KR20150061585A - Colored curable resin composition - Google Patents

Abstract

A colored curable resin composition comprises: a silicon atom; a coloring agent (A) comprising a dye (A1) with maximum absorption wavelength of 500-600 nm with respect to chloroform; a resin (B); a polymerizable compound (C); and a polymerization initiator (D).

Description

COLORED CURABLE RESIN COMPOSITION [0002]

The present invention relates to a colored curable resin composition.

BACKGROUND ART Dyes are used for color display by using reflected light or transmitted light in the fields of textile materials, liquid crystal displays, inkjets, and the like. As such dyes, rhodamine B having a xanthene skeleton and represented by the following chemical formula (Rb) is widely known (Yoshida Yutaka, " New Dye Chemistry " Page 274].

The present invention includes the following inventions.

[1] A colorant (A) comprising a dye (A1) having a silicon atom and having a maximum absorption wavelength in chloroform of 500 nm to 600 nm,

The resin (B)

The polymerizable compound (C)

The polymerization initiator (D)

And a coloring curable resin.

[2] The colored curable resin composition according to [1], wherein the dye (A1) is a dye having a xanthene skeleton having a substituent, and the substituent comprises an organic silicon group.

[3] The colored curable resin composition according to [2], wherein the organic silicon group has a silyloxy group.

[4] The colored curable resin composition according to any one of [1] to [3], wherein the dye (A1) is a compound represented by the formula (II).

[In the formula (II), R ²¹ to R ²⁴ each independently represent a hydrogen atom, a monovalent saturated hydrocarbon group having 1 to 10 carbon atoms, a phenyl group which may have a substituent, or a group represented by the formula (ii). Provided that at least one of R ²¹ to R ²⁴ is a group represented by the formula (ii).

-R ⁵⁰ -Si (R ²⁹ ) ₃ (ii)

(R ²⁹ represents an alkoxy group having 1 to 4 carbon atoms or a hydrogen atom, a hydroxyl group, having 1 to 4 carbon atoms, * represents a bonding number (結合手) with a nitrogen atom. A plurality of R ²⁹ may be the same respectively Or may be different.

R ⁵⁰ represents an alkanediyl group having 1 to 10 carbon atoms, and -CH ₂ - which constitutes the alkanediyl group is -O-, -CO-, -NR ¹¹ -, -OCO-, -COO-, -OCONH- , -CONH-, or -NHCO-).

In R ²¹ to R ²⁴ , a hydrogen atom contained in a monovalent saturated hydrocarbon group having 1 to 10 carbon atoms may be substituted with a halogen atom, and -CH ₂ - included in the saturated hydrocarbon group may be -O-, -CO-, NR ¹¹ -, -OCO-, -COO-, -OCONH-, -CONH- or -NHCO-.

R ²⁵ and R ²⁶ each independently represent a hydrogen atom or an alkyl group having 1 to 6 carbon atoms.

R ²⁷ and R ²⁸ are each independently selected from _{^{-OH, -SO 3 -, -SO 3}} H, -SO 3 - Z +, -CO 2 -, -CO 2 H, -CO 2 - Z +, -CO 2 R ¹⁴ shows a -SO ₃ R ¹⁵ or -SO ₂ NR ¹² R ^13.

R ¹⁴ and R ¹⁵ each independently represent a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a halogen atom.

Z ⁺ represents ⁺ N (R ¹⁶ ) ₄ , Na ⁺ or K ⁺ .

R ¹¹ , R ¹² and R ¹³ each independently represent a hydrogen atom or a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms.

R ¹⁶ each independently represents a hydrogen atom or a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms.

and p represents an integer of 0 to 4.]

[5] The alkanediyl group having 1 to 10 carbon atoms represented by R ⁵⁰ is a group represented by -CH ₂ - in which -CH ₂ - is -O-, -CO-, -NR ¹¹ -, -OCO-, -COO-, -OCONH-, -CONH - or -NHCO-. ≪ / RTI >

[6] The colored curable resin composition according to [4] or [5], wherein in the formula (ii), R ⁵⁰ is an alkanediyl group having 1 to 8 carbon atoms and R ²⁹ is a hydroxyl group or an alkoxy group having 1 to 4 carbon atoms.

[7] The monovalent saturated hydrocarbon group having 1 to 10 carbon atoms represented by R ²¹ to R ²⁴ is a group represented by -CH ₂ - in the group consisting of -OCO-, -COO-, -OCONH-, -CONH- and -NHCO- The colored curable resin composition according to any one of [4] to [6], which is a compound which may be substituted with at least one group selected.

[8] A coated film formed using the colored curable resin composition according to any one of [1] to [7].

[9] A color filter formed by using the colored curable resin composition according to any one of [1] to [7].

[10] A display device including the color filter according to [9].

[11] The compound represented by the formula (II).

[In the formula (II), R ²¹ to R ²⁴ each independently represent a hydrogen atom, a monovalent saturated hydrocarbon group having 1 to 10 carbon atoms, a phenyl group which may have a substituent, or a group represented by the formula (ii). Provided that at least one of R ²¹ to R ²⁴ is a group represented by the formula (ii).

-R ⁵⁰ -Si (R ²⁹ ) ₃ (ii)

(Wherein R ²⁹ represents a hydrogen atom, a hydroxy group, an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms, and * indicates the number of bonds with a nitrogen atom. The plurality of R ^{29 s} may be the same or different .

R ⁵⁰ represents an alkanediyl group having 1 to 10 carbon atoms, and -CH ₂ - which constitutes the alkanediyl group is -O-, -CO-, -NR ¹¹ -, -OCO-, -COO-, -OCONH- , -CONH-, or -NHCO-).

In R ²¹ to R ²⁴ , the hydrogen atom contained in the monovalent saturated hydrocarbon group having 1 to 10 carbon atoms may be substituted with a halogen atom, and -CH ₂ - included in the monovalent hydrocarbon group may be replaced by -O-, -CO-, NR ¹¹ -, -OCO-, -COO-, -OCONH-, -CONH- or -NHCO-.

R ²⁵ and R ²⁶ each independently represent a hydrogen atom or an alkyl group having 1 to 6 carbon atoms.

R ²⁷ and R ²⁸ are each independently selected from _{^{-OH, -SO 3 -, -SO 3}} H, -SO 3 - Z +, -CO 2 -, -CO 2 H, -CO 2 - Z +, -CO 2 R ¹⁴ shows a -SO ₃ R ¹⁵ or -SO ₂ NR ¹² R ^13.

R ¹⁴ and R ¹⁵ each independently represent a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a halogen atom.

Z ⁺ represents ⁺ N (R ¹⁶ ) ₄ , Na ⁺ or K ⁺ .

R ¹¹ , R ¹² and R ¹³ each independently represent a hydrogen atom or a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms.

R ¹⁶ each independently represents a hydrogen atom or a monovalent saturated hydrocarbon group of 1 to 20 carbon atoms.

and p represents an integer of 0 to 4.]

[12] The alkanediyl group having 1 to 10 carbon atoms represented by R ⁵⁰ is preferably -CH ₂ -, -O-, -CO-, -NR ¹¹ -, -OCO-, -COO-, -OCONH-, -CONH - or -NHCO-. ≪ / RTI >

[13] The compound according to [11] or [12], wherein in Formula (ii), R ⁵⁰ is an alkanediyl group having 1 to 8 carbon atoms and R ²⁹ is a hydroxy group or an alkoxy group having 1 to 4 carbon atoms.

[14] A process for producing a compound represented by the formula (II), which comprises the step of reacting a compound represented by the formula (IV) with a compound represented by the formula (V).

[In the formulas, X ² represents a halogen atom or a trifluoromethylsulfonyloxy group.

R ²¹ , R ²² , R ²³ and R ²⁴ each independently represent a hydrogen atom, a monovalent saturated hydrocarbon group having 1 to 10 carbon atoms, a phenyl group which may have a substituent, or a group represented by the formula (ii). Provided that at least one of R ²¹ , R ²² , R ²³ or R ²⁴ is a group represented by the formula (ii).

-R ⁵⁰ -Si (R ²⁹ ) ₃ (ii)

(Wherein R ²⁹ represents a hydrogen atom, a hydroxy group, an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms, and * indicates the number of bonds with a nitrogen atom. The plurality of R ^{29 s} may be the same or different .

