JP2005232296A - Ink composition, inkjet recording method and recorded matter - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an ink composition using a phthalocyanine cyano dye, capable of improving indoor storability (gas resistance) of an image produced using the composition. <P>SOLUTION: The ink composition comprises at least water, the phthalocyanine cyano dye of formula (I), an aromatic compound having a sulfone group of formula (a) and/or formula (b) and/or its salt. In an inkjet recording method, liquid droplets of an ink composition are discharged and adhered to a recording medium, wherein the above ink composition is used as the ink composition. The recorded matter is recorded using the above ink composition. <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

  The present invention relates to an ink composition capable of improving indoor storage stability (gas resistance) of an image to be produced, and more specifically, an ink composition containing a phthalocyanine cyan dye that can effectively prevent discoloration of an image. Related to things.

  Conventionally, an ink composition using a phthalocyanine-based cyan dye has been widely used as an ink composition for developing an excellent cyan color image. In addition, recently, an ink composition that develops such an image is used together with one or more ink compositions for developing other colors to form an image, and the resulting image (color) It is widespread that images are posted indoors.

  However, in the ink composition using the phthalocyanine cyan dye, the phthalocyanine cyan dye is inferior in resistance to oxidizing gases such as ozone, nitrogen oxide and sulfur oxide present in the air, particularly ozone resistance. Therefore, when an image of a plurality of colors is formed together with the ink composition of other colors and the image is posted indoors, there is a problem that the image formed from the cyan dye is prematurely discolored.

Various ink compositions have been developed to prevent such discoloration of phthalocyanine. For example, WO99 / 50363 discloses a cyanide comprising a copper phthalocyanine cyan dye, an imidazole derivative, an antioxidant, a sugar, naphthalene-1-sulfonic acid having a hydroxyl group or an amino group at the 4-position. An ink composition has been disclosed as means for improving light resistance (Patent Document 1). However, this ink composition has not been evaluated for resistance to ozone gas, and there are hydroxyl groups and amino groups in the molecules of the components used, resulting in an image formed by nitrogen oxides (NOx gas). There is a problem of causing a greening or blackening phenomenon.
WO99 / 50363

  Accordingly, an object of the present invention is to provide an ink composition capable of improving the indoor storage stability (gas resistance) of an image produced by an ink composition using a phthalocyanine cyan dye.

  As a result of intensive studies, the present inventors have found that an ink composition containing a specific phthalocyanine cyan dye as a cyan dye and containing an aromatic compound having a specific sulfone group can achieve the object. Obtained knowledge.

The present invention has been made based on the above findings,
1. At least water, a phthalocyanine cyan dye represented by the following formula (I), an aromatic compound having a sulfone group represented by the following general formula (a) and / or (b) and / or a salt thereof: An ink composition comprising: is provided.

（式中、Ｘ₁₁、Ｘ₁₂、Ｘ₁₃およびＸ₁₄は、それぞれ独立に、−ＳＯ₂ＮＲ₁Ｒ₂及び／又はスルホン基を表す。但しＸ₁₁、Ｘ₁₂、Ｘ₁₃及びＸ₁₄のすべてが同時にスルホン基になることはない。ここで、Ｒ₁は、複数個存在する場合それぞれ独立に、水素原子、置換もしくは無置換のアルキル基、置換もしくは無置換のシクロアルキル基、置換もしくは無置換のアルケニル基、置換もしくは無置換のアラルキル基、置換もしくは無置換のアリール基、または置換もしくは無置換のヘテロ環基を表す。Ｒ₂は、複数個存在する場合それぞれ独立に、置換もしくは無置換のアルキル基、置換もしくは無置換のシクロアルキル基、置換もしくは無置換のアルケニル基、置換もしくは無置換のアラルキル基、置換もしくは無置換のアリール基、または置換もしくは無置換のヘテロ環基を表す。Ｒ₁とＲ₂は互いに結合して５〜６員含窒素ヘテロ環を形成してもよい。

Wherein X ₁₁ , X ₁₂ , X ₁₃ and X ₁₄ each independently represent —SO ₂ NR ₁ R ₂ and / or a sulfone group, provided that all of X ₁₁ , X ₁₂ , X ₁₃ and X ₁₄ At the same time, when there are a plurality of R _{1 s} , each independently represents a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted group. R ₂ represents an independently substituted or unsubstituted alkenyl group, substituted or unsubstituted aralkyl group, substituted or unsubstituted aryl group, or substituted or unsubstituted heterocyclic group. An alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted aryl group, or a R ₁ and R ₂ may be bonded to each other to form a 5- or 6-membered nitrogen-containing heterocyclic ring.

Y ₁₁ , Y ₁₂ , Y ₁₃ , Y ₁₄ , Y ₁₅ , Y ₁₆ , Y ₁₇ and Y ₁₈ are each independently a hydrogen atom, halogen atom, alkyl group, cycloalkyl group, alkenyl group, aralkyl group, aryl group , Heterocyclic group, cyano group, hydroxy group, nitro group, amino group, alkylamino group, alkoxy group, aryloxy group, amide group, arylamino group, ureido group, sulfamoylamino group, alkylthio group, arylthio group, Alkoxycarbonylamino group, sulfonamido group, carbamoyl group, alkoxycarbonyl group, heterocyclic oxy group, azo group, acyloxy group, carbamoyloxy group, silyloxy group, aryloxycarbonyl group, aryloxycarbonylamino group, imide group, heterocyclic ring Thio group, phosphoryl group, acyl group or ionic hydrophilic Represents a group, each group may further have a substituent.

a ₁₁ ~a ₁₄ each represent a number of substituents X ₁₁ to X _14, independently, it is an integer of 0 to 2, but all are not 0 at the same time.

  M is a hydrogen atom, a metal element or an oxide, hydroxide or halide thereof.

_{However, X 11, X 12, X} 13, X 14, Y 11, Y 12, Y 13, Y 14, Y 15, Y 16, Y 17 and Y
_At least one of ₁₈ is an ionic hydrophilic group or a group having an ionic hydrophilic group as a substituent. )

（式中、Ｍ¹は塩を構成する対イオンを示し、Ｘは１〜３の整数を示し、Ｒ¹及びＲ²はそれぞれ水素原子、炭素数１〜６のアルキル基又は炭素数１〜６のアルコキシ基を示し、Ｒ¹及びＲ²は同一でも異なっていても良い。）

(Wherein, M ¹ is shown a counter ion constituting the salt, X is an integer of 1 to 3, R ¹ and R ² are each a hydrogen atom, 1-6 alkyl group carbon atoms or 1 to 6 carbon atoms And R ¹ and R ² may be the same or different.)

（式中、Ｍ²は塩を構成する対イオンを示し、Ｙは１〜４の整数を示し、Ｒ³及びＲ⁴はそれぞれ水素原子、炭素数１〜６のアルキル基又は炭素数１〜６のアルコキシ基を示し、Ｒ³及びＲ⁴は同一でも異なっていても良い。）

(Wherein, M ² represents a counter ion constituting the salt, Y is an integer of 1 to 4, R ³ and R ⁴ are each a hydrogen atom, 1-6 alkyl group carbon atoms or 1 to 6 carbon atoms And R ³ and R ⁴ may be the same or different.)

The present invention also provides the following ink composition, ink cartridge, ink jet recording method, and recorded matter.
2. The phthalocyanine cyan dye represented by the formula (I) is a phthalocyanine dye represented by the following formula (II): The ink composition described in 1.

（式中、Ｒ₁₁、Ｒ₁₂、Ｒ₁₃およびＲ₁₄は、それぞれ独立に、水素原子、置換もしくは無置換のアルキル基、置換もしくは無置換のシクロアルキル基、置換もしくは無置換のアルケニル基、置換もしくは無置換のアラルキル基、置換もしくは無置換のアリール基、または置換もしくは無置換のヘテロ環基を表す。

Wherein R ₁₁ , R ₁₂ , R ₁₃ and R ₁₄ are each independently a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted alkenyl group, substituted Alternatively, it represents an unsubstituted aralkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group.

V ₁ , V ₂ , V ₃ and V ₄ are each independently a substituted or unsubstituted alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted aralkyl group, It represents a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group.

Y ₃₁ , Y ₃₂ , Y ₃₃ , Y ₃₄ , Y ₃₅ , Y ₃₆ , Y ₃₇ and Y ₃₈ are each independently a hydrogen atom, halogen atom, alkyl group, cycloalkyl group, alkenyl group, aralkyl group, aryl group , Heterocyclic group, cyano group, hydroxy group, nitro group, amino group, alkylamino group, alkoxy group, aryloxy group, amide group, arylamino group, ureido group, sulfamoylamino group, alkylthio group, arylthio group, Alkoxycarbonylamino group, sulfonamido group, carbamoyl group, alkoxycarbonyl group, heterocyclic oxy group, azo group, acyloxy group, carbamoyloxy group, silyloxy group, aryloxycarbonyl group, aryloxycarbonylamino group, imide group, heterocyclic ring Thio group, phosphoryl group, acyl group or ionic hydrophilic Represents a group, each group may further have a substituent.

  M has the same meaning as M in formula (I).

Of R ₁₁ , R ₁₂ , R ₁₃ , R ₁₄ , V ₁ , V ₂ , V ₃ , V ₄ , Y ₃₁ , Y ₃₂ , Y ₃₃ , Y ₃₄ , Y ₃₅ , Y ₃₆ , Y ₃₇ and Y ₃₈ At least one is an ionic hydrophilic group or a group having an ionic hydrophilic group as a substituent. )

3. The ink composition according to 1 or 2, wherein the aromatic compound having a sulfone group and / or a salt thereof has two or more sulfone groups.

