, tetracycline, etc.), sodium dehydroacetate, sodium benzoate, ethyl p-hydroxybenzoate, and salts thereof Can be used. In addition, as the antiseptic, those described in the antibacterial and microscopic handbook (Technical Hall: 1986), the antibacterial and antifungal encyclopedia (edited by the Japanese Society for Antibacterial and Antifungal Society), etc. can be used.
As a preservative, a phenol derivative and a heterocyclic compound are preferable, a heterocyclic compound is more preferable, and a heterocyclic compound (Proxel XL-II, Proxel GXL (S)) is further preferable.
Preservatives can be added singly or in combination of two or more. Various preservatives such as oil-soluble structures and water-soluble structures can be used, but water-soluble preservatives are preferred.
Among these, it is preferable that at least one preservative is a heterocyclic compound. In the present invention, when two or more kinds of preservatives are used in combination, the effect of the present invention is more satisfactorily exhibited. For example, the combination of a heterocyclic compound and an antibiotic, the combination of a heterocyclic compound and a phenol derivative, etc. are mentioned preferably. The content ratio when combining two kinds of preservatives is not particularly limited, but the range of preservative A (heterocyclic compound) / preservative B (phenol derivative) = 0.01 to 100 (mass ratio) is included. preferable.
Although the addition amount of the preservative to the aqueous solution can be used within a wide range, it is preferably 0.001 to 10% by mass, more preferably 0.1 to 5% by mass. By setting the content of the preservative within the above range, there is an effect of suppressing the growth of bacteria in the aqueous solution.

[(B) Azo compound represented by formula (1)]
The azo compound represented by the general formula (1) (hereinafter sometimes referred to as “compound represented by the general formula (1)”) will be described.
General formula (1)

(In General Formula (1), G represents a nitrogen atom or —C (R ₁ ) ═. R ₁ represents a hydrogen atom, a sulfo group, a carboxy group, a substituted or unsubstituted carbamoyl group, or a cyano group. R ₂ represents a monovalent substituent, A represents a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, or a substituted or unsubstituted nitrogen-containing 5-membered or 6-membered heterocyclic group. (The nitrogen-containing 5-membered or 6-membered heterocyclic group may further have a condensed ring structure, and M independently represents a hydrogen atom or a monovalent counter cation.)

G in the general formula (1) represents a nitrogen atom or —C (R ₁ ) ═. R ₁ represents a hydrogen atom, a sulfo group, a carboxy group, a substituted or unsubstituted carbamoyl group, or a cyano group. When the carbamoyl group has a substituent, the substituent is an alkyl group (preferably having 1 to 4 carbon atoms). And more preferably a methyl group, an ethyl group) and an aryl group (preferably an aryl group having 6 to 10 carbon atoms, more preferably a phenyl group). R ₁ is preferably a carboxy group, a carbamoyl group, or a cyano group, more preferably a carbamoyl group or a cyano group, and most preferably a cyano group.
From the viewpoint of light resistance and ozone gas resistance, G preferably represents a nitrogen atom or —C (CN) ═.

M in the general formula (1) independently represents a hydrogen atom or a monovalent counter cation. Examples of the monovalent counter cation include ammonium ion, alkali metal ion (eg, lithium ion, sodium ion, potassium ion) and organic cation (eg, tetramethylammonium ion, tetramethylguanidinium ion, tetramethylphosphonium). Is mentioned.
From the viewpoint of suppressing bronze gloss, M preferably represents a monovalent counter cation, more preferably represents an alkali metal ion, and still more preferably represents a lithium ion, a sodium ion or a potassium ion.

In the present invention, the compound represented by the general formula (1) may be in the form of a salt, and the salt formed is preferably a lithium salt, sodium salt, potassium salt or ammonium salt, such as lithium salt, sodium salt. Further preferred are salts or potassium salts. Furthermore, the salt formed may be a single salt or a mixed salt.
When the azo compound represented by the general formula (1) is a mixed salt, a mixed salt of a lithium salt and a sodium salt from the viewpoint of solubility in water, viscosity of an aqueous solution, surface tension, and storage stability of a high concentration aqueous solution, A mixed salt of a lithium salt and a potassium salt, a mixed salt of a sodium salt and a potassium salt, a lithium salt, a sodium salt, or a mixed salt of a potassium salt is preferable, and M in the general formula (1) is a lithium ion, a sodium ion, Alternatively, an embodiment in which potassium ions are mixed may be an embodiment in which compounds in which all M in the general formula (1) represent lithium ions, sodium ions, or potassium ions are mixed.
The ratio of cations of the mixed salt can be measured by ion chromatography analysis.

R ₂ in the general formula (1) represents a monovalent substituent. Examples of the monovalent substituent represented by R ₂ include a substituent selected from the above substituent group A ′. From the viewpoint of suppressing bronze gloss, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, Alternatively, a substituted or unsubstituted heterocyclic group is preferable, and a substituted or unsubstituted alkyl group or a substituted or unsubstituted aryl group is more preferable. As said alkyl group, a C1-C6 alkyl group is preferable, a C1-C4 alkyl group is more preferable, a methyl group, an ethyl group, and n-propyl group are still more preferable, and an ethyl group is especially preferable. As said aryl group, a C6-C10 aryl group is preferable, a phenyl group and a naphthyl group are more preferable, and a phenyl group is further more preferable. As the heterocyclic group, a pyridyl group is preferable.
In the case where the alkyl group, aryl group, or heterocyclic group has a substituent, examples of the substituent include a monovalent substituent, and an ionic hydrophilic group, an arylamino group, and an alkylamino group are preferable. -SO ₃ M or -CO ₂ M (M represents a hydrogen atom or a monovalent counter cation, specific examples and preferred ranges are the same as those described above) are more preferable, and -CO ₂ M is particularly preferable. .
R ₂ is particularly preferably an alkyl group having —CO ₂ M as a substituent, or a phenyl group having —CO ₂ M as a substituent at least in the ortho position.
Specific preferred examples of R ₂ are shown below, but the invention is not limited thereto. In the following specific examples, * represents a bond.

A in the general formula (1) represents a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, or a substituted or unsubstituted nitrogen-containing 5-membered or 6-membered heterocyclic group. The nitrogen-containing 5-membered or 6-membered heterocyclic group may further have a condensed ring structure.
In the case where A represents a nitrogen-containing 5-membered or 6-membered heterocyclic group, the nitrogen-containing 5-membered or 6-membered heterocyclic group includes one from a 5-membered aromatic or non-aromatic heterocyclic compound. A monovalent group from which a hydrogen atom has been removed is preferred, and a 5-membered aromatic heterocyclic group having 2 to 4 carbon atoms is more preferred. Examples of the nitrogen-containing 5-membered heterocyclic group include a pyrrole ring, a pyrazole ring, an imidazole ring, a triazole ring, a thiazole ring, an isothiazole ring, a thiadiazole ring, an oxazole ring, and a thiazole ring. Is preferred. Examples of the nitrogen-containing 6-membered heterocyclic group include a pyridine ring, a pyrazine ring, a pyrimidine ring, and a triazine ring when the substitution position is not limited.
The nitrogen-containing 5-membered or 6-membered heterocyclic group may further have a condensed ring structure, and preferably a benzene ring may be condensed. A having a condensed ring structure is preferably a benzothiazole ring.

When the phenyl group, naphthyl group, or nitrogen-containing 5-membered or 6-membered heterocyclic group represented by A has a substituent, examples of the substituent include a substituent selected from the above substituent group J, and ionic hydrophilicity Or an electron-attracting group having a σp value of 0.3 or more is preferable, a halogen atom (preferably a chlorine atom), a nitro group, —SO ₃ M or —CO ₂ M (M is a hydrogen atom or a monovalent group) The specific examples and preferred ranges thereof are the same as those described above.
Specific examples of the electron withdrawing group having a Hammett σp value of 0.3 or more include an acyl group, an acyloxy group, a carbamoyl group, an alkyloxycarbonyl group, an aryloxycarbonyl group, a cyano group, a nitro group, and a dialkylphosphono group. Group, diarylphosphono group, diarylphosphinyl group, alkylsulfinyl group, arylsulfinyl group, alkylsulfonyl group, arylsulfonyl group, sulfonyloxy group, acylthio group, sulfamoyl group, thiocyanate group, thiocarbonyl group, halogenated alkyl group , Halogenated alkoxy groups, halogenated aryloxy groups, halogenated alkylamino groups, halogenated alkylthio groups, aryl groups substituted with other electron withdrawing groups with a σp value of 0.3 or more, nitro groups, heterocycles Group, halogen atom, azo group, or Examples include selenocyanate groups. A cyano group, a methylsulfonyl group, a phenylsulfonyl group, a methoxycarbonyl group, a carbamoyl group, and a nitro group are preferable, and a cyano group, a methylsulfonyl group, and a nitro group are more preferable. If the σp value is an electron withdrawing group in this range, the hue of the azo compound can be adjusted, light fastness and ozone gas fastness can be improved, and an effect can be obtained in that it is used as a water-soluble dye for inkjet recording black ink. Can do. The upper limit of Hammett's substituent constant σp value is preferably an electron withdrawing group of 1.0 or less.

  Although the preferable specific example of A is shown below, it is not limited to these. In the following specific examples, * represents a bond.

  The compound represented by the general formula (1) is also preferably a compound represented by the following general formula (2-1).

Hereinafter, the compound represented by formula (2-1) or a salt thereof will be described in detail.
General formula (2-1)

(In General Formula (2-1), G ¹ represents a nitrogen atom or —C (CN) ═. A represents a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, or a substituted or unsubstituted group. Represents a nitrogen 5-membered or 6-membered heterocyclic group, and the nitrogen-containing 5-membered or 6-membered heterocyclic group may further have a condensed ring structure, and each M independently represents a hydrogen atom or a monovalent group. Represents the counter cation.)

  Examples of A and M in the general formula (2-1) are independently the same as examples of A and M in the general formula (1), and preferred examples are also the same.

The compound represented by the general formula (1) or (2-1) is preferably a compound represented by the following general formula (3-1).
Hereinafter, the compound represented by Formula (3-1) or a salt thereof will be described in detail.
Formula (3-1)

(In General Formula (3-1), G ¹ represents a nitrogen atom or —C (CN) ═. X ₁ , X ₂ , X ₃ , X ₄ , and X ₅ are each independently a hydrogen atom, or Represents a monovalent substituent, and each M independently represents a hydrogen atom or a monovalent counter cation.)

  Examples of M in the general formula (3-1) are each independently the same as the examples of M in the general formula (2-1), and preferred examples are also the same.

In General Formula (3-1), X ₁ , X ₂ , X ₃ , X ₄ , and X ₅ each independently represent a hydrogen atom or a monovalent substituent. Examples of the substituent when X ₁ , X ₂ , X ₃ , X ₄ , and X ₅ represent a monovalent substituent include groups selected from the above substituent group J.
X ₁ , X ₂ , X ₃ , X ₄ and X ₅ are each independently a hydrogen atom, an ionic hydrophilic group, a cyano group, a substituted or unsubstituted alkylsulfonyl group, a substituted or unsubstituted arylsulfonyl group, nitro Group, halogen atom, substituted or unsubstituted alkoxycarbonyl group, substituted or unsubstituted carbamoyl group, preferably substituted or unsubstituted sulfamoyl group, hydrogen atom, ionic hydrophilic group, cyano group, methanesulfonyl group More preferably a phenylsulfonyl group, a nitro group, a halogen atom, a methoxycarbonyl group or a carbamoyl group, particularly preferably a hydrogen atom, an ionic hydrophilic group, a nitro group, a halogen atom or a cyano group, Most preferably, they are atoms, ionic hydrophilic groups, nitro groups, or halogen atoms.

In General Formula (3-1), at least one of X ₁ , X ₂ , X ₃ , X ₄ , and X ₅ is an electron withdrawing property in which the σp value of an ionic hydrophilic group or Hammett is 0.3 or more. A group, preferably a halogen atom (preferably a chlorine atom), a nitro group, —SO ₃ M or —CO ₂ M (M represents a hydrogen atom or a monovalent counter cation, and specific examples and preferred ranges thereof are the same as above). More preferred.

  The compound represented by the general formula (1) or (2-1) is also preferably a compound represented by the following general formula (4-1).

Hereinafter, the compound represented by Formula (4-1) or a salt thereof will be described in detail.
Formula (4-1)

(In General Formula (4-1), G ¹ represents a nitrogen atom or —C (CN) ═. Y ₁ , Y ₂ , Y ₃ , Y ₄ , Y ₅ , Y ₆ , and Y ₇ are each independent. Represents a hydrogen atom or a monovalent substituent, and each M independently represents a hydrogen atom or a monovalent counter cation.)

  The example of M in General formula (4-1) is the same as the example of M in the said General formula (1), and its preferable example is also the same.

Y ₁ , Y ₂ , Y ₃ , Y ₄ , Y ₅ , Y ₆ , and Y ₇ in the general formula (4-1) each independently represent a hydrogen atom or a monovalent substituent. Examples of the substituent when Y ₁ , Y ₂ , Y ₃ , Y ₄ , Y ₅ , Y ₆ , and Y ₇ represent a monovalent substituent include a group selected from the above substituent group J. .
Y ₁ , Y ₂ , Y ₃ , Y ₄ , Y ₅ , Y ₆ , and Y ₇ are each independently a hydrogen atom, ionic hydrophilic group, cyano group, substituted or unsubstituted alkylsulfonyl group, substituted or unsubstituted Preferably an arylsulfonyl group, a nitro group, a halogen atom, a substituted or unsubstituted alkoxycarbonyl group, a substituted or unsubstituted carbamoyl group, a substituted or unsubstituted sulfamoyl group, a hydrogen atom, an ionic hydrophilic group, More preferably, it is a cyano group, a methanesulfonyl group, a phenylsulfonyl group, a nitro group, a halogen atom, a methoxycarbonyl group, or a carbamoyl group, and is a hydrogen atom, an ionic hydrophilic group, a nitro group, a halogen atom, or a cyano group. Particularly preferred is a hydrogen atom, an ionic hydrophilic group, a nitro group, or a halogen atom. .

In General Formula (4-1), at least one of Y ₁ , Y ₂ , Y ₃ , Y ₄ , Y ₅ , Y ₆ , and Y ₇ has an σp value of an ionic hydrophilic group or Hammett of 0.3. The above electron withdrawing groups are preferable, and a halogen atom (preferably a chlorine atom), a nitro group, —SO ₃ M or —CO ₂ M (M represents a hydrogen atom or a monovalent counter cation, and specific examples and preferred ranges) Is more preferably the same as above.

  The compound represented by the general formula (1) or (2-1) is also preferably a compound represented by the following general formula (5-1).

Hereinafter, the compound represented by Formula (5-1) or a salt thereof will be described in detail.
General formula (5-1)

(In General Formula (5-1), G ¹ represents a nitrogen atom or —C (CN) ═. Z ₁ , Z ₂ , Z ₃ , and Z ₄ are each independently a hydrogen atom or a monovalent group. Represents a substituent, and each M independently represents a hydrogen atom or a monovalent counter cation.)

  The example of M in General formula (5-1) is the same as the example of M in the said General formula (1), and its preferable example is also the same.

Z ₁ , Z ₂ , Z ₃ , and Z ₄ in the general formula (5-1) each independently represent a hydrogen atom or a monovalent substituent. Examples of the substituent in the case where Z ₁ , Z ₂ , Z ₃ , and Z ₄ represent a monovalent substituent include a group selected from the above substituent group J.
Z ₁ , Z ₂ , Z ₃ and Z ₄ are each independently a hydrogen atom, ionic hydrophilic group, cyano group, substituted or unsubstituted alkylsulfonyl group, substituted or unsubstituted arylsulfonyl group, nitro group, halogen An atom, a substituted or unsubstituted alkoxycarbonyl group, a substituted or unsubstituted carbamoyl group, a substituted or unsubstituted sulfamoyl group is preferable, a hydrogen atom, an ionic hydrophilic group, a cyano group, a methanesulfonyl group, a phenylsulfonyl Group, nitro group, halogen atom, methoxycarbonyl group, carbamoyl group, more preferably hydrogen atom, ionic hydrophilic group, nitro group, halogen atom, or cyano group, hydrogen atom, ion Most preferably a hydrophilic hydrophilic group, a nitro group, or a halogen atom.

In general formula (5-1), at least one of Z ₁ , Z ₂ , Z ₃ , and Z ₄ is preferably an ionic hydrophilic group or an electron-withdrawing group having a Hammett's σp value of 0.3 or more. , A halogen atom (preferably a chlorine atom), a nitro group, —SO ₃ M or —CO ₂ M (M represents a hydrogen atom or a monovalent counter cation, and specific examples and preferred ranges thereof are the same as above).

  The compound represented by the general formula (1) is also preferably a compound represented by the following general formula (2-2).

Hereinafter, the compound represented by Formula (2-2) or a salt thereof will be described in detail.
General formula (2-2)

(In General Formula (2-2), G ¹ represents a nitrogen atom or —C (CN) ═. R ₁₁ , R ₁₂ , R ₁₃ , and R ₁₄ are each independently a hydrogen atom or a monovalent group. A represents a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, or a substituted or unsubstituted nitrogen-containing 5-membered or 6-membered heterocyclic group. The membered heterocyclic group may further have a condensed ring structure, and each M independently represents a hydrogen atom or a monovalent counter cation.)

  Examples of A and M in the general formula (2-2) are each independently the same as examples of A and M in the general formula (1), and preferred examples are also the same.

In General Formula (2-2), R ₁₁ , R ₁₂ , R ₁₃ , and R ₁₄ each independently represent a hydrogen atom or a monovalent substituent. When R ₁₁ , R ₁₂ , R ₁₃ , and R ₁₄ represent a monovalent substituent, an ionic hydrophilic group, an arylamino group, and an alkylamino group are preferable, an ionic hydrophilic group is more preferable, and —SO ₃ More preferably, M or —CO ₂ M (M represents a hydrogen atom or a monovalent counter cation, and specific examples and preferred ranges thereof are the same as those described above).

  The compounds represented by the general formulas (1) and (2-2) are preferably compounds represented by the following general formula (3-2).

Hereinafter, the compound represented by formula (3-2) or a salt thereof will be described in detail.
Formula (3-2)

(In General Formula (3-2), G ¹ represents a nitrogen atom or —C (CN) ═. X ₁ , X ₂ , X ₃ , X ₄ , and X ₅ each independently represent a hydrogen atom, or R ₁₁ , R ₁₂ , R ₁₃ , and R ₁₄ each independently represents a hydrogen atom or a monovalent substituent, and M independently represents a hydrogen atom or a monovalent substituent. Represents the counter cation.)

Examples of R ₁₁ , R ₁₂ , R ₁₃ , R ₁₄ , and M in the general formula (3-2) are each independently R ₁₁ , R ₁₂ , R ₁₃ , R in the general formula (2-2). ₁₄ and M, and preferred examples are also the same.
In the general formula (3-2), examples of X ₁ , X ₂ , X ₃ , X ₄ , and X ₅ are each independently X ₁ , X ₂ , X ₃ , X _4, and the same as the examples of X _5, and preferred examples thereof are also the same.

  The compound represented by the general formula (1) or (2-2) is also preferably a compound represented by the following general formula (4-2).

Hereinafter, the compound represented by formula (4-2) or a salt thereof will be described in detail.
Formula (4-2)

(In General Formula (4-2), G ¹ represents a nitrogen atom or —C (CN) ═. Y ₁ , Y ₂ , Y ₃ , Y ₄ , Y ₅ , Y ₆ , and Y ₇ are each independently R ₁₁ , R ₁₂ , R ₁₃ , and R ₁₄ each independently represents a hydrogen atom or a monovalent substituent, and M represents each independently a hydrogen atom. Or represents a monovalent counter cation.)

Examples of R ₁₁ , R ₁₂ , R ₁₃ , R ₁₄ , and M in General Formula (4-2) are each independently R ₁₁ , R ₁₂ , R ₁₃ , R in General Formula (2-2). ₁₄ and M, and preferred examples are also the same.
In General Formula (4-2), examples of Y ₁ , Y ₂ , Y ₃ , Y ₄ , Y ₅ , Y ₆ , and Y ₇ are each independently Y ₁ in General Formula (4-1), The examples are the same as Y ₂ , Y ₃ , Y ₄ , Y ₅ , Y ₆ , and Y ₇ , and preferred examples are also the same.

The compound represented by the general formula (1) or (2-2) is also preferably a compound represented by the following general formula (5-2).
General formula (5-2)

(In General Formula (5-2), G ¹ represents a nitrogen atom or —C (CN) ═. Z ₁ , Z ₂ , Z ₃ , and Z ₄ are each independently a hydrogen atom or a monovalent group. R ₁₁ , R ₁₂ , R ₁₃ , and R ₁₄ each independently represent a hydrogen atom or a monovalent substituent, and M independently represents a hydrogen atom or a monovalent counter cation. Represents.)

Examples of R ₁₁ , R ₁₂ , R ₁₃ , R ₁₄ , and M in the general formula (5-2) are each independently R ₁₁ , R ₁₂ , R ₁₃ , R in the general formula (2-2). ₁₄ and M, and preferred examples are also the same.
In General Formula (5-2), examples of Z ₁ , Z ₂ , Z ₃ , and Z ₄ are each independently Z ₁ , Z ₂ , Z ₃ , and Z _{4 in} General Formula (5-1). This is the same as the above example, and the preferred example is also the same.

  The present invention also relates to the azo compound represented by the general formula (1). An aqueous solution and a water-soluble ink composition using the azo compound of the present invention as a coloring matter (coloring agent) can be used for colors such as dyes and pigments. It means a composition containing a material and a dispersant (such as a solvent) thereof, and can be suitably used particularly for image formation.

  The azo compound represented by the general formula (1) is the general formula (2-1), (3-1), (4-1), (5-1), (2-2), (3- It is preferable that it is an azo compound represented by 2), (4-2), or (5-2). Specific examples and preferred ranges of each symbol in each general formula are as described above.