R ⁵⁰ represents an alkanediyl group having 1 to 10 carbon atoms, and -CH ₂ - which constitutes the alkanediyl group is -O-, -CO-, -NR ¹¹ -, -OCO-, -COO-, -OCONH- , -CONH-, or -NHCO-).

In R ²¹ , R ²² , R ²³ and R ²⁴ , the hydrogen atom contained in the monovalent saturated hydrocarbon group having 1 to 10 carbon atoms may be substituted with a halogen atom, and -CH ₂ - included in the saturated hydrocarbon group may be replaced by -O- , -CO-, -NR ¹¹ -, -OCO-, -COO-, -OCONH-, -CONH- or -NHCO-.

R ²⁵ and R ²⁶ each independently represent a hydrogen atom or an alkyl group having 1 to 6 carbon atoms.

R ²⁷ and R ²⁸ are each independently selected from _{^{-OH, -SO 3 -, -SO 3}} H, -SO 3 - Z +, -CO 2 -, -CO 2 H, -CO 2 - Z +, -CO 2 R ¹⁴ shows a -SO ₃ R ¹⁵ or -SO ₂ NR ¹² R ^13.

R ¹⁴ and R ¹⁵ each independently represent a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a halogen atom.

Z ⁺ represents ⁺ N (R ¹⁶ ) ₄ , Na ⁺ or K ⁺ .

R ¹¹ , R ¹² and R ¹³ each independently represent a hydrogen atom or a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms.

R ¹⁶ each independently represents a hydrogen atom or a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms.

and p represents an integer of 0 to 4.]

[15] The production method according to [14], wherein the compound represented by the formula (IV) is reacted with the compound represented by the formula (V) in an organic solvent having a solubility in water at 20 ° C of not more than 200 g / ℓ.

[16] A process for producing a compound represented by the formula (II-1) which comprises a step of reacting a compound represented by the formula (VI), a compound represented by the formula (III) and a compound represented by the formula (V).

[In the formulas, X ¹ and X ² each independently represent a halogen atom or a trifluoromethylsulfonyloxy group.

R ²⁵ and R ²⁶ each independently represent a hydrogen atom or an alkyl group having 1 to 6 carbon atoms.

R ²⁸ is _{^{-OH, -SO 3 -, -SO 3}} H, -SO 3 - Z +, -CO 2 -, -CO 2 H, -CO 2 - Z +, -CO 2 R 14, -SO 3 R ¹⁵ or -SO ₂ represents a NR ¹² R ^13.

R ¹² and R ¹³ each independently represent a hydrogen atom or a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms.

R ¹⁴ and R ¹⁵ each independently represent a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a halogen atom.

Z ⁺ represents ⁺ N (R ¹⁶ ) ₄ , Na ⁺ or K ⁺ .

R ¹⁶ each independently represents a hydrogen atom or a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms.

p represents an integer of 0 to 4;

R ³⁰ represents -SO ₂ - or -CO-.

R ²¹ , R ²² , R ²³ and R ²⁴ each independently represent a hydrogen atom, a monovalent saturated hydrocarbon group having 1 to 10 carbon atoms, a phenyl group which may have a substituent, or a group represented by the formula (ii). Provided that at least one of R ²¹ , R ²² , R ²³ or R ²⁴ is a group represented by the formula (ii).

-R ⁵⁰ -Si (R ²⁹ ) ₃ (ii)

(Wherein R ²⁹ represents a hydrogen atom, a hydroxy group, an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms, and * indicates the number of bonds with a nitrogen atom. The plurality of R ^{29 s} may be the same or different .

R ⁵⁰ represents an alkanediyl group having 1 to 10 carbon atoms, and -CH ₂ - which constitutes the alkanediyl group is -O-, -CO-, -NR ¹¹ -, -OCO-, -COO-, -OCONH- , -CONH-, or -NHCO-).

In R ²¹ , R ²² , R ²³ and R ²⁴ , the hydrogen atom contained in the monovalent saturated hydrocarbon group having 1 to 10 carbon atoms may be substituted with a halogen atom, and -CH ₂ - included in the saturated hydrocarbon group may be replaced by -O- , -CO-, -NR ¹¹ -, -OCO-, -COO-, -OCONH-, -CONH- or -NHCO-.

R ¹¹ each independently represents a hydrogen atom or a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms.

And R ³¹ represents -SO ₃ ^- or -CO ₂ ^- .

(17) A process for producing a compound represented by the formula (VI), a compound represented by the formula (III) and a compound represented by the formula (V) in an organic solvent having a solubility in water at 20 ° C. of 200 g / Gt; [16]. ≪ / RTI >

The compound represented by the formula (VII) and the compound represented by the formula (V) can be obtained by reacting the compound represented by the formula (VI) with the compound represented by the formula (III) Wherein the compound represented by the formula (II-1) is reacted with the compound represented by the formula (II-1).

In the formulas (VI), (III), (VII), (V) and (II-1)

X ¹ and X ² each independently represent a halogen atom or a trifluoromethylsulfonyloxy group.

R ²⁵ and R ²⁶ each independently represent a hydrogen atom or an alkyl group having 1 to 6 carbon atoms.

R ²⁸ is _{^{-OH, -SO 3 -, -SO 3}} H, -SO 3 - Z +, -CO 2 -, -CO 2 H, -CO 2 - Z +, -CO 2 R 14, -SO 3 R ¹⁵ or -SO ₂ represents a NR ¹² R ^13.

R ¹² and R ¹³ each independently represent a hydrogen atom or a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms.

R ¹⁴ and R ¹⁵ each independently represent a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a halogen atom.

Z ⁺ represents ⁺ N (R ¹⁶ ) ₄ , Na ⁺ or K ⁺ .

R ¹⁶ each independently represents a hydrogen atom or a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms.

p represents an integer of 0 to 4;

R ³⁰ represents -SO ₂ - or -CO-.

R ²¹ , R ²² , R ²³ and R ²⁴ each independently represent a hydrogen atom, a monovalent saturated hydrocarbon group having 1 to 10 carbon atoms, a phenyl group which may have a substituent, or a group represented by the formula (ii). Provided that at least one of R ²¹ , R ²² , R ²³ or R ²⁴ is a group represented by the formula (ii).

-R ⁵⁰ -Si (R ²⁹ ) ₃ (ii)

(Wherein R ²⁹ represents a hydrogen atom, a hydroxy group, an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms, and * indicates the number of bonds with a nitrogen atom. The plurality of R ^{29 s} may be the same or different .

R ⁵⁰ represents an alkanediyl group having 1 to 10 carbon atoms, and -CH ₂ - which constitutes the alkanediyl group is -O-, -CO-, -NR ¹¹ -, -OCO-, -COO-, -OCONH- , -CONH-, or -NHCO-).

In R ²¹ , R ²² , R ²³ and R ²⁴ , the hydrogen atom contained in the monovalent saturated hydrocarbon group having 1 to 10 carbon atoms may be substituted with a halogen atom, and -CH ₂ - contained in the saturated hydrocarbon may be replaced by -O- , -CO-, -NR ¹¹ -, -OCO-, -COO-, -OCONH-, -CONH- or -NHCO-.

R ¹¹ each independently represents a hydrogen atom or a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms.

And R ³¹ represents -SO ₃ ^- or -CO ₂ ^- .

The color filter formed from the colored curable resin composition of the present invention is excellent in heat resistance.

The colored curable resin composition of the present invention comprises a colorant (A), the colorant (A) is a dye (A1) having a silicon atom and a maximum absorption wavelength in chloroform of 500 nm to 600 nm A1) " in some cases).

Examples of the dye (A1) include compounds represented by the following formulas described in [0193] of JP-A No. 2010-526897.

As the dye (A1), a dye having a maximum absorption wavelength in chloroform of 500 nm to 580 nm is preferable, and a dye of 500 nm to 560 nm is particularly preferable.

Among the dyes (A1)

A dye having at least one skeleton selected from the group consisting of a triarylmethane skeleton, a cyanine skeleton and a xanthene skeleton is preferable,

A dye having a silicon atom and having a xanthene skeleton is more preferable.

The dye having a silicon atom and having a xanthene skeleton preferably has a substituent including an organic silicon group.