4). The aromatic compound having a sulfonic group and / or a salt thereof is 1,3-benzenedisulfonic acid, naphthalene-1,5-disulfonic acid, naphthalene-1,6-disulfonic acid, naphthalene-2,6-disulfonic acid, 4. The ink composition according to 3, which is at least one selected from the group consisting of naphthalene-2,7-disulfonic acid, naphthalene-1,3,6-trisulfonic acid, and salts thereof.

5). The ink composition according to any one of 1 to 4, comprising 0.1 to 10% by weight of the aromatic compound having a sulfone group and / or a salt thereof based on the total amount of the ink composition.

6). The content ratio of the phthalocyanine cyan dye and the aromatic compound having a sulfone group and / or a salt thereof is in the range of 1: 0.1 to 1:10, according to any one of 1 to 5. Ink composition.

7). The ink composition according to any one of 1 to 6, further comprising a nonionic surfactant.

8). 8. The ink composition according to 7, wherein the nonionic surfactant is an acetylene glycol surfactant.

9. The ink composition according to 7 or 8, comprising 0.1 to 5% by weight of the nonionic surfactant based on the total amount of the ink composition.

10. The ink composition according to any one of 1 to 9, further comprising a penetration enhancer.

11. 11. The ink composition according to 10, wherein the penetration enhancer is a glycol ether.

12. The ink composition according to any one of 1 to 11, wherein the pH of the ink composition at 20 ° C is 8.0 to 10.5.

13. The ink composition according to any one of 1 to 12, which is used in an inkjet recording method.

14 14. The ink composition according to 13, wherein the ink jet recording method is a recording method using an ink jet head that forms ink droplets by mechanical deformation of an electrostrictive element.

15. An ink cartridge comprising at least the ink composition according to any one of 15.1 to 14.

16. An ink jet recording method for performing recording by discharging droplets of an ink composition and attaching the droplets to a recording medium, wherein the ink composition according to any one of 1 to 14 is used as the ink composition An inkjet recording method characterized by the above.

17. A recorded matter recorded using the ink composition according to any one of 17.1 to 14.

  Hereinafter, the ink composition of the present invention will be described in detail based on preferred embodiments thereof.

  As described above, the ink composition of the present invention is represented by at least water, a phthalocyanine cyan dye represented by the above formula (I), and the above general formula (a) and / or (b). It comprises an aromatic compound having a sulfone group and / or a salt thereof.

  Since the ink composition of the present invention has such a configuration, it is possible to effectively prevent early fading of a cyan image, and thus the indoor storage stability (gas resistance) of the image created thereby. Can be improved.

  The ink composition of the present invention contains at least a phthalocyanine cyan dye represented by the above formula (I) and the above general formula (a) and / or in an aqueous medium comprising water or a water-soluble organic solvent. It contains an aromatic compound having a sulfone group represented by (b) and / or a salt thereof, and may contain a moisturizing agent, a viscosity adjusting agent, a pH adjusting agent and other additives as necessary.

  First, the cyan dye used in the ink composition of the present invention, that is, the phthalocyanine cyan dye represented by the following formula (I) will be described in detail.

前記一般式（Ｉ）において、Ｘ₁₁、Ｘ₁₂、Ｘ₁₃およびＸ₁₄は、それぞれ独立に、−ＳＯ₂ＮＲ₁Ｒ₂又はスルホン基を表し、特に−ＳＯ₂ＮＲ₁Ｒ₂が好ましい。但しＸ₁₁、Ｘ₁₂、Ｘ₁₃及びＸ₁₄のすべてが同時にスルホン基になることはない。Ｒ₁とＲ₂は互いに結合して５〜６員含窒素ヘテロ環を形成してもよい。

In the general formula (I), X ₁₁ , X ₁₂ , X ₁₃ and X ₁₄ each independently represent —SO ₂ NR ₁ R ₂ or a sulfone group, and —SO ₂ NR ₁ R ₂ is particularly preferred. However, all of X ₁₁ , X ₁₂ , X ₁₃ and X ₁₄ do not become a sulfone group at the same time. R ₁ and R ₂ may combine with each other to form a 5- to 6-membered nitrogen-containing heterocycle.

Each R ₁ independently represents a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heterocyclic group, particularly preferably a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group, among which a hydrogen atom, a substituted An alkyl group, a substituted aryl group and a substituted heterocyclic group are preferred, a hydrogen atom, a substituted alkyl group and a substituted aryl group are more preferred, and a hydrogen atom is most preferred.

Each R ₂ independently represents a substituted or unsubstituted alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted aryl group, or Represents a substituted or unsubstituted heterocyclic group, and among them, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, a substituted or unsubstituted heterocyclic group is preferable, and a substituted alkyl group, substituted aryl group, substituted A heterocyclic group is preferred, a substituted alkyl group and a substituted aryl group are particularly preferred, and a substituted alkyl group is most preferred.

The substituted or unsubstituted alkyl group represented by R ₁ and R ₂ is preferably an alkyl group having 1 to 30 carbon atoms. Examples of the substituent are those in which R ₁ , R ₂ , Y ₁₁ , Y ₁₂ , Y ₁₃ , Y ₁₄ , Y ₁₅ , Y ₁₆ , Y ₁₇ and Y _{18 described later} can further have a substituent. The same thing as a substituent is mentioned.

The substituted or unsubstituted cycloalkyl group represented by R ₁ and R ₂ is preferably a cycloalkyl group having 5 to 30 carbon atoms. Examples of the substituent are those in which R ₁ , R ₂ , Y ₁₁ , Y ₁₂ , Y ₁₃ , Y ₁₄ , Y ₁₅ , Y ₁₆ , Y ₁₇ and Y _{18 described later} can further have a substituent. The same thing as a substituent is mentioned.

The substituted or unsubstituted alkenyl group represented by R ₁ and R ₂ is preferably an alkenyl group having 2 to 30 carbon atoms. Examples of the substituent are those in which R ₁ , R ₂ , Y ₁₁ , Y ₁₂ , Y ₁₃ , Y ₁₄ , Y ₁₅ , Y ₁₆ , Y ₁₇ and Y _{18 described later} can further have a substituent. The same thing as a substituent is mentioned.

The substituted or unsubstituted aralkyl group represented by R ₁ and R ₂ is preferably an aralkyl group having 7 to 30 carbon atoms. Examples of the substituent are those in which R ₁ , R ₂ , Y ₁₁ , Y ₁₂ , Y ₁₃ , Y ₁₄ , Y ₁₅ , Y ₁₆ , Y ₁₇ and Y _{18 described later} can further have a substituent. The same thing as a substituent is mentioned.

The substituted or unsubstituted aryl group represented by R ₁ and R ₂ is preferably an aryl group having 6 to 30 carbon atoms. Examples of the substituent are those in which R ₁ , R ₂ , Y ₁₁ , Y ₁₂ , Y ₁₃ , Y ₁₄ , Y ₁₅ , Y ₁₆ , Y ₁₇ and Y _{18 described later} can further have a substituent. The same thing as a substituent is mentioned.

The heterocyclic group represented by R ₁ and R ₂ is preferably a 5-membered or 6-membered ring, which may be further condensed. Further, it may be an aromatic heterocycle or a non-aromatic heterocycle. In the following, the heterocyclic group represented by R ₁ and R ₂ is exemplified in the form of a heterocyclic ring by omitting the substitution position, but the substitution position is not limited. Substitution at the 3rd and 4th positions is possible. Pyridine, pyrazine, pyrimidine, pyridazine, triazine, quinoline, isoquinoline, quinazoline, cinnoline, phthalazine, quinoxaline, pyrrole, indole, furan, benzofuran, thiophene, benzothiophene, pyrazole, imidazole, benzimidazole, triazole, oxazole, benzoxazole, thiazole Benzothiazole, isothiazole, benzisothiazole, thiadiazole, isoxazole, benzisoxazole, pyrrolidine, piperidine, piperazine, imidazolidine, thiazoline and the like. Among them, an aromatic heterocyclic group is preferable, and preferable examples thereof are exemplified in the same manner as described above. Examples include thiazole and thiadiazole.

These may have a substituent, and examples of the substituent include R ₁ , R ₂ , Y ₁₁ , Y ₁₂ , Y ₁₃ , Y ₁₄ , Y ₁₅ , Y ₁₆ , Y ₁₇ and Y _{18 described later.} Are the same as the substituents in the case where can further have a substituent.

Y ₁₁ , Y ₁₂ , Y ₁₃ , Y ₁₄ , Y ₁₅ , Y ₁₆ , Y ₁₇ and Y ₁₈ are each independently a hydrogen atom, halogen atom, alkyl group, cycloalkyl group, alkenyl group, aralkyl group, aryl group , Heterocyclic group, cyano group, hydroxy group, nitro group, amino group, alkylamino group, alkoxy group, aryloxy group, amide group, arylamino group, ureido group, sulfamoylamino group, alkylthio group, arylthio group, Alkoxycarbonylamino group, sulfonamido group, carbamoyl group, alkoxycarbonyl group, heterocyclic oxy group, azo group, acyloxy group, carbamoyloxy group, silyloxy group, aryloxycarbonyl group, aryloxycarbonylamino group, imide group, heterocyclic ring Thio group, phosphoryl group, acyl group, carboxyl group, Other represents a sulfone group, each of which may further have a substituent.