General formula (1), (2-1), (2-2), (3-1), (3-2), (4-1), (4-2), (5-1), or ( In the compound represented by 5-2), the maximum absorption wavelength (λ _max ) of an absorption spectrum measured using water as a solvent is preferably 550 nm to 700 nm, and more preferably 580 nm to 650 nm.
In the present invention, the general formulas (1), (2-1), (2-2), (3-1), (3-2), (4-1), (4-2), (5 The compound represented by -1) or (5-2) preferably has three or more ionic hydrophilic groups. More preferably, it has 3-6 ionic hydrophilic groups, and still more preferably 4-5 ionic hydrophilic groups. As a result, the water solubility and aqueous solution storage stability of the azo compound of the present invention are improved, the required performance as a water-soluble dye for inkjet recording black ink is satisfied at a high level, and the inkjet printed matter when used as an inkjet recording ink is further improved. There is an effect that the image quality can be further improved.
In the present invention, the general formulas (1), (2-1), (2-2), (3-1), (3-2), (4-1), (4-2), (5 The compound represented by (-1) or (5-2) can be applied even if it contains an isotope (for example, 2H, 3H, 13C, 15N).

  The following general formulas (1), (2-1), (2-2), (3-1), (3-2), (4-1), (4-2), (5-1) Specific examples of the compound represented by (5-2) are shown below, but are not limited to the following examples.

  The azo compound represented by the general formula (1) can be synthesized by a coupling reaction between a diazo component and a coupler, and these are disclosed in JP2003-306623A and JP2005-139427A. There is description in the gazette.

[(C) pH adjuster]
The aqueous solution of the present invention can further contain (c) a pH adjuster.
As the pH adjuster, a neutralizer (organic base, inorganic alkali) can be used. For the purpose of improving the storage stability of the inkjet ink, the pH adjuster is preferably added so that the inkjet ink has a pH of 7.0 to 9.0, so that the pH is 7.5 to 8.5. It is more preferable to add.
It can be set as desired pH by making content of a pH adjuster into said range.

Examples of the pH adjuster include basic organic bases and inorganic bases, and acidic bases such as organic acids and inorganic acids.
Basic compounds include sodium hydroxide, potassium hydroxide, lithium hydroxide, sodium carbonate, potassium carbonate, lithium carbonate, sodium bicarbonate (sodium bicarbonate), potassium bicarbonate, lithium bicarbonate, sodium acetate, potassium acetate, phosphorus Inorganic compounds such as sodium acid, sodium monohydrogen phosphate, aqueous ammonia, methylamine, ethylamine, diethylamine, triethylamine, ethanolamine, diethanolamine, triethanolamine, ethylenediamine, piperidine, diazabicyclooctane, diazabicycloundecene, pyridine It is also possible to use organic bases such as quinoline, picoline, lutidine and collidine, and alkali metal salts of organic acids such as lithium benzoate and potassium phthalate.
Examples of acidic compounds include inorganic compounds such as hydrochloric acid, sulfuric acid, phosphoric acid, boric acid, sodium hydrogen sulfate, potassium hydrogen sulfate, potassium dihydrogen phosphate, sodium dihydrogen phosphate, acetic acid, tartaric acid, benzoic acid, trifluoroacetic acid. Organic compounds such as methanesulfonic acid, ethanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, saccharic acid, phthalic acid, picolinic acid and quinolinic acid can also be used.
As a pH adjuster, sodium hydrogencarbonate, potassium hydrogencarbonate, and lithium hydrogencarbonate are preferable, sodium hydrogencarbonate and lithium hydrogencarbonate are more preferable, and lithium hydrogencarbonate is still more preferable.

In the present invention, other colorants may be used in combination with the azo compound represented by the general formula (1) to adjust to a more preferable hue. Arbitrary dyes (for example, yellow dye, magenta dye, cyan dye, etc.) can be used as the dye to be used in combination. For example, in yellow dyes, aryl or heteryl azo dyes having substituted benzenes, substituted naphthalenes, heterocycles such as pyrazolone and pyridone, open-chain active methylene compounds, etc. as coupling components (hereinafter referred to as coupler components); Examples include azomethine dyes having open-chain active methylene compounds as coupler components; methine dyes such as benzylidene dyes and monomethine oxonol dyes; and quinone dyes such as naphthoquinone dyes and anthraquinone dyes. Examples of other dye species include quinophthalone dyes, nitro / nitroso dyes, acridine dyes, and acridinone dyes. Particularly preferred in combination is a dye (S) having a λmax of 350 nm to 500 nm, and the above-mentioned and later-described yellow dyes can be used. Among them, an azo having 2 to 6 azo groups in one molecule is preferable. It is a dye. In the present invention, a yellow pigment can also be used.
In magenta dyes, aryl or heteryl azo dyes having phenols, naphthols, anilines, heterocycles such as pyridine and pyrazine, open-chain active methylene compounds, etc. as coupler components; for example, open-chain active methylene compounds as coupler components Azomethine dyes having the above; and anthrapyridone dyes. Particularly preferred are azo dyes having a hetero ring in the chromophore or an anthrapyridone dye.
For cyan dyes, aryl or hetaryl azo dyes having phenols, naphthols, anilines, etc. as coupler components; for example, azomethine dyes having phenols, naphthols, heterocyclic rings such as pyrrolotriazole, etc. as coupler components; cyanine dyes; Polymethine dyes such as oxonol dyes and merocyanine dyes; Carbonium dyes such as diphenylmethane dyes, triphenylmethane dyes and xanthene dyes; phthalocyanine dyes; anthraquinone dyes; indigo / thioindigo dyes and the like. Particularly preferred are phthalocyanine dyes.

  In particular, from the standpoint of fastness, a dye having an oxidation potential nobler than 1.0 V or an associative dye is preferable. Specific examples of preferable dyes used in combination include the dyes described in JP-A No. 2005-146244.

As the heterocyclic azo dye, a known yellow dye and magenta dye can be used in addition to the azo compound represented by the general formula (1). These yellow dyes and magenta dyes, which are heterocyclic azo dyes, preferably have at least one of the above properties (oxidation potential and association property), and more preferably have all the properties. The oxidation potential of these dyes is more preferably noble than 1.1 V (vs SCE), particularly preferably noble than 1.15 V (vs SCE).
Examples of yellow dyes that are heterocyclic azo dyes include JP-A-2004-83903 (paragraph numbers [0048] to [0062]), JP-A 2003-277661 (paragraph numbers [0041] to [0050]), and 2003-277661. Nos. (Paragraph numbers [0042] to [0047]) and US application publication US2003 / 0213405 (paragraph number [0108]).

  In the aqueous solution of the present invention, the main solvent is water, preferably the water content in the total solvent is 50% by mass to 100% by mass, more preferably the water content in the total solvent is 60% by mass to 100% by mass. The aqueous solution of the present invention may contain a water-miscible organic solvent and a lipophilic medium in addition to water.

  In the aqueous solution of the present invention, (b) the azo compound represented by the general formula (1) or a salt thereof is dissolved or dispersed in a solvent, preferably dissolved.

In the aqueous solution of the present invention, (b) the content of the azo compound represented by the general formula (1) or a salt thereof is 1% by mass to 25% by mass, preferably 2% by mass with respect to the total mass of the aqueous solution. % To 20% by mass, more preferably 2% to 15% by mass. By setting the content of (b) in the above range, there is an effect that the storage stability of the aqueous solution is good and the preparation of the water-soluble ink for inkjet is easy.
The aqueous solution of the present invention preferably has a pH at 25 ° C. of 7.0 to 9.0, more preferably 7.5 to 8.5. By adjusting the pH to the above range, there are the effects that high solution stability of the azo compound in the aqueous solution can be imparted and the preparation of the water-soluble ink for inkjet is easy.
The aqueous solution of the present invention may be referred to as “ink stock solution”.

  The aqueous solution of the present invention is preferably prepared by dissolving in an aqueous medium when the azo compound represented by the general formula (1) is water-soluble, and the azo compound represented by the general formula (1) is When it is oil-soluble, it is preferably prepared by dissolving and / or dispersing in an aqueous medium and a lipophilic medium. The aqueous medium is a solvent mainly containing water, and optionally contains an organic solvent such as a water-miscible organic solvent. This organic solvent may have a function as a viscosity reducing agent. The lipophilic medium is mainly composed of an organic solvent. The water-miscible organic solvent and the lipophilic medium will be described later.

When producing an aqueous solution, it is preferable to add the process (filtering process) which removes the dust which is solid content by filtration. A filtration filter is used for this operation, and a filter having an effective diameter of 1 μm or less, preferably 0.3 μm or less is used as the filtration filter at this time. Various materials can be used as the filter material, but in the case of an aqueous solution of a water-soluble dye, it is preferable to use a filter prepared for an aqueous solvent. Among them, it is particularly preferable to use a jacket type filter made of a polymer material that is difficult to generate dust. As a filtration method, the jacket may be passed by liquid feeding, and either pressure filtration or vacuum filtration can be used.
In this invention, the viscosity reducing agent may be used and the said filtration process can be performed without resistance.

  Various methods such as dissolution by stirring, dissolution by ultrasonic irradiation, and dissolution by shaking can be used as a method for dissolving the dye and other components in the step of preparing the aqueous solution and the preparation step. Of these, the stirring method is particularly preferably used. In the case of stirring, various methods such as fluidized stirring known in the art and stirring using shearing force using an inverted agitator or dissolver can be used. On the other hand, a stirring method using a shearing force with the bottom surface of the container, such as a magnetic stirrer, can also be preferably used.

  The use of the aqueous solution of the present invention is not particularly limited, but it is preferably used as an ink composition, and more preferably used for an ink jet recording ink.

[Ink composition]
The ink composition of the present invention contains the aqueous solution of the present invention.

The content of the compound represented by the general formula (1) in the ink composition is preferably 0.2 to 20% by mass, more preferably 0.5 to 10% by mass, and 1.0 to 8.0% by mass. % Is particularly preferred.
The ink composition of the present invention preferably contains 0.2 to 20% by mass of all dyes, more preferably 0.5 to 10% by mass, and particularly preferably 1.0 to 8.0% by mass. contains.

In the ink composition of the present invention, the pH of the ink composition at 25 ° C. is preferably adjusted to 7.0 to 10.0 with a pH adjuster, and the pH is adjusted to 7.5 to 9.5. More preferably. When pH is 7.5 or more, the solubility of dye improves and it can prevent clogging of a nozzle. Moreover, if pH is 9.5 or less, there exists a tendency for the long-term storage stability of an ink to be excellent.
Examples of the pH adjuster used in the ink composition include those used in the aqueous solution of the present invention, preferably lithium hydrogen carbonate, sodium hydrogen carbonate, and potassium hydrogen carbonate, more preferably lithium hydrogen carbonate, sodium hydrogen carbonate. .
The use of the ink composition of the present invention is not particularly limited, and is an ink composition for printing such as inkjet, an ink sheet in a heat-sensitive recording material, a color toner for electrophotography, an LCD, a display such as PDP, and the like. Although it can be preferably used for the preparation of a color filter used in an image pickup device such as a CCD and a dyeing solution for dyeing various fibers, an ink composition for inkjet recording is particularly preferable.
The above aqueous solution can be used in the method for producing the ink composition.
The ink composition is preferably black ink, but should not be limited to black ink, and can include ink of any color by mixing with other dyes or pigments.
The method for producing an ink composition includes a step (hereinafter also referred to as a liquid preparation step) of producing a desired ink composition having the above viscosity range using at least an aqueous solution.
The liquid preparation step is a step of preparing the aqueous solution obtained as described above into an ink composition having a specific viscosity and desired use, and may be a final product or an intermediate product. It may be. This preparation step includes at least a step of diluting the aqueous solution with a medium, preferably an aqueous medium. The aqueous solution containing the oil-soluble dye is not particularly limited in the medium used in this dilution step, but is preferably prepared as an aqueous ink composition by being emulsified and dispersed in an aqueous medium. The medium may contain various components of a necessary concentration, the components may be added to the aqueous solution separately, or both of them may be combined.
Since the ink composition produced according to the present invention is produced using an aqueous solution having a high dye concentration, the solubility of the dye is improved as compared with the ink composition produced by a usual method, and as a result, the ejection stability is improved. Will improve.

Next, the dye used for the aqueous solution and ink composition of the present invention will be described. The dye is not particularly limited, but the half-value width (Wλ, _1/2 ) in an absorption spectrum of a diluted solution having a λmax of 500 nm to 700 nm and an absorbance normalized to 1.0 is 100 nm or more, preferably 120 nm. It is preferable to include at least one azo compound represented by the general formula (1) which is not less than 500 nm and more preferably not less than 120 nm and not more than 350 nm.

The azo compound represented by the general formula (1) alone has a high image quality “(good) black” = black that does not depend on the observation light source and any of the color tones of B, G, and R is difficult to be emphasized. Can be used alone as a raw material for an aqueous solution or an ink composition, however, the ink composition is usually used in combination with a dye that covers a region where the absorption of the dye is low. Is common. Usually, in the case of an ink composition using an azo compound represented by the general formula (1), it is preferably used in combination with another dye having a main absorption (λmax of 350 nm to 500 nm) in the yellow region. Further, it is also possible to prepare an ink composition in combination with other dyes.
Other dyes can be used in the aqueous solution, but are preferably mixed and used in the preparation of the ink composition from the viewpoint of storage stability.

  In the present invention, a black ink composition satisfying the following conditions is preferable in order to satisfy 1) excellent weather resistance and / or 2) that black balance is not lost even after fading.

First, a black square symbol of JIS code 2223 is printed at 48 points using the black ink composition, and the reflection density (D _vis ) measured by the status A filter (visual filter) is defined as the initial density. An example of a reflection density measuring machine equipped with a status A filter is an X-Rite density measuring machine. Here, when measuring the density of “black”, the measured value by D _vis is used as the standard observation reflection density. From this time (t) until the reflection density (D _vis ) reaches 80% of the initial reflection density value, this print is forcibly faded using an ozone fading tester capable of always generating 5 ppm of ozone. The forced fading rate constant (k _vis ) is obtained from the relational expression “0.8 = exp (−k _vis · t)”.
In the present invention, the rate constant (k _vis ) is 5.0 × 10 ⁻² [hour ⁻¹ ] or less, preferably 3.0 × 10 ⁻² [hour ⁻¹ ] or less, more preferably 1.0 × 10 ^{−. 2} [hour ⁻¹ ] An ink composition having the following ^value is prepared.

Also, a black square symbol of JIS code 2223 is printed at 48 points using a black ink composition, and this is a density measurement value measured by a status A filter, which is not D _vis C (cyan), M (magenta), The reflection density (D _R , D _G , D _B ) of the three colors Y (yellow) is also defined as the initial density. Here, (D _R , D _G , D _B ) indicates (C reflection density by the red filter, M reflection density by the green filter, and Y reflection density by the blue filter). This print is forcibly faded using an ozone fading tester capable of always generating 5 ppm of ozone according to the above method, and the respective reflection densities (D _R , D _G , D _B ) are 80% of the initial density value. Similarly, the forced fading rate constants (k _R , k _G , k _B ) are determined from the time until. When the three rate constants are obtained and the ratio (R) between the maximum value and the minimum value is obtained (for example, when k _R is the maximum value and k _G is the minimum value, R = k _R / k _G ) The ink composition is prepared so that the ratio (R) is 1.2 or less, preferably 1.1 or less, more preferably 1.05 or less.

  Note that the “printed matter in which the black square symbol of the JIS code 2223 is printed at 48 points” used above gives an image large enough to cover the aperture of the measuring instrument in order to give a sufficient size for density measurement. It is printed.

Examples of the dye used in the aqueous solution of the present invention, and thus the ink composition, include a dye having an azo group bonded to a heterocyclic ring (hereinafter also referred to as “heterocyclic azo dye”) and an associative phthalocyanine dye (hereinafter referred to as a heterocyclic ring). The dyes used in the present invention, such as azo dyes and the phthalocyanine dyes, are also collectively referred to as dyes for the present invention). The present invention preferably contains at least one heterocyclic azo dye or the phthalocyanine dye, but other dyes and / or pigments may be used in combination.
In addition, the dye used in the present invention preferably has an oxidation potential of 1.0 V (vs SCE) or more.
A person skilled in the art can easily measure the value (Eox) of the oxidation potential. Regarding this method, see, for example, P.I. Delahay, “New Instrumental Methods in Electrochemistry” (published by Interscience Publishers, 1954) J. et al. "Electrochemical Methods" by Bard et al. (Published by John Wiley & Sons in 1980) and "Electrochemical Measurement Method" by Akira Fujishima et al. (Published by Gihodo Publishing Co., Ltd. in 1984).

Specifically, the oxidation potential is measured by placing a test sample in a solvent such as dimethylformamide or acetonitrile containing a supporting electrolyte such as sodium perchlorate or tetrapropylammonium perchlorate in the range of 1 × 10 ⁻² to 1 × 10 ⁻⁶ mol / It is measured as a value relative to SCE (saturated calomel electrode) using various voltammetry (polarography using a dropping mercury electrode, cyclic voltammetry, a method using a rotating disk electrode, etc.). Although this value may be deviated by several tens of mil volts due to the influence of the liquid potential difference or the liquid resistance of the sample solution, the reproducibility of the potential can be ensured by inserting a standard sample (for example, hydroquinone).
In the present invention, SCE (saturated calomel) is used as a reference electrode in N, N-dimethylformamide (concentration of dye is 0.001 mol / liter) containing 0.1 mol / liter of tetrapropylammonium perchlorate as a supporting electrolyte. Electrode), a value (vs SCE) measured using a graphite electrode as a working electrode and a platinum electrode as a counter electrode was defined as an oxidation potential of the dye.

  The value of Eox represents the ease of electron transfer from the sample to the electrode, and the larger the value (the oxidation potential is noble), the less the electron transfer from the sample to the electrode, in other words, the less easily oxidized. . In relation to the structure of the compound, the oxidation potential becomes more noble by introducing an electron withdrawing group, and the oxidation potential becomes lower by introducing an electron donating group. In the present invention, in order to lower the reactivity with ozone as an electrophile, it is desirable to introduce an electron withdrawing group into the dye skeleton to make the oxidation potential more noble.

  Moreover, as a dye used in the present invention, ε1 / ε2 is preferably 1.1 or more, more preferably 1.1 to 1.5, and particularly preferably 1.2 to 1.5 in the following associative evaluation method. .

(Assembly evaluation method of dye)
The association property of the dye can be evaluated as follows. When a 0.01 mmol / L dye solution was measured using a cell with an optical path length of 1 cm, a molecular absorption coefficient (ε1) of the solution absorption spectrum and a 20 mmol / L dye solution with an optical path length of 5 μm were used. The ratio of the solution absorption spectrum to the molecular extinction coefficient (ε2), ε1 / ε2, is an indicator of dye association. The higher this number, the easier the dye will associate. A dye having a value of 1.1 or more exhibits excellent performance in ozone resistance and light resistance due to dye association.
The above solvent used in the dye solution is a pure solution if the dye is water-soluble, using ultrapure water having a specific resistance value of 18 MΩ · cm or more such as deionized water, and if the dye is oil-soluble Is measured using an organic solvent in which the dye is soluble, or a dispersion or emulsion in ultrapure water similar to the case of the water-soluble dye.

  Examples of dyes that can be used in the present invention include the following. A single dye is used in combination in order to adjust the color tone. The ink composition obtained from each of the yellow, magenta, cyan, and black ink stock solutions of the present invention can be used not only for forming a single color image but also for forming a full color image. In order to form a full-color image, a two-color ink composition can be used for each color. Furthermore, ink compositions of intermediate colors such as red, green, blue, and violet can also be used. The ink composition of the present invention can constitute an ink set for obtaining a full-color image. Alternatively, the ink composition can form part of an ink set. In other words, any ink composition other than the present invention may be combined with the ink composition of the present invention to constitute an ink set.

In addition, in order to obtain a full-color image together with the dye, another colorant may be used in combination with the ink composition of the present invention in order to adjust the color tone.
Any colorant can be used as the colorant that can be used in the ink set of the present invention or the colorant that can be used in combination with the dye. Examples of the dye that can be used in combination include the dyes described so far and the following.
As yellow dyes, for example, phenols, naphthols, anilines, pyrazolones, pyridones, aryl or heteryl azo dyes having open-chain active methylene compounds as coupling components; for example, open-chain active methylene compounds as coupling components Azomethine dyes; methine dyes such as benzylidene dyes and monomethine oxonol dyes; quinone dyes such as naphthoquinone dyes and anthraquinone dyes, and other dye species such as quinophthalone dyes, nitro-nitroso dyes And dyes, acridine dyes, acridinone dyes and the like. These dyes may be those that exhibit yellow only after a part of the chromophore is dissociated, in which case the counter cation may be an alkali metal or an inorganic cation such as ammonium, pyridinium, It may be an organic cation such as a quaternary ammonium salt, and may further be a polymer cation having them in a partial structure.

  Examples of magenta dyes include, for example, aryl or heteryl azo dyes having phenols, naphthols, and anilines as coupling components; azomethine dyes having pyrazolones and pyrazolotriazoles as coupling components; for example, arylidene dyes, styryl dyes, and merocyanine Dyes, methine dyes such as oxonol dyes; carbonium dyes such as diphenylmethane dyes, triphenylmethane dyes, xanthene dyes, quinone dyes such as naphthoquinone, anthraquinone, anthrapyridone, etc. And ring dyes. These dyes may exhibit magenta only after part of the chromophore is dissociated, and the counter cation in that case may be an alkali metal or an inorganic cation such as ammonium, pyridinium, It may be an organic cation such as a quaternary ammonium salt, and may further be a polymer cation having them in a partial structure.

  Examples of the cyan dye include azomethine dyes such as indoaniline dyes and indophenol dyes; polymethine dyes such as cyanine dyes, oxonol dyes and merocyanine dyes; carbonium dyes such as diphenylmethane dyes, triphenylmethane dyes and xanthene dyes; phthalocyanine Dyes; anthraquinone dyes; for example, aryl or heteryl azo dyes having phenols, naphthols and anilines as coupling components, and indigo / thioindigo dyes. These dyes may exhibit cyan only after a part of the chromophore is dissociated, and the counter cation in that case may be an alkali metal or an inorganic cation such as ammonium, pyridinium, It may be an organic cation such as a quaternary ammonium salt, and may further be a polymer cation having them in a partial structure.