Here, the organic silicon group represents a group having a carbon-silicon bond. As the organic silicon group, a silyloxy group is preferable. Examples of the silyloxy group include a silyloxy group having an alkyl group having 1 to 4 carbon atoms such as trimethylsilyloxy group and triethylsilyloxy group; And a silyloxy group having an alkoxy group having 1 to 4 carbon atoms, such as trimethoxysilyl group and triethoxysilyl group.

Among the dyes (A1), compounds represented by the formula (II) [hereinafter sometimes referred to as " compound (II) " Compound (II) also includes its tautomer.

In the formula (II), R ²¹ to R ²⁴ each independently represent a hydrogen atom, a monovalent saturated hydrocarbon group having 1 to 10 carbon atoms, a phenyl group which may have a substituent, or a group represented by the formula (ii). Provided that at least one of R ²¹ to R ²⁴ is a group represented by the formula (ii).

-R ⁵⁰ -Si (R ²⁹ ) ₃ (ii)

(Wherein R ²⁹ represents a hydrogen atom, a hydroxy group, an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms, and * indicates the number of bonds with a nitrogen atom. The plurality of R ^{29 s} may be the same or different .

R ⁵⁰ represents an alkanediyl group having 1 to 10 carbon atoms, and -CH ₂ - which constitutes the alkanediyl group is -O-, -CO-, -NR ¹¹ -, -OCO-, -COO-, -OCONH- , -CONH-, or -NHCO-).

In R ²¹ to R ²⁴ , a hydrogen atom contained in a monovalent saturated hydrocarbon group having 1 to 10 carbon atoms may be substituted with a halogen atom, and -CH ₂ - included in the saturated hydrocarbon group may be -O-, -CO-, NR ¹¹ -, -OCO-, -COO-, -OCONH-, -CONH- or -NHCO-.

R ²⁵ and R ²⁶ each independently represent a hydrogen atom or an alkyl group having 1 to 6 carbon atoms.

R ²⁷ and R ²⁸ are each independently selected from _{^{-OH, -SO 3 -, -SO 3}} H, -SO 3 - Z +, -CO 2 -, -CO 2 H, -CO 2 - Z +, -CO 2 R ¹⁴ shows a -SO ₃ R ¹⁵ or -SO ₂ NR ¹² R ^13.

R ¹⁴ and R ¹⁵ each independently represent a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a halogen atom.

Z ⁺ represents ⁺ N (R ¹⁶ ) ₄ , Na ⁺ or K ⁺ .

R ¹¹ , R ¹² and R ¹³ each independently represent a hydrogen atom or a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms.

R ¹⁶ each independently represents a hydrogen atom or a monovalent saturated hydrocarbon group of 1 to 20 carbon atoms.

p represents an integer of 0 to 4;

The compound represented by the formula (II) includes a compound represented by the formula (I) [hereinafter sometimes referred to as " compound (I) ") and tautomers thereof.

The compound represented by the formula (I) is a compound in which, in the formula (II), R ⁵⁰ is an alkanediyl group having 1 to 8 carbon atoms and R ²⁹ is a hydroxyl group or an alkoxy group having 1 to 4 carbon atoms.

In formula (I), each of R ¹ to R ⁴ independently represents a hydrogen atom, a monovalent saturated hydrocarbon group having 1 to 10 carbon atoms, a phenyl group which may have a substituent, or a group represented by the formula (i). Provided that at least one of R ¹ to R ⁴ is a group represented by the formula (i).

(wherein n represents an integer of 1 to 8, R ⁹ represents a hydrogen atom or an alkyl group of 1 to 4 carbon atoms, and * represents the number of bonds with a nitrogen atom.)

In R ¹ to R ⁴ , a hydrogen atom contained in a monovalent saturated hydrocarbon group having 1 to 10 carbon atoms may be substituted with a halogen atom, and -CH ₂ - included in the saturated hydrocarbon group may be replaced by -O-, NR < ¹¹ > -.

R ⁵ and R ⁶ each independently represent a hydrogen atom or an alkyl group having 1 to 6 carbon atoms.

R ⁷ and R ⁸ are each independently selected from _{^{-OH, -SO 3 -, -SO 3}} H, -SO 3 - Z +, -CO 2 -, -CO 2 H, -CO 2 - Z +, -CO 2 R ¹⁴ shows a -SO ₃ R ¹⁵ or -SO ₂ NR ¹² R ^13.

R ¹⁴ and R ¹⁵ each independently represent a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a halogen atom.

Z ⁺ represents ⁺ N (R ¹⁶ ) ₄ , Na ⁺ or K ⁺ .

R ¹¹ , R ¹² and R ¹³ each independently represent a hydrogen atom or a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms.

R ¹⁶ each independently represents a hydrogen atom or a monovalent saturated hydrocarbon group of 1 to 20 carbon atoms.

m represents an integer of 0 to 4;

In the formula (II) and the formula (I), as the monovalent saturated hydrocarbon group having 1 to 10 carbon atoms represented by R ²¹ to R ²⁴ and R ¹ to R ⁴ ,

Examples of the aryl group include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, a sec- , 1-methylbutyl group, 1,1,3,3-tetramethylbutyl group, 1,5-dimethylhexyl group, 1,6-dimethylheptyl group, 2-ethylhexyl group and 1,1,5,5- And an alkyl group having 1 to 10 carbon atoms such as a tetramethylhexyl group.

As the monovalent saturated hydrocarbon group having 1 to 10 carbon atoms represented by R ²¹ to R ²⁴ and R ¹ to R ⁴ , a methyl group, ethyl group, propyl group or butyl group is preferable.

The hydrogen atom contained in the monovalent saturated hydrocarbon group having 1 to 10 carbon atoms represented by R ²¹ to R ²⁴ and R ¹ to R ⁴ may be substituted with a halogen atom.

Examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom.

Examples of the monovalent saturated hydrocarbon group having 1 to 10 carbon atoms substituted with a halogen atom include a fluoromethyl group, a difluoromethyl group, a trifluoromethyl group, a perfluoroethyl group and a chlorobutyl group.

-CH ₂ - included in the monovalent saturated hydrocarbon group having 1 to 10 carbon atoms represented by R ²¹ to R ²⁴ and R ¹ to R ⁴ may be substituted with -O-, -CO- or -NR ¹¹ -.

As the monovalent saturated hydrocarbon group having 1 to 10 carbon atoms represented by R ¹¹ ,

A linear alkyl group having 1 to 20 carbon atoms such as methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, dodecyl, hexadecyl and eicosyl;

Branched alkyl groups having 3 to 20 carbon atoms such as isopropyl, isobutyl, sec-butyl, tert-butyl, isopentyl, neopentyl and 2-ethylhexyl;

And alicyclic saturated hydrocarbon groups having 3 to 20 carbon atoms such as cyclopropyl group, cyclopentyl group, cyclohexyl group, cycloheptyl group, cyclooctyl group and tricyclodecyl group.

As the group in which -CH ₂ - included in the monovalent saturated hydrocarbon group having 1 to 10 carbon atoms is substituted with -O-,

(* Denotes the number of bonds).

Examples of the group in which -CH ₂ - contained in the monovalent saturated hydrocarbon group having 1 to 10 carbon atoms is substituted with -CO- include,

(* Denotes the number of bonds).

As the group in which -CH ₂ - included in the monovalent saturated hydrocarbon group having 1 to 10 carbon atoms is substituted with -NR ¹¹ -

(* Denotes the number of bonds).

-CH ₂ - included in the monovalent saturated hydrocarbon group having 1 to 10 carbon atoms represented by R ²¹ to R ²⁴ and R ¹ to R ⁴ is -OCO-, -COO-, -OCONH-, -CONH- and -NHCO - > may be substituted with at least one group selected from the group consisting of -

As the group in which -CH ₂ - included in the monovalent saturated hydrocarbon group having 1 to 10 carbon atoms is substituted with -OCO-,

(* Denotes the number of bonds).

As the group in which -CH ₂ - included in the above-mentioned monovalent saturated hydrocarbon group having 1 to 10 carbon atoms is substituted with -COO-,

(* Denotes the number of bonds).

As the group in which -CH ₂ - included in the monovalent saturated hydrocarbon group having 1 to 10 carbon atoms is substituted with -OCONH-,

(* Denotes the number of bonds).