  Among them, a hydrogen atom, a halogen atom, an alkyl group, an aryl group, a cyano group, an alkoxy group, an amide group, a ureido group, a sulfonamide group, a carbamoyl group, an alkoxycarbonyl group, a carboxyl group, and a sulfone group are preferable, and in particular, a hydrogen atom, A halogen atom, a cyano group, a carboxyl group and a sulfone group are preferred, and a hydrogen atom is most preferred.

When R ₁ , R ₂ , Y ₁₁ , Y ₁₂ , Y ₁₃ , Y ₁₄ , Y ₁₅ , Y ₁₆ , Y ₁₇ and Y ₁₈ are groups that can further have a substituent, as listed below Further substituents may be included.

  Halogen atom (for example, chlorine atom, bromine atom); C1-C12 straight or branched alkyl group, C7-C18 aralkyl group, C2-C12 alkenyl group, C2-C12 A linear or branched alkynyl group, a cycloalkyl group having 3 to 12 carbon atoms which may have a side chain, a cycloalkenyl group having 3 to 12 carbon atoms which may have a side chain (specific examples of the above groups) Specific examples include, for example, methyl, ethyl, propyl, isopropyl, t-butyl, 2-methylsulfonylethyl, 3-phenoxypropyl, trifluoromethyl, cyclopentyl): aryl groups (eg, phenyl, 4-t-butylphenyl, 2 , 4-di-t-amylphenyl); heterocyclic groups (eg imidazolyl, pyrazolyl, triazolyl, 2-furyl, 2-thienyl, 2-pyrimidi) Alkoxy group (eg, methoxy, ethoxy, 2-methoxyethoxy, 2-methylsulfonylethoxy); aryloxy group (eg, phenoxy, 2-methylphenoxy, 4-t-butylphenoxy, 3- Nitrophenoxy, 3-t-butyloxycarbonylphenoxy, 3-methoxycarbonylphenoxy); acylamino groups (eg acetamide, benzamide, 4- (3-t-butyl-4-hydroxyphenoxy) butanamide); alkylamino groups (eg , Methylamino, butylamino, diethylamino, methylbutylamino); anilino group (eg, phenylamino, 2-chloroanilino); ureido group (eg, phenylureido, methylureido, N, N-dibutylureido); Moylamino group (for example, N, N-dipropylsulfamoylamino); alkylthio group (for example, methylthio, octylthio, 2-phenoxyethylthio); arylthio group (for example, phenylthio, 2-butoxy-5-t-octylphenylthio) , 2-carboxyphenylthio); alkyloxycarbonylamino group (for example, methoxycarbonylamino); sulfonamide group (for example, methanesulfonamide, benzenesulfonamide, p-toluenesulfonamide); carbamoyl group (for example, N-ethyl) Carbamoyl, N, N-dibutylcarbamoyl); sulfamoyl groups (eg, N-ethylsulfamoyl, N, N-dipropylsulfamoyl, N, N-diethylsulfamoyl); sulfonyl groups (eg, methylsulfonyl) , Octylsulfonyl, phenylsulfonyl, 4-methylphenylsulfonyl); alkyloxycarbonyl groups (for example, methoxycarbonyl, butyloxycarbonyl); heterocyclic oxy groups (for example, 1-phenyltetrazol-5-oxy, 2-tetrahydropyranyl) Oxy); 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-benzothiazolylthio, 2,4-di-phenoxy-1,3,5-triazole-6-thio) , 2-pyridylthio); sulfinyl group (eg, 3-phenoxypropylsulfinyl); phosphonyl group (eg, phenoxyphosphonyl, octyloxyphosphonyl, phenylphosphonyl); aryloxycarbonyl group (eg, phenoxycarbonyl); acyl group (For example, acetyl, 3-phenylpropanoyl, benzoyl); ionic hydrophilic group (for example, carboxyl group, sulfone group, quaternary ammonium group, sulfonylsulfamoyl group and acylsulfamoyl group); other cyano group, Examples include hydroxy, nitro, and amino groups It is. Among these substituents, a hydroxy group, an alkoxy group, a sulfamoyl group, a sulfonamide group, an acylamino group, a carbamoyl group, a cyano group, and an ionic hydrophilic group are preferable, and among them, a hydroxy group, a sulfamoyl group, and an ionic hydrophilic group are preferable. Particularly preferred.

A ₁₁ ~a ₁₄ in the general formula (I), each represent the number of substituents X ₁₁ to X _14, each independently, represent an integer of 0 to 2. However, all of a _{11 to} a ₁₄ do not become 0 at the same time. a ₁₁ ~a ₁₄ are particularly preferably each 1.

  M represents a hydrogen atom, a metal element, a metal oxide, a metal hydroxide, or a metal halide.

In addition to hydrogen atoms, preferable as M are metal elements such as Li, Na, K, Mg, Ti, Zr, V, Nb, Ta, Cr, Mo, W, Mn, Fe, Co, Ni, Ru, Rh, Pd, Os, Ir, Pt, Cu, Ag, Au, Zn, Cd, Hg, Al, Ga, In, Si, Ge, Sn, Pb, Sb, Bi and the like can be mentioned. Preferred oxides include VO and GeO. Preferred examples of the hydroxide include Si (OH) ₂ , Cr (OH) ₂ , Sn (OH) _{2 and the} like. Further, as the _{halides, AlCl, SiCl 2, VCl,} VCl 2, VOCl, FeCl, GaCl, ZrCl , and the like. Of these, Cu, Ni, Zn, Al and the like are preferable, and Cu is most preferable.

  Further, in the phthalocyanine compound represented by the general formula (I), Pc (phthalocyanine ring) is a dimer (for example, Pc-MLMMM-Pc) or 3 via L (a divalent linking group). A monomer may be formed, and a plurality of M present at that time may be the same or different.

The divalent linking group represented by L includes an oxy group —O—, a thio group —S—, a carbonyl group —CO—, a sulfonyl group —SO ₂ —, an imino group —NH—, a methylene group —CH ₂ —, And a group formed by combining them is preferred.

  In the above general formula (I), the molecular weight of the phthalocyanine compound is preferably in the range of 750 to 3000, more preferably in the range of 995 to 2500, of which the molecular weight is preferably 995 to 2000, and particularly the molecular weight in the range of 995 to 1800. Is most preferred.

  The phthalocyanine compound represented by the general formula (I) is dimer (for example, Pc-MLMMPc) or trimer with Pc (phthalocyanine ring) via L (divalent linking group). The preferred molecular weight, for example, the particularly preferred molecular weight is 2 times (in the case of a dimer) or 3 times (in the case of a trimer) the particularly preferred molecular weight (in the range of 995 to 1800) described above. is there. Here, the preferable molecular weight of the dimer or trimer is a value including the linking group L.

The phthalocyanine compound represented by the general formula (I) includes at least X ₁₁ , X ₁₂ , X ₁₃ , X ₁₄ , Y ₁₁ , Y ₁₂ , Y ₁₃ , Y ₁₄ , Y ₁₅ , Y ₁₆ , Y ₁₇ and Y ₁₈ . One is an ionic hydrophilic group or a group having an ionic hydrophilic group as a substituent.

The ionic hydrophilic group as a substituent, a sulfonic group (-SO ₃ ^- X ^+), a carboxyl group (-CO ₂ ^- X ^+), and quaternary ammonium group (-N ⁺ RR'R "X ^-) , acylsulfamoyl groups ^{_{(-SO 2 N + X - COR}} ), a sulfonylcarbamoyl group _{^{(-CON + X - SO 2 R}} ), sulfonylsulfamoyl groups ^{_{(-SO 2 N + X - SO}} 2 R) or the like Preferred are a sulfone group, a carboxyl group, and a quaternary ammonium group, and particularly preferred is a sulfone group, and the sulfone group, carboxyl group, acylsulfamoyl group, sulfonylcarbamoyl group, and sulfonylsulfamoyl group are in a salt state. Examples of counter ions that form salts include alkali metal ions (eg, sodium ions, potassium ions, lithium ions), ammonium ions. , Organic cations (eg, tetramethylguanidinium ion), organic and / or inorganic anions (eg, halogen ion, methanesulfonic acid ion, benzenesulfonic acid ion), where X in parentheses is hydrogen. An atom or counter ion, R, R ′, R ″ represents a substituent.

  Since the phthalocyanine compound represented by the general formula (I) has at least one ionic hydrophilic group or a group having an ionic hydrophilic group as a substituent in one molecule, it is soluble in an aqueous medium. Or dispersibility becomes favorable. From such a viewpoint, as the phthalocyanine compound represented by the general formula (I), those having at least two ionic hydrophilic groups in one molecule are preferable, and at least one of a plurality of ionic hydrophilic groups is used. Is more preferably a sulfone group, and most preferably those having at least two sulfone groups in one molecule.

Particularly preferred compounds as the phthalocyanine compound represented by the general formula (I) are compounds having the following combinations (a) to (g).
(A) Regarding X _{11 to} X ₁₄ , these are each independently preferably —SO ₂ NR ₁ R ₂ .
(B) R ₁ is preferably a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group, and among them, a hydrogen atom, a substituted alkyl group, a substituted aryl group, A substituted heterocyclic group is preferred, and a hydrogen atom is most preferred.
(C) R ₂ is preferably a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group, and among them, a substituted alkyl group, a substituted aryl group, or a substituted heterocyclic group is preferred. Most preferred are substituted alkyl groups. Furthermore, it is more preferable that at least one of R ₁ and R ₂ has an ionic hydrophilic group or a group having an ionic hydrophilic group as a substituent.
(D) Y _{11 to} Y ₁₈ are each independently a hydrogen atom, a halogen atom, an alkyl group, an aryl group, a cyano group, an alkoxy group, an amide group, a ureido group, a sulfonamide group, a carbamoyl group, a sulfamoyl group. Group, alkoxycarbonyl group, carboxyl group, and sulfone group are preferable, hydrogen atom, halogen atom, cyano group, carboxyl group, and sulfone group are particularly preferable, and hydrogen atom is most preferable.
(E) is preferably a ₁₁ ~a ₁₄ are each 1.
(F) M is preferably Cu, Ni, Zn, or Al, and most preferably Cu.
(G) The molecular weight of the phthalocyanine compound is preferably in the range of 750 to 3000, more preferably in the range of 995 to 2500, of which the molecular weight in the range of 995 to 2000 is preferred, and the molecular weight in the range of 995 to 1800 is most preferred. preferable.