  In addition, water-soluble dyes such as direct dyes, acid dyes, food dyes, basic dyes, and reactive dyes can be used in combination. Among these, C.I. I. Direct Red 1, 2, 4, 9, 11, 23, 26, 31, 37, 39, 62, 63, 72, 75, 76, 79, 80, 81, 83, 84, 87, 89, 92, 95, 111, 173, 184, 207, 211, 212, 214, 218, 21, 223, 224, 225, 226, 227, 232, 233, 240, 241, 242, 243, 247, 254, C.I. I. Direct violet 7, 9, 47, 48, 51, 66, 90, 93, 94, 95, 98, 100, 101, C.I. I. Direct yellow 4, 8, 9, 11, 12, 27, 28, 29, 33, 35, 39, 41, 44, 50, 53, 58, 59, 68, 86, 87, 93, 95, 96, 98, 100, 106, 108, 109, 110, 120, 130, 132, 142, 144, 157, 161, 163, C.I. I. Direct Blue 1, 10, 15, 22, 25, 55, 67, 68, 71, 76, 77, 78, 80, 84, 86, 87, 90, 98, 106, 108, 109, 151, 156, 158, 159, 160, 168, 189, 192, 193, 194, 199, 200, 201, 202, 203, 207, 211, 213, 214, 218, 225, 229, 236, 237, 244, 248, 249, 251, 252, 264, 270, 280, 288, 289, 290, 291, C.I. I. Direct Black 9, 17, 19, 22, 32, 51, 56, 62, 69, 77, 80, 91, 94, 97, 108, 112, 113, 114, 117, 118, 121, 122, 125, 132, 146, 154, 166, 168, 173, 199, C.I. I. Acid Red 1, 8, 35, 42, 52, 57, 62, 80, 81, 82, 87, 94, 111, 114, 115, 118, 119, 127, 128, 131, 143, 144, 151, 152, 154, 158, 186, 245, 249, 254, 257, 261, 263, 266, 289, 299, 301, 305, 336, 337, 361, 396, 397, C.I. I. Acid Violet 5, 34, 43, 47, 48, 90, 103, 126, C.I. I. Acid Yellow 17, 19, 23, 25, 39, 40, 42, 44, 49, 50, 61, 64, 76, 79, 110, 127, 135, 143, 151, 159, 169, 174, 190, 195, 196, 197, 199, 218, 219, 222, 227, C.I. I. Acid Blue 9, 25, 40, 41, 62, 72, 76, 78, 80, 82, 87, 92, 106, 112, 113, 120, 127: 1, 129, 138, 143, 175, 181, 185, 205, 207, 220, 221, 230, 232, 247, 249, 258, 260, 264, 271, 277, 278, 279, 280, 288, 290, 326, C.I. I. Acid Black 7, 24, 29, 48, 52: 1, 172, C.I. I. Reactive Red 3, 6, 13, 17, 19, 21, 22, 23, 24, 29, 35, 37, 40, 41, 43, 45, 49, 55, 63, 106, 107, 112, 113, 114 , 126, 127, 128, 129, 130, 131, 137, 160, 161, 174, 180, C.I. I. Reactive violet 1, 3, 4, 5, 6, 7, 8, 9, 16, 17, 22, 23, 24, 26, 27, 33, 34, C.I. I. Reactive Yellow 2, 3, 13, 14, 15, 17, 18, 23, 24, 25, 26, 27, 29, 35, 37, 41, 42, C.I. I. Reactive Blue 2, 3, 5, 7, 8, 10, 13, 14, 15, 17, 18, 19, 21, 25, 26, 27, 28, 29, 38, 82, 89, 158, 182, 190 203, 216, 220, 244, C.I. I. Reactive Black 4, 5, 8, 14, 21, 23, 26, 31, 32, 34, C.I. I. Basic Red 12, 13, 14, 15, 18, 22, 23, 24, 25, 27, 29, 35, 36, 38, 39, 45, 46, C.I. I. Basic violet 1, 2, 3, 7, 10, 15, 16, 20, 21, 25, 27, 28, 35, 37, 39, 40, 48, C.I. I. Basic yellow 1, 2, 4, 11, 13, 14, 15, 19, 21, 23, 24, 25, 28, 29, 32, 36, 39, 40, C.I. I. Basic Blue 1, 3, 5, 7, 9, 22, 26, 41, 45, 46, 47, 54, 57, 60, 62, 65, 66, 69, 71, C.I. I. Basic black 8, etc. are mentioned.

  In addition to the dye represented by the above formula, dyes described in the following publications can also be preferably used. JP-A-10-130557, JP-A-9-255906, JP-A-6-234944, JP-A-7-97541, EP 982371, WO 00/43450, WO 00/43451, WO 00/43452, WO 00 / 43453, WO 03/106572, WO 03/104332, JP 2003-238862, JP 2004-83609, JP 2002-302619, JP 2002-327131, JP 2002-265809, WO 01 / 48090, WO 04/087815, WO 02/90441, WO 03/027185, WO 04/085541, JP 2003-321627, JP 2002-332418, JP 2002-332419, WO 02/059215, WO 02 / 059216, WO 04/087814, WO 04/046252, WO 04/046265, U.S. Patent No. 6652637, WO 03/106572, WO 03/104332, WO 00/58407, Patent 3558213, Patent No. 3558212, Patent No. 3558212 No. 3558211, JP 2004-285351, WO 04/078860, JP 2004-323605, WO 04/104108.

Furthermore, in the present invention, a pigment can be used in combination with a dye.
As the pigment that can be used in the present invention, commercially available pigments and known pigments described in various documents can be used. For the literature, Color Index (Edited by The Society of Dyers and Colorists), “Revised New Handbook of Pigments” edited by the Japan Pigment Technology Association (published in 1989), “Latest Pigment Applied Technology” published by CMC (published in 1986), “Printing Ink Technology” CMC Publishing (1984), W. Herbst, K.M. Industrial Organic Pigments (VCH) by Hunger
Verlagsgesellschaft, published in 1993). Specifically, for organic pigments, azo pigments (azo lake pigments, insoluble azo pigments, condensed azo pigments, chelate azo pigments), polycyclic pigments (phthalocyanine pigments, anthraquinone pigments, perylene and perinone pigments, indigo pigments, quinacridone Pigments, dioxazine pigments, isoindolinone pigments, quinophthalone pigments, diketopyrrolopyrrole pigments), dyed lake pigments (acid or basic dye lake pigments), azine pigments, etc. C.I. of yellow pigment I. Pigment Yellow 34, 37, 42, 53, and other red pigments such as C.I. I. Pigment Red 101, 108, C.I. I. Pigment Blue 27, 29, 17: 1, etc., black pigments such as C.I. I. Pigment Black 7, magnetite, and other white pigments such as C.I. I. Pigment White 4, 6, 18, 21 and the like.

  As a pigment having a preferable color tone for image formation, a phthalocyanine pigment, an anthraquinone-based indanthrone pigment (for example, CI Pigment Blue 60), and a dyed lake pigment-based triarylcarbonium pigment are preferable for a blue or cyan pigment. Phthalocyanine pigments (preferred examples include copper phthalocyanine such as CI Pigment Blue 15: 1, 15: 2, 15: 3, 15: 4, 15: 6, monochloro or low chlorinated copper) Among the phthalocyanines and alnium phthalocyanines, the pigments described in European Patent No. 860475, the metal-free phthalocyanine which is CI Pigment Blue 16, the phthalocyanines whose central metals are Zn, Ni and Ti, among them, CI pigment is preferable. Bl e 15: 3, 15: 4 and aluminum phthalocyanine) are most preferred.

  For red to purple pigments, azo pigments (preferred examples include CI Pigment Red 3, 5, 11, 22, 38, 48: 1, 48: 2, 48: 3, 48: 4, 49: 1, 52: 1, 53: 1, 57: 1, 63: 2, 144, 146, and 184). I. Pigment Red 57: 1, 146, 184), quinacridone pigments (preferred examples include CI Pigment Red 122, 192, 202, 207, 209, CI Pigment Violet 19, 42, particularly preferred are CI Pigment Red 122), dyed lake pigment-based triarylcarbonium pigments (preferred examples include xanthene-based CI Pigment Red 81: 1, CI Pigment Violet). 1, 2, 3, 27, 39), dioxazine pigments (for example, CI Pigment Violet 23, 37), diketopyrrolopyrrole pigments (for example, CI Pigment Red 254), perylene Pigments (e.g. CI Pi ment Violet 29), anthraquinone pigments (e.g., C.I. Pigment Violet 5: 1, the 31, the 33), thioindigo (e.g. C.I. Pigment Red 38, the 88) is preferably used.

Examples of yellow pigments include azo pigments (preferred examples include monoazo pigment-based CI Pigment Yellow 1, 3, 74, 98, disazo pigment-based CI Pigment.
Yellow 12, 13, 14, 16, 17, 83, synthetic azo C.I. I. Pigment Yellow 93, 94, 95, 128, 155, benzimidazolone C.I. I. Pigment Yellow 120, 151, 154, 156, 180, etc., among which preferable ones do not use benzidine compounds as raw materials, isoindoline / isoindolinone pigments (preferred examples include CI Pigment Yellow 109, 110, 137, 139, etc.), quinophthalone pigments (preferred examples include CI Pigment Yellow 138), and furapantron pigments (eg, CI Pigment Yellow 24) are preferably used.

  Preferred examples of the black pigment include inorganic pigments (preferably carbon black and magnetite as examples) and aniline black. In addition, an orange pigment (such as CI Pigment Orange 13, 16) or a green pigment (such as CI Pigment Green 7) may be used.

The pigment that can be used in the present invention may be the above-mentioned bare pigment or a surface-treated pigment. Surface treatment methods include resin or wax surface coating, surfactant deposition, reactive substances (eg radicals derived from silane coupling agents, epoxy compounds, polyisocyanates, diazonium salts, etc.) pigments A method of bonding to the surface is conceivable and is described in the following documents and patents.
(1) Properties and applications of metal soap (Sachishobo)
(2) Printing ink printing (CMC Publishing 1984)
(3) Latest pigment application technology (CMC Publishing 1986)
(4) U.S. Pat. Nos. 5,554,739 and 5,571,311 (5) JP-A Nos. 9-151342, 10-140065, 10-292143, and 11-166145 Self-dispersing pigments prepared by allowing a diazonium salt described in US Patent 4) to act on carbon black, or encapsulated pigments prepared by the method described in Japanese Patent (5) above are ink compositions. This is particularly effective because dispersion stability can be obtained without using an extra dispersant in the product.

In the present invention, the pigment may be further dispersed using a dispersant. Various known dispersants can be used in accordance with the pigment to be used, for example, a surfactant-type low-molecular dispersant or a polymer-type dispersant. Examples of the dispersant include those described in JP-A-3-69949, European Patent 549486 and the like. In addition, when a dispersant is used, a pigment derivative called a synergist may be added to promote adsorption of the dispersant to the pigment. The particle size of the pigment that can be used in the present invention is preferably in the range of 0.01 to 10 μm after dispersion, and more preferably 0.05 to 1 μm.
As a method for dispersing the pigment, a known dispersion technique used in ink production or toner production can be used. Examples of the dispersing machine include vertical or horizontal agitator mills, attritors, colloid mills, ball mills, three roll mills, pearl mills, super mills, impellers, dispersers, KD mills, dynatrons, and pressure kneaders. Details are described in "Latest Pigment Application Technology" (CMC Publishing, 1986).

  Examples of water-soluble dyes used in the present invention include magenta dyes described in JP-A No. 2002-371214, phthalocyanine dyes described in JP-A No. 2002-309118, JP-A Nos. 2003-12952 and 2003-12956. It is also preferable to use the dyes described in water-soluble phthalocyanine dyes.

  The ink composition of the present invention contains a dye in a medium, preferably in an aqueous medium. The aqueous medium is added with water or a solvent such as a water-miscible organic solvent as necessary. The water-miscible organic solvent may be a viscosity reducing agent in the ink stock solution as described above.

  The water-miscible organic solvent that can be used in the present invention is a material having functions such as an anti-drying agent, a penetration accelerator, and a wetting agent for an ink composition for inkjet recording in the field, and is mainly a high-boiling water. A miscible organic solvent is used. Such compounds include alcohols (eg, methanol, ethanol, propanol, isopropanol, butanol, isobutanol, sec-butanol, t-butanol, pentanol, hexanol, cyclohexanol, benzyl alcohol), polyhydric alcohols (eg, , Ethylene glycol, diethylene glycol, triethylene glycol, polyethylene glycol, propylene glycol, dipropylene glycol, polypropylene glycol, butylene glycol, hexanediol, pentanediol, glycerin, hexanetriol, thiodiglycol), glycol derivatives (eg, ethylene glycol monomethyl) Ether, ethylene glycol monoethyl ether, ethylene glycol monobutyl ether Diethylene glycol monomethyl 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 Monomethyl ether, triethylene glycol monoethyl ether, ethylene glycol monophenyl ether), amine (for example, ethanolamine, diethanolamine, triethanolamine, N-methyldiethanolamine, N-ethyldiethanolamine, morpholine, N-ethylmorpholine, ethylenediamine, diethylenetriamine) , Reethylenetetramine, polyethyleneimine, tetramethylpropylenediamine) and other polar solvents (eg, 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). In addition, the said water miscible organic solvent may use 2 or more types together.

  Among these, alcohol solvents are particularly preferable. The ink composition of the present invention preferably contains a water-miscible organic solvent having a boiling point of 150 ° C. or higher, and examples thereof include 2-pyrrolidone selected from the above. These water-miscible organic solvents are preferably contained in the ink composition in a total amount of 5 to 60% by mass, particularly preferably 10 to 45% by mass.

By incorporating a surfactant into the ink composition of the present invention and adjusting the liquid physical properties of the ink composition, the ejection stability of the ink composition is improved, the water resistance of the image is improved, and the printed ink composition It is possible to have an excellent effect in preventing bleeding.
Examples of the surfactant include anionic surfactants such as sodium dodecyl sulfate, sodium dodecyloxysulfonate, and sodium alkylbenzene sulfonate, and cationic surfactants such as cetyl pyridinium chloride, trimethyl cetyl ammonium chloride, and tetrabutyl ammonium chloride. And nonionic surfactants such as polyoxyethylene nonylphenyl ether, polyoxyethylene naphthyl ether, polyoxyethylene octylphenyl ether, and the like. Among these, nonionic surfactants are particularly preferably used.

  The content of the surfactant is 0.001 to 20% by mass, preferably 0.005 to 10% by mass, and more preferably 0.01 to 5% by mass with respect to the ink composition.

When the dye is an oil-soluble dye, the ink composition of the present invention can be prepared by emulsifying and dispersing an ink stock solution in which the oil-soluble dye is dissolved in a high-boiling organic solvent in an aqueous medium. The boiling point of the high-boiling organic solvent used in the present invention is 150 ° C. or higher, preferably 170 ° C. or higher.
For example, phthalic acid esters (for example, dibutyl phthalate, dioctyl phthalate, dicyclohexyl phthalate, di-2-ethylhexyl phthalate, decyl phthalate, bis (2,4-di-tert-amylphenyl) isophthalate, bis (1, 1-diethylpropyl) phthalate), esters of phosphoric acid or phosphones (eg diphenyl phosphate, triphenyl phosphate, tricresyl phosphate, 2-ethylhexyl diphenyl phosphate, dioctyl butyl phosphate, tricyclohexyl phosphate, tri-2-ethylhexyl phosphate , Tridodecyl phosphate, di-2-ethylhexylphenyl phosphate), benzoic acid esters (eg 2-ethylhexyl benzoate, 2,4-dicarbonate) Lobenzoate, dodecylbenzoate, 2-ethylhexyl-p-hydroxybenzoate), amides (eg, N, N-diethyldodecanamide, N, N-diethyllaurylamide), alcohols or phenols (isostearyl alcohol, 2, 4-di-tert-amylphenol), aliphatic esters (eg, dibutoxyethyl succinate, di-2-ethylhexyl succinate, 2-hexyldecyl tetradecanoate, tributyl citrate, diethyl azelate, isostearyl lactate , Trioctyl citrate), aniline derivatives (N, N-dibutyl-2-butoxy-5-tert-octylaniline, etc.), chlorinated paraffins (paraffins having a chlorine content of 10% to 80%), trimesic acid esters Class (for example, Tributyl rimesate), dodecylbenzene, diisopropylnaphthalene, phenols (eg, 2,4-di-tert-amylphenol, 4-dodecyloxyphenol, 4-dodecyloxycarbonylphenol, 4- (4-dodecyloxyphenylsulfonyl)) Phenol), carboxylic acids (eg, 2- (2,4-di-tert-amylphenoxybutyric acid, 2-ethoxyoctanedecanoic acid), alkylphosphoric acids (eg, di-2 (ethylhexyl) phosphoric acid, diphenylphosphoric acid) The high-boiling organic solvent can be used in an amount of 0.01 to 3 times, preferably 0.01 to 1.0 times the mass ratio of the oil-soluble dye.
These high-boiling organic solvents may be used alone or in a mixture of several types (eg tricresyl phosphate and dibutyl phthalate, trioctyl phosphate and di (2-ethylhexyl) sebacate, dibutyl phthalate and poly (Nt-butyl). Acrylamide)].

Examples of other high boiling point organic solvents used in the present invention and / or methods for synthesizing these high boiling point organic solvents are disclosed in, for example, US Pat. Nos. 2,322,027, 2,533,514, and 2 772,163, 2,835,579, 3,594,171, 3,676,137, 3,689,271, 3,700,454 3,748,141, 3,764,336, 3,765,897, 3,912,515, 3,936,303, 4, No. 004,928, No. 4,080,209, No. 4,127,413, No. 4,193,802, No. 4,207,393, No. 4,220,711, No. 4,239,851, No. 4,278,757, No. 4, 53,979, 4,363,873, 4,430,421, 4,430,422, 4,464,464, 4,483,918, 4,540,657, 4,684,606, 4,728,599, 4,745,049, 4,935,321, 5,013 , 639, European Patent Nos. 276,319A, 286,253A, 289,820A, 309,158A, 309,159A, 309,160A, 509 No. 311A, No. 510,576A, East German Patent No. 147,009, No. 157,147, No. 159,573, No. 225,240A, British Patent No. 2,091,124A, JP-A-48-47335, 50- No. 6530, No. 51-25133, No. 51-26036, No. 51-27921, No. 51-27922, No. 51-149028, No. 52-46816, No. 53-1520, No. 53-1521 53-15127, 53-146622, 54-91325, 54-106228, 54-118246, 55-59464, 56-64333, 56-81836, 59-204041, 61-84641, 62-118345, 62-247364, 63-167357, 63-214744, 63-301941, 63-94552, 64-945 9454, 64-68745, JP-A-1-101543, 1-1202454, 2-792, 2- No. 4239, No. 2-43541, No. 4-29237, No. 4-30165, No. 4-232946, No. 4-346338 and the like.
The high boiling point organic solvent is used in an amount of 0.01 to 3.0 times, preferably 0.01 to 1.0 times the mass ratio of the oil-soluble dye.

  In the present invention, the oil-soluble dye and the high boiling point organic solvent are preferably emulsified and dispersed in an aqueous medium. In the emulsification dispersion, a low boiling organic solvent can be used depending on the case from the viewpoint of emulsification. The low boiling point organic solvent is an organic solvent having a boiling point of about 30 ° C. or higher and 150 ° C. or lower at normal pressure. For example, esters (eg ethyl acetate, butyl acetate, ethyl propionate, β-ethoxyethyl acetate, methyl cellosolve acetate), alcohols (eg isopropyl alcohol, n-butyl alcohol, secondary butyl alcohol), ketones (eg methyl isobutyl) Ketones, methyl ethyl ketone, cyclohexanone), amides (for example, dimethylformamide, N-methylpyrrolidone), ethers (for example, tetrahydrofuran, dioxane) and the like are preferably used, but are not limited thereto.

  The emulsification dispersion is used to disperse an oil phase in which a dye is dissolved in a mixed solvent of a high-boiling organic solvent and, optionally, a low-boiling organic solvent, in an aqueous phase mainly composed of water to form fine oil droplets in the oil phase. (The oil layer may be used as an ink stock solution, or the oil layer dispersed in the water phase may be used as an ink stock solution). At this time, components such as a surfactant, a wetting agent, a dye stabilizer, an emulsion stabilizer, an antiseptic, and an antifungal agent can be added to either or both of the aqueous phase and the oil phase as necessary. . As an emulsification method, a method of adding an oil phase to an aqueous phase is common, but a so-called phase inversion emulsification method in which an aqueous phase is dropped into an oil phase can also be preferably used. The emulsification method can also be applied when the dye is water-soluble and the component is oil-soluble.

  When emulsifying and dispersing, various surfactants can be used. Anionic interfaces such as fatty acid salts, alkyl sulfate esters, alkyl benzene sulfonates, alkyl naphthalene sulfonates, dialkyl sulfosuccinates, alkyl phosphate esters, naphthalene sulfonate formalin condensates, polyoxyethylene alkyl sulfates, etc. Activator, polyoxyethylene alkyl ether, polyoxyethylene alkyl allyl ether, polyoxyethylene fatty acid ester, sorbitan fatty acid ester, polyoxyethylene sorbitan fatty acid ester, polyoxyethylene alkylamine, glycerin fatty acid ester, oxyethyleneoxypropylene block copolymer Nonionic surfactants such as Further, SURFYNOLS (Air Products & Chemicals), which is an acetylene-based polyoxyethylene oxide surfactant, is also preferably used. An amine oxide type amphoteric surfactant such as N, N-dimethyl-N-alkylamine oxide is also preferred. Further, pages (37) to (38) of JP-A-59-157,636, Research Disclosure No. The surfactants described in 308119 (1989) can also be used.

For the purpose of stabilization immediately after emulsification, a water-soluble polymer can be added in combination with the surfactant. As the water-soluble polymer, polyvinyl alcohol, polyvinyl pyrrolidone, polyethylene oxide, polyacrylic acid, polyacrylamide or a copolymer thereof is preferably used. It is also preferable to use natural water-soluble polymers such as polysaccharides, casein, and gelatin. Further, for stabilization of the dye dispersion, acrylic acid esters, methacrylic acid esters, vinyl esters, acrylamides, methacrylamides, olefins, styrenes, vinyl ethers that are substantially insoluble in an aqueous medium, Polyvinyl, polyurethane, polyester, polyamide, polyurea, polycarbonate and the like obtained by polymerization of acrylonitrile can also be used in combination. These polymers preferably contain —SO ₃ ^— and —COO ^— . When these polymers that do not substantially dissolve in an aqueous medium are used in combination, it is preferably used in an amount of 20% by mass or less, more preferably 10% by mass or less of the high boiling point organic solvent.