As the group in which -CH ₂ - included in the above-mentioned monovalent saturated hydrocarbon group having 1 to 10 carbon atoms is substituted with -CONH-, for example,

(* Denotes the number of bonds).

Examples of the group in which -CH ₂ - included in the monovalent saturated hydrocarbon group having 1 to 10 carbon atoms is substituted with -NHCO- include,

(* Denotes the number of bonds).

The phenyl group represented by R ²¹ to R ²⁴ and R ¹ to R ⁴ may have a substituent.

As the substituent, a halogen ^{atom, -R 10, -OH, -OR 18} , -SO 3 H, -SO 3 - Z +, -CO 2 H, -CO 2 R 14, -SR 10, -SO 2 R ^17, -SO ₃ R ^15, there may be mentioned, or -SO ₂ NR ¹² R ^13.

In this substituent, R ¹⁰ represents a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms, and R ¹² to R ¹⁸ are the same as defined above.

Examples of the monovalent saturated hydrocarbon group having 1 to 20 carbon atoms represented by R ¹⁰ and R ¹² to R ¹⁸ include a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, , A straight chain alkyl group having 1 to 20 carbon atoms such as a dodecyl group, a hexadecyl group and an icosyl group;

Branched alkyl groups having 3 to 20 carbon atoms such as isopropyl, isobutyl, sec-butyl, tert-butyl, isopentyl, neopentyl and 2-ethylhexyl;

And alicyclic saturated hydrocarbon groups having 3 to 20 carbon atoms such as cyclopropyl group, cyclopentyl group, cyclohexyl group, cycloheptyl group, cyclooctyl group and tricyclodecyl group.

Examples of -OR ¹⁸ include a methoxy group, ethoxy group, propoxy group, butoxy group, pentyloxy group, hexyloxy group, heptyloxy group, octyloxy group, 2-ethylhexyloxy group and eicosyloxy group.

-SO ₃ ^- Z ⁺ is preferably -SO ₃ ^{- +} N (R ¹³ ) ₄ .

Examples of -CO ₂ R ¹⁴ include a methoxycarbonyl group, ethoxycarbonyl group, propoxycarbonyl group, tert-butoxycarbonyl group, hexyloxycarbonyl group and eicosyloxycarbonyl group.

Examples of -SR ¹⁰ include a methylsulfanyl group, an ethylsulfanyl group, a butylsulfanyl group, a hexylsulfanyl group, a decylsulfanyl group and an icosylsulfanyl group.

Examples of -SO ₂ R ¹⁷ include a methylsulfonyl group, an ethylsulfonyl group, a butylsulfonyl group, a hexylsulfonyl group, a decylsulfonyl group and an icosylsulfonyl group.

Examples of -SO ₃ R ¹⁵ include a methoxysulfonyl group, an ethoxysulfonyl group, a propoxysulfonyl group, a tert-butoxysulfonyl group, a hexyloxysulfonyl group, and an icosyloxysulfonyl group.

A -SO ₂ NR ¹² R ¹³ is, N- methyl-sulfamoyl, N- ethyl sulfamoyl, N- propyl sulfamoyl, N- isopropyl-sulfamoyl, N- butyl sulfamoyl, N- isobutyl Butylsulfamoyl group, N-pentylsulfamoyl group, N- (1-ethylpropyl) sulfamoyl group, N- (1,1-dimethylpropyl) sulfamoyl group, ), Sulfamoyl group, N- (1,2-dimethylpropyl) sulfamoyl group, N- (2,2-dimethylpropyl) sulfamoyl group, N- Methylbutyl) sulfamoyl group, N- (3-methylbutyl) sulfamoyl group, N-cyclopentylsulfamoyl group, N-hexylsulfamoyl group, N- (3,3-dimethylbutyl) sulfamoyl group, N-heptylsulfamoyl group, N- (1-methylhexyl) sulfamoyl group, N- (1,4-dimethylpentyl) sulfamoyl group, (1, 2, 2-tetramethylbutyl) sulfamoyl group such as N- (2-ethylhexyl) sulfamoyl group, N- A monosubstituted sulfamoyl group;

N, N-dimethylsulfamoyl group, N, N-ethylmethylsulfamoyl group, N, N-diethylsulfamoyl group, N, N-propylmethylsulfamoyl group, N, N-diethylamino groups such as N, N-tert-butylmethylsulfamoyl group, N, N-butylethylsulfamoyl group, N, N-bis (1-methylpropyl) sulfamoyl group, N-2-substituted sulfamoyl group.

The substituent of the phenyl group represented by R ²¹ to R ²⁴ and R ¹ to R ⁴ is preferably -R ¹⁰ , more preferably a monovalent saturated hydrocarbon group having 1 to 10 carbon atoms, more preferably an alkyl group having 1 to 5 carbon atoms desirable.

At least one of R ²¹ to R ²⁴ is a group represented by the formula (ii).

In the group represented by the formula (ii), R ²⁹ represents a hydrogen atom, a hydroxy group, an alkyl group having 1 to 4 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.

Examples of the alkyl group having 1 to 4 carbon atoms represented by R ²⁹ include a methyl group, an ethyl group, a propyl group and a butyl group.

Examples of the alkoxy group having 1 to 4 carbon atoms represented by R ²⁹ include a methoxy group, ethoxy group, propoxy group and t-butoxy group.

As R ²⁹ in the group represented by the formula (ii), a methyl group, an ethyl group, a methoxy group and an ethoxy group are preferable, and a methoxy group and an ethoxy group are more preferable.

Examples of the alkanediyl group having 1 to 10 carbon atoms represented by R ⁵⁰ include a methylene group, an ethylene group, a trimethylene group, a tetramethylene group, a pentamethylene group, a hexamethylene group, an isopropylene group, an isobutylene group, A methylene group, an isopentylene group, an isohexylene group, an iso-octylene group, and a 2-ethylhexylene group. Of these, an alkanediyl group having 1 to 6 carbon atoms is preferable, and an alkanediyl group having 1 to 4 carbon atoms Is more preferable.

Examples of the group represented by the formula (ii) include groups represented by the formulas (ii-13) to (ii-24) and the formulas (i-1) to (i-12).

In the formula (ii), groups in which -CH ₂ - constituting R ⁵⁰ are substituted with -O- include the groups shown below (* represents the number of bonds).

In the formula (ii), groups in which -CH ₂ - constituting R ⁵⁰ are substituted with -CO- include the groups shown below (* represents the number of bonds).

In the formula (ii), groups in which -CH ₂ - constituting R ⁵⁰ is substituted with -NR ¹¹ - include the groups shown below (* represents the number of bonds).

In the formula (ii), groups in which -CH ₂ - constituting R ⁵⁰ is substituted with -OCO- include the groups shown below (* represents the number of bonds).

In the formula (ii), groups in which -CH ₂ - constituting R ⁵⁰ is substituted with -COO- include the groups shown below (* represents the number of bonds).

In the formula (ii), groups in which -CH ₂ - constituting R ⁵⁰ is substituted with -OCONH- include the groups shown below (* represents the number of bonds).

In the formula (ii), groups in which -CH ₂ - constituting R ⁵⁰ is substituted with -CONH- include the groups shown below (* represents the number of bonds).

In the formula (ii), groups in which -CH ₂ - constituting R ⁵⁰ are substituted with -NHCO- include the groups shown below (* represents the number of bonds).

As the formula (ii), a group represented by the following formula is preferable.

At least one of R ¹ to R ⁴ is a group represented by the formula (i).

In the formula (i), examples of the alkyl group having 1 to 4 carbon atoms represented by R ⁹ include a methyl group, an ethyl group, a propyl group and a butyl group.

As R ⁹ , a hydrogen atom, a methyl group, an ethyl group and a propyl group are preferable, and a hydrogen atom, a methyl group and an ethyl group are more preferable.

Examples of the group represented by the formula (i) include groups represented by the formulas (i-1) to (i-12).

The group represented by the formula (i) is preferably a group represented by the formula (i-2), (i-3), (i-5) or (i-6).

Examples of the alkyl group having 1 to 6 carbon atoms represented by R ²⁵ , R ²⁶ , R ⁵ and R ⁶ include methyl group, ethyl group, propyl group, butyl group, pentyl group, hexyl group, isopropyl group, A tert-butyl group, an isopentyl group, and a neopentyl group.