  As for the preferred combination of substituents of the compound represented by the general formula (I), a compound in which at least one of various substituents is the preferred group is preferred, and more various substituents are preferred groups. Certain compounds are more preferred, and compounds in which all substituents are the preferred groups are most preferred.

Among the phthalocyanine compounds represented by the general formula (I), a phthalocyanine compound having a structure represented by the following general formula (II) is more preferable. The phthalocyanine compound represented by the general formula (II) used in the present invention is described in detail below.
Formula (II)

前記一般式(II)中、Ｒ₁₁、Ｒ₁₂、Ｒ₁₃およびＲ₁₄は、それぞれ独立に、水素原子、置換
もしくは無置換のアルキル基、置換もしくは無置換のシクロアルキル基、置換もしくは無
置換のアルケニル基、置換もしくは無置換のアラルキル基、置換もしくは無置換のアリー
ル基、または置換もしくは無置換のヘテロ環基を表す。

In the general formula (II), R ₁₁ , R ₁₂ , R ₁₃ and R ₁₄ are each independently a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted group. An alkenyl group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group is represented.

Preferred examples of R ₁₁ , R ₁₂ , R ₁₃ and R ₁₄ are the same as R ₁ in the general formula (I).

V ₁ , V ₂ , V ₃ and V ₄ are each independently a substituted or unsubstituted alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted aralkyl group, It represents a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group.

Preferred examples of V ₁ , V ₂ , V ₃ and V ₄ are the same as R ₂ in the general formula (I).

Y _{31 to} Y ₃₈ are each independently represented by Y ₁₁ , Y ₁₂ , Y ₁₃ , Y ₁₄ ,
Y ₁₅ , Y ₁₆ , Y ₁₇ and Y ₁₈ have the same meanings, and preferred examples are also the same.

  M has the same meaning as M in formula (I), and preferred examples are also the same.

_{However, R 11, R 12, R} 13, R 14, V 1, V 2, V 3, V 4, Y 31, Y 32, Y 33, Y 34, Y 35
, Y ₃₆ , Y ₃₇ and Y ₃₈ are ionic hydrophilic groups or groups having an ionic hydrophilic group as a substituent.

Examples of the ionic hydrophilic group, X ₁₁ in the general formula _{(I), X 12, X} 13, are the same as examples of X _14, and preferred examples thereof are also the same.

Since the phthalocyanine compound represented by the general formula (II) has at least one ionic hydrophilic group or a group having an ionic hydrophilic group as a substituent in one molecule, it is soluble in an aqueous medium. Or dispersibility becomes favorable. From such a viewpoint, the phthalocyanine compound represented by the general formula (II) preferably has at least two ionic hydrophilic groups in one molecule, and has at least one of a plurality of ionic hydrophilic groups. Those having a sulfone group are more preferable, and among them, those having at least two sulfone groups in one molecule are most preferable.

In the general formula (II), the molecular weight of the phthalocyanine compound is preferably in the range of 750 to 3000, more preferably in the range of 995 to 2500, of which 995-2.
A molecular weight of 000 is preferred, and a molecular weight in the range of 995 to 1800 is most preferred.

However, in the phthalocyanine compound represented by the general formula (II) in the present invention, Pc (phthalocyanine ring) is dimerized via L (divalent linking group) (for example, Pc-MLMLM-Pc). )
Or in the case of forming a trimer, a preferred molecular weight, for example a particularly preferred molecular weight
It is 2 times (in the case of a dimer) or 3 times (in the case of a trimer) of a particularly preferable molecular weight (in the range of 995 to 1800) described above. Here, the preferable molecular weight of the dimer or trimer is a value including the linking group L.

Particularly preferred compounds as the phthalocyanine compound represented by the general formula (II) are compounds having the following combinations (a) to (e).
(A) R ₁₁ , R ₁₂ , R ₁₃ and R ₁₄ are preferably a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group, and among them, a hydrogen atom , A substituted alkyl group, a substituted aryl group and a substituted heterocyclic group are preferred, and a hydrogen atom is most preferred.
(B) V ₁ , V ₂ , V ₃ and V ₄ are preferably a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group, and among them, a substituted alkyl group or a substituted group An aryl group and a substituted heterocyclic group are preferred, and a substituted alkyl group is most preferred. Further, at least one of R ₁₁ , R ₁₂ , R ₁₃ , R ₁₄ , V ₁ , V ₂ , V ₃ and V ₄ is an ionic hydrophilic group or has an ionic hydrophilic group as a substituent. More preferably, it is a group.
(C) Regarding Y _{31 to} Y ₃₈ , these are each independently a hydrogen atom, a halogen atom, an alkyl group, an aryl group, a cyano group, an alkoxy group, an amide group, a ureido group, a sulfonamide group, a carbamoyl group, and a sulfamoyl group. Group, alkoxycarbonyl group, carboxyl group,
And a sulfone group are preferable, and a hydrogen atom, a halogen atom, a cyano group, a carboxyl group, and a sulfone group are particularly preferable, and a hydrogen atom is most preferable.
(D) M is preferably Cu, Ni, Zn, or Al, and most preferably Cu.
(E) The molecular weight of the phthalocyanine compound is preferably in the range of 750 to 2500, more preferably 99
A molecular weight in the range of 5 to 2500 is preferred, a molecular weight in the range of 995 to 2000 is preferred, and a molecular weight in the range of 995 to 1800 is most preferred.

Regarding the preferred combination of substituents of the compound represented by the general formula (II), a compound in which at least one of various substituents is the preferred group is preferred, and more various substituents are preferred groups. Certain compounds are more preferred, and compounds in which all substituents are the preferred groups are most preferred.

Among the phthalocyanine compounds represented by the general formula (II), a phthalocyanine compound having a structure represented by the following general formula (III) is more preferable. The general formula (III) used in the present invention is as follows.
The phthalocyanine compound represented by) will be described in detail.

  Among the phthalocyanine compounds represented by the general formula (II), a phthalocyanine compound having a structure represented by the following general formula (III) is more preferable. Hereinafter, the phthalocyanine compound represented by the general formula (III) preferably used in the present invention will be described in detail.

前記一般式(III)中、Ｒ₂₁、Ｒ₂₂、Ｒ₂₃およびＲ₂₄は、それぞれ独立に、水素原子、置換もしくは無置換のアルキル基、置換もしくは無置換のシクロアルキル基、置換もしくは無置換のアルケニル基、置換もしくは無置換のアラルキル基、置換もしくは無置換のアリール基、または置換もしくは無置換のヘテロ環基を表し、特に水素原子、置換アルキル基、置換アリール基、置換ヘテロ環基が好ましく、その中でも水素原子、置換アルキル基が好ましく、水素原子が最も好ましい。

In the general formula (III), R ₂₁ , R ₂₂ , R ₂₃ and R ₂₄ are each independently a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted group. Represents an alkenyl group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group, particularly preferably a hydrogen atom, a substituted alkyl group, a substituted aryl group, or a substituted heterocyclic group; Among these, a hydrogen atom and a substituted alkyl group are preferable, and a hydrogen atom is most preferable.

V ₁₁ , V ₁₂ , V ₁₃ and V ₁₄ are each independently a substituted or unsubstituted alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted aralkyl group, A substituted or unsubstituted aryl group or a substituted or unsubstituted heterocyclic group is represented, and a substituted alkyl group, a substituted aryl group, and a substituted heterocyclic group are particularly preferable, and a substituted alkyl group is most preferable.

The alkyl group represented by R ₂₁ , R ₂₂ , R ₂₃ , R ₂₄ , V ₁₁ , V ₁₂ , V ₁₃ and V ₁₄ includes an alkyl group having a substituent and an unsubstituted alkyl group. As the alkyl group, an alkyl group having 1 to 12 carbon atoms when a substituent is removed is preferable. Examples of the substituent include a hydroxy group, an alkoxy group, a cyano group, and a halogen atom and an ionic hydrophilic group. Examples of the alkyl group include methyl, ethyl, isopropyl, t-butyl, hydroxyethyl, methoxyethyl, cyanoethyl, trifluoroethyl, 3-sulfopropyl and 4-sulfobutyl.

The cycloalkyl group represented by R ₂₁ , R ₂₂ , R ₂₃ , R ₂₄ , V ₁₁ , V ₁₂ , V ₁₃ and V ₁₄ includes a cycloalkyl group having a substituent and an unsubstituted cycloalkyl group. The cycloalkyl group is preferably a cycloalkyl group having 5 to 12 carbon atoms when a substituent is removed. Examples of the substituent include an ionic hydrophilic group. Examples of the cycloalkyl group include a cyclohexyl group.