When an oil-soluble dye or a high-boiling organic solvent is dispersed by emulsification to obtain an aqueous ink composition, control of the particle size is particularly important. In order to increase color purity and density when an image is formed by inkjet, it is essential to reduce the average particle size. The volume average particle size is preferably 1 μm or less, more preferably 5 to 100 nm.
In addition to static light scattering, dynamic light scattering, and centrifugal sedimentation, the methods for measuring the volume average particle size and particle size distribution of the dispersed particles are described on pages 417 to 418 of Experimental Chemistry Course 4th edition. It can be easily measured by a known method such as using a method. For example, it is diluted with distilled water so that the particle concentration in the ink composition is 0.1 to 1% by mass, and a commercially available volume average particle size measuring device (for example, Microtrac UPA (manufactured by Nikkiso Co., Ltd.)) Can be measured easily. Furthermore, the dynamic light scattering method using the laser Doppler effect is particularly preferable because it can measure the particle size up to a small size.
The volume average particle diameter is an average particle diameter weighted by the particle volume, and is the sum of the diameter of each particle multiplied by the volume of the particle divided by the total volume of the particles. The volume average particle diameter is described on page 119 of “Chemistry of Polymer Latex (by Soichi Muroi, Polymer Press Society)”.

  It was also found that the presence of coarse particles also plays a very important role in printing performance. That is, it has been found that the coarse particles clog the nozzles of the head, or even if they do not clog, the ink composition will cause non-ejection and ejection deviation, which will have a significant effect on printing performance. In order to prevent this, it is important to reduce the number of particles of 5 μm or more to 10 or less and 1 μm or more to 1000 or less in 1 μl of the ink composition when the ink composition is formed. As a method for removing these coarse particles, a known centrifugal separation method, microfiltration method, or the like can be used. These separation means may be performed immediately after the emulsification dispersion, or may be performed immediately after filling the ink dispersion after adding various components such as a wetting agent and a surfactant to the emulsification dispersion. A mechanical emulsifier can be used as an effective means for reducing the average particle size and eliminating coarse particles.

As the emulsifying device, known devices such as a simple stirrer, impeller stirring method, in-line stirring method, mill method such as colloid mill, and ultrasonic method can be used, but the use of a high-pressure homogenizer is particularly preferable. The high-pressure homogenizer is described in detail in US Pat. No. 4,533,254, JP-A-6-47264, and the like, but as a commercially available device, a Gorin homogenizer (APV GAULIN INC.), A microfluidizer ( MICROFLUIDEX INC.), Optimizer (Sugino Machine Co., Ltd.) and the like.
In addition, a high-pressure homogenizer equipped with a mechanism for atomizing in an ultrahigh-pressure jet stream as described in US Pat. No. 5,720,551 in recent years is particularly effective for the emulsification dispersion of the present invention. As an example of an emulsification apparatus using this ultra-high pressure jet stream, DeBEE2000 (BEE
INTERNATIONAL LTD. ).

The pressure when emulsifying with the high-pressure emulsifying dispersion device is 50 MPa or more, preferably 60 MPa or more, more preferably 180 MPa or more.
For example, it is a particularly preferable method that two or more types of emulsifiers are used in combination by a method such as emulsification with a stirring emulsifier and then passing through a high-pressure homogenizer. Also preferred is a method of once emulsifying and dispersing with these emulsifying apparatuses, adding components such as a wetting agent and a surfactant, and then passing again through the high-pressure homogenizer while the cartridge is filled with the ink composition. When a low boiling point organic solvent is contained in addition to the high boiling point organic solvent, it is preferable to remove the low boiling point solvent from the viewpoint of the stability of the emulsion and safety and health. Various known methods can be used as the method for removing the low boiling point solvent depending on the type of the solvent. That is, an evaporation method, a vacuum evaporation method, an ultrafiltration method and the like. This step of removing the low-boiling organic solvent is preferably performed as soon as possible immediately after emulsification.

  The method for preparing the inkjet ink composition is described in detail in JP-A Nos. 5-148436, 5-295212, 7-97541, 7-82515, and 7-118584. And can be used to prepare the ink composition of the present invention.

  The ink composition of the present invention can contain a functional component for imparting various functions to the ink composition. For example, as the functional component, the above-mentioned various solvents, an anti-drying agent for preventing clogging due to dry operation at the ink composition ejection port, a penetration enhancer for allowing the ink composition to penetrate well into paper, Examples include ultraviolet absorbers, antioxidants, viscosity modifiers, surface tension modifiers, dispersants, dispersion stabilizers, antifungal agents, rust inhibitors, pH adjusters, antifoaming agents, chelating agents, and the like. The ink composition can be appropriately selected and used in an appropriate amount. These functional components include a single compound that can exhibit one or more functions. Therefore, in the following blending ratio of the functional component, the handling of the functional component in the case where the function is duplicated shall include the compound in each functional component independently.

  The drying inhibitor used in the present invention is preferably a water-soluble organic solvent having a vapor pressure lower than that of water. Specific examples include ethylene glycol, propylene glycol, diethylene glycol, polyethylene glycol, thiodiglycol, dithiodiglycol, 2-methyl-1,3-propanediol, 1,2,6-hexanetriol, acetylene glycol derivatives, glycerin. Polyhydric alcohols typified by trimethylolpropane, etc., lower alkyl ethers of polyhydric alcohols such as ethylene glycol monomethyl (or ethyl) ether, diethylene glycol monomethyl (or ethyl) ether, triethylene glycol monoethyl (or butyl) ether 2-pyrrolidone, N-methyl-2-pyrrolidone, 1,3-dimethyl-2-imidazolidinone, heterocycles such as N-ethylmorpholine, sulfolane, dimethyl sulfoxide, - sulfur-containing compounds such as sulfolane, diacetone alcohol, polyfunctional compounds such as diethanolamine, and urea derivatives. Of these, polyhydric alcohols such as glycerin and diethylene glycol are more preferred. Moreover, said drying inhibitor may be used independently and may be used together 2 or more types. These drying inhibitors are preferably contained in the ink composition in an amount of 10 to 50% by mass.

  Examples of penetration enhancers used in the present invention include alcohols such as ethanol, isopropanol, butanol, di (tri) ethylene glycol monobutyl ether, 1,2-hexanediol, sodium lauryl sulfate, sodium oleate, and nonionic surfactants. Etc. can be used. If these are contained in the ink composition in an amount of 10 to 30% by mass, sufficient effects are obtained, and it is preferable to use them in a range of addition amounts that do not cause printing bleeding or paper loss (print-through).

  Examples of the ultraviolet absorber used for improving the storability of the image in the present invention include JP-A Nos. 58-185677, 61-190537, JP-A-2-782, and JP-A-5-97075. Benzotriazole compounds described in JP-A-9-34057, etc., benzophenone compounds described in JP-A No. 46-2784, JP-A No. 5-194443, US Pat. No. 3,214,463, etc. 48-30492, 56-21114, and cinnamic acid compounds described in JP-A-10-88106, JP-A-4-298503, JP-A-8-53427, and 8-239368. And triazine compounds described in JP-A-10-182621, JP-A-8-501291, etc. Jar No. Compounds described in No. 24239, compounds that emit fluorescence by absorbing ultraviolet rays typified by stilbene-based compounds and benzoxazole-based compounds, so-called fluorescent brighteners, can also be used.

  In the present invention, various organic and metal complex anti-fading agents can be used as the antioxidant used to improve image storage stability. Organic anti-fading agents include hydroquinones, alkoxyphenols, dialkoxyphenols, phenols, anilines, amines, indanes, chromans, alkoxyanilines, heterocycles, etc. Complex, zinc complex and the like. More specifically, Research Disclosure No. No. 17643, No. VII, I to J, ibid. 15162, ibid. No. 18716, page 650, left column, ibid. No. 36544, page 527, ibid. No. 307105, page 872, ibid. The compounds described in the patent cited in No. 15162 and the compounds included in the general formulas and compound examples of the representative compounds described in pages 127 to 137 of JP-A-62-215272 can be used.

  Examples of the rust inhibitor used in the present invention include acidic sulfite, sodium thiosulfate, ammonium thioglycolate, diisopropylammonium nitrite, pentaerythritol tetranitrate, dicyclohexylammonium nitrite, and benzotriazole. These are preferably used in the ink composition in an amount of 0.02 to 5.00% by mass.

The conductivity of the ink composition of the present invention is in the range of 0.01 to 10 S / m. Among these, a preferable range is a conductivity of 0.05 to 5 S / m.
The conductivity can be measured by an electrode method using commercially available saturated potassium chloride. The conductivity can be controlled mainly by the ion concentration in the aqueous solution. When the salt concentration is high, desalting can be performed using an ultrafiltration membrane or the like. Moreover, when adjusting conductivity by adding salt etc., it can adjust by adding various organic substance salt and inorganic substance salt.
Inorganic salts include potassium halide, sodium halide, sodium sulfate, potassium sulfate, sodium hydrogen sulfate, potassium hydrogen sulfate, sodium nitrate, potassium nitrate, sodium hydrogen carbonate, potassium hydrogen carbonate, sodium phosphate, sodium monohydrogen phosphate, Inorganic compounds such as boric acid, potassium dihydrogen phosphate, sodium dihydrogen phosphate, sodium acetate, potassium acetate, potassium tartrate, sodium tartrate, sodium benzoate, potassium benzoate, sodium p-toluenesulfonate, potassium saccharinate Organic compounds such as potassium phthalate and sodium picolinate can also be used.
The conductivity can also be adjusted by selecting the components of the aqueous medium described later.

The viscosity of the ink composition of the present invention is preferably 1 to 30 mPa · s at 25 ° C. More preferably, it is 2-15 mPa * s, Most preferably, it is 2-10 mPa * s. If it exceeds 30 mPa · s, the fixing speed of the recorded image becomes slow, and the discharge performance also deteriorates. If it is less than 1 mPa · s, the recorded image is blurred and the quality is lowered.
The viscosity can be arbitrarily adjusted by adding the ink solvent. Examples of the ink solvent include glycerin, diethylene glycol, triethanolamine, 2-pyrrolidone, diethylene glycol monobutyl ether, and triethylene glycol monobutyl ether.
A viscosity modifier may be used. Examples of the viscosity modifier include water-soluble polymers such as celluloses and polyvinyl alcohol, and nonionic surfactants. In more detail, “Viscosity Preparation Technology” (Technical Information Association, 1999), Chapter 9, and “Chemicals for Inkjet Printers (98 Supplement)-Material Development Trends and Prospects Survey” (CMC, 1997) 162- Page 174.

  The method for measuring the viscosity of the liquid is described in detail in JIS Z8803, but can be easily measured with a commercially available viscometer. For example, the rotary type includes Tokyo Keiki B-type viscometer and E-type viscometer. In this invention, it measured at 25 degreeC by the vibration type VM-100AL type of Yamaichi Electric. The unit of viscosity is Pascal second (Pa · s), but millipascal second (mPa · s) is usually used.

The surface tension of the ink composition used in the present invention is preferably 20 to 50 mN / m, more preferably 20 to 40 mN / m at 25 ° C. for both dynamic and static surface tension. If the surface tension exceeds 50 mN / m, the ejection quality, bleeding at the time of color mixing, print quality such as whiskers, etc. will be significantly reduced. In addition, when the surface tension of the ink composition is less than 20 mN / m, printing may be defective due to adhesion of the ink composition to the hard surface during ejection.
For the purpose of adjusting the surface tension, various cations, anions, nonionic surfactants and betaine surfactants can be added. Moreover, 2 or more types of surfactant can be used together.

  As a static surface tension measuring method, a capillary rising method, a dropping method, a hanging ring method and the like are known. In the present invention, a vertical plate method is used as a static surface tension measuring method. When a thin plate of glass or platinum is partially immersed in the liquid and hung vertically, the surface tension of the liquid acts downward along the length of contact between the liquid and the plate. The surface tension can be measured by balancing this force with an upward force.

  Examples of the dynamic surface tension measurement method include “New Experimental Chemistry Course, Vol. 18, Interface and Colloid” [Maruzen Co., Ltd., p. 69-90 (1977)], the vibration jet method, the meniscus dropping method, the maximum bubble pressure method and the like are known, and further, the liquid film destruction as described in JP-A-3-2064 is known. In the present invention, a bubble pressure differential pressure method is used as a dynamic surface tension measurement method. The measurement principle and method will be described below.

  When bubbles are generated in the solution that has become homogeneous by stirring, a new gas-liquid interface is generated, and the surfactant molecules in the solution gather on the surface of the water at a constant rate. When the bubble rate (bubble generation rate) is changed, if the generation rate slows down, more surfactant molecules gather on the surface of the bubble, so the maximum bubble pressure just before the bubble pops is reduced, The maximum bubble pressure (surface tension) relative to the bubble rate can be detected. As a preferable dynamic surface tension measurement, a method is used in which bubbles are generated in a solution using two large and small probes, the differential pressure in the maximum bubble pressure state of the two probes is measured, and the dynamic surface tension is calculated. Can be mentioned.

The non-volatile component in the ink composition of the present invention is 10 to 70% by mass of the total amount of the ink composition. The ejection stability of the ink composition, print image quality, various image fastnesses, and It is preferable from the viewpoint of bleeding and stickiness reduction on the printing surface, and is more preferably 20 to 60% by mass from the viewpoint of ejection stability of the ink composition and reduction of bleeding of the image after printing.
Here, the non-volatile component means a liquid, a solid component or a high molecular weight component having a boiling point of 150 ° C. or higher under 1 atm. Non-volatile components of ink-jet ink compositions are dyes, high-boiling solvents, polymer latex added as necessary, surfactants, dye stabilizers, antifungal agents, buffering agents, etc., and many of these non-volatile components Reduces the dispersion stability of the ink composition other than the dye stabilizer and also remains on the inkjet image-receiving paper after printing. And has the property of exacerbating image bleeding under high humidity conditions.

  In the present invention, a high molecular weight compound can also be contained. Here, the high molecular weight compound means all high molecular compounds having a number average molecular weight of 5000 or more contained in the ink composition. These polymer compounds are soluble in water-soluble polymer compounds that are substantially soluble in aqueous media, water-dispersible polymer compounds such as polymer latex and polymer emulsion, and polyhydric alcohols that are used as auxiliary solvents. Alcohol-soluble polymer compounds and the like can be mentioned, and any compound that can be dissolved or dispersed substantially uniformly in the ink composition is included in the polymer compound of the present invention.

Specific examples of the water-soluble polymer compound include polyvinyl alcohol, silanol-modified polyvinyl alcohol, carboxymethyl cellulose, hydroxyethyl cellulose, polyvinyl pyrrolidone, polyethylene oxide, water-soluble polymers such as polyoxyalkylene oxide such as polypropylene oxide, and polyalkylene oxide derivatives. polysaccharides, starch, cationized starch, casein, natural water-soluble polymers such as gelatin, polyacrylic acid, polyacrylamide or aqueous acrylic resins such as a copolymer thereof, aqueous alkyd resins, -SO in the molecule ₃ ^-, -COO ^- has a group, substantially water-soluble polymer compound soluble in an aqueous medium.
Examples of the polymer latex include styrene-butadiene latex, styrene-acrylic latex, and polyurethane latex. Furthermore, an acrylic emulsion etc. are mentioned as a polymer emulsion. These water-soluble polymer compounds can be used alone or in combination of two or more.

As described above, the water-soluble polymer compound is used as a viscosity modifier to adjust the viscosity of the ink composition in a viscosity region having good ejection characteristics. As the viscosity increases, the ejection stability of the ink composition decreases, and the nozzle becomes easily clogged by precipitates as the ink composition ages.
The addition amount of the polymer compound of the viscosity modifier depends on the molecular weight of the compound to be added (the higher the molecular weight, the smaller the addition amount may be), but the addition amount is 0 to 5% by mass with respect to the total amount of the ink composition. The content is preferably 0 to 3% by mass, more preferably 0 to 1% by mass.

  Further, in the present invention, the above-mentioned cation, anion, nonionic and betaine surfactants are necessary as a dispersant and dispersion stabilizer, and fluorine-based, silicone-based compounds and chelating agents represented by EDTA are required as an antifoaming agent. Can be used according to.

The reflection type medium that is a printing medium preferably used in the present invention will be further described. Examples of reflective media include recording paper and recording film. The support for recording paper and recording film is made of chemical pulp such as LBKP and NBKP, mechanical pulp such as GP, PGW, RMP, TMP, CTMP, CMP, and CGP, and waste paper pulp such as DIP. Additives such as known pigments, binders, sizing agents, fixing agents, cationic agents, paper strength enhancers, etc. can be mixed and manufactured using various devices such as long net paper machines and circular net paper machines. is there. As the support, in addition to these supports, either synthetic paper or plastic film sheet may be used. The thickness of the support is preferably 10 to 250 μm and the basis weight is preferably 10 to 250 g / m ² .
An image receiving layer and a back coat layer may be provided on the support as they are to provide an image receiving material for the ink composition and the ink set of the present invention, or after a size press or anchor coat layer is provided with starch, polyvinyl alcohol or the like, A back coat layer may be provided as an image receiving material. Further, the support may be flattened by a calendar device such as a machine calendar, a TG calendar, or a soft calendar.
As the support, paper and plastic film laminated on both sides with polyolefin (eg, polyethylene, polystyrene, polybutene and copolymers thereof) or polyethylene terephthalate are more preferably used. It is preferable to add a white pigment (eg, titanium oxide, zinc oxide) or a tinting dye (eg, cobalt blue, ultramarine blue, neodymium oxide) to the polyolefin.

  The image receiving layer provided on the support contains a porous material and an aqueous binder. The image receiving layer preferably contains a pigment, and the pigment is preferably a white pigment. White pigments include calcium carbonate, kaolin, talc, clay, diatomaceous earth, synthetic amorphous silica, aluminum silicate, magnesium silicate, calcium silicate, aluminum hydroxide, alumina, lithopone, zeolite, barium sulfate, calcium sulfate, titanium dioxide, Examples thereof include inorganic white pigments such as zinc sulfide and zinc carbonate, organic pigments such as styrene pigments, acrylic pigments, urea resins and melamine resins. A porous white inorganic pigment is particularly preferable, and synthetic amorphous silica having a large pore area is particularly preferable. As the synthetic amorphous silica, either anhydrous silicic acid obtained by a dry production method (gas phase method) or hydrous silicic acid obtained by a wet production method can be used.

  Specific examples of the recording paper containing the pigment in the image receiving layer include JP-A Nos. 10-81064, 10-119423, 10-157277, 10-217601, 11-348409, and JP-A-2001-138621. 2000-43401, 2000-2111235, 2000-309157, 2001-96897, 2001-138627, JP-A-11-91242, 8-2087, 8-2090, 8-2091, 8-9. 2093, 8-174992, 11-192777, JP-A-2001-301314, and the like can be used.

  The aqueous binder contained in the image receiving layer includes water-soluble polyvinyl alcohol, silanol-modified polyvinyl alcohol, starch, cationized starch, casein, gelatin, carboxymethylcellulose, hydroxyethylcellulose, polyvinylpyrrolidone, polyalkylene oxide, polyalkylene oxide derivatives, etc. Examples thereof include water-dispersible polymers such as polymers, styrene butadiene latexes, and acrylic emulsions. These aqueous binders can be used alone or in combination of two or more. In the present invention, among these, polyvinyl alcohol and silanol-modified polyvinyl alcohol are particularly preferable in terms of adhesion to the pigment and resistance to peeling of the ink receiving layer.

  The image receiving layer can contain a mordant, a water resistance agent, a light resistance improver, a gas resistance improver, a surfactant, a hardener and other additives in addition to the pigment and the aqueous binder.

The mordant added to the image receiving layer is preferably immobilized. For that purpose, a polymer mordant is preferably used.
For the polymer mordant, JP-A-48-28325, 54-74430, 54-124726, 55-22766, 55-142339, 60-23850, 60-23835, 60-23852, 60-23853, 60-57836, 60-60643, 60-118834, 60-122940, 60-122941, 60-122942, 60- No. 235134, JP-A-1-161236, U.S. Pat.Nos. 2,484,430, 2,548,564, 3,148,061, 3,309,690, 4,115,124, 4,124,386, 4,193,800, 4,283,853, 4,282,305, It is described in each specification of the same No. 4450224. An image receiving material containing a polymer mordant described in JP-A-1-161236, pages 212 to 215 is particularly preferred. When the polymer mordant described in the publication is used, an image with excellent image quality is obtained and the light resistance of the image is improved.

  The water-proofing agent is effective for making the image water-resistant. As these water-proofing agents, cationic resins are particularly desirable. Examples of such a cationic resin include polyamide polyamine epichlorohydrin, polyethyleneimine, polyamine sulfone, dimethyldiallylammonium chloride polymer, and cationic polyacrylamide. The content of these cationic resins is preferably 1 to 15% by mass, particularly 3 to 10% by mass, based on the total solid content of the ink receiving layer.

Examples of the light resistance improver and gas resistance improver include phenol compounds, hindered phenol compounds, thioether compounds, thiourea compounds, thiocyanate compounds, amine compounds, hindered amine compounds, TEMPO compounds, hydrazine compounds, hydrazide compounds, amidine compounds, Vinyl group-containing compounds, ester compounds, amide compounds, ether compounds, alcohol compounds, sulfinic acid compounds, saccharides, water-soluble reducing compounds, organic acids, inorganic acids, hydroxy group-containing organic acids, benzotriazole compounds, benzophenone compounds, triazine compounds , Heterocyclic compounds, water-soluble metal salts, organometallic compounds, metal complexes and the like.
Specific examples of these compounds include JP-A-10-182621, JP-A-2001-260519, JP-A-2000-260519, JP-B-4-34953, JP-B-4-34513, and JP-B-4-34512. , JP-A-11-170686, JP-A-60-67190, JP-A-7-276808, JP-A-2000-94829, JP-T 8-512258, JP-A-11-321090, etc. Is given.

The surfactant functions as a coating aid, a peelability improver, a slippage improver or an antistatic agent. The surfactant is described in JP-A Nos. 62-173463 and 62-183457.
An organic fluoro compound may be used in place of the surfactant. The organic fluoro compound is preferably hydrophobic. Examples of the organic fluoro compound include a fluorine-based surfactant, an oily fluorine-based compound (eg, fluorine oil), and a solid fluorine compound resin (eg, tetrafluoroethylene resin). The organic fluoro compounds are described in JP-B-57-9053 (columns 8 to 17), JP-A-61-20994, and 62-135826.