R ^27, R ^28, -SO ₃ represented by R ⁷ and R ^{8 -} roneun Z ^+, is preferably -SO ₃ Na or -SO ₃ K.

As -CO ₂ ^- Z ⁺ represented by R ²⁷ , R ²⁸ , R ⁷ and R ⁸ , -CO ₂ Na or -CO ₂ K is preferable.

Examples of -CO ₂ R ¹⁴ represented by R ²⁷ , R ²⁸ , R ⁷ and R ⁸ include a methoxycarbonyl group, an ethoxycarbonyl group, a propoxycarbonyl group, a tert-butoxycarbonyl group, a hexyloxycarbonyl group and an eicosyloxycarbonyl group. have.

Examples of -SO ₃ R ¹⁵ represented by R ²⁷ , R ²⁸ , R ⁷ and R ⁸ include a methoxysulfonyl group, an ethoxysulfonyl group, a propoxysulfonyl group, a tert-butoxysulfonyl group, a hexyloxysulfonyl group, And an icosyloxysulfonyl group.

Examples of -SO ₂ NR ¹² R ¹³ represented by R ²⁷ , R ²⁸ , R ⁷ and R ⁸ include N-methylsulfamoyl group, N-ethylsulfamoyl group, N-propylsulfamoyl group, N- Butylsulfamoyl group, N-tert-butylsulfamoyl group, N-pentylsulfamoyl group, N- (1-ethylpropyl) sulfamoyl group, N-butylsulfamoyl group, N-isobutylsulfamoyl group, N- ) Sulfamoyl group, N- (1,1-dimethylpropyl) sulfamoyl group, N- (1,2-dimethylpropyl) sulfamoyl group, N- (2,2- (2-methylbutyl) sulfamoyl group, N- (3-methylbutyl) sulfamoyl group, N-cyclopentylsulfamoyl group, N-hexylsulfamoyl group, N- (1, 3-dimethylbutyl) sulfamoyl group, N- (3,3-dimethylbutyl) sulfamoyl group, N-heptylsulfamoyl group, N- (2-ethylhexyl) sulfamoyl group, N- (1,5-dimethyl) hexylsulfamoyl group, N- (1,1,2,2-tetramethylpiperidinyl) , 2-tetramethylbutyl) sulphamoyl group and the like. Sulfamoyl group;

N, N-dimethylsulfamoyl group, N, N-ethylmethylsulfamoyl group, N, N-diethylsulfamoyl group, N, N-propylmethylsulfamoyl group, N, N-diethylamino groups such as N, N-tert-butylmethylsulfamoyl group, N, N-butylethylsulfamoyl group, N, N-bis (1-methylpropyl) sulfamoyl group, N-2-substituted sulfamoyl group.

The monovalent saturated hydrocarbon group having 1 to 20 carbon atoms represented by R ¹⁴ and R ¹⁵ is preferably a methyl group, an ethyl group, a propyl group or a butyl group.

The hydrogen atom contained in the monovalent saturated hydrocarbon group having 1 to 20 carbon atoms represented by R ¹⁴ and R ¹⁵ may be substituted with a halogen atom.

Examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom.

Examples of the monovalent saturated hydrocarbon group having 1 to 20 carbon atoms substituted with a halogen atom include a fluoromethyl group, a difluoromethyl group, a trifluoromethyl group, a perfluoroethyl group, and a chlorobutyl group.

Z ⁺ is preferably ⁺ N (R ¹⁶ ) ₄ .

⁺ N (R ¹⁶⁾ 4 in the _four R ¹⁶ are preferably all the same. The total carbon number of the four R < ¹⁶ > s is preferably from 20 to 80, more preferably from 20 to 60. [

As the monovalent saturated hydrocarbon group having 1 to 20 carbon atoms and represented by R ¹² , R ¹³ and R ¹⁶ , a methyl group, an ethyl group, a propyl group, a butyl group or a 2-ethylhexyl group is preferable.

At least one of R ²¹ to R ²⁴ is a group represented by the formula (ii), and other R ²¹ to R ²⁴ include a methyl group, an ethyl group, a propyl group,

(* Represents the number of bonds with nitrogen atoms).

At least one of R ¹ to R ⁴ is a group represented by the formula (i), and other R ¹ to R ⁴ include a methyl group, an ethyl group, a propyl group,

(* Represents the number of bonds with nitrogen atoms).

R ²⁵ , R ²⁶ , R ⁵ and R ⁶ are preferably a hydrogen atom, a methyl group or an ethyl group, and more preferably a hydrogen atom.

R ^27, R ^28, R ⁷ and R ⁸ is preferably _{^{-CO 2 -, -CO 2 H,}} -SO 3 H, -SO - , and _3, and preferably -SO ₃ H, -SO _^than-3 is .

Each of R ¹⁴ and R ¹⁵ is preferably a methyl group, an ethyl group, a propyl group or a butyl group.

Each of R ¹¹ , R ¹² and R ¹³ is preferably a hydrogen atom, a methyl group, an ethyl group, a propyl group, a butyl group or a 2-ethylhexyl group.

R ¹⁶ is preferably a hydrogen atom, a methyl group, an ethyl group, a propyl group or a butyl group.

p and m are preferably an integer of 0 to 2, more preferably 0 or 1, and even more preferably 0.

Specific examples of the compound (II) include those shown below.

As the compound (II)

(I-1) to (I-4), the compounds represented by formulas (I-13) to (I-16), the compounds represented by formulas (I- (I-40), Formula (I-49) to Formula (I-54), Formula (I-55) to Formula (I- Compounds represented by the formulas (I-117) to (I-123) are preferable,

(I-1) to (I-4), the compounds represented by formulas (I-13) to (I-16), the compounds represented by formulas (I- Compounds represented by formulas (I-62), (I-87) to (I-94), (I-117) and (I-119) to (I-123) are more preferable.

As specific examples of the compound (I)

There may be mentioned the compounds represented by the above formulas (I-1) to (I-54) or the compounds represented by formulas (I-117) to (I-119).

(I-1) to (I-4), the compounds represented by formulas (I-13) to (I-16), the compounds represented by formulas (I- Compounds represented by formulas (I-37) to (I-40), (I-49) to (I-54) (1-14), (I-13) to (I-16), (I-25) to (I-28), (I-117) 119) is more preferable.

The compound (II) is a compound represented by the formula (IV)

(Wherein R ²¹ , R ²² , R ²⁵ , R ²⁶ , R ²⁸ , R ²⁷ and p each have the same meaning as defined above, and X ² represents a halogen atom or a trifluoromethylsulfonyloxy group.

(Hereinafter sometimes referred to as " compound (IV) "), a compound represented by formula (V)

(Wherein R ²³ and R ²⁴ each have the same meaning as defined above.)

(Hereinafter sometimes referred to as " compound (V) ").

The halogen atom represented by X < ² > includes a fluorine atom, a chlorine atom, a bromine atom and an iodine atom, preferably a chlorine atom.

X ² is preferably a chlorine atom.

R ²⁷ is preferably -SO ₃ ^- .

As the compound (IV), a compound represented by the following formula can be given.

As the compound (V), a compound represented by the following formula can be given.

The reaction of the compound (IV) with the compound (V) is usually carried out in an organic solvent. The organic solvent is preferably an organic solvent having a solubility in water at 20 占 폚 of 200 g / liter or less.

Examples of the organic solvent having a solubility in water at 20 占 폚 of 200 g / liter or less include aliphatic hydrocarbon solvents such as n-pentane, n-hexane, n-heptane and cyclohexane; Aromatic hydrocarbon solvents such as toluene and xylene; Halogenated hydrocarbon solvents such as carbon tetrachloride, chlorobenzene, dichlorobenzene, chloroform and methylene chloride; Nitrated hydrocarbon solvents such as nitrobenzene; Ketone solvents such as methyl isobutyl ketone; Ester solvents such as ethyl acetate, butyl acetate and propylene glycol monomethyl ether acetate, and mixed solvents thereof.

The organic solvent having a solubility in water at 20 占 폚 of not more than 200 g / l can be selected from n-pentane, n-hexane, n-heptane, cyclohexane, ethyl acetate, methylisobutylketone, chloroform, carbon tetrachloride, benzene, Propylene glycol monomethyl ether acetate, and propylene glycol monomethyl ether acetate.