The alkenyl group represented by R ₂₁ , R ₂₂ , R ₂₃ , R ₂₄ , V ₁₁ , V ₁₂ , V ₁₃ and V ₁₄ includes an alkenyl group having a substituent and an unsubstituted alkenyl group. The alkenyl group is preferably an alkenyl group having 2 to 12 carbon atoms when a substituent is removed. Examples of the substituent include an ionic hydrophilic group. Examples of the alkenyl group include a vinyl group and an allyl group.

The aralkyl group represented by R ₂₁ , R ₂₂ , R ₂₃ , R ₂₄ , V ₁₁ , V ₁₂ , V ₁₃ and V ₁₄ includes an aralkyl group having a substituent and an unsubstituted aralkyl group. As the aralkyl group, an aralkyl group having 7 to 12 carbon atoms when a substituent is removed is preferable. Examples of the substituent include an ionic hydrophilic group. Examples of the aralkyl group include a benzyl group and a 2-phenethyl group.

The aryl group represented by R ₂₁ , R ₂₂ , R ₂₃ , R ₂₄ , V ₁₁ , V ₁₂ , V ₁₃ and V ₁₄ includes an aryl group having a substituent and an unsubstituted aryl group. As the aryl group, an aryl group having 6 to 12 carbon atoms when a substituent is removed is preferable. Examples of the substituent include an alkyl group, an alkoxy group, a halogen atom, an alkylamino group, and an ionic hydrophilic group. Examples of the aryl group include phenyl, p-tolyl, p-methoxyphenyl, o-chlorophenyl and m- (3-sulfopropylamino) phenyl.

The heterocyclic group represented by R ₂₁ , R ₂₂ , R ₂₃ , R ₂₄ , V ₁₁ , V ₁₂ , V ₁₃ and V ₁₄ includes a heterocyclic group having a substituent and an unsubstituted heterocyclic group.

The heterocyclic groups represented by R ₂₁ , R ₂₂ , R ₂₃ , R ₂₄ , V ₁₁ , V ₁₂ , V ₁₃ and V ₁₄ are each independently a saturated heterocyclic ring or an unsaturated heterocyclic ring. Also good.

The heterocyclic groups represented by R ₂₁ , R ₂₂ , R ₂₃ , R ₂₄ , V ₁₁ , V ₁₂ , V ₁₃ and V ₁₄ may each independently form a condensed ring with another ring.

The heterocyclic group represented by R ₂₁ , R ₂₂ , R ₂₃ , R ₂₄ , V ₁₁ , V ₁₂ , V ₁₃ and V ₁₄ is preferably a 5-membered or 6-membered heterocyclic group.

Preferred examples of the heterocyclic group represented by R ₂₁ , R ₂₂ , R ₂₃ , R ₂₄ , V ₁₁ , V ₁₂ , V ₁₃ and V ₁₄ and condensed rings thereof include 5- to 6-membered nitrogen-containing heterocycles (further other rings And a condensed ring can be formed).

The heterocyclic group represented by R ₂₁ , R ₂₂ , R ₂₃ , R ₂₄ , V ₁₁ , V ₁₂ , V ₁₃ and V ₁₄ is exemplified in the form of a heterocyclic ring with the substitution position omitted, but the substitution position is limited. For example, pyridine can be substituted at the 2-position, 3-position, and 4-position.

  Pyridine, pyrazine, pyrimidine, pyridazine, quinoline, isoquinoline, quinazoline, cinnoline, phthalazine, quinoxaline, pyrrole, benzopyrrole, indole, furan, benzofuran, thiophene, benzothiophene, pyrazole, benzopyrazole, imidazole, benzimidazole, triazole, Examples include oxazole, benzoxazole, thiazole, benzothiazole, isothiazole, benzisothiazole, thiadiazole, isoxazole, benzisoxazole, pyrrolidine, piperidine, piperazine, imidazolidine, thiazoline and the like. Among them, an aromatic heterocyclic group is preferable, and preferable examples thereof are exemplified in the same manner as described above. Thiadiazole is mentioned.

Examples of the substituent when the heterocyclic group represented by R ₂₁ , R ₂₂ , R ₂₃ , R ₂₄ , V ₁₁ , V ₁₂ , V ₁₃ and V ₁₄ further has a substituent include an alkyl group (R—), an alkoxy group (RO-), an alkylamino group (RNH-, RR'N-), a carbamoyl group (-CONHR), a sulfamoyl group (-SO ₂ NHR), sulfonylamino groups (-NHSO ₂ R), a halogen atom, ion (In addition, R and R ′ represent an alkyl group and a phenyl group, and these may have an ionic hydrophilic group).

  M has the same meaning as M in formula (I), and preferred examples are also the same.

However, at least one of R ₂₁ , R ₂₂ , R ₂₃ , R ₂₄ , V ₁₁ , V ₁₂ , V ₁₃ and V ₁₄ has an ionic hydrophilic group as a substituent.

The example of an ionic hydrophilic group is synonymous with the example of X < ₁₁ >, X < ₁₂ >, X <_13> , X < ₁₄ > in the said general formula (I), and its preferable example is also the same.

  The molecular weight of the phthalocyanine compound is preferably in the range of 750 to 2500, more preferably in the range of 995 to 2500, of which the molecular weight in the range of 995 to 2000 is preferable, and the molecular weight in the range of 995 to 1800 is most preferable.

  Since the phthalocyanine compound represented by the general formula (III) is an ionic hydrophilic group or a group having an ionic hydrophilic group as a substituent in one molecule, it can be dissolved in an aqueous medium. Or dispersibility is improved. From such a viewpoint, the phthalocyanine compound represented by the general formula (III) preferably has at least two ionic hydrophilic groups in one molecule, and at least one of a plurality of ionic hydrophilic groups. Those having a sulfone group are preferred, and among them, those having at least two sulfone groups in one molecule of the phthalocyanine compound are most preferred.

Particularly preferred compounds as the phthalocyanine compound represented by the general formula (III) are compounds having the following combinations (a) to (e).
(A) R ₂₁ , R ₂₂ , R ₂₃ and R ₂₄ are each independently a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted alkenyl. Represents a group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted aryl group, a substituted or unsubstituted heterocyclic group, particularly preferably a hydrogen atom, a substituted alkyl group, a substituted aryl group, or a substituted heterocyclic group. A hydrogen atom is most preferred.
(B) With respect to V ₁₁ , V ₁₂ , V ₁₃ and V ₁₄ , these are each independently a substituted or unsubstituted alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted alkenyl group, a substituted Or an unsubstituted aralkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group, particularly preferably a substituted alkyl group, a substituted aryl group, or a substituted heterocyclic group, and among them, an ionic hydrophilic group Most preferred is an alkyl group as a substituent.
(C) M is preferably Cu, Ni, Zn, or Al, and most preferably Cu.
(D) The molecular weight of the phthalocyanine compound is preferably in the range of 750 to 2500, more preferably in the range of 995 to 2500, of which the molecular weight in the range of 995 to 2000 is preferred, and the molecular weight in the range of 995 to 1800 is most preferred. preferable.
(E) Since the phthalocyanine compound represented by the general formula (III) has at least one ionic hydrophilic group in the molecule, the solubility or dispersibility in an aqueous medium is good. From such a viewpoint, the phthalocyanine compound represented by the general formula (III) preferably has at least two ionic hydrophilic groups in one molecule, and is at least one of a plurality of ionic hydrophilic groups. Is a sulfone group, and among them, one having at least two sulfone groups in one molecule is most preferable.

  As for the preferred combination of substituents of the compound represented by the general formula (III), a compound in which at least one of various substituents is the preferred group is preferred, and more various substituents are preferred groups. Certain compounds are more preferred, and compounds in which all substituents are the preferred groups are most preferred.

In general, it is known to use various phthalocyanine derivatives in an ink composition for ink jet recording. The phthalocyanine derivative represented by the following general formula (IV) inevitably has a substitution position (R ₁ : 1 position to R ₁₆ : 16 position) of the substituent R _n (n = 1 to 16) at the time of synthesis. In some cases, these substitution position isomers are regarded as the same derivative without being distinguished from each other. Further, even when isomers are included in the substituent of R, they are often regarded as the same phthalocyanine derivative without distinction.
Formula (IV)

本明細書中で定義するフタロシアニン系色素において構造が異なる場合とは、一般式（IV）で説明すると、置換基（Ｒ_n（ｎ＝１〜１６））の構成原子種が異なる場合、置換基Ｒ_nの数が異なる場合または置換基Ｒ_nの位置が異なる場合のいずれかである。

The case where the structures of the phthalocyanine dyes defined in the present specification are different from each other is described by the general formula (IV). When the constituent atomic species of the substituent (R _n (n = 1 to 16)) are different, Either the number of R _n is different or the position of the substituent R _n is different.

In the present invention, derivatives having different structures (particularly substitution positions) of the phthalocyanine dye represented by the general formula (IV) are classified and defined as the following three types.
β-position substitution type: (phthalocyanine compound having a specific substituent at positions 2 and / or 3, position 6 and / or 7, position 10 and / or 11, position 14 and / or 15).
α-position substitution type: (phthalocyanine compound having a specific substituent at positions 1 and / or 4, 5 and / or 8, 9 and / or 12, 13 and / or 16).
α, β-position mixed substitution type: (phthalocyanine compound having a specific substituent without regularity at positions 1 to 16).

  In the present specification, when a derivative of a phthalocyanine dye having a different structure (especially a substitution position) is described, the β-position substitution type, α-position substitution type, and α, β-position mixed substitution type are used.

  Examples of the phthalocyanine derivative used in the present invention include “Phthalocyanine—Chemistry and Function” (P. 1-62), C.K. C. Leznoff-A. B. P. Lever co-authored, published by VCH, “Phthalogicanes-Properties and Applications” (P. 1-54), etc., can be synthesized by combining quoted or similar methods.