  As the hardener, materials described in JP-A-1-161236, page 222, JP-A-9-263036, JP-A-10-119423, and JP-A-2001-310547 can be used.

  Examples of other additives to be added to the image receiving layer include pigment dispersants, thickeners, antifoaming agents, dyes, fluorescent whitening agents, preservatives, pH adjusters, and matting agents. The ink receiving layer may be one layer or two layers.

The recording paper and the recording film can be provided with a back coat layer, and examples of components that can be added to this layer include a white pigment, an aqueous binder, and other components.
Examples of white pigments contained in the backcoat layer include light calcium carbonate, heavy calcium carbonate, kaolin, talc, calcium sulfate, barium sulfate, titanium dioxide, zinc oxide, zinc sulfide, zinc carbonate, satin white, and aluminum silicate. , Diatomaceous earth, calcium silicate, magnesium silicate, synthetic amorphous silica, colloidal silica, colloidal alumina, pseudoboehmite, aluminum hydroxide, alumina, lithopone, zeolite, hydrous halloysite, magnesium carbonate, magnesium hydroxide, white inorganic pigment, styrene And organic pigments such as polyethylene plastic pigments, acrylic plastic pigments, polyethylene, microcapsules, urea resins, and melamine resins.

  As the aqueous binder contained in the backcoat layer, styrene / maleate copolymer, styrene / acrylate copolymer, polyvinyl alcohol, silanol modified polyvinyl alcohol, starch, cationized starch, casein, gelatin, carboxymethylcellulose Water-soluble polymers such as hydroxyethyl cellulose and polyvinyl pyrrolidone, and water-dispersible polymers such as styrene butadiene latex and acrylic emulsion. Examples of other components contained in the backcoat layer include an antifoaming agent, an antifoaming agent, a dye, a fluorescent brightening agent, a preservative, and a water-proofing agent.

  A polymer fine particle dispersion may be added to the constituent layers (including the back layer) of the inkjet recording paper and recording film. The polymer fine particle dispersion is used for the purpose of improving the physical properties of the film such as dimensional stabilization, curling prevention, adhesion prevention, and film cracking prevention. The polymer fine particle dispersion is described in JP-A Nos. 62-245258, 62-136648, and 62-110066. When a polymer fine particle dispersion having a low glass transition temperature (40 ° C. or lower) is added to a layer containing a mordant, cracking and curling of the layer can be prevented. Further, even when a polymer fine particle dispersion having a high glass transition temperature is added to the back layer, curling can be prevented.

  The ink composition of the present invention can also be used for purposes other than inkjet recording. For example, it can be used for display image materials, image forming materials for interior decoration materials, and image forming materials for outdoor decoration materials.

  Display image materials include posters, wallpaper, small decorative items (such as figurines and dolls), commercial flyers, wrapping paper, wrapping materials, paper bags, plastic bags, packaging materials, signs, transportation (automobiles, buses, trains, etc.) ) Refers to various things such as images drawn and attached to the side, clothes with logos, and so on. When the dye of the present invention is used as a material for forming a display image, the image includes all patterns of dyes that can be recognized by humans, such as abstract designs, characters, and geometric patterns, in addition to images in a narrow sense.

  The interior decoration material refers to various items such as wallpaper, decorative accessories (such as figurines and dolls), lighting fixture members, furniture members, floor and ceiling design members. When the dye of the present invention is used as an image forming material, the image includes all patterns of dyes that can be recognized by humans such as abstract designs, characters, and geometric patterns in addition to images in a narrow sense.

  The outdoor decoration material refers to various materials such as wall materials, roofing materials, signboards, gardening materials, outdoor decoration accessories (such as figurines and dolls), and members of outdoor lighting equipment. When the dye of the present invention is used as an image forming material, the image includes not only images in a narrow sense but also all patterns of dyes that can be recognized by humans, such as abstract designs, characters, and geometric patterns.

  In the above applications, examples of media on which a pattern is formed include various materials such as paper, fiber, cloth (including non-woven fabric), plastic, metal, and ceramics. As the dyeing form, the dye can be fixed in the form of mordanting, printing, or a reactive dye having a reactive group introduced. Among these, it is preferable that the mordanting is performed.

In the production of an ink stock solution or an ink composition, ultrasonic vibration can be applied to the dissolution step of additives such as dyes.
Ultrasonic vibration means that ultrasonic energy equal to or higher than the energy received by the recording head is preliminarily applied during the manufacturing process of the ink composition in order to prevent the ink composition from generating bubbles due to the pressure applied by the recording head. In addition to removing bubbles.
The ultrasonic vibration is usually an ultrasonic wave having a frequency of 20 kHz or higher, preferably 40 kHz or higher, more preferably 50 kHz. The energy applied to the liquid by ultrasonic vibration is usually 2 × 10 ⁷ J / m ³ or more, preferably 5 × 10 ⁷ J / m ³ or more, more preferably 1 × 10 ⁸ J / m ³ or more. . Further, the application time of ultrasonic vibration is usually about 10 minutes to 1 hour.
The step of applying ultrasonic vibration shows an effect at any time after the dye is put into the medium. Even if ultrasonic vibration is applied after the completed ink composition is stored once, the effect is exhibited. However, adding ultrasonic vibration when dissolving and / or dispersing the dye in the medium has a greater effect of removing bubbles, and the ultrasonic vibration promotes dissolution and / or dispersion of the dye in the medium. Therefore, it is preferable.
That is, the step of applying at least ultrasonic vibration can be performed in any case, either during or after the step of dissolving and / or dispersing the dye in the medium. In other words, the step of applying at least ultrasonic vibration can be arbitrarily performed once or more after the ink composition is prepared until it becomes a product.
As an embodiment, the step of dissolving and / or dispersing in the medium preferably includes a step of dissolving the dye in a medium of a part of the whole medium and a step of mixing the remaining medium, and at least one of the above It is preferable to apply ultrasonic vibration to this step, and it is more preferable to apply at least ultrasonic vibration to the step of dissolving the dye in a part of the medium.
The step of mixing the remaining solvent may be a single step or a plurality of steps. In addition, it is preferable to use heat degassing or vacuum degassing in combination with the production of the ink composition according to the present invention because the effect of removing bubbles in the ink composition is improved. The heating degassing step or the vacuum degassing step is preferably performed simultaneously with or after the step of mixing the remaining medium. Examples of the ultrasonic vibration generating means in the step of applying ultrasonic vibration include known devices such as an ultrasonic disperser.

When preparing the ink stock solution or ink composition of the present invention, a step of removing dust which is a solid content by filtration, which is performed after further preparation, is important. A filtration filter is used for this work. The filtration filter at this time is a filter having an effective diameter of 1 μm or less, preferably 0.3 μm or less and 0.05 μm or more, particularly preferably 0.3 μm or less and 0.25 μm or more. Use. Various materials can be used as the filter material, but in the case of an ink composition of a water-soluble dye, it is preferable to use a filter prepared for an aqueous solvent. Among them, it is particularly preferable to use a filter made of a polymer material that hardly generates dust. As the filtration method, the solution may be passed through a solution, and either pressure filtration or vacuum filtration can be used.
After this filtration, air is often taken into the solution. Since bubbles caused by air often cause image disturbance in ink jet recording, it is preferable to separately provide the aforementioned defoaming step. As the defoaming method, the filtered solution may be allowed to stand, or various methods such as ultrasonic defoaming and vacuum defoaming using a commercially available apparatus can be used. In the case of defoaming with ultrasonic waves, the defoaming operation is preferably performed for about 30 seconds to 2 hours, more preferably about 5 minutes to 1 hour.
These operations are preferably performed using a space such as a clean room or a clean bench in order to prevent dust from entering during the operation. In the present invention, it is particularly preferable to perform this operation in a space of class 1000 or less as the cleanliness. Here, “cleanness” refers to a value measured by a dust counter.

  The droplet ejection volume of the ink composition on the recording material in the invention is from 0.1 pl to 100 pl. A preferable range of the droplet ejection volume is 0.5 pl or more and 50 pl or less, and a particularly preferable range is 2 pl or more and 50 pl or less.

[Ink for ink jet recording, ink jet recording method, ink cartridge for ink jet recording, ink jet recording apparatus and ink jet recorded matter]
The ink for inkjet recording of the present invention contains the above aqueous solution or ink composition of the present invention.
The inkjet recording method of the present invention is a method for forming a colored image (sometimes simply referred to as an image) on a recording material (recording material) using an inkjet recording ink.
In the present invention, there is no limitation on the ink jet recording method as long as the image recording is performed by an ink jet printer using the ink composition or ink set of the present invention, and a known method such as electrostatic attraction is used. The charge control method for discharging the ink composition, the drop-on-demand method (pressure pulse method) that uses the vibration pressure of the piezo element, the electrical signal is converted into an acoustic beam, and the ink composition is irradiated and the radiation pressure is used. It is used in acoustic ink jet systems that eject ink compositions, thermal ink jet (bubble jet (registered trademark)) systems that use the pressure generated by heating the ink composition to form bubbles.
Inkjet recording methods include a method of ejecting a large number of low-density ink compositions called photo inks in a small volume, a method of improving image quality using a plurality of ink compositions having substantially the same hue and different concentrations, and colorless and transparent. The method using the ink composition is included. The droplet ejection volume of the ink composition is mainly controlled by the print head.

  For example, in the case of the thermal ink jet method, the droplet ejection volume can be controlled by the structure of the print head. That is, droplets can be ejected in a desired size by changing the sizes of the ink chamber, the heating unit, and the nozzle. Even in the case of the thermal ink jet method, it is possible to realize droplet ejection of a plurality of sizes by providing a plurality of print heads having different heating parts and nozzle sizes. In the case of the drop-on-demand method using a piezo element, the droplet ejection volume can be changed due to the structure of the print head as in the thermal ink jet method, but the waveform of the drive signal that drives the piezo element is controlled as described later. By doing so, droplets of a plurality of sizes can be ejected with a print head having the same structure.

The ejection frequency when the ink composition of the present invention is ejected onto a recording material is preferably 1 KHz or more.
In order to record a high-quality image such as a photograph, it is necessary to set the droplet ejection density to 600 dpi (number of dots per inch) or more in order to reproduce a sharp image with small ink droplets.
On the other hand, when the ink composition is ejected by a head having a plurality of nozzles, the number of heads that can be driven simultaneously is about several tens to 200 in the type in which the recording paper and the head are moved and recorded in directions orthogonal to each other. There is a restriction that the number of heads called line heads is fixed even in the hundreds. This is because there are restrictions on driving power, and heat generated by the head affects the image, so that a large number of head nozzles cannot be driven simultaneously.
Here, the recording speed can be increased by increasing the drive frequency. In the case of the thermal ink jet method, the droplet ejection frequency can be controlled by controlling the frequency of the head drive signal for heating the head.
In the case of the piezo method, this is possible by controlling the frequency of a signal for driving the piezo. The driving of the piezo head will be described. For the image signal to be printed, the droplet size, droplet ejection speed, and droplet ejection frequency are determined by the printer control unit, and a signal for driving the print head is created. The drive signal is supplied to the print head. The droplet ejection size, droplet ejection speed, and droplet ejection frequency are controlled by a signal for driving the piezo. Here, the droplet ejection size and droplet ejection speed are determined by the shape and amplitude of the drive waveform, and the frequency is determined by the signal repetition period.
When this droplet ejection frequency is set to 10 kHz, the head is driven every 100 microseconds, and recording of one line is completed in 400 microseconds. By setting the moving speed of the recording paper to move 1/600 inch in 400 microseconds, that is, approximately 42 microns, it is possible to print at a speed of one sheet in 1.2 seconds.

The present invention also relates to an ink jet recording ink cartridge filled with the above ink jet recording ink.
As for the configuration of the printing apparatus and the printer used in the present invention, for example, a mode as disclosed in JP-A-11-170527 is preferable. For the ink cartridge, for example, the one disclosed in Japanese Patent Laid-Open No. 5-229133 is suitable. With respect to the suction and the configuration of a cap or the like that covers the print head at that time, for example, the one disclosed in JP-A-7-276671 is preferable. Further, it is preferable that a filter for eliminating bubbles as disclosed in JP-A-9-277552 is provided in the vicinity of the head.
The surface of the nozzle is preferably subjected to water repellent treatment as described in JP-A-2002-292878. The application may be a printer connected to a computer or an apparatus specialized for printing photographs.
In the ink jet recording method applied to the present invention, it is preferable that the average droplet ejection speed when ejecting the ink composition onto a recording material is 2 m / sec or more, preferably 5 m / sec or more. The droplet ejection speed is controlled by controlling the shape and amplitude of the waveform that drives the head. In addition, by using a plurality of drive waveforms properly, it is possible to eject droplets of a plurality of sizes with the same head.

Hereinafter, a recording paper and a recording film, which are examples of a recording material used for ink-jet printing using the ink of the present invention, will be described.
The support in recording paper and recording film is made of chemical pulp such as LBKP and NBKP, mechanical pulp such as GP, PGW, RMP, TMP, CTMP, CMPMP, CGP, and waste paper pulp such as DIP. Additives such as known pigments, binders, sizing agents, fixing agents, cationic agents, paper strength enhancers, etc. can be mixed and manufactured using various devices such as long net paper machines and circular net paper machines. is there. In addition to these supports, either synthetic paper or plastic film sheets may be used. The thickness of the support is preferably 10 to 250 μm and the basis weight is preferably 10 to 250 g / m ² . The support may be provided with an ink receiving layer and a backcoat layer as they are, or after a size press or anchor coat layer is provided with starch, polyvinyl alcohol or the like, an ink receiving layer and a backcoat layer may be provided. Further, the support may be flattened by a calendar device such as a machine calendar, a TG calendar, or a soft calendar. In the present invention, as the support, paper and plastic films laminated on both sides with polyolefin (for example, polyethylene, polystyrene, polyethylene terephthalate, polybutene and copolymers thereof) are more preferably used. It is preferable to add a white pigment (for example, titanium oxide or zinc oxide) or a tinting dye (for example, cobalt blue, ultramarine blue, or neodymium oxide) to the polyolefin.

  The ink jet recorded matter of the present invention is formed by forming a colored image on a recording material using the above-described ink for ink jet recording of the present invention. Here, the image formation can be suitably obtained by adopting an ink jet recording method using the above-described ink jet recording apparatus.

  The present invention will be described more specifically with reference to the following examples. The materials, reagents, ratios, equipment, operations, and the like shown in the following examples can be appropriately changed without departing from the spirit of the present invention. Therefore, the scope of the present invention is not limited to the specific examples shown below. In the following examples, “%” and “parts” represent “% by mass” and “parts by mass” unless otherwise specified, and the molecular weight indicates the mass average molecular weight.

[Synthesis Example 1]
A synthesis scheme of BLACK-1 is shown below.

(1) Synthesis of intermediate (b-1):
To a three-necked flask, 200 g of 3-aminoacetophenone (a-1), 117.4 g of malononitrile, 114 g of ammonium acetate, 142 g of acetic acid and 500 mL of toluene were added, and the temperature was raised to an internal temperature of 100 ° C. After stirring for 2 hours, the internal temperature was cooled to 25 ° C., 500 mL of methanol was added, and the precipitated crystals were separated by filtration. The crystals were washed twice with 100 mL of methanol and dried at 50 ° C. to obtain 210 g of yellow crystal intermediate (b-1).

(2) Synthesis of intermediate (d-1):
Intermediate (b-1) 50.0g, sulfur 8.58g, and methanol 150mL were added to the three necked flask. To this suspension, 13.8 g of triethylamine was added dropwise, and the temperature was raised to an internal temperature of 60 ° C. After stirring for 3 hours, a methanol solution of intermediate (c-1) cooled to an internal temperature of 15 ° C. was obtained. To the methanol solution of the obtained intermediate (c-1), 27.3 g of succinic anhydride was added and stirred at room temperature for 1 hour. The precipitated crystals were separated by filtration, washed twice with 10 mL of methanol, and dried at 50 ° C. to obtain 37.9 g of yellow crystal intermediate (d-1).

(3) Synthesis of intermediate (f-1):
6.0 g of 5-aminoisophthalic acid (e-1) was suspended in 36 mL of water, and 9.4 mL of 12N hydrochloric acid was added dropwise at room temperature. After cooling to an internal temperature of 4 ° C. in an ice bath, 5 mL of an aqueous solution of 2.51 g of sodium nitrite was added dropwise at an internal temperature of 5 ° C. or lower and stirred for 30 minutes. Thereafter, 0.7 g of amidosulfuric acid was added, followed by stirring at an internal temperature of 5 ° C. for 10 minutes to obtain a diazonium solution. Separately, 10.9 g of intermediate (d-1) was suspended in 178 mL of water, and the above diazonium solution was added dropwise at room temperature over 20 minutes. The mixture was heated to an internal temperature of 40 ° C., stirred at 40 ° C. for 30 minutes, and then cooled to room temperature. The crystals were separated by filtration and washed with 20 mL of water and 10 mL of isopropyl alcohol. Drying at 50 ° C. yielded 17.6 g of brown crystals of intermediate (f-1).

(4) Synthesis of BLACK-1:
To a suspension of 17.6 g of intermediate (f-1), 20.7 g of intermediate (g) and 420 mL of water, 10.1 g of isoamyl nitrite was added dropwise at room temperature. After stirring for 2 hours at an internal temperature of 25 ° C., a 4M aqueous lithium hydroxide solution was added dropwise until the pH reached 8.3. Subsequently, 1.0 L of isopropyl alcohol was added dropwise, the crystals were filtered off, and washed twice with 100 mL of isopropyl alcohol. The isolated crystal was added to 100 mL of water, and 300 mL of isopropyl alcohol was added dropwise thereto. After stirring for 5 minutes, the crystals were filtered off and washed twice with 30 mL of isopropyl alcohol. The obtained crystals were dried at 50 ° C. to obtain 27.6 g of BLACK-1 black crystals. As a result of MS spectrum, 194.6 corresponding to [(M-5) / 5] ⁻ in the free form of BLACK-1 was observed. The absorption spectrum of the compound in an aqueous solution was 591 nm.

[Synthesis Example 2]
(1) Synthesis of BLACK-2 After dissolving 2.0 g of black crystals of BLACK-1 in 40 mL of water and passing a cation exchange resin (Amberlite IR-120, manufactured by Organo Corporation) filled with sodium ions. And concentrated. The obtained crystals were dried at 50 ° C. to obtain 1.9 g of BLACK-2 black crystals.

[Synthesis Example 3]
(1) Synthesis of BLACK-3 After dissolving 2.0 g of black crystals of BLACK-1 in 40 mL of water and passing through a cation exchange resin (Amberlite IR-120, manufactured by Organo Corporation) filled with potassium ions. And concentrated. The obtained crystals were dried at 50 ° C. to obtain 2.0 g of BLACK-3 black crystals.

[Synthesis Example 4]
A synthesis scheme of BLACK-4 is shown below.

(1) Synthesis of intermediate (b-2):
To 78 mL of an aqueous solution of 7.8 g of thiourea, 25.0 g of 2-bromo-3′-nitroacetophenone (a-2; Wako Pure Chemical Industries) was added and stirred at 70 ° C. for 5 hours. After the crystals were separated by filtration, 240 mL of 5% aqueous sodium hydroxide solution was added, and the mixture was stirred at room temperature for 3 hours, and then the crystals were separated by filtration. After drying at 50 ° C., 31.1 g of yellow crystals of intermediate (b-2) were obtained.

(2) Synthesis of intermediate (c-2):
To the three-necked flask, 82.1 g of reduced iron, 7.1 g of ammonium chloride, 50 mL of water and 360 mL of isopropyl alcohol were added, refluxed for 30 minutes, 30.0 g of intermediate (b-2) was added, and the mixture was stirred at reflux for 2 hours. did. After filtration, the filtrate was concentrated to dryness to obtain 17.5 g of yellow crystals of intermediate (c-2).

(3) Synthesis of intermediate (d-2):
To a three-necked flask, 5.0 g of intermediate (c-2), 2.6 g of succinic anhydride, and 50 mL of acetonitrile were added and stirred at reflux. After stirring under reflux for 1 hour, the mixture was cooled to room temperature, and the precipitated crystals were separated by filtration and washed twice with 10 mL of acetonitrile. The obtained crystals were dried at 50 ° C. to obtain 7.2 g of yellow crystal intermediate (d-2).

(4) Synthesis of intermediate (f-2):
1.8 g of 5-aminoisophthalic acid (e-1) was suspended in 18 mL of water, and 2.5 mL of 12N hydrochloric acid was added dropwise at room temperature. After cooling to an internal temperature of 4 ° C. in an ice bath, 1.5 mL of an aqueous solution of 0.7 g of sodium nitrite was dropped at an internal temperature of 5 ° C. or less, and the mixture was stirred for 30 minutes. Thereafter, 0.09 g of urea was added and subsequently stirred at an internal temperature of 5 ° C. for 10 minutes to obtain a diazonium solution. Separately, 2.9 g of intermediate (d-2) was dissolved in 120 mL of dimethylacetamide, and the previous diazonium solution was added dropwise at 4 ° C. over 10 minutes. After stirring at 4 ° C. for 3 hours, the temperature was raised to room temperature. To this solution, 120 mL of water was added dropwise, and the resulting crystals were separated by filtration and washed with 10 mL of water and 10 mL of isopropyl alcohol. It dried at 50 degreeC and 4.7g of brown crystals of the intermediate body (f-2) were obtained.

(5) Synthesis of BLACK-4:
To a suspension of 2.0 g of intermediate (f-2), 2.5 g of intermediate (g) and 50 mL of water, 1.2 g of isoamyl nitrite was added dropwise at room temperature. After stirring at an internal temperature of 20 ° C. for 3 hours, a 4M lithium hydroxide aqueous solution was added dropwise until the pH reached 8.3. Subsequently, 240 mL of isopropyl alcohol was added dropwise, the crystals were filtered off, and washed twice with 10 mL of isopropyl alcohol. The isolated crystal was added to 30 mL of water, and 135 mL of isopropyl alcohol was added dropwise thereto. After stirring for 5 minutes, the crystals were filtered off and washed twice with 10 mL of isopropyl alcohol. The obtained crystals were dried at 50 ° C. to obtain 2.1 g of BLACK-4 black crystals. As a result of MS spectrum, 189.8 corresponding to [(M-5) / 5] ⁻ in the free form of BLACK-4 was observed. The absorption spectrum of the compound in an aqueous solution was 574 nm.