When two or more solvents are used, it is preferable that the solubility of the entire solvent in water is 200 g / liter or less.

The reaction of compound (IV) with compound (V) is usually carried out by mixing compound (IV) with compound (V). The compound (IV) is preferably mixed with the compound (V), and the compound (IV) is preferably added with the compound (V) (V) is added dropwise to a mixture of an organic solvent and an organic solvent.

The reaction temperature in the reaction of the compound (IV) with the compound (V) is usually 0 ° C to 180 ° C, preferably 0 ° C to 150 ° C, more preferably 20 ° C to 130 ° C, More preferably 100 < 0 > C. The reaction time is usually 1 hour to 50 hours, preferably 1 hour to 24 hours, more preferably 1 hour to 8 hours.

The amount of the compound (V) to be used is usually 1 mol or more and 10 mol or less, preferably 1 mol or more and 3 mol or less, and more preferably 1 mol or more and 2 mol or less, per 1 mol of the compound (IV).

Examples of the method for extracting the compound (II) from the reaction mixture include a method of precipitating the compound (II) from the reaction mixture and filtering out the deposited precipitate. The crystals obtained by filtration are preferably washed with water, an organic solvent or the like and dried. Further, if necessary, purification may be carried out by a known technique such as recrystallization.

Examples of the method of precipitating the compound (II) include a method of concentrating the reaction mixture, a method of cooling the reaction mixture, a method of adding the reaction mixture to a poor solvent (poor solvent), and the like, Is preferably added.

The poor solvent is preferably an organic solvent having a solubility in water at 20 占 폚 of 200 g / liter or less.

When the reaction of the compound (IV) with the compound (V) is carried out in an organic solvent having a solubility in water at 20 DEG C of not more than 200 g / L, the poor solvent has a solubility in water Low.

The compound (II) wherein R ²⁷ is -SO ₃ ^- or -CO ₂ ^- [hereinafter sometimes referred to as compound (II-1)

(In the above formulas, R ²⁵ , R ²⁶ , R ²⁸ and p have the same meanings as defined above.

X ¹ and X ² each independently represent a halogen atom or a trifluoromethylsulfonyloxy group.

R ³⁰ represents -SO ₂ - or -CO-.)

(Hereinafter sometimes referred to as " compound (VI) "), a compound represented by the formula (III)

(Wherein R ²¹ and R ²² have the same meanings as defined above.)

(Hereinafter sometimes referred to as " compound (III) ") and a compound represented by the formula (V)

(Wherein R ²³ and R ²⁴ each have the same meaning as defined above.)

In the presence of a base.

The halogen atom represented by X &^lt; ¹ > includes a fluorine atom, a chlorine atom, a bromine atom and an iodine atom, preferably a chlorine atom.

X ¹ and X ² are preferably the same.

X ¹ and X ² are each independently preferably a halogen atom, more preferably a chlorine atom.

R ³⁰ is preferably -SO ₂ -.

As the compound (III), the same compounds as the compound (V) can be mentioned.

The reaction of compound (VI), compound (III) and compound (V) is usually carried out in an organic solvent. The organic solvent is preferably an organic solvent having a solubility in water at 20 캜 of 200 g / ℓ or less.

Examples of the organic solvent having a solubility in water at 20 占 폚 of 200 g / liter or less include aliphatic hydrocarbon solvents such as n-pentane, n-hexane, n-heptane and cyclohexane; Aromatic hydrocarbon solvents such as toluene and xylene; Halogenated hydrocarbon solvents such as carbon tetrachloride, chlorobenzene, dichlorobenzene, chloroform and methylene chloride; Nitrated hydrocarbon solvents such as nitrobenzene; Ketone solvents such as methyl isobutyl ketone; Ester solvents such as ethyl acetate, butyl acetate, and propylene glycol monomethyl ether acetate, and mixed solvents thereof.

The organic solvent having a solubility in water at 20 占 폚 of not more than 200 g / l can be selected from n-pentane, n-hexane, n-heptane, cyclohexane, ethyl acetate, methylisobutylketone, chloroform, carbon tetrachloride, benzene, Propylene glycol monomethyl ether acetate, and propylene glycol monomethyl ether acetate.

When two or more solvents are used, it is preferable that the solubility of the entire solvent in water is 200 g / liter or less.

The amount of the compound (III) to be used is generally 1 mole or more and 30 moles or less, preferably 1 mole or more and 20 moles or less, more preferably 1 mole or more and 10 moles or less, Preferably 1 mol or more and 3 mol or less, and particularly preferably 1 mol or more and 2 mol or less.

The amount of the compound (V) to be used is generally 1 mol or more and 30 mol or less, preferably 1 mol or more and 20 mol or less, more preferably 1 mol or more and 10 mol or less, relative to 1 mol of the compound (VI) Preferably 1 mol or more and 3 mol or less, and particularly preferably 1 mol or more and 2 mol or less.

The reaction of compound (VI), compound (III) and compound (V) is usually carried out by mixing compound (VI), compound (III) and compound (V).

The mixing of the compound (VI), the compound (III) and the compound (V) is preferably carried out by adding the compound (III) and the compound (V) to the compound (VI) It is more preferable to drop the compound (V), and it is more preferable to drop the compound (III) and the compound (V) into the mixture of the compound (VI) and the organic solvent.

The reaction temperature in the reaction of the compound (VI), the compound (III) and the compound (V) is usually 0 ° C to 150 ° C, preferably 10 ° C to 110 ° C, more preferably 20 ° C to 100 ° C, More preferably from 20 캜 to 80 캜. The reaction time is usually 1 hour to 50 hours, preferably 1 hour to 12 hours, more preferably 1 hour to 8 hours.

As a method for extracting the compound (II-1) from the obtained reaction mixture, for example, there is a method of precipitating the compound (II-1) from the reaction mixture and filtering out the deposited precipitate. The crystals obtained by filtration are preferably washed with water, an organic solvent or the like and dried. Further, if necessary, purification may be carried out by a known technique such as recrystallization.

Examples of the method of precipitating the compound (II-1) include a method of concentrating the reaction mixture, a method of cooling the reaction mixture, a method of adding the reaction mixture to the poor solvent, and the like. Method is preferable.

The poor solvent is preferably an organic solvent having a solubility in water at 20 占 폚 of 200 g / liter or less.

When the reaction of the compound (IV) with the compound (V) is carried out in an organic solvent having a solubility in water at 20 DEG C of not more than 200 g / L, the poor solvent has a solubility in water Low.

Compound (II-1) can be produced by reacting compound (VI) with compound (III) to obtain a compound represented by formula (VII) [hereinafter referred to as compound (VII) ) With a compound (V).

[Wherein R ²¹ , R ²² , R ²⁵ , R ²⁶ , R ²⁸ , X ² and p have the same meanings as defined above, respectively.

And R ³¹ represents -SO ₃ ^- or -CO ₂ ^- .

The amount of the compound (III) to be used is generally 1 mole or more and 30 moles or less, preferably 1 mole or more and 20 moles or less, more preferably 1 mole or more and 10 moles or less, Preferably 1 mol or more and 3 mol or less, and particularly preferably 1 mol or more and 2 mol or less.

The reaction of compound (VI) with compound (III) is usually carried out in an organic solvent.

Examples of the organic solvent include aliphatic hydrocarbon solvents such as n-pentane, n-hexane, n-heptane, and cyclohexane; Aromatic hydrocarbon solvents such as toluene and xylene; Halogenated hydrocarbon solvents such as carbon tetrachloride, chlorobenzene, dichlorobenzene, chloroform and methylene chloride; Alcohol solvents such as methanol, ethanol and butanol; Nitrated hydrocarbon solvents such as nitrobenzene; Ketone solvents such as methyl isobutyl ketone; Amide solvents such as 1-methyl-2-pyrrolidone; Ester solvents such as ethyl acetate, butyl acetate, and propylene glycol monomethyl ether acetate, and mixed solvents thereof.

The organic solvent preferably has a solubility in water at 20 占 폚 of 200 g / liter or less and is preferably an organic solvent selected from the group consisting of n-pentane, n-hexane, n-heptane, cyclohexane, ethyl acetate, methylisobutylketone, chloroform, Benzene, toluene, and propylene glycol monomethyl ether acetate.