  The phthalocyanine compound represented by the general formula (I) used in the present invention is as described in WO 00/17275, 00/08103, 00/08101, 98/41853, JP-A-10-36471, and the like. For example, it can be synthesized through sulfonation, sulfonyl chlorideation, and amidation reaction of an unsubstituted phthalocyanine compound.

  In this case, sulfonation can occur at any position of the phthalocyanine nucleus, and the number of sulfonation is difficult to control.

  Therefore, when the sulfone group is introduced under such reaction conditions, the position and number of the sulfone group introduced into the product cannot be specified, and a mixture in which the number of substituents and the substitution position are different is always given.

  Therefore, when synthesizing the compound of the present invention using it as a raw material, the number and substitution position of the heterocyclic substituted sulfamoyl group cannot be specified, so that the compound is a mixture containing several kinds of compounds having different numbers of substitution groups and substitution positions. can get.

  Among the phthalocyanine compounds represented by the general formulas (I) to (III), for example, the phthalocyanine compound represented by the following general formula (V) includes, for example, a phthalonitrile derivative represented by the following general formula (VI) and / Or synthesized by reacting a diiminoisoindoline derivative represented by the following general formula (VII) with a metal derivative represented by the general formula (VIII).

On the other hand, a phthalocyanine compound represented by the general formula (V) is obtained by reacting a 4-sulfophthalic acid-sodium salt represented by the general formula (IX) with a metal derivative represented by the general formula (VIII). After synthesizing copper (II) -tetrasulfonic acid-4sodium, it can be synthesized by derivatizing to the corresponding sulfonyl chloride and reacting with the target amine and / or aniline derivative (for example, G ₁ , G ₂ , G ₃ and G ₄ are G ₁ : {-SO ₂ N (R ₂₁ ) (V ₁₁ )}, G ₂ : {-SO ₂ N (R ₂₂ ) (V ₁₂ )}, G ₃ : {-SO _{2 N (R 23) (V} 13)}, G 4: {- SO 2 N (R 24) when the (V _14)}).

In addition, l, m, n, and p in the general formula (V) are synonymous with t in the general formula (VI) and / or the general formula (VII), and t is an integer of 1 to 2. G ₁ , G ₂ , G ₃ and G ₄ in the general formula (V) are each independently G ₁ in the general formula (III): {—SO ₂ N (R ₂₁ ) (V ₁₁ )} _{, G 2: {- SO 2} N (R 22) (V 12)}, G 3: {- SO 2 N (R 23) (V 13)}, G 4: {- SO 2 N (R 24) ( represents the V _14)}.

このようにして得られる前記一般式（Ｖ）で表される化合物は通常、Ｒ₁（ＳＯ₂−Ｚ₁）、Ｒ₂（ＳＯ₂−Ｚ₂）、Ｒ₃（ＳＯ₂−Ｚ₃）、Ｒ₄（ＳＯ₂−Ｚ₄）の各置換位置における異性体である下記一般式（ａ）−１〜（ａ）−４で表される化合物の混合物となっている。

The compound represented by the general formula (V) thus obtained is usually R ₁ (SO ₂ -Z ₁ ), R ₂ (SO ₂ -Z ₂ ), R ₃ (SO ₂ -Z ₃ ), It is a mixture of compounds represented by the following general formulas (a) -1 to (a) -4, which are isomers at each substitution position of R ₄ (SO ₂ —Z ₄ ).

  Furthermore, when preparing a dye using two or more types of general formula (VI) and / or general formula (VII) having different substituents, the compound represented by general formula (V) is the type of substituent. , The dye mixture in different positions.

本発明に用いるシアン染料の例としては、特開２００２−２５６１６７号、同２００２−２７５３８６号、同２００２−２８５０５０号、同２００２−２９４０９７号、同２００２−３０２６２３号、同２００２−３０９１１８号、同２００３−２１３１６７号、同２００３−２１３１６８号公報に記載の該当する構造の化合物を挙げることができるが、特に好ましいものは下記表に挙げるものである。表１に記載の化合物については、上記公報に記載の方法で合成できる。もちろん、出発化合物、色素中間体および合成方法について、これらに限定されるものではない。

Examples of cyan dyes used in the present invention include JP-A Nos. 2002-256167, 2002-275386, 2002-285050, 2002-294097, 2002-302623, 2002-309118, and 2003. The compounds having the corresponding structure described in JP-A Nos. 213167 / 2003-213168 can be mentioned, and particularly preferable ones are listed in the following table. About the compound of Table 1, it is compoundable by the method as described in the said gazette. Of course, the starting compound, the dye intermediate and the synthesis method are not limited to these.

染料の含有量は、一般式（Ｉ）で表される化合物の種類、溶媒成分の種類等により決められるが、インク組成物全重量に対し、好ましくは０．１〜１０重量％、さらに好ましくは０．５〜５重量％の範囲である。０．１重量％以上とすることで、記録媒体上での発色性又は画像濃度を確保でき、１０重量％以下とすることで、インク組成物の粘度調整が容易となり吐出信頼性や目詰まり性等の特性が容易に確保できる。

The content of the dye is determined by the type of the compound represented by the general formula (I), the type of the solvent component, etc., but is preferably 0.1 to 10% by weight, more preferably based on the total weight of the ink composition. It is in the range of 0.5 to 5% by weight. By setting the content to 0.1% by weight or more, it is possible to ensure color developability or image density on the recording medium, and by setting the content to 10% by weight or less, the viscosity of the ink composition can be easily adjusted, and ejection reliability and clogging properties Such characteristics can be easily secured.

  In the ink composition of the present invention, discoloration observed when solid printing is performed using the ink composition containing the above phthalocyanine cyan dye (the phthalocyanine cyan dye is inferior in gas resistance, particularly ozone resistance). In order to suppress the phenomenon caused by (2), at least one aromatic compound having a specific sulfone group and / or a salt thereof is contained.

  In the present invention, an aromatic compound having a specific sulfone group and / or a salt thereof is used in combination with the phthalocyanine cyan dye represented by the above formula (I), so that the color change and fading of an image derived from ozone gas can be achieved. It suppresses and drastically improves the fading resistance of the image.

  In the present invention, the cyan ink composition is, of course, any ink composition that contains water, the phthalocyanine-based cyan dye, and an aromatic compound having a specific sulfone group or a salt thereof. Even if the ink composition has a color different from cyan, such as a black ink composition, it is possible to effectively prevent the discoloration color seen in solid printing. In order to produce these various ink compositions, they can be used in combination with other conventionally known dyes.

The aromatic compound having a sulfone group or a salt thereof used in the ink composition of the present invention is an aromatic compound having a sulfone group represented by the following general formula (a) and / or (b) and / or a salt thereof. It is. By containing aromatic compounds and / or salts thereof having the sulfonic group, without causing greening-blackening phenomenon from NO _x gas, to suppress the discoloration of the image derived from the ozone gas resistance of the image Fading property can be improved.

（式中、Ｍ¹は塩を構成する対イオンを示し、Ｘは１〜３の整数を示し、Ｒ¹及びＲ²はそれぞれ水素原子、炭素数１〜６のアルキル基又は炭素数１〜６のアルコキシ基を示し、Ｒ¹及びＲ²は同一でも異なっていても良い。）

(Wherein, M ¹ is shown a counter ion constituting the salt, X is an integer of 1 to 3, R ¹ and R ² are each a hydrogen atom, 1-6 alkyl group carbon atoms or 1 to 6 carbon atoms And R ¹ and R ² may be the same or different.)

（式中、Ｍ²は塩を構成する対イオンを示し、Ｙは１〜４の整数を示し、Ｒ³及びＲ⁴はそれぞれ水素原子、炭素数１〜６のアルキル基又は炭素数１〜６のアルコキシ基を示し、Ｒ³及びＲ⁴は同一でも異なっていても良い。）
前記一般式（ａ）及び／又は（ｂ）で表されるスルホン基を有する芳香族化合物及び／又はその塩としては、分子構造中にスルホン基を少なくとも１つ有する芳香族化合物又はその塩であればいかなるものでも良いが、スルホン基を２つ以上有するもの、特に、１，３−ベンゼンジスルホン酸、ナフタレン−１，５−ジスルホン酸、ナフタレン−１，６−ジスルホン酸、ナフタレン−２，６−ジスルホン酸、ナフタレン−２，７−ジスルホン酸、ナフタレン−１，３，６−トリスルホン酸、及びそれらの塩からなる群より選択される少なくとも１種が、得られる画像の耐オゾン性の改善の点で好ましい。

(Wherein, M ² represents a counter ion constituting the salt, Y is an integer of 1 to 4, R ³ and R ⁴ are each a hydrogen atom, 1-6 alkyl group carbon atoms or 1 to 6 carbon atoms And R ³ and R ⁴ may be the same or different.)
The aromatic compound having a sulfone group represented by the general formula (a) and / or (b) and / or a salt thereof may be an aromatic compound having at least one sulfone group in the molecular structure or a salt thereof. Any one having two or more sulfone groups, particularly 1,3-benzenedisulfonic acid, naphthalene-1,5-disulfonic acid, naphthalene-1,6-disulfonic acid, naphthalene-2,6- At least one selected from the group consisting of disulfonic acid, naphthalene-2,7-disulfonic acid, naphthalene-1,3,6-trisulfonic acid, and salts thereof can improve the ozone resistance of the resulting image. This is preferable.