[Synthesis Example 5]
(1) Synthesis of BLACK-5 After dissolving 1.2 g of BLACK-4 black crystals in 20 mL of water and passing through a cation exchange resin (Amberlite IR-120, manufactured by Organo) filled with sodium ions. And concentrated. The obtained crystals were dried at 50 ° C. to obtain 1.1 g of BLACK-5 black crystals.

[Synthesis Example 6]
(1) Synthesis of BLACK-6 After dissolving 1.2 g of black crystals of BLACK-4 in 20 mL of water and passing through a cation exchange resin (Amberlite IR-120, manufactured by Organo Corporation) filled with potassium ions. And concentrated. The obtained crystal was dried at 50 ° C. to obtain 1.3 g of BLACK-6 black crystal.

[Synthesis Example 7]
A synthesis scheme of BLACK-8 is shown below.

(1) Synthesis of intermediates (b-1) and (d-1):
The compound was synthesized by the method described in Synthesis Example (1) above.

(2) Synthesis of intermediate (f-3):
3-aminobenzenesulfonic acid (e-3) 3.0g was suspended in water 15mL, and 4M lithium hydroxide aqueous solution 4.3mL was added. After cooling to an internal temperature of 5 ° C. in an ice bath, 2.5 mL of an aqueous solution of 1.3 g of sodium nitrite was added dropwise at an internal temperature of 10 ° C. or lower and stirred for 10 minutes. Separately, 5.8 mL of 12N hydrochloric acid and 10 mL of water were mixed and cooled to an internal temperature of 4 ° C. with an ice bath. Here, the solution of 3-aminobenzenesulfonic acid was dropped at 5 ° C. or lower. After stirring at 5 ° C. or lower for 30 minutes, 0.4 g of amidosulfuric acid was added, and subsequently stirred at an internal temperature of 5 ° C. for 10 minutes to obtain a diazonium solution. Separately, 5.5 g of intermediate (d-1) was suspended in 100 mL of water, and the previous diazonium solution was added dropwise at room temperature over 5 minutes. The mixture was heated to 40 ° C., stirred at 40 ° C. for 30 minutes, and then cooled to room temperature. The obtained crystals were separated by filtration and washed with 10 mL of water and 10 mL of isopropyl alcohol. It dried at 50 degreeC and obtained 8.7g of brown crystals of the intermediate (f-3).

(3) Synthesis of BLACK-8:
8.7 g of the intermediate (f-3) was suspended in 50 mL of water, and 4M lithium hydroxide aqueous solution was added at room temperature until the pH reached 6.5. Then, 1.3 g of sodium nitrite was added, and 5 mL at room temperature was added. Stir for minutes. Separately, 8.8 g of intermediate (g) was dissolved in 30 mL of water, 2.9 mL of 12N hydrochloric acid was added, and the solution of the intermediate (f-3) was added thereto at room temperature over 10 minutes. After stirring for 1 hour at an internal temperature of 25 ° C., a 4M aqueous lithium hydroxide solution was added dropwise until pH 8.3 was reached. Subsequently, 500 mL of isopropyl alcohol was added dropwise, and the crystals were separated by filtration and washed twice with 50 mL of isopropyl alcohol. The isolated crystal was added to 150 mL of water, and 225 mL of isopropyl alcohol was added dropwise thereto. After stirring for 5 minutes, the crystals were filtered off and washed twice with 20 mL of isopropyl alcohol. The obtained crystals were dissolved in 100 mL of water, passed through a cation exchange resin (manufactured by Organo, Amberlite IR-120) filled with lithium ions, and then concentrated. The obtained crystals were dried at 50 ° C. to obtain 6.1 g of BLACK-8 black crystals. As a result of MS spectrum, 241.5 corresponding to [(M-4) / 4] ⁻ of the free form of BLACK-8 was observed. The absorption spectrum of the compound in an aqueous solution was 585 nm.

[Synthesis Example 8]
(1) Synthesis of BLACK-9 After dissolving 2.0 g of black crystals of BLACK-8 in 40 mL of water and passing through a cation exchange resin (Amberlite IR-120, manufactured by Organo) filled with sodium ions. And concentrated. The obtained crystals were dried at 50 ° C. to obtain 1.8 g of BLACK-9 black crystals.

[Synthesis Example 9]
(1) Synthesis of BLACK-10 After dissolving 2.0 g of black crystals of BLACK-8 in 40 mL of water and passing through a cation exchange resin (Amberlite IR-120, manufactured by Organo Corporation) filled with potassium ions. And concentrated. The obtained crystals were dried at 50 ° C. to obtain 1.9 g of BLACK-10 black crystals.

[Synthesis Example 10]
A synthesis scheme of BLACK-11 is shown below.

(1) Synthesis of intermediates (b-1) and (d-1):
The compound was synthesized by the method described in Synthesis Example (1) above.

(2) Synthesis of intermediate (f-4):
2.5 g of 2-amino-1,5-benzenedisulfonic acid (e-4) was suspended in 20 mL of water, and 2.5 mL of 12N hydrochloric acid was added dropwise at room temperature. After cooling to an internal temperature of 4 ° C. in an ice bath, 1.5 mL of an aqueous solution of 0.7 g of sodium nitrite was dropped at an internal temperature of 5 ° C. or less, and the mixture was stirred for 30 minutes. Thereafter, 0.2 g of amidosulfuric acid was added, followed by stirring at an internal temperature of 5 ° C. for 10 minutes to obtain a diazonium solution. Separately, it was suspended in 3.2 g of intermediate (d-1), 20 mL of water and 20 mL of methanol, 2.5 mL of 4M lithium hydroxide aqueous solution was added, and the previous diazonium solution was added dropwise thereto at room temperature over 20 minutes. The mixture was heated to an internal temperature of 50 ° C., stirred at 50 ° C. for 2 hours, and then cooled to room temperature. The crystals were filtered off and washed with 50 mL of isopropyl alcohol. It dried at 50 degreeC and 2.0g of brown crystals of the intermediate body (f-4) were obtained.

(3) Synthesis of BLACK-11:
After suspending 2.0 g of intermediate (f-4) in 10 mL of water and adding a 4M aqueous lithium hydroxide solution at room temperature until the pH reached 8.4, 0.25 g of sodium nitrite was added, and room temperature was maintained for 10 minutes. And stirred. Separately, 1.6 g of intermediate (g) was dissolved in 6.0 mL of water, 0.6 mL of 12N hydrochloric acid was added, and the solution of the previous intermediate (f-4) was added thereto at room temperature over 10 minutes. After stirring for 1 hour at an internal temperature of 25 ° C., a 4M aqueous lithium hydroxide solution was added dropwise until pH 8.3 was reached. Subsequently, 80 mL of isopropyl alcohol was added dropwise, the crystals were filtered off, and washed twice with 20 mL of isopropyl alcohol. The isolated crystal was added to 20 mL of water, and 90 mL of isopropyl alcohol was added dropwise thereto. After stirring for 5 minutes, the crystals were filtered off and washed twice with 10 mL of isopropyl alcohol. The obtained crystals were dissolved in 20 mL of water, passed through a cation exchange resin (Amberlite IR-120, manufactured by Organo Corporation) filled with lithium ions, and then concentrated. The obtained crystals were dried at 50 ° C. to obtain 2.2 g of BLACK-11 black crystals. As a result of MS spectrum, 209.0 corresponding to [(M-5) / 5] ⁻ of the free form of BLACK-11 was observed. The absorption spectrum of the compound in an aqueous solution was 600 nm.

[Synthesis Example 11]
A synthesis scheme of BLACK-14 is shown below.

(1) Synthesis of intermediates (b-1) and (d-1):
The compound was synthesized by the method described in Synthesis Example (1) above.

(2) Synthesis of intermediate (f-5):
3.0 g of 3-amino-4-chlorobenzenesulfonic acid (e-5) was suspended in 20 mL of water, and 3.6 mL of 4M lithium hydroxide aqueous solution was added. After cooling to an internal temperature of 5 ° C. with an ice bath, 2 mL of an aqueous solution of 1.1 g of sodium nitrite was added dropwise at an internal temperature of 10 ° C. or lower, and the mixture was stirred for 10 minutes. Separately, 4.8 mL of 12N hydrochloric acid and 10 mL of water were mixed and cooled to an internal temperature of 4 ° C. in an ice bath. Here, the solution of 3-amino-4-chlorobenzenesulfonic acid was dropped at 5 ° C. or lower. After stirring at 5 ° C. or lower for 30 minutes, 0.28 g of amidosulfuric acid was added, and subsequently stirred at an internal temperature of 5 ° C. for 10 minutes to obtain a diazonium solution. Separately, 4.6 g of the intermediate (d-1) was suspended in 100 mL of water, and the above diazonium solution was added dropwise at room temperature over 5 minutes. The mixture was heated to 40 ° C., stirred at 40 ° C. for 30 minutes, and then cooled to room temperature. The obtained crystals were separated by filtration and washed with 10 mL of water and 10 mL of isopropyl alcohol. It dried at 50 degreeC and obtained 7.7g of brown crystals of the intermediate body (f-5).

(3) Synthesis of BLACK-14:
7.7 g of the intermediate (f-5) was suspended in 100 mL of water, and 4 M lithium hydroxide aqueous solution was added at room temperature until the pH reached 6.5. Then, 1.1 g of sodium nitrite was added, and 5 g at room temperature was added. Stir for minutes. Separately, 7.2 g of intermediate (g) was dissolved in 50 mL of water, 2.4 mL of 12N hydrochloric acid was added thereto, and the solution of the intermediate (f-5) was added thereto at room temperature over 10 minutes. After stirring for 1 hour at an internal temperature of 25 ° C., a 4M aqueous lithium hydroxide solution was added dropwise until pH 8.3 was reached. Subsequently, 300 mL of isopropyl alcohol was added dropwise, the crystals were filtered off, and washed twice with 30 mL of isopropyl alcohol. The isolated crystal was added to 60 mL of water, and 120 mL of isopropyl alcohol was added dropwise thereto. After stirring for 5 minutes, the crystals were filtered off and washed twice with 10 mL of isopropyl alcohol. The obtained crystals were dissolved in 100 mL of water, passed through a cation exchange resin (manufactured by Organo, Amberlite IR-120) filled with lithium ions, and then concentrated. The obtained crystals were dried at 50 ° C. to obtain 5.1 g of BLACK-14 black crystals. As a result of MS spectrum, 250.0 corresponding to [(M-4) / 4] ⁻ in the free form of BLACK-14 was observed. The absorption spectrum of the compound in an aqueous solution was 596 nm.

[Synthesis Example 12]
A synthesis scheme of BLACK-15 is shown below.

(1) Synthesis of intermediates (b-1) and (d-1):
The compound was synthesized by the method described in Synthesis Example (1) above.

(2) Synthesis of intermediate (f-6):
3.0 g of sodium 2-amino-4-nitrobenzenesulfonate (e-6) was suspended in 10 mL of acetic acid and 5 mL of propionic acid. After cooling to an internal temperature of 5 ° C. in an ice bath, 3.9 g of 43% nitrosylsulfuric acid was added dropwise at an internal temperature of 10 ° C. or less. After stirring at an internal temperature of 5 ° C. for 1 hour, 0.08 g of urea was added, and then stirred at an internal temperature of 5 ° C. for 10 minutes. Separately, 3.9 g of the intermediate (d-1) was suspended in 60 mL of water, and 3.1 mL of 4M lithium hydroxide aqueous solution was added, and then the above diazonium solution was added dropwise at room temperature over 5 minutes. After stirring at an internal temperature of 25 ° C. for 1 hour, the obtained crystals were separated by filtration and washed twice with 10 mL of water. By drying at 50 ° C., 6.8 g of brown crystals of intermediate (f-6) were obtained.

(3) Synthesis of BLACK-15:
6.8 g of intermediate (f-5) was suspended in 50 mL of water, and 4M aqueous lithium hydroxide solution was added at room temperature until the pH reached 6.3. Then, 0.9 g of sodium nitrite was added, and 5 g at room temperature was added. Stir for minutes. Separately, 6.3 g of intermediate (g) was dissolved in 50 mL of water, 2.1 mL of 12N hydrochloric acid was added thereto, and the solution of the intermediate (f-6) was added thereto at room temperature over 10 minutes. After stirring for 1 hour at an internal temperature of 25 ° C., a 4M aqueous lithium hydroxide solution was added dropwise until pH 8.3 was reached. Subsequently, 300 mL of isopropyl alcohol was added dropwise, the crystals were filtered off, and washed twice with 50 mL of isopropyl alcohol. The isolated crystal was added to 70 mL of water, and 140 mL of isopropyl alcohol was added dropwise thereto. After stirring for 5 minutes, the crystals were filtered off and washed twice with 35 mL of isopropyl alcohol. The obtained crystals were dissolved in 100 mL of water, passed through a cation exchange resin (manufactured by Organo, Amberlite IR-120) filled with lithium ions, and then concentrated. The obtained crystal was dried at 50 ° C. to obtain 3.1 g of BLACK-15 black crystal. As a result of MS spectrum, 252.8 corresponding to [(M-4) / 4] ⁻ in the free form of BLACK-15 was observed. The absorption spectrum of the compound in an aqueous solution was 611 nm.

[Synthesis Example 13]
A synthesis scheme of BLACK-16 is shown below.

(1) Synthesis of intermediates (b-1) and (d-1):
The compound was synthesized by the method described in Synthesis Example (1) above.

(2) Synthesis of intermediate (f-7):
4.9 g of 3-amino-1,5-naphthalenedisulfonic acid monosodium (e-7) was dissolved in 25 mL of water, and 4.3 mL of 12N hydrochloric acid was added dropwise at room temperature. After cooling to an internal temperature of 4 ° C. in an ice bath, 2 mL of an aqueous solution of 1.1 g of sodium nitrite was added dropwise at an internal temperature of 5 ° C. or lower and stirred for 30 minutes to obtain a diazonium solution. Separately, 4.7 g of the intermediate (d-1) was suspended in 89 mL of water, and 3.8 mL of 4M lithium hydroxide aqueous solution was added, and then the above diazonium solution was added dropwise at room temperature over 20 minutes. After stirring at an internal temperature of 25 ° C. for 4 hours, the crystals were separated by filtration and washed with 30 mL of isopropyl alcohol. It dried at 50 degreeC and 6.1g of brown crystals of the intermediate body (f-7) were obtained.

(3) Synthesis of BLACK-16:
Intermediate (f-7) (3.0 g) was suspended in water (10 mL), and 4 M lithium hydroxide aqueous solution was added at room temperature until the pH reached 6.8. Then, sodium nitrite (0.35 g) was added, and room temperature was increased to 5 at room temperature. Stir for minutes. Separately, 2.4 g of intermediate (g) was dissolved in 7 mL of water, 0.8 mL of 12N hydrochloric acid was added, and the solution of the above intermediate (f-7) was added thereto at room temperature over 10 minutes. After stirring for 1 hour at an internal temperature of 25 ° C., a 4M aqueous lithium hydroxide solution was added dropwise until pH 8.3 was reached. Subsequently, 50 mL of isopropyl alcohol was added dropwise, the crystals were filtered off, and washed twice with 10 mL of isopropyl alcohol. The isolated crystal was added to 50 mL of water, and 100 mL of isopropyl alcohol was added dropwise thereto. After stirring for 5 minutes, the crystals were filtered off and washed twice with 20 mL of isopropyl alcohol. The obtained crystals were dissolved in 50 mL of water, passed through a cation exchange resin (Amberlite IR-120, manufactured by Organo Corporation) filled with lithium ions, and then concentrated. The obtained crystals were dried at 50 ° C. to obtain 2.5 g of BLACK-16 black crystals. As a result of the MS spectrum, 219.0 corresponding to the free [[M-5) / 5] ⁻ of BLACK-16 was observed. The absorption spectrum of the compound in an aqueous solution was 613 nm.

[Synthesis Example 14]
(1) Synthesis of BLACK-17 After dissolving 1.2 g of black crystals of BLACK-16 in 20 mL of water and passing through a cation exchange resin (Amberlite IR-120, manufactured by Organo Corporation) filled with sodium ions. And concentrated. The obtained crystals were dried at 50 ° C. to obtain 1.3 g of BLACK-17 black crystals.

[Synthesis Example 15]
(1) Synthesis of BLACK-18 After 1.2 g of black crystals of BLACK-16 were dissolved in 20 mL of water, a cation exchange resin (Amberlite IR-120, manufactured by Organo Corporation) filled with potassium ions was passed through. And concentrated. The obtained crystals were dried at 50 ° C. to obtain 1.3 g of BLACK-18 black crystals.

[Synthesis Example 16]
A synthesis scheme of BLACK-21 is shown below.

(1) Synthesis of intermediates (b-1) and (d-1):
The compound was synthesized by the method described in Synthesis Example (1) above.

(2) Synthesis of intermediate (f-8):
5.2 g of 3-amino-7-nitro-1,5-naphthalenedisulfonic acid (e-8) was dissolved in 25 mL of water, and 4.3 mL of 12N hydrochloric acid was added dropwise at room temperature. After cooling to an internal temperature of 4 ° C. in an ice bath, 2 mL of an aqueous solution of 1.1 g of sodium nitrite was added dropwise at an internal temperature of 5 ° C. or lower and stirred for 30 minutes to obtain a diazonium solution. Separately, 4.7 g of the intermediate (d-1) was suspended in 89 mL of water, and 3.8 mL of 4M lithium hydroxide aqueous solution was added, and then the above diazonium solution was added dropwise at room temperature over 20 minutes. After stirring at an internal temperature of 25 ° C. for 4 hours, the crystals were separated by filtration and washed with 30 mL of isopropyl alcohol. It dried at 50 degreeC and obtained 6.3g of brown crystals of the intermediate (f-8).

(3) Synthesis of BLACK-21:
Intermediate (f-8) (3.2 g) was suspended in water (10 mL), and a 4M aqueous lithium hydroxide solution was added at room temperature until the pH reached 6.8. Then, sodium nitrite (0.35 g) was added, and Stir for minutes. Separately, 2.4 g of intermediate (g) was dissolved in 7 mL of water, 0.8 mL of 12N hydrochloric acid was added thereto, and the solution of the intermediate (f-8) was added thereto at room temperature over 10 minutes. After stirring for 1 hour at an internal temperature of 25 ° C., a 4M aqueous lithium hydroxide solution was added dropwise until pH 8.3 was reached. Subsequently, 50 mL of isopropyl alcohol was added dropwise, the crystals were filtered off, and washed twice with 10 mL of isopropyl alcohol. The isolated crystal was added to 50 mL of water, and 100 mL of isopropyl alcohol was added dropwise thereto. After stirring for 5 minutes, the crystals were filtered off and washed twice with 20 mL of isopropyl alcohol. The obtained crystals were dissolved in 50 mL of water, passed through a cation exchange resin (Amberlite IR-120, manufactured by Organo Corporation) filled with lithium ions, and then concentrated. The obtained crystals were dried at 50 ° C. to obtain 2.8 g of BLACK-21 black crystals. As a result of MS spectrum, 228.0 corresponding to the free form [(M-5) / 5] ⁻ of BLACK-21 was observed. The absorption spectrum of the compound in an aqueous solution was 620 nm.

[Synthesis Example 17]
A synthesis scheme of BLACK-22 is shown below.

(1) Synthesis of intermediates (b-1) and (d-1):
The compound was synthesized by the method described in Synthesis Example (1) above.

(2) Synthesis of intermediate (f-9):
2.9 g of 2-amino-6-sulfobenzothiazole (e-9) was suspended in 10 mL of acetic acid and 5 mL of propionic acid. After cooling to an internal temperature of 5 ° C. in an ice bath, 3.9 g of 43% nitrosylsulfuric acid was added dropwise at an internal temperature of 10 ° C. or less. After stirring at an internal temperature of 5 ° C. for 1 hour, 0.08 g of urea was added, and then stirred at an internal temperature of 5 ° C. for 10 minutes. Separately, 3.9 g of the intermediate (d-1) was suspended in 60 mL of water, and 3.1 mL of 4M lithium hydroxide aqueous solution was added, and then the above diazonium solution was added dropwise at room temperature over 5 minutes. After stirring at an internal temperature of 25 ° C. for 1 hour, the obtained crystals were separated by filtration and washed twice with 15 mL of water. It dried at 50 degreeC and 6.0g of brown crystals of the intermediate body (f-9) were obtained.

(3) Synthesis of BLACK-22:
2.7 g of the intermediate (f-9) was suspended in 10 mL of water, and 4M lithium hydroxide aqueous solution was added at room temperature until the pH reached 6.8. Then, 0.35 g of sodium nitrite was added, and 5 mL at room temperature was added. Stir for minutes. Separately, 2.4 g of the intermediate (g) was dissolved in 7 mL of water, 0.8 mL of 12N hydrochloric acid was added, and the solution of the intermediate (f-9) was added thereto at room temperature over 10 minutes. After stirring for 1 hour at an internal temperature of 25 ° C., a 4M aqueous lithium hydroxide solution was added dropwise until pH 8.3 was reached. Subsequently, 55 mL of isopropyl alcohol was added dropwise, the crystals were filtered off, and washed twice with 10 mL of isopropyl alcohol. The isolated crystal was added to 30 mL of water, and 60 mL of isopropyl alcohol was added dropwise thereto. After stirring for 5 minutes, the crystals were filtered off and washed twice with 15 mL of isopropyl alcohol. The obtained crystals were dissolved in 30 mL of water, passed through a cation exchange resin (Amberlite IR-120, manufactured by Organo Corporation) filled with lithium ions, and then concentrated. The obtained crystals were dried at 50 ° C. to obtain 2.3 g of BLACK-22 black crystals. As a result of the MS spectrum, 255.8 corresponding to [(M-4) / 4] ⁻ in the free form of BLACK-22 was observed. The absorption spectrum of the compound in an aqueous solution was 638 nm.

[Synthesis Example 18]
A synthesis scheme of BLACK-24 is shown below.

(1) Synthesis of intermediate (b-1):
The compound was synthesized by the method described in Synthesis Example (1) above.