When two or more solvents are used, it is preferable that the solubility of the entire solvent in water is 200 g / liter or less.

The reaction of compound (VI) with compound (III) is usually carried out by mixing compound (VI) with compound (III). The compound (III) is preferably added to the compound (VI), more preferably the compound (III) is added to the compound (VI) And the compound (III) is added dropwise to a mixture of an organic solvent and an organic solvent.

The compound (VII) may be extracted from the obtained reaction mixture, or the obtained reaction mixture may be reacted with the compound (V). It is preferable to extract the compound (VII).

As a method for extracting the compound (VII) from the obtained reaction mixture, for example, a method of concentrating the reaction mixture can be mentioned. If necessary, the obtained reaction mixture may be neutralized. If necessary, the extracted compound (VII) may be washed and dried with water, an organic solvent or the like.

The reaction of compound (VII) with compound (VI) is usually carried out in an organic solvent.

The organic solvent is preferably an organic solvent having a solubility in water at 20 占 폚 of 200 g / liter or less.

Examples of the organic solvent having a solubility in water at 20 占 폚 of 200 g / liter or less include aliphatic hydrocarbon solvents such as n-pentane, n-hexane, n-heptane and cyclohexane; Aromatic hydrocarbon solvents such as toluene and xylene; Halogenated hydrocarbon solvents such as carbon tetrachloride, chlorobenzene, dichlorobenzene, chloroform and methylene chloride; Nitrated hydrocarbon solvents such as nitrobenzene; Ketone solvents such as methyl isobutyl ketone; Ester solvents such as ethyl acetate, butyl acetate, and propylene glycol monomethyl ether acetate; And mixed solvents thereof.

The organic solvent having a solubility in water at 20 占 폚 of not more than 200 g / l can be selected from n-pentane, n-hexane, n-heptane, cyclohexane, ethyl acetate, methylisobutylketone, chloroform, carbon tetrachloride, benzene, And an organic solvent selected from the group consisting of propylene glycol monomethyl ether acetate and propylene glycol monomethyl ether acetate.

When two or more solvents are used, it is preferable that the solubility of the entire solvent in water is 200 g / liter or less.

The amount of the compound (V) to be used is generally 1 mol or more and 50 mol or less, preferably 1 mol or more and 30 mol or less, and more preferably 1 mol or more and 20 mol or less, relative to 1 mol of the compound (III).

The reaction of the compound (VII) with the compound (V) can be generally carried out by mixing the compound (VII) with the compound (V). The compound (V) is preferably added to the compound (VII), more preferably the compound (V) is added dropwise to the compound (VII) It is more preferable to drop the compound (V) in a mixture of an organic solvent and an organic solvent.

The reaction time in the reaction of the compound (VII) with the compound (V) is usually 0 ° C to 180 ° C, preferably 30 ° C to 180 ° C, more preferably 20 ° C to 130 ° C. The reaction time is usually 1 hour to 50 hours, preferably 1 hour to 24 hours, more preferably 1 hour to 8 hours.

As a method for extracting the compound (II-1) from the obtained reaction mixture, for example, there is a method of precipitating the compound (II-1) from the reaction mixture and filtering out the deposited precipitate. The crystals obtained by filtration are preferably washed with water, an organic solvent or the like and dried. Further, if necessary, purification may be carried out by a known technique such as recrystallization.

Examples of the method of precipitating the compound (II-1) include a method of concentrating the reaction mixture, a method of cooling the reaction mixture, a method of adding the reaction mixture to the poor solvent, and the like. Method is preferable.

The poor solvent is preferably an organic solvent having a solubility in water at 20 占 폚 of 200 g / liter or less.

When the reaction of the compound (IV) with the compound (V) is carried out in an organic solvent having a solubility in water at 20 DEG C of not more than 200 g / L, the poor solvent has a solubility in water Low.

The compound (II) is useful as a dye. And is particularly useful as a coloring agent for a colored curable resin composition used for a color filter of a display device such as a liquid crystal display, because of its high solubility in an organic solvent.

In the colored curable resin composition of the present invention, the content of the dye (A) is preferably 0.025 mass% or more and 48 mass% or less, more preferably 0.08 mass% or more and 42 mass% And more preferably not less than 30% by mass.

Here, the "total amount of solid content" in the present specification means the amount excluding the content of the solvent in the total amount of the colored curable resin composition. The total amount of the solid content and the content of each component in the total amount can be measured by known analytical means such as liquid chromatography or gas chromatography.

The colored curable resin composition of the present invention comprises a colorant (A), a resin (B), a polymerizable compound (C), and a polymerization initiator (D).

As the colorant (A), it is preferable to include the pigment (P) in addition to the dye (A1). Further, it may contain a dye (A2) different from the dye (A1).

The content of the dye (A1) in the colorant (A) is preferably 0.01 mass% or more and 90 mass% or less, and more preferably 0.1 mass% or more and 80 mass% or less, based on the total amount of the colorant (A).

The content of the compound (II) in the colorant (A) is preferably 0.5% by mass or more and 80% by mass or less, more preferably 1% by mass or more and 70% by mass or less based on the total amount of the colorant (A) And more preferably not less than 50% by mass.

≪ Pigment (P) >

The pigment (P) is not particularly limited and known pigments can be used. For example, the pigment is classified into pigments in the Color Index (The Society of Dyers and Colourists).

As the pigment, for example, C.I. 13, 14, 15, 16, 17, 20, 24, 31, 53, 83, 86, 93 (hereinafter abbreviated as "Pigment Yellow 1" Yellow pigments such as 94, 109, 110, 117, 125, 128, 137, 138, 139, 147, 148, 150, 153, 154, 166, 173, 194 and 214;

C.I. Orange pigments such as Pigment Orange 13, 31, 36, 38, 40, 42, 43, 51, 55, 59, 61, 64, 65, 71, 73;

C.I. Pigment Red 9, 97, 105, 122, 123, 144, 149, 166, 168, 175, 176, 177, 180, 192, 209, 215, 216, 224, 242, 254, 255, 264, Red pigment;

C.I. Pigment Blue 15, 15: 3, 15: 4, 15: 6, 60 and 80;

C.I. Violet pigments such as Pigment Violet 1, 19, 23, 29, 32, 36, 38;

C.I. Green pigments such as Pigment Green 7, 36, and 58;

C.I. Brown pigments such as Pigment Brown 23 and 25;

C.I. Pigment black 1, pigment black 7, and the like.

These pigments may be used alone or in combination of two or more kinds.

As the pigment, C.I. Yellow pigments such as Pigment Yellow 138, 139 and 150, C.I. Red pigments such as Pigment Red 177, 242, 254, and C.I. Pigment Blue 15, 15: 3, 15: 4, 15: 6 and 60, and C.I. Violet pigments such as Pigment Violet 1, 19, 23, 29, 32, 36, 38 and the like are preferable. By including the above-mentioned pigment, the transmission spectrum of the color filter using the colored curable resin composition of the present invention can be easily optimized, and the light resistance and chemical resistance of the color filter are improved.

≪ Dye (A2) >

Examples of the dye (A2) include dyes such as oil soluble dyes, acid dyes, basic dyes, direct dyes, mordant dyes, amine salts of acid dyes and sulfonamide derivatives of acid dyes. The Society of Dyers and Colourists), and known dyes described in Dyeing Note (Shika Sensha). According to the chemical structure, the azo dye, the cyanine dye, the triphenylmethane dye, the xanthene dye, the phthalocyanine dye, the naphthoquinone dye, the quinoneimine dye, the methine dye, the azomethine dye, the squarylium dye, , Styryl dyes, coumarin dyes, quinoline dyes, and nitro dyes. Of these, organic solvent-soluble dyes are preferred.