  A salt of an aromatic compound having a sulfone group is added in the form of a salt and can be contained in the ink composition. Also, the aromatic compound having a sulfone group and a base are added separately. It can also be contained in the ink composition. Such a salt is not particularly limited to its counter ion, and examples thereof include metal salts and ammonium salts. Alkali metal salts are particularly preferable, specifically, sodium salts, lithium salts and potassium salts. Examples include salts.

  The content of the aromatic compound having a sulfone group and / or a salt thereof is appropriately determined depending on the type of aromatic compound having the sulfone group and / or the salt thereof, the type of the dye, the type of the solvent component, etc. Preferably it is 0.1 to 10 weight% with respect to the total weight of a composition, More preferably, it is the range of 0.5 to 10 weight%.

  In the ink composition of the present invention, the content ratio of the phthalocyanine cyan dye and the aromatic compound having a sulfone group and / or a salt thereof effectively improves the gas resistance and improves the reliability of the ink. In terms of ensuring, it is preferable to be within a range of 1: 0.1 to 1:10, particularly 1: 0.2 to 1: 5.

  The pH (20 ° C.) of the ink composition is preferably 8.0 or more in order to stably dissolve the predetermined dye and the aromatic compound having a sulfone group and / or the salt thereof. In consideration of material resistance with various members in contact with the ink composition, the pH of the ink composition is preferably 10.5 or less. In order to make these matters better compatible, it is more preferable to adjust the pH of the ink composition to 8.0 to 10.5, particularly 8.5 to 10.0.

  The ink composition of the present invention may further contain a humectant selected from water-soluble organic solvents and / or saccharides having a vapor pressure lower than that of pure water.

  By including the humectant, the ink can be moisturized by suppressing evaporation of moisture in the ink jet recording system. In addition, if it is a water-soluble organic solvent, the viscosity can be easily changed without improving ejection stability or changing ink characteristics.

  The water-soluble organic solvent refers to a medium having an ability to dissolve a solute, and is selected from organic and water-soluble solvents having a vapor pressure smaller than that of water. Specifically, ethylene glycol, propylene glycol, butanediol, pentanediol, 2-butene-1,4-diol, 2-methyl-2,4-pentanediol, glycerin, 1,2,6-hexanetriol, diethylene glycol Desirable are polyhydric alcohols such as triethylene glycol and dipropylene glycol, ketones such as acetonyl acetone, esters such as γ-butyrolactone and triethyl phosphate, furfuryl alcohol, tetrahydrofurfuryl alcohol, thiodiglycol and the like. .

  As the saccharide, maltitol, sorbitol, gluconolactone, maltose and the like are preferable.

  The humectant is preferably added in the range of 5 to 50% by weight, more preferably 5 to 30% by weight, and still more preferably 5 to 20% by weight with respect to the total amount of the ink composition. If it is 5% by weight or more, moisture retention can be obtained, and if it is 50% by weight or less, it is easy to adjust the viscosity used for inkjet recording.

  The ink composition of the present invention preferably contains a nitrogen-containing organic solvent as a solvent. Examples of the nitrogen-containing organic solvent include 1,3-dimethyl-2-imidazolidinone, 2-pyrrolidone, N-methyl-2-pyrrolidone, and ε-caprolactam. Among them, 2-pyrrolidone is preferably used. be able to. They can be used alone or in combination of two or more.

  The content is preferably 0.5 to 10% by weight, more preferably 1 to 5% by weight. By making the content 0.5% by weight or more, it is possible to improve the solubility of the coloring material of the present invention by adding, and by making the content 10% by weight or less, various kinds of ink compositions that come into contact with it. The material resistance with the member is not deteriorated.

  In addition, the ink composition of the present invention contains a nonionic surfactant as an additive effective for obtaining rapid fixing (penetration) of the ink and maintaining the roundness of one dot. Is preferred.

  Examples of nonionic surfactants that can be used in the present invention include acetylene glycol surfactants. Specific examples of acetylene glycol surfactants include Surfinol 465, Surfinol 104 (manufactured by Air Products and Chemicals Inc.), Olphine E1010, Olphine PD001, Olphine STG (manufactured by Nissin Chemical Industry Co., Ltd.). Product name). The addition amount is preferably 0.1 to 5% by weight, more preferably 0.5 to 2% by weight. When the addition amount is 0.1% by weight or more, sufficient penetrability can be obtained, and when the addition amount is 5% by weight or less, it is easy to prevent image blurring.

  The ink composition of the present invention preferably further comprises a penetration enhancer from the viewpoint that the permeability can be improved. By adding glycol ethers as the penetration enhancer, the penetrability is further increased and the bleed at the boundary with the adjacent color ink is reduced when color printing is performed, thereby obtaining a very clear image. Can do.

  Glycol ethers include ethylene glycol monobutyl ether, diethylene glycol monobutyl ether, triethylene glycol monoethyl ether, propylene glycol monomethyl ether, dipropylene glycol monoethyl ether, propylene glycol monobutyl ether, dipropylene glycol monobutyl ether, triethylene glycol monobutyl ether. Etc. The addition amount is 3 to 30% by weight, preferably 5 to 15% by weight. If the amount added is less than 3% by weight, the effect of preventing bleeding may not be obtained. If the amount exceeds 30% by weight, not only the image will bleed, but also oily separation will occur, so the dissolution aid for these glycol ethers will be required, which will increase the viscosity of the ink. Becomes difficult.

  Furthermore, the ink composition of the present invention includes a pH adjuster such as triethanolamine or alkali metal hydroxide, a hydrotrope such as urea and its derivatives, a water-soluble polymer such as sodium alginate, if necessary. A water-soluble resin, a fluorine-based surfactant, an antifungal agent, an antirust agent, an antiseptic, and the like may be added.

  As a method for preparing the ink composition of the present invention, for example, each component is sufficiently mixed and dissolved, pressure-filtered through a membrane filter having a pore size of 0.8 μm, and then degassed using a vacuum pump. There is.

  The present invention can also provide an ink cartridge including at least the ink composition described above. According to the ink cartridge of the present invention, it is possible to improve indoor storage stability (gas resistance) of a formed image, and to facilitate handling such as transport of ink that can effectively prevent early color fading of the image. Is possible.

  Next, the recording method of the present invention using the above-described ink composition will be described. In the recording method of the present invention, an ink jet recording method in which an ink composition is ejected as droplets from fine holes and the droplets are attached to a recording medium for recording can be used particularly preferably. Needless to say, it can also be used for applications such as pen plotters.

  As the ink jet recording method, any of the conventionally known methods can be used, and in particular, a method of ejecting droplets using vibration of a piezoelectric element (using an ink jet head that forms ink droplets by mechanical deformation of an electrostrictive element). Recording method) and a method using thermal energy, it is possible to perform excellent image recording.

  In addition, the recorded matter of the present invention is recorded using the above-described ink composition, is excellent in image indoor storage (gas resistance), and does not cause premature discoloration.

  The ink composition of the present invention can improve the indoor storage stability (gas resistance) of the obtained image, and has an excellent effect of being able to effectively prevent early color change and fading of the image.

  Hereinafter, the present invention will be described more specifically with reference to examples and comparative examples of the present invention, but the present invention is not limited to these examples.

[Examples 1 to 13 and Comparative Examples 1 to 9]
The ink compositions of Examples 1 to 13 and Comparative Examples 1 to 9 were mixed and dissolved at the blending ratios shown in Table 2, and subjected to pressure filtration with a membrane filter having a pore size of 1 μm. A product was prepared.

なお、表２中に示すインク組成物の各成分はインク組成物全量に対する各成分の重量％を示し、残量は水である。また、実施例に用いた色材は前記の表１に示す化合物（化合物Ａ〜Ｆ）であり、比較例に用いた色材はＣ．Ｉ．ダイレクトブルー１９９である。

In addition, each component of the ink composition shown in Table 2 indicates weight% of each component with respect to the total amount of the ink composition, and the remaining amount is water. The color materials used in the examples are the compounds (compounds A to F) shown in Table 1 above, and the color materials used in the comparative examples are C.I. I. Direct Blue 199.

  Using the ink compositions described in Examples 1 to 13 and Comparative Examples 1 to 9, an inkjet printer PM970C (manufactured by Seiko Epson Corporation), an ink jet recording medium (PM photographic paper: manufactured by Seiko Epson Corporation) Each of the following evaluations was performed.

≪Ozone resistance test≫
Using the above cartridge, printed matter obtained by performing printing while adjusting the applied duty so that the OD (Optical Density) is in the range of 0.9 to 1.1 is obtained as an ozone weather meter OMS-H type ( Using a trade name, manufactured by Suga Test Instruments Co., Ltd.), the printed matter was exposed for a predetermined time (12, 24 hours) under the conditions of 24 ° C., relative humidity 60% RH, and ozone concentration 20 ppm.

  After the exposure, the OD of each printed matter was measured using a densitometer (Spectrolino: manufactured by Gretag), the optical density residual ratio (ROD) was determined by the following formula, and evaluated according to the following criteria.

ROD (%) = (D / D ₀ ) × 100
D: OD after exposure test
D ₀ : OD before exposure test
(However, the measurement conditions are Filter: Red, light source: D50, viewing angle: 2 degrees)

[Criteria]
Evaluation A: ROD is 90% or more Evaluation B: ROD is 80% or more and less than 90% Evaluation C: ROD is 70% or more and less than 80% Evaluation D: ROD is 70% or less

≪Nitrogen oxide resistance test≫
Using the cartridges filled with the ink compositions of Examples 1 to 13 and Comparative Examples 1 to 9, the applied duty was adjusted so that the OD (Optical Density) was in the range of 0.9 to 1.1. Using a gas corrosion tester GS-UV type (trade name, manufactured by Suga Test Instruments Co., Ltd.), the printed matter obtained by printing is printed under the conditions of 24 ° C., relative humidity 60% RH, and nitrogen dioxide concentration 10 ppm. The print was exposed for a predetermined time (12, 24 hours).