(2) Synthesis of intermediate (d-11):
To the three-necked flask, 9.1 g of intermediate (b-1), 1.6 g of sulfur and 30 mL of methanol were added. To this suspension, 2.5 g of triethylamine was added dropwise, and the temperature was raised to an internal temperature of 60 ° C. After stirring for 3 hours, a methanol solution of intermediate (c-1) cooled to an internal temperature of 15 ° C. was obtained. To the methanol solution of the obtained intermediate (c-1), 8.2 g of phthalic anhydride was added and stirred at room temperature for 1 hour. The precipitated crystals were separated by filtration, washed twice with 5 mL of methanol, and dried at 50 ° C. to obtain 9.4 g of yellow crystal intermediate (d-11).

(3) Synthesis of intermediate (f-11):
3.0 g of 5-aminoisophthalic acid (e-1) was suspended in 18 mL of water, and 4.7 mL of 12N hydrochloric acid was added dropwise at room temperature. After cooling to an internal temperature of 4 ° C. in an ice bath, 2.5 mL of an aqueous solution of 1.3 g of sodium nitrite was added dropwise at an internal temperature of 5 ° C. or lower and stirred for 30 minutes. Thereafter, 0.34 g of amidosulfuric acid was added, followed by stirring at an internal temperature of 5 ° C. for 10 minutes to obtain a diazonium solution. Separately, 6.3 g of the intermediate (d-11) was suspended in 90 mL of water, 4.3 mL of 4M lithium hydroxide aqueous solution was added, and the diazonium solution was added dropwise at room temperature over 20 minutes. The mixture was heated to an internal temperature of 40 ° C., stirred at 40 ° C. for 30 minutes, and then cooled to room temperature. The crystals were separated by filtration and washed with 15 mL of water and 15 mL of isopropyl alcohol. By drying at 50 ° C., 8.9 g of brown crystals of the intermediate (f-11) were obtained.

(4) Synthesis of BLACK-24:
To a suspension of 5.9 g of the intermediate (f-11), 6.9 g of the intermediate (g) and 140 mL of water, 3.4 g of isoamyl nitrite was added dropwise at room temperature. After stirring for 2 hours at an internal temperature of 25 ° C., a 4M aqueous lithium hydroxide solution was added dropwise until the pH reached 8.3. Subsequently, 300 mL of isopropyl alcohol was added dropwise, the crystals were filtered off, and washed twice with 30 mL of isopropyl alcohol. The isolated crystal was added to 40 mL of water, and 100 mL of isopropyl alcohol was added dropwise thereto. After stirring for 5 minutes, the crystals were filtered off and washed twice with 20 mL of isopropyl alcohol. The obtained crystals were dried at 50 ° C. to obtain 8.8 g of BLACK-24 black crystals. As a result of MS spectrum, 204.2 corresponding to [(M-5) / 5] ⁻ in the free form of BLACK-24 was observed. The absorption spectrum of the compound in an aqueous solution was 591 nm.

[Synthesis Example 19]
(1) Synthesis of BLACK-25 After dissolving 2.0 g of black crystals of BLACK-24 in 40 mL of water and passing through a cation exchange resin (Amberlite IR-120, manufactured by Organo) filled with sodium ions. And concentrated. The obtained crystals were dried at 50 ° C. to obtain 1.8 g of BLACK-25 black crystals.

[Synthesis Example 20]
(1) Synthesis of BLACK-26 After dissolving 2.0 g of black crystals of BLACK-24 in 40 mL of water and passing through a cation exchange resin (Amberlite IR-120, manufactured by Organo Corporation) filled with potassium ions. And concentrated. The obtained crystals were dried at 50 ° C. to obtain 2.0 g of BLACK-26 black crystals.

[Synthesis Example 21]
A synthesis scheme of BLACK-28 is shown below.

(1) Synthesis of intermediates (b-1) and (d-11):
Synthesized by the method described in Synthesis Example (19) above.

(2) Synthesis of intermediate (f-12):
2.5 g of monosodium 3-amino-1,5-naphthalenedisulfonate (e-7) was dissolved in 15 mL of water, and 2.1 mL of 12N hydrochloric acid was added dropwise at room temperature. After cooling to an internal temperature of 4 ° C. in an ice bath, 1 mL of an aqueous solution of 0.6 g of sodium nitrite was dropped at an internal temperature of 5 ° C. or less, and the mixture was stirred for 30 minutes to obtain a diazonium solution. Separately, 2.7 g of intermediate (d-11) was suspended in 45 mL of water, 1.9 mL of 4M aqueous lithium hydroxide solution was added, and the diazonium solution was added dropwise at room temperature over 20 minutes. After stirring at an internal temperature of 25 ° C. for 4 hours, the crystals were separated by filtration and washed with 15 mL of isopropyl alcohol. It dried at 50 degreeC and 5.1g of brown crystals of the intermediate body (f-12) were obtained.

(3) Synthesis of BLACK-28:
Intermediate (f-12) (3.2 g) was suspended in water (10 mL), 4M aqueous lithium hydroxide solution was added at room temperature until the pH reached 6.6, sodium nitrite (0.35 g) was added, and Stir for minutes. Separately, 2.4 g of the intermediate (g) was dissolved in 7 mL of water, 0.8 mL of 12N hydrochloric acid was added, and the solution of the intermediate (f-12) was added thereto at room temperature over 10 minutes. After stirring for 1 hour at an internal temperature of 25 ° C., a 4M aqueous lithium hydroxide solution was added dropwise until pH 8.3 was reached. Subsequently, 50 mL of isopropyl alcohol was added dropwise, the crystals were filtered off, and washed twice with 10 mL of isopropyl alcohol. The isolated crystal was added to 40 mL of water, and 80 mL of isopropyl alcohol was added dropwise thereto. After stirring for 5 minutes, the crystals were filtered off and washed twice with 20 mL of isopropyl alcohol. The obtained crystals were dissolved in 40 mL of water, passed through a cation exchange resin (Amberlite IR-120, manufactured by Organo Corporation) filled with lithium ions, and then concentrated. The obtained crystals were dried at 50 ° C. to obtain 2.8 g of BLACK-28 black crystals. Result of MS spectrum, a free form of BLACK-28 [(M-5 ) / 5] - corresponding to 228.6 was observed in. The absorption spectrum of the compound in an aqueous solution was 612 nm.

[Synthesis Example 22]
A synthesis scheme of BLACK-30 is shown below.

(1) Synthesis of intermediates (b-2) and (c-2):
Synthesis was performed by the method described in Synthesis Example (2) above.

(2) Synthesis of intermediate (d-13):
To a three-necked flask, 5.0 g of intermediate (c-2), 5.7 g of 3,4-dichlorophthalic anhydride, and 50 mL of acetonitrile were added and stirred at reflux. After stirring under reflux for 1 hour, the mixture was cooled to room temperature, and the precipitated crystals were separated by filtration and washed twice with 10 mL of acetonitrile. The obtained crystal was dried at 50 ° C. to obtain 9.2 g of a yellow crystal intermediate (d-13).

(3) Synthesis of intermediate (f-13):
Dissolve 5.0 g of sodium 7-amino-1,3-naphthalenedisulfonate (e-13) in 20 mL of water, cool to an internal temperature of 5 ° C. in an ice bath, and add 1.1 g of sodium nitrite at an internal temperature of 10 ° C. or lower. 2 mL of an aqueous solution was added dropwise and stirred for 10 minutes. Separately, 3.6 mL of 12N hydrochloric acid and 8 mL of water were mixed and cooled to an internal temperature of 4 ° C. with an ice bath. The previous solution of sodium 7-amino-1,3-naphthalenedisulfonate was added dropwise at 5 ° C. or lower. After stirring at 5 ° C. or lower for 30 minutes, 0.28 g of amidosulfuric acid was added, and subsequently stirred at an internal temperature of 5 ° C. for 10 minutes to obtain a diazonium solution. Separately, 5.9 g of intermediate (d-13) was suspended in 30 mL of water and 30 mL of methanol, and the above diazonium solution was added dropwise at room temperature over 5 minutes. The mixture was heated to 40 ° C., stirred at 40 ° C. for 30 minutes, and then cooled to room temperature. The obtained crystals were separated by filtration and washed with 10 mL of water and 10 mL of isopropyl alcohol. It dried at 50 degreeC and 10.1g of brown crystals of the intermediate body (f-13) were obtained.

(4) Synthesis of BLACK-30:
Intermediate (f-13) (7.2 g) was suspended in water (40 mL), and a 4M aqueous lithium hydroxide solution was added at room temperature until the pH reached 6.8. Then, sodium nitrite (1.0 g) was added, and the mixture was stirred at room temperature for 5 minutes. Stir for minutes. Separately, 7.3 g of intermediate (g) was dissolved in 25 mL of water, 4.8 mL of 12N hydrochloric acid was added, and the solution of the intermediate (f-13) was added thereto at room temperature over 10 minutes. After stirring for 1 hour at an internal temperature of 25 ° C., a 4M aqueous lithium hydroxide solution was added dropwise until pH 8.3 was reached. Subsequently, 150 mL of isopropyl alcohol was added dropwise, the crystals were filtered off, and washed twice with 30 mL of isopropyl alcohol. The isolated crystal was added to 100 mL of water, and 200 mL of isopropyl alcohol was added dropwise thereto. After stirring for 5 minutes, the crystals were filtered off and washed twice with 30 mL of isopropyl alcohol. The obtained crystals were dissolved in 80 mL of water, passed through a cation exchange resin (Amberlite IR-120, manufactured by Organo Corporation) filled with lithium ions, and then concentrated. The obtained crystals were dried at 50 ° C. to obtain 6.8 g of BLACK-30 black crystals. As a result of the MS spectrum, 237.4 corresponding to the free [[M-5) / 5] ⁻ of BLACK-30 was observed. The absorption spectrum of the compound in an aqueous solution was 598 nm.

[Synthesis Example 23]
A synthesis scheme of BLACK-33 is shown below.

(1) Synthesis of intermediate (b-1):
Synthesis was performed by the method described in Synthesis Example (1) above.

(2) Synthesis of intermediate (d-14):
10.0 g of intermediate (b-1), 1.7 g of sulfur, and 30 mL of methanol were added to the three-necked flask. To this suspension, 2.8 g of triethylamine was added dropwise, and the temperature was raised to an internal temperature of 60 ° C. After stirring for 3 hours, a methanol solution of intermediate (c-1) cooled to an internal temperature of 15 ° C. was obtained. To a methanol solution of the obtained intermediate (c-1), 8.2 g of 2-sulfobenzoic anhydride was added and stirred at room temperature for 1 hour. The precipitated crystals were separated by filtration, washed twice with 5 mL of methanol, and dried at 50 ° C. to obtain 10.6 g of yellow crystal intermediate (d-14).

(3) Synthesis of intermediate (f-14):
2.9 g of 2-amino-6-sulfobenzothiazole (e-9) was suspended in 10 mL of acetic acid and 5 mL of propionic acid. After cooling to an internal temperature of 5 ° C. in an ice bath, 3.9 g of 43% nitrosylsulfuric acid was added dropwise at an internal temperature of 10 ° C. or less. After stirring at an internal temperature of 5 ° C. for 1 hour, 0.08 g of urea was added, and then stirred at an internal temperature of 5 ° C. for 10 minutes. Separately, 4.9 g of the intermediate (d-14) was suspended in 60 mL of water, and 3.1 mL of 4M lithium hydroxide aqueous solution was added, and then the above diazonium solution was added dropwise at room temperature over 5 minutes. After stirring at an internal temperature of 25 ° C. for 1 hour, the obtained crystals were separated by filtration and washed twice with 15 mL of water. It dried at 50 degreeC and obtained 6.3g of brown crystals of the intermediate (f-14).

(4) Synthesis of BLACK-33:
Intermediate (f-14) (3.0 g) was suspended in water (10 mL), and a 4M aqueous lithium hydroxide solution was added at room temperature until the pH reached 6.8. Then, sodium nitrite (0.35 g) was added, and the mixture was stirred at room temperature for 5 minutes. Stir for minutes. Separately, 2.4 g of the intermediate (g) was dissolved in 7 mL of water, 0.8 mL of 12N hydrochloric acid was added, and the solution of the intermediate (f-14) was added thereto at room temperature over 10 minutes. After stirring for 1 hour at an internal temperature of 25 ° C., a 4M aqueous lithium hydroxide solution was added dropwise until pH 8.3 was reached. Subsequently, 60 mL of isopropyl alcohol was added dropwise, the crystals were filtered off, and washed twice with 10 mL of isopropyl alcohol. The isolated crystal was added to 30 mL of water, and 75 mL of isopropyl alcohol was added dropwise thereto. After stirring for 5 minutes, the crystals were filtered off and washed twice with 15 mL of isopropyl alcohol. The obtained crystals were dissolved in 40 mL of water, passed through a cation exchange resin (Amberlite IR-120, manufactured by Organo Corporation) filled with lithium ions, and then concentrated. The obtained crystals were dried at 50 ° C. to obtain 2.2 g of BLACK-33 black crystals. As a result of MS spectrum, 276.8 corresponding to [(M-4) / 4] ⁻ in the free form of BLACK-33 was observed. The absorption spectrum of the compound in an aqueous solution was 640 nm.

[Synthesis Example 24]
A synthesis scheme of BLACK-34 is shown below.

(1) Synthesis of intermediate (b-1):
Synthesis was performed by the method described in Synthesis Example (1) above.

(2) Synthesis of intermediate (d-15):
10.0 g of intermediate (b-1), 1.7 g of sulfur, and 30 mL of methanol were added to the three-necked flask. To this suspension, 2.8 g of triethylamine was added dropwise, and the temperature was raised to an internal temperature of 60 ° C. After stirring for 3 hours, a methanol solution of intermediate (c-1) cooled to an internal temperature of 15 ° C. was obtained. 11.0 g of trimellitic anhydride was added to the methanol solution of the obtained intermediate (c-1), and the mixture was stirred at room temperature for 1 hour. The precipitated crystals were separated by filtration, washed twice with 5 mL of methanol, and dried at 50 ° C. to obtain 11.6 g of an intermediate (d-15) of yellow crystals.

(3) Synthesis of intermediate (f-15):
3.0 g of sodium 2-amino-4-nitrobenzenesulfonate (e-6) was suspended in 10 mL of acetic acid and 5 mL of propionic acid. After cooling to an internal temperature of 5 ° C. in an ice bath, 3.9 g of 43% nitrosylsulfuric acid was added dropwise at an internal temperature of 10 ° C. or less. After stirring at an internal temperature of 5 ° C. for 1 hour, 0.08 g of urea was added, and then stirred at an internal temperature of 5 ° C. for 10 minutes. Separately, 5.2 g of the intermediate (d-15) was suspended in 30 mL of water, and 3.1 mL of 4M lithium hydroxide aqueous solution was added, and then the above diazonium solution was added dropwise at room temperature over 5 minutes. After stirring at an internal temperature of 25 ° C. for 1 hour, the obtained crystals were separated by filtration and washed twice with 10 mL of water. It dried at 50 degreeC and 4.6g of brown crystals of the intermediate body (f-15) were obtained.

(4) Synthesis of BLACK-34:
After suspending 2.0 g of the intermediate (f-15) in 30 mL of water and adding a 4M lithium hydroxide aqueous solution at room temperature until the pH becomes 7.5, 0.23 g of sodium nitrite was added, and 5 mL at room temperature was added. Stir for minutes. Separately, 1.6 g of intermediate (g) was dissolved in 50 mL of water, 0.5 mL of 12N hydrochloric acid was added thereto, and the solution of the intermediate (f-15) was added thereto at room temperature over 10 minutes. After stirring for 1 hour at an internal temperature of 25 ° C., a 4M aqueous lithium hydroxide solution was added dropwise until pH 8.3 was reached. Subsequently, 100 mL of isopropyl alcohol was added dropwise, the crystals were filtered off, and washed twice with 20 mL of isopropyl alcohol. The isolated crystal was added to 15 mL of water, and 45 mL of isopropyl alcohol was added dropwise thereto. After stirring for 5 minutes, the crystals were filtered off and washed twice with 10 mL of isopropyl alcohol. The obtained crystals were dissolved in 20 mL of water, passed through a cation exchange resin (Amberlite IR-120, manufactured by Organo Corporation) filled with lithium ions, and then concentrated. The obtained crystals were dried at 50 ° C. to obtain 1.3 g of BLACK-34 black crystals. As a result of MS spectrum, 220.4 corresponding to [(M-5) / 5] ⁻ in the free form of BLACK-34 was observed. The absorption spectrum of the compound in an aqueous solution was 611 nm.

[Synthesis Example 25]
(1) Synthesis of BLACK-35 After dissolving 1.2 g of black crystals of BLACK-34 in 20 mL of water and passing through a cation exchange resin (Amberlite IR-120, manufactured by Organo Corporation) filled with sodium ions. And concentrated. The obtained crystals were dried at 50 ° C. to obtain 1.2 g of BLACK-35 black crystals.

[Synthesis Example 26]
(1) Synthesis of BLACK-36 After dissolving 1.2 g of black crystals of BLACK-34 in 20 mL of water and passing through a cation exchange resin (Amberlite IR-120, manufactured by Organo) filled with potassium ions. And concentrated. The obtained crystals were dried at 50 ° C. to obtain 1.3 g of BLACK-36 black crystals.

[Synthesis Example 27]
A synthesis scheme of BLACK-37 is shown below.

(1) Synthesis of intermediates (b-1) and (d-15):
Synthesized by the method described in Synthesis Example (25) above.

(2) Synthesis of intermediate (f-16):
1.9 g of 2-aminobenzonitrile (e-16) was suspended in 45 mL of water, and 7.9 mL of 12N hydrochloric acid was added dropwise at room temperature. After cooling to an internal temperature of 4 ° C. in an ice bath, 2.5 mL of an aqueous solution of 1.2 g of sodium nitrite was added dropwise at an internal temperature of 5 ° C. or less, and the mixture was stirred for 30 minutes. Thereafter, 0.15 g of amidosulfuric acid was added, followed by stirring at an internal temperature of 5 ° C. for 10 minutes to obtain a diazonium solution. Separately, 6.1 g of the intermediate (d-15) was suspended in 70 mL of water, 7.5 mL of 4M lithium hydroxide aqueous solution was added, and the above diazonium solution was added dropwise at room temperature over 20 minutes. After stirring at an internal temperature of 25 ° C. for 1 hour, the crystals were separated by filtration and washed with 15 mL of water and 15 mL of isopropyl alcohol. The obtained crystal was dried at 50 ° C. to obtain 6.9 g of a brown crystal of intermediate (f-16).

(3) Synthesis of Black-37:
2.7 g of intermediate (f-16) and 2.5 g of intermediate (g) were dissolved in 30 mL of dimethylacetamide and cooled to 15 ° C. At an internal temperature of 15 ° C., 0.79 g of isoamyl nitrite was added dropwise. After stirring at an internal temperature of 15 ° C. for 2 hours, 200 mL of isopropyl alcohol was added dropwise, and the crystals were separated by filtration. 30 mL of water was added to the isolated crystal, and a 4M lithium hydroxide aqueous solution was added dropwise until the pH reached 8.3. Subsequently, 90 mL of isopropyl alcohol was added dropwise and the mixture was stirred for 5 minutes, and then the crystals were separated by filtration and washed twice with 10 mL of isopropyl alcohol. The obtained crystals were dried at 50 ° C. to obtain 8.8 g of BLACK-37 black crystals. As a result of MS spectrum, 250.8 corresponding to [(M-4) / 4] ⁻ in the free form of BLACK-37 was observed. The absorption spectrum of the compound in an aqueous solution was 609 nm.

[Synthesis Example 28]
A synthesis scheme of BLACK-39 is shown below.

(1) Synthesis of intermediates (b-2), (c-2), and (d-17):
Synthesis was performed by the method described in Synthesis Example (17) above.

(2) Synthesis of intermediate (f-18):
1.8 g of 2-amino-5-nitrothiazole (e-18) was suspended in 10 mL of acetic acid and 5 mL of propionic acid. After cooling to an internal temperature of 5 ° C. in an ice bath, 3.9 g of 43% nitrosylsulfuric acid was added dropwise at an internal temperature of 10 ° C. or less. After stirring at an internal temperature of 5 ° C. for 1 hour, 0.08 g of urea was added, and then stirred at an internal temperature of 5 ° C. for 10 minutes. Separately, 4.8 g of the intermediate (d-17) was suspended in 30 mL of water, and 3.1 mL of 4M lithium hydroxide aqueous solution was added, and then the above diazonium solution was added dropwise at room temperature over 5 minutes. After stirring at an internal temperature of 25 ° C. for 1 hour, the obtained crystals were separated by filtration and washed twice with 10 mL of water. It dried at 50 degreeC and 4.4g of brown crystals of the intermediate body (f-18) were obtained.

(3) Synthesis of BLACK-39:
Intermediate (f-18) (2.1 g) was suspended in water (30 mL), and a 4M aqueous lithium hydroxide solution was added at room temperature until the pH reached 7.5. Then, sodium nitrite (0.28 g) was added, and the mixture was stirred at room temperature for 5 minutes. Stir for minutes. Separately, 1.9 g of intermediate (g) was dissolved in 50 mL of water, 0.5 mL of 12N hydrochloric acid was added thereto, and the solution of the intermediate (f-18) was added thereto at room temperature over 10 minutes. After stirring for 1 hour at an internal temperature of 25 ° C., a 4M aqueous lithium hydroxide solution was added dropwise until pH 8.3 was reached. Subsequently, 90 mL of isopropyl alcohol was added dropwise, the crystals were filtered off, and washed twice with 20 mL of isopropyl alcohol. The isolated crystal was added to 20 mL of water, and 60 mL of isopropyl alcohol was added dropwise thereto. After stirring for 5 minutes, the crystals were filtered off and washed twice with 10 mL of isopropyl alcohol. The obtained crystals were dissolved in 20 mL of water, passed through a cation exchange resin (Amberlite IR-120, manufactured by Organo Corporation) filled with lithium ions, and then concentrated. The obtained crystals were dried at 50 ° C. to obtain 1.6 g of BLACK-39 black crystals. As a result of MS spectrum, 251.5 corresponding to [(M-4) / 4] ⁻ in the free form of BLACK-39 was observed. The absorption spectrum of the compound in an aqueous solution was 633 nm.

[Synthesis Example 29]
A synthesis scheme of BLACK-41 is shown below.

(1) Synthesis of intermediate (b-1):
The compound was synthesized by the method described in Synthesis Example (1) above.