After exposure, the CIE-L ^* a ^* b ^* coordinates of each printed material are measured using a densitometer (Spectrolino: manufactured by Gretag), and the color difference (ΔE) is determined by the following formula, and evaluated according to the following criteria. did.

ΔE = {(L ^* −L ₀ ^* ) ² + (a ^* −a ₀ ^* ) ² + (b ^* −b ₀ ^* ) ² } ^1/2
L ^* , a ^* , b ^* : Each coordinate value after the exposure test L ₀ ^* , a ₀ ^* , b ₀ ^* : Each coordinate value before the exposure test

[Criteria]
Evaluation A: ΔE is less than 3 Evaluation B: ΔE is 3 or more and less than 10 Evaluation C: ΔE is 10 or more and less than 20 Evaluation D: ΔE is 20 or more

≪Clogging resistance≫
Ink was filled in an ink jet printer PM970C (manufactured by Seiko Epson Corporation), and printing was continued for 10 minutes. After confirming that ink was ejected from the nozzles, printing was stopped. The printer was left for 2 weeks in an environment of 40 ° C. and 25% RH for each of the ink compositions of Examples 1 to 13 and Comparative Examples 1 to 9 without capping the head. After leaving, nozzle cleaning operation was performed, and then printing was performed. The ink clogging characteristics were evaluated by the number of cleaning operations until there was no defective printing such as blurring or missing, and printing equivalent to the initial printing became possible.

[Criteria]
Evaluation A: When printing equivalent to the initial value is obtained by 1 to 5 cleaning operations Evaluation B: When printing equivalent to the initial value is obtained by 6 to 10 cleaning operations Evaluation C: Cleaning operation 11 to 15 times In the case where printing equivalent to the initial value is obtained, Evaluation D: Even if the cleaning operation is performed 16 times or more, printing equivalent to the initial value is impossible. Table 3 shows the evaluation results obtained.

  The present invention is an ink composition using a specific phthalocyanine cyan dye, which can improve indoor storage stability (gas resistance) of a formed image, and effectively prevent early discoloration of the image. INDUSTRIAL APPLICABILITY The present invention has industrial applicability as an ink composition that can be used, and an ink jet recording method and recorded matter using the ink composition.

FIG. 1 is a graph showing spectral characteristics (absorption wavelength) of a dye (CI Direct Blue 199) (* 1) contained in an ink composition of a comparative example.

Claims (17)

At least water, a phthalocyanine cyan dye represented by the following formula (I), an aromatic compound having a sulfone group represented by the following general formula (a) and / or (b) and / or a salt thereof: An ink composition comprising:

Wherein X ₁₁ , X ₁₂ , X ₁₃ and X ₁₄ each independently represent —SO ₂ NR ₁ R ₂ and / or a sulfone group, provided that all of X ₁₁ , X ₁₂ , X ₁₃ and X ₁₄ At the same time, when there are a plurality of R _{1 s} , each independently represents a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted group. R ₂ represents an independently substituted or unsubstituted alkenyl group, substituted or unsubstituted aralkyl group, substituted or unsubstituted aryl group, or substituted or unsubstituted heterocyclic group. An alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted aryl group, or a R ₁ and R ₂ may be bonded to each other to form a 5- or 6-membered nitrogen-containing heterocyclic ring.
Y ₁₁ , Y ₁₂ , Y ₁₃ , Y ₁₄ , Y ₁₅ , Y ₁₆ , Y ₁₇ and Y ₁₈ are each independently a hydrogen atom, halogen atom, alkyl group, cycloalkyl group, alkenyl group, aralkyl group, aryl group , Heterocyclic group, cyano group, hydroxy group, nitro group, amino group, alkylamino group, alkoxy group, aryloxy group, amide group, arylamino group, ureido group, sulfamoylamino group, alkylthio group, arylthio group, Alkoxycarbonylamino group, sulfonamido group, carbamoyl group, alkoxycarbonyl group, heterocyclic oxy group, azo group, acyloxy group, carbamoyloxy group, silyloxy group, aryloxycarbonyl group, aryloxycarbonylamino group, imide group, heterocyclic ring Thio group, phosphoryl group, acyl group or ionic hydrophilic Represents a group, each group may further have a substituent.
a ₁₁ ~a ₁₄ each represent a number of substituents X ₁₁ to X _14, independently, it is an integer of 0 to 2, but all are not 0 at the same time.
M is a hydrogen atom, a metal element or an oxide, hydroxide or halide thereof.
Provided that at least one of X ₁₁ , X ₁₂ , X ₁₃ , X ₁₄ , Y ₁₁ , Y ₁₂ , Y ₁₃ , Y ₁₄ , Y ₁₅ , Y ₁₆ , Y ₁₇ and Y ₁₈ is an ionic hydrophilic group Or a group having an ionic hydrophilic group as a substituent. )

(Wherein, M ¹ is shown a counter ion constituting the salt, X is an integer of 1 to 3, R ¹ and R ² are each a hydrogen atom, 1-6 alkyl group carbon atoms or 1 to 6 carbon atoms And R ¹ and R ² may be the same or different.)

(Wherein, M ² represents a counter ion constituting the salt, Y is an integer of 1 to 4, R ³ and R ⁴ are each a hydrogen atom, 1-6 alkyl group carbon atoms or 1 to 6 carbon atoms And R ³ and R ⁴ may be the same or different.) 2. The ink composition according to claim 1, wherein the phthalocyanine cyan dye represented by the formula (I) is a phthalocyanine dye represented by the following formula (II).

Wherein R ₁₁ , R ₁₂ , R ₁₃ and R ₁₄ are each independently a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted alkenyl group, substituted Alternatively, it represents an unsubstituted aralkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group.
V ₁ , V ₂ , V ₃ and V ₄ are each independently a substituted or unsubstituted alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted aralkyl group, It represents a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group.
Y ₃₁ , Y ₃₂ , Y ₃₃ , Y ₃₄ , Y ₃₅ , Y ₃₆ , Y ₃₇ and Y ₃₈ are each independently a hydrogen atom, halogen atom, alkyl group, cycloalkyl group, alkenyl group, aralkyl group, aryl group , Heterocyclic group, cyano group, hydroxy group, nitro group, amino group, alkylamino group, alkoxy group, aryloxy group, amide group, arylamino group, ureido group, sulfamoylamino group, alkylthio group, arylthio group, Alkoxycarbonylamino group, sulfonamido group, carbamoyl group, alkoxycarbonyl group, heterocyclic oxy group, azo group, acyloxy group, carbamoyloxy group, silyloxy group, aryloxycarbonyl group, aryloxycarbonylamino group, imide group, heterocyclic ring Thio group, phosphoryl group, acyl group or ionic hydrophilic Represents a group, each group may further have a substituent.
M has the same meaning as M in formula (I).
Of R ₁₁ , R ₁₂ , R ₁₃ , R ₁₄ , V ₁ , V ₂ , V ₃ , V ₄ , Y ₃₁ , Y ₃₂ , Y ₃₃ , Y ₃₄ , Y ₃₅ , Y ₃₆ , Y ₃₇ and Y ₃₈ At least one is an ionic hydrophilic group or a group having an ionic hydrophilic group as a substituent. )   The ink composition according to claim 1, wherein the aromatic compound having a sulfone group and / or a salt thereof has two or more sulfone groups.   The aromatic compound having a sulfonic group and / or a salt thereof is 1,3-benzenedisulfonic acid, naphthalene-1,5-disulfonic acid, naphthalene-1,6-disulfonic acid, naphthalene-2,6-disulfonic acid, The ink composition according to claim 3, which is at least one selected from the group consisting of naphthalene-2,7-disulfonic acid, naphthalene-1,3,6-trisulfonic acid, and salts thereof.   The ink composition according to any one of claims 1 to 4, comprising 0.1 to 10% by weight of the aromatic compound having a sulfone group and / or a salt thereof based on the total amount of the ink composition.   The content ratio of the phthalocyanine-based cyan dye and the aromatic compound having a sulfone group and / or a salt thereof is in the range of 1: 0.1 to 1:10. The ink composition as described.   The ink composition according to any one of claims 1 to 6, further comprising a nonionic surfactant.   The ink composition according to claim 7, wherein the nonionic surfactant is an acetylene glycol surfactant.   The ink composition according to claim 7 or 8, comprising 0.1 to 5% by weight of the nonionic surfactant based on the total amount of the ink composition.   The ink composition according to any one of claims 1 to 9, further comprising a penetration enhancer.   The ink composition according to claim 10, wherein the penetration enhancer is a glycol ether.   The ink composition according to claim 1, wherein the pH of the ink composition at 20 ° C. is 8.0 to 10.5.   The ink composition according to any one of claims 1 to 12, which is used in an inkjet recording method.   The ink composition according to claim 13, wherein the ink jet recording method is a recording method using an ink jet head that forms ink droplets by mechanical deformation of an electrostrictive element.   An ink cartridge comprising at least the ink composition according to claim 1.   An ink jet recording method for performing recording by discharging droplets of an ink composition and attaching the droplets to a recording medium, wherein the ink composition according to claim 1 is used as the ink composition. An ink jet recording method comprising: A recorded matter recorded using the ink composition according to claim 1.

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