(2) Synthesis of intermediate (d-19):
10.0 g of intermediate (b-1), 1.7 g of sulfur, and 30 mL of methanol were added to the three-necked flask. To this suspension, 2.8 g of triethylamine was added dropwise, and the temperature was raised to an internal temperature of 60 ° C. After stirring for 3 hours, a methanol solution of intermediate (c-1) cooled to an internal temperature of 15 ° C. was obtained. To a methanol solution of the obtained intermediate (c-1), 4.5 g of acetyl chloride was added and stirred at room temperature for 1 hour. The precipitated crystals were separated by filtration, washed twice with 5 mL of methanol, and dried at 50 ° C. to obtain 8.6 g of yellow crystal intermediate (d-19).

(3) Synthesis of intermediate (D-19):
Intermediate (d-19) (5.0 g) was suspended in water (100 mL), and concentrated sulfuric acid (10 mL) was added dropwise at room temperature. The internal temperature was heated to 80 ° C, and the mixture was stirred at 80 ° C for 6 hours. After cooling to room temperature, the crystals were filtered off to obtain 3.8 g of yellow crystal intermediate (D-19).

(4) Synthesis of intermediate (f-19):
4.9 g of 3-amino-1,5-naphthalenedisulfonic acid monosodium (e-7) was dissolved in 25 mL of water, and 4.3 mL of 12N hydrochloric acid was added dropwise at room temperature. After cooling to an internal temperature of 4 ° C. in an ice bath, 2 mL of an aqueous solution of 1.1 g of sodium nitrite was added dropwise at an internal temperature of 5 ° C. or lower and stirred for 30 minutes to obtain a diazonium solution. Separately, 4.1 g of the intermediate (D-19) was suspended in 100 mL of water, and the above diazonium solution was added dropwise at room temperature over 20 minutes. After stirring at an internal temperature of 25 ° C. for 4 hours, the crystals were separated by filtration and washed with 30 mL of isopropyl alcohol. Drying at 50 ° C. yielded 4.1 g of brown crystals of intermediate (f-19).

(5) Synthesis of BLACK-41:
2.8 g of intermediate (f-19) was suspended in 10 mL of water, and 4M lithium hydroxide aqueous solution was added at room temperature until the pH reached 6.8. Then, 0.35 g of sodium nitrite was added, and 5 mL at room temperature was added. Stir for minutes. Separately, 2.4 g of intermediate (g) was dissolved in 7 mL of water, 0.8 mL of 12N hydrochloric acid was added thereto, and the solution of the intermediate (f-19) was added thereto at room temperature over 10 minutes. After stirring for 1 hour at an internal temperature of 25 ° C., a 4M aqueous lithium hydroxide solution was added dropwise until pH 8.3 was reached. Subsequently, 50 mL of isopropyl alcohol was added dropwise, the crystals were filtered off, and washed twice with 10 mL of isopropyl alcohol. The isolated crystal was added to 50 mL of water, and 100 mL of isopropyl alcohol was added dropwise thereto. After stirring for 5 minutes, the crystals were filtered off and washed twice with 20 mL of isopropyl alcohol. The obtained crystals were dissolved in 50 mL of water, passed through a cation exchange resin (Amberlite IR-120, manufactured by Organo Corporation) filled with lithium ions, and then concentrated. The obtained crystals were dried at 50 ° C. to obtain 1.9 g of BLACK-41 black crystals. As a result of the MS spectrum, 264.0 corresponding to [(M-4) / 4] ⁻ in the free form of BLACK-41 was observed. The absorption spectrum of the compound in an aqueous solution was 602 nm.

[Preparation of aqueous solution]
The aqueous solution of the present invention is herein referred to as “ink stock solution”.
In addition, pH was adjusted to 8.1-8.3 using 4 mol / L lithium hydroxide aqueous solution for aqueous solution.

[Example-1]
1.0 g of the compound of the present invention (BLACK-1) is dissolved in 9.0 g of ultrapure water while stirring at room temperature, and then added and dissolved in portions, followed by preservative (Proxel XL-II: Fujifilm Imaging Colorant) Product) was added in a solid content of 1.0 mg. The pH was adjusted to 8.2 using a 4 mol / L lithium hydroxide aqueous solution, and then unnecessary substances were filtered using a membrane filter having an effective diameter of 0.2 μm to obtain an ink stock solution-1.

[Example-2]
Except that (BLACK-2) was used in place of the compound (BLACK-1) of the present invention, the same operation as in Example-1 was performed to obtain Ink Stock Solution-2.

[Example-3]
Except that (BLACK-3) was used instead of the compound (BLACK-1) of the present invention, the same operation as in Example-1 was performed to obtain Ink Stock Solution-3.

[Example-4]
Except that (BLACK-4) was used in place of the compound (BLACK-1) of the present invention, the same operation as in Example-1 was performed to obtain Ink Stock Solution-4.

[Example-5]
Except that (BLACK-5) was used instead of the compound (BLACK-1) of the present invention, the same operation as in Example-1 was performed to obtain an ink stock solution-5.

[Example-6]
Except that (BLACK-6) was used instead of the compound (BLACK-1) of the present invention, the same operation as in Example-1 was carried out to obtain an ink stock solution-6.

[Example-7]
Except that (BLACK-8) was used instead of the compound (BLACK-1) of the present invention, the same operation as in Example-1 was carried out to obtain an ink stock solution-7.

[Example-8]
Except that (BLACK-9) was used in place of the compound (BLACK-1) of the present invention, the same operation as in Example-1 was performed to obtain an ink stock solution-8.

[Example-9]
Except that (BLACK-10) was used in place of the compound (BLACK-1) of the present invention, the same operation as in Example-1 was performed to obtain an ink stock solution-9.

[Example-10]
Except that (BLACK-11) was used in place of the compound (BLACK-1) of the present invention, the same operation as in Example-1 was performed to obtain an ink stock solution-10.

[Example-11]
Except that (BLACK-14) was used instead of the compound (BLACK-1) of the present invention, the same operation as in Example-1 was performed to obtain an ink stock solution-11.

[Example-12]
Except that (BLACK-15) was used instead of the compound (BLACK-1) of the present invention, the same operation as in Example-1 was carried out to obtain an ink stock solution-12.

[Example-13]
Except that (BLACK-16) was used in place of the compound (BLACK-1) of the present invention, the same operation as in Example-1 was performed to obtain an ink stock solution-13.

[Example-14]
Except that (BLACK-17) was used instead of the compound (BLACK-1) of the present invention, the same operation as in Example-1 was performed to obtain an ink stock solution-14.

[Example-15]
Except that (BLACK-18) was used instead of the compound (BLACK-1) of the present invention, the same operation as in Example-1 was performed to obtain an ink stock solution-15.

[Example-16]
Except that (BLACK-21) was used instead of the compound (BLACK-1) of the present invention, the same operation as in Example 1 was carried out to obtain Ink Stock Solution-16.

[Example-17]
Except that (BLACK-22) was used in place of the compound (BLACK-1) of the present invention, the same operation as in Example-1 was performed to obtain an ink stock solution-17.

[Example-19]
Except that (BLACK-24) was used in place of the compound (BLACK-1) of the present invention, the same operation as in Example-1 was performed to obtain an ink stock solution-19.

[Example-20]
Except that (BLACK-25) was used in place of the compound (BLACK-1) of the present invention, the same operation as in Example-1 was performed to obtain an ink stock solution-20.

[Example-21]
Except that (BLACK-26) was used instead of the compound (BLACK-1) of the present invention, the same operation as in Example-1 was performed to obtain an ink stock solution-21.

[Example-22]
Except that (BLACK-28) was used in place of the compound (BLACK-1) of the present invention, the same operation as in Example-1 was performed to obtain an ink stock solution-22.

[Example-23]
Except that (BLACK-30) was used instead of the compound (BLACK-1) of the present invention, the same operation as in Example-1 was performed to obtain an ink stock solution-23.

[Example-24]
Except that (BLACK-33) was used instead of the compound (BLACK-1) of the present invention, the same operation as in Example 1 was performed to obtain an ink stock solution-24.

[Example-25]
Except that (BLACK-34) was used in place of the compound (BLACK-1) of the present invention, the same operation as in Example-1 was performed to obtain an ink stock solution-25.

[Example-26]
Except that (BLACK-35) was used in place of the compound (BLACK-1) of the present invention, the same operation as in Example-1 was performed to obtain Ink Stock Solution-26.

[Example-27]
Except that (BLACK-36) was used instead of the compound (BLACK-1) of the present invention, the same operation as in Example 1 was carried out to obtain an ink stock solution-27.

[Example-28]
Except that (BLACK-37) was used in place of the compound (BLACK-1) of the present invention, the same operation as in Example 1 was performed to obtain Ink Stock Solution-28.

[Example-30]
Except that (BLACK-39) was used instead of the compound (BLACK-1) of the present invention, the same operation as in Example 1 was carried out to obtain an ink stock solution-30.

[Example-31]
An ink stock solution-31 was obtained in the same manner as in Example 1 except that (BLACK-41) was used instead of the compound (BLACK-1) of the present invention.

[Comparative Example-1]
A comparative ink stock solution-01 was obtained by performing the same operation as in Example 1 except that the following compound (Dye-01) was used instead of the compound (BLACK-1) of the present invention.
Dye-01

[Comparative Example-2]
A comparative ink stock solution-02 was obtained in the same manner as in Example 1 except that the following compound (Dye-02) was used instead of the compound (BLACK-1) of the present invention.
Dye-02

[Preparation of ink composition]
10.0 g of ink stock solution-1 obtained in Example-1, 5.0 g of ultrapure water, 1.6 g of glycerin, 0.2 g of triethylene glycol, 0.1 g of propylene glycol, 1,2- Add 0.4 g of hexanediol, 1.6 g of triethylene glycol monobutyl ether, 0.3 g of Orphine E1010 (manufactured by Nissin Chemical Co., Ltd.), 0.8 g of 2-pyrrolidone, 0.02 g of lithium hydrogen carbonate, After stirring for 30 minutes, the pH was adjusted to 8.2 using a 4 mol / L lithium hydroxide aqueous solution, and the resulting solution was filtered using a membrane filter having an effective aperture of 1.0 μm. Ink composition 1 was obtained.
Ink composition 1 is similar to ink composition 2 except that ink stock solution-1 is replaced with ink stock solution-2 to ink stock solution-31, comparative ink stock solution-01, and comparative ink stock solution-02, respectively. Composition 31, comparative ink composition 01, and comparative ink composition 02 were obtained.

[Evaluation of suppression of bronze gloss]
An ink jet printer Stylus Color 880 (trademark) (trade name, manufactured by Seiko Epson Corporation) was used, and each of Ink Composition 1 to Ink Composition 31, Comparative Ink Composition 01, and Comparative Ink Composition 02 was used. , Inkjet recording media (Exclusive paper A: Photographic paper Crispia <High gloss> (trade name, manufactured by Seiko Epson Corporation), Special paper B: Canon photo paper / Glossy professional [Platinum grade] (Product name, manufactured by Canon Inc.) ), Special Paper C: Image Acrylic Photo Finishing Pro (trade name, manufactured by FUJIFILM Corporation)) is printed with a solid black color so that the applied amount is 1.5 to 2.2 mg per square inch. The obtained printed matter was measured using a gloss meter (PG-1M, manufactured by Nippon Denshoku Industries Co., Ltd.) (measurement angle 60 degrees), and the gloss was measured. Meta. Printing was performed in two environments of 20 ° C. 40% RH and 35 ° C. 60% RH. Using the obtained glossiness and the increased value calculated based on the following formula as a criterion for determining the degree of occurrence of bronze phenomenon, the determination was made based on the following criterion.
Increase value = Glossiness (printed material)-Glossiness (recording medium)
[Criteria]
Evaluation A: Less than 15 Evaluation B: 15 or more and less than 35 Evaluation C: 35 or more and less than 55 Evaluation D: 55 or more

(Print density evaluation)
For the dedicated paper on which the image was formed, the OD value was measured using a reflection densitometer (X-Rite 310TR), and the print density was evaluated based on the maximum value of OD.
(Criteria)
Evaluation A: Maximum value of OD is 2.2 or more Evaluation B: Maximum value of OD is 2.0 or more and less than 2.2 Evaluation C: Maximum value of OD is less than 2.0

  From the results shown above, the ink composition of the comparative example showed practically satisfactory performance for suppressing the bronze gloss and the print density of the obtained print, but the ink composition of the present invention is obtained. It can be seen that the bronze gloss suppression and the print density of the printed material are very excellent even when any of the dedicated papers A to C is used as the recording medium, and a higher level is satisfied. .

Claims (25)

It contains (a) an antiseptic and (b) at least one azo compound represented by the following general formula (1) or a salt thereof, and the content of (b) is 1% by mass to 25% by mass. Aqueous solution.
General formula (1)

(In General Formula (1), G represents a nitrogen atom or —C (R ₁ ) ═. R ₁ represents a hydrogen atom, a sulfo group, a carboxy group, a substituted or unsubstituted carbamoyl group, or a cyano group. R ₂ represents a monovalent substituent, A represents a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, or a substituted or unsubstituted nitrogen-containing 5-membered or 6-membered heterocyclic group. (The nitrogen-containing 5-membered or 6-membered heterocyclic group may further have a condensed ring structure, and M independently represents a hydrogen atom or a monovalent counter cation.) The aqueous solution according to claim 1, wherein the azo compound represented by the general formula (1) is an azo compound represented by the following general formula (2-1).
General formula (2-1)

(In General Formula (2-1), G ¹ represents a nitrogen atom or —C (CN) ═. A represents a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, or a substituted or unsubstituted group. Represents a nitrogen 5-membered or 6-membered heterocyclic group, and the nitrogen-containing 5-membered or 6-membered heterocyclic group may further have a condensed ring structure, and each M independently represents a hydrogen atom or a monovalent group. Represents the counter cation.) The aqueous solution according to claim 1 or 2, wherein the azo compound represented by the general formula (1) or (2-1) is an azo compound represented by the following general formula (3-1).
Formula (3-1)

(In General Formula (3-1), G ¹ represents a nitrogen atom or —C (CN) ═. X ₁ , X ₂ , X ₃ , X ₄ , and X ₅ are each independently a hydrogen atom, or Represents a monovalent substituent, and each M independently represents a hydrogen atom or a monovalent counter cation.) The aqueous solution according to claim 1 or 2, wherein the azo compound represented by the general formula (1) or (2-1) is an azo compound represented by the following general formula (4-1).
Formula (4-1)

(In General Formula (4-1), G ¹ represents a nitrogen atom or —C (CN) ═. Y ₁ , Y ₂ , Y ₃ , Y ₄ , Y ₅ , Y ₆ , and Y ₇ are each independent. Represents a hydrogen atom or a monovalent substituent, and each M independently represents a hydrogen atom or a monovalent counter cation.) The aqueous solution according to claim 1 or 2, wherein the azo compound represented by the general formula (1) or (2-1) is an azo compound represented by the following general formula (5-1).
General formula (5-1)

(In General Formula (5-1), G ¹ represents a nitrogen atom or —C (CN) ═. Z ₁ , Z ₂ , Z ₃ , and Z ₄ are each independently a hydrogen atom or a monovalent group. Represents a substituent, and each M independently represents a hydrogen atom or a monovalent counter cation.) The aqueous solution according to claim 1, wherein the azo compound represented by the general formula (1) is an azo compound represented by the following general formula (2-2).
General formula (2-2)

(In General Formula (2-2), G ¹ represents a nitrogen atom or —C (CN) ═. R ₁₁ , R ₁₂ , R ₁₃ , and R ₁₄ are each independently a hydrogen atom or a monovalent group. A represents a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, or a substituted or unsubstituted nitrogen-containing 5-membered or 6-membered heterocyclic group. The membered heterocyclic group may further have a condensed ring structure, and each M independently represents a hydrogen atom or a monovalent counter cation.) The aqueous solution according to claim 1 or 6, wherein the azo compound represented by the general formula (1) or (2-2) is an azo compound represented by the following general formula (3-2).
Formula (3-2)

(In General Formula (3-2), G ¹ represents a nitrogen atom or —C (CN) ═. X ₁ , X ₂ , X ₃ , X ₄ , and X ₅ each independently represent a hydrogen atom, or R ₁₁ , R ₁₂ , R ₁₃ , and R ₁₄ each independently represents a hydrogen atom or a monovalent substituent, and M independently represents a hydrogen atom or a monovalent substituent. Represents the counter cation.) The aqueous solution according to claim 1 or 6, wherein the azo compound represented by the general formula (1) or (2-2) is an azo compound represented by the following general formula (4-2).
Formula (4-2)

(In General Formula (4-2), G ¹ represents a nitrogen atom or —C (CN) ═. Y ₁ , Y ₂ , Y ₃ , Y ₄ , Y ₅ , Y ₆ , and Y ₇ are each independently R ₁₁ , R ₁₂ , R ₁₃ , and R ₁₄ each independently represents a hydrogen atom or a monovalent substituent, and M represents each independently a hydrogen atom. Or represents a monovalent counter cation.) The aqueous solution according to claim 1 or 6, wherein the azo compound represented by the general formula (1) or (2-2) is an azo compound represented by the following general formula (5-2).
General formula (5-2)

(In General Formula (5-2), G ¹ represents a nitrogen atom or —C (CN) ═. Z ₁ , Z ₂ , Z ₃ , and Z ₄ are each independently a hydrogen atom or a monovalent group. R ₁₁ , R ₁₂ , R ₁₃ , and R ₁₄ each independently represent a hydrogen atom or a monovalent substituent, and M independently represents a hydrogen atom or a monovalent counter cation. Represents.)   The general formula (1), (2-1), (2-2), (3-1), (3-2), (4-1), (4-2), (5-1), or The aqueous solution according to any one of claims 1 to 9, wherein the azo compound represented by (5-2) has three or more ionic hydrophilic groups.   Furthermore, (c) The aqueous solution of any one of Claims 1-10 containing a pH adjuster.   The aqueous solution according to any one of claims 1 to 11, which has a pH of 7.0 to 9.0 at 25 ° C.   An ink composition comprising the aqueous solution according to claim 1.   An ink for inkjet recording comprising the aqueous solution according to any one of claims 1 to 12 or the ink composition according to claim 13.   An inkjet recording method for forming a colored image on a recording material using the inkjet recording ink according to claim 14.   An ink cartridge for ink jet recording filled with the ink for ink jet recording according to claim 14.   An ink-jet recorded matter in which a colored image is formed on a recording material using the ink for ink-jet recording according to claim 14. An azo compound represented by the following general formula (2-1) or a salt thereof.
General formula (2-1)

(In General Formula (2-1), G ¹ represents a nitrogen atom or —C (CN) ═. A represents a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, or a substituted or unsubstituted group. Represents a nitrogen 5-membered or 6-membered heterocyclic group, and the nitrogen-containing 5-membered or 6-membered heterocyclic group may further have a condensed ring structure, and each M independently represents a hydrogen atom or a monovalent group. Represents the counter cation.) The azo compound or a salt thereof according to claim 18, wherein the general formula (2-1) is represented by the following general formula (3-1).
Formula (3-1)

(In General Formula (3-1), G ¹ represents a nitrogen atom or —C (CN) ═. X ₁ , X ₂ , X ₃ , X ₄ , and X ₅ are each independently a hydrogen atom, or Represents a monovalent substituent, and each M independently represents a hydrogen atom or a monovalent counter cation.) The azo compound or a salt thereof according to claim 18, wherein the general formula (2-1) is represented by the following general formula (4-1).
Formula (4-1)

(In General Formula (4-1), G ¹ represents a nitrogen atom or —C (CN) ═. Y ₁ , Y ₂ , Y ₃ , Y ₄ , Y ₅ , Y ₆ , and Y ₇ are each independent. Represents a hydrogen atom or a monovalent substituent, and each M independently represents a hydrogen atom or a monovalent counter cation.) The azo compound or a salt thereof according to claim 18, wherein the general formula (2-1) is represented by the following general formula (5-1).
General formula (5-1)

(In General Formula (5-1), G ¹ represents a nitrogen atom or —C (CN) ═. Z ₁ , Z ₂ , Z ₃ , and Z ₄ are each independently a hydrogen atom or a monovalent group. Represents a substituent, and each M independently represents a hydrogen atom or a monovalent counter cation.) An azo compound represented by the following general formula (2-2) or a salt thereof.
General formula (2-2)

(In General Formula (2-2), G ¹ represents a nitrogen atom or —C (CN) ═. R ₁₁ , R ₁₂ , R ₁₃ , and R ₁₄ are each independently a hydrogen atom or a monovalent group. A represents a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, or a substituted or unsubstituted nitrogen-containing 5-membered or 6-membered heterocyclic group. The membered heterocyclic group may further have a condensed ring structure, and each M independently represents a hydrogen atom or a monovalent counter cation.) The azo compound or a salt thereof according to claim 22, wherein the general formula (2-2) is represented by the following general formula (3-2).
Formula (3-2)

(In General Formula (3-2), G ¹ represents a nitrogen atom or —C (CN) ═. X ₁ , X ₂ , X ₃ , X ₄ , and X ₅ each independently represent a hydrogen atom, or R ₁₁ , R ₁₂ , R ₁₃ , and R ₁₄ each independently represents a hydrogen atom or a monovalent substituent, and M independently represents a hydrogen atom or a monovalent substituent. Represents the counter cation.) The azo compound or a salt thereof according to claim 22, wherein the general formula (2-2) is represented by the following general formula (4-2).
Formula (4-2)

(In General Formula (4-2), G ¹ represents a nitrogen atom or —C (CN) ═. Y ₁ , Y ₂ , Y ₃ , Y ₄ , Y ₅ , Y ₆ , and Y ₇ are each independently R ₁₁ , R ₁₂ , R ₁₃ , and R ₁₄ each independently represents a hydrogen atom or a monovalent substituent, and M represents each independently a hydrogen atom. Or represents a monovalent counter cation.) The azo compound or a salt thereof according to claim 22, wherein the general formula (2-2) is represented by the following general formula (5-2).
General formula (5-2)

(In General Formula (5-2), G ¹ represents a nitrogen atom or —C (CN) ═. Z ₁ , Z ₂ , Z ₃ , and Z ₄ are each independently a hydrogen atom or a monovalent group. R ₁₁ , R ₁₂ , R ₁₃ , and R ₁₄ each independently represent a hydrogen atom or a monovalent substituent, and M independently represents a hydrogen atom or a monovalent counter cation. Represents.)