Specifically, C.I. Solvent Yellow 4, 14, 15, 23, 24, 38, 62, 63, 68, 82, 94, 98, 99, 162;

C.I. Solvent Red 45, 49, 125, 130, 218;

C.I. Solvent Orange 2, 7, 11, 15, 26, 56;

C.I. Solvent Blue 4, 5, 37, 67, 70, 90;

C.I. Solvent Green 1, 4, 5, 7, 34, 35, etc. C.I. Solvent dyes,

C.I. Acid Yellow 1, 3, 7, 9, 11, 17, 23, 25, 29, 34, 36, 38, 40, 42, 54, 65, 72, 73, 76, 79, 98, 99, 112, 134, 135, 138, 139, 140, 144, 150, 155, 157, 160, 161, 163, 168, 169, 172, 177, 178, 179, 184, 190, 193, 196, 197, 199, 202, 203, 204, 205, 207, 212, 214, 220, 221, 228, 230, 232, 235, 238, 240, 242, 243, 251;

C.I. Acid Red 1, 4, 8, 14, 17, 18, 26, 27, 29, 31, 34, 35, 37, 42, 44, 50, 51, 52, 57, 66, 73, 87, 215, 198, 206, 211, 215, 216, 217, 218, 219, 288, 289, 308, 312, 315, 316, 339, 341, 345, 346, 349, 276, 268, 270, 274, 277, 280, 382, 383, 388, 394, 401, 412, 417, 418, 422, 426;

C.I. Acid Orange 6, 7, 8, 10, 12, 26, 50, 51, 52, 56, 62, 63, 64, 74, 75, 94, 95, 107, 108, 169, 173;

C.I. Acid Violet 6B, 7, 9, 17, 19, 30, 102;

C.I. Acid Blue 1, 7, 9, 15, 18, 22, 29, 42, 59, 60, 62, 70, 72, 74, 82, 83, 86, 87, 90, 92, 93, 166, 167, 168, 170, 171, 184, 187, 192, 199, 210, 229, 234, 236, 242, 243, 256, 259, 267, 285, 296, 315, 335;

C.I. C.I., such as Acid Green 1, 3, 5, 9, 16, 50, 58, 63, 65, 80, 104, 105, Acid dyes,

C.I. Direct Yellow 2, 33, 34, 35, 38, 39, 43, 47, 50, 54, 58, 68, 69, 70, 71, 86, 93, 94, 95, 98, 136, 138, 141;

C.I. Direct Red 79, 82, 83, 84, 91, 92, 96, 97, 98, 99, 105, 106, 107, 172, 173, 176, 177, 179, 181, 182, 184, 204, 213, 218, 220, 221, 222, 232, 233, 234, 241, 243, 246, 250;

C.I. Direct Orange 26, 34, 39, 41, 46, 50, 52, 56, 57, 61, 64, 65, 68, 70, 96, 97, 106, 107;

C.I. Direct Violet 47, 52, 54, 59, 60, 65, 66, 79, 80, 81, 82, 84, 89, 90, 93, 95, 96, 103, 104;

C.I. Direct Blue 1, 2, 6, 8, 15, 22, 25, 41, 57, 71, 76, 78, 80, 81, 84, 85, 86, 90, 93, 94, 95, 97, 120, 137, 149, 150, 153, 155, 156, 158, 159, 160, 161, 162, 163, 164, 198, 199, 200, 201, 202, 203, 207, 209, 210, 202, 203, 207, 242, 243, 244, 245, 246, 247, 248, 249, 250, 251, 252, 256, 257, 259, 260, 268, 274, 275, 293;

C.I. Direct Green 25, 27, 31, 32, 34, 37, 63, 65, 66, 67, 68, 69, 72, 77, Direct dyes,

C.I. Disperse Yellow 54, C.I. Disperse dyes,

C.I. Basic Red 1, 10;

C.I. Basic Blue 1, 3, 5, 7, 9, 19, 24, 25, 26, 28, 29, 40, 41, 54, 58, 59, 64, 65, 66, 67, 68;

C.I. Basic Green 1; C.I. Basic dyes,

C.I. Reactive Yellow 2, 76, 116;

C.I. Reactive Orange 16;

C.I. Reactive red 36; C.I. Reactive dyes,

C.I. Modern Yellow 5, 8, 10, 16, 20, 26, 30, 31, 33, 42, 43, 45, 56, 61, 62, 65;

C.I. 43, 38, 39, 41, 43, 43, 43, 43, 42, 43, , 45, 46, 48, 53, 56, 63, 71, 74, 85, 86, 88, 90, 94, 95;

C.I. Modern orange 3, 4, 5, 8, 12, 13, 14, 20, 21, 23, 24, 28, 29, 32, 34, 35, 36, 37, 42, 43, 47, 48;

C.I. Modern Violet 1, 2, 4, 5, 7, 14, 22, 24, 30, 31, 32, 37, 40, 41, 44, 45, 47, 48, 53, 58;

C.I. 1, 2, 3, 7, 9, 12, 13, 15, 16, 19, 20, 21, 22, 26, 30, 31, 39, 40, 41, 43, 44, 49, 53, 61 , 74, 77, 83, 84;

C.I. C.I., such as Modern Green 1, 3, 4, 5, 10, 15, 26, 29, 33, 34, 35, 41, Modern dyes,

C.I. C.I. Bat dye

And the like.

Among them, a blue dye, a violet dye and a red dye are preferable.

These dyes may be suitably selected in accordance with the spectral spectrum of a desired color filter. These dyes may be used alone, or two or more dyes may be used in combination.

The content of the colorant (A) is preferably 1% by mass or more and 70% by mass or less, more preferably 1% by mass or more and 60% by mass or less, and still more preferably 1% % Or less. If the content of the colorant (A) is within the above range, desired spectral or color density can be obtained.

≪ Resin (B) >

The resin (B) is preferably an alkali-soluble resin (B). The alkali-soluble resin (B) [hereinafter sometimes referred to as " resin (B) ") is a resin derived from at least one monomer (a) selected from the group consisting of an unsaturated carboxylic acid and an unsaturated carboxylic acid anhydride Units. ≪ / RTI >

Examples of the resin (B) include the following resins [K1] to [K6].

At least one monomer (a) [hereinafter sometimes referred to as "(a)") selected from the group consisting of a resin [K1] unsaturated carboxylic acid and an unsaturated carboxylic acid anhydride, a cyclic ether having 2 to 4 carbon atoms And a monomer (b) having an ethylenically unsaturated bond (hereinafter occasionally referred to as "(b)");

(A) and (b), and a monomer (c) copolymerizable with (a), which is different from (a) and (b) ≪ / RTI >

Resin [K3] Copolymer of (a) and (c);

Resin [K4] Resin (b) is reacted with a copolymer of (a) and (c);

Resin [K5] Resin (a) is reacted with a copolymer of (b) and (c);

Resin [K6] Resin (a) is reacted with a copolymer of (b) and (c) and the carboxylic acid anhydride is further reacted.

(a) include, for example, unsaturated monocarboxylic acids such as acrylic acid, methacrylic acid, crotonic acid, o-, m-, and p-vinylbenzoic acid;

Maleic acid, fumaric acid, citraconic acid, mesaconic acid, itaconic acid, 3-vinylphthalic acid, 4-vinylphthalic acid, 3,4,5,6-tetrahydrophthalic acid, 1,2,3,6-tetrahydrophthalic acid, Unsaturated dicarboxylic acids such as tetrahydrophthalic acid and 1,4-cyclohexene dicarboxylic acid;

5-norbornene-2,3-dicarboxylic acid, 5-carboxybicyclo [2.2.1] hept-2-ene, 5,6-dicarboxybicyclo [2.2.1] hept- 5-ethylbicyclo [2.2.1] hept-2-ene, 5-carboxy-6-methylbicyclo [2.2.1] hept- [2.2.1] hept-2-ene, and 5-carboxy-6-ethylbicyclo [2.2.1] hept-2-ene;

Maleic anhydride, citraconic anhydride, itaconic anhydride, 3-vinylphthalic anhydride, 4-vinylphthalic anhydride, 3,4,5,6-tetrahydrophthalic anhydride, 1,2,3,6-tetrahydrophthalic anhydride , Unsaturated dicarboxylic acid anhydrides such as dimethyl tetrahydrophthalic anhydride and 5,6-dicarboxybicyclo [2.2.1] hept-2-eno anhydride;

(Meth) acryloyloxyalkyl (meth) acrylate of a divalent or higher polyvalent carboxylic acid such as mono [2- (meth) acryloyloxyethyl] succinate, mono [2- ] Esters;

unsaturated acrylates containing a hydroxyl group and a carboxyl group in the same molecule, such as? - (hydroxymethyl) acrylic acid; And the like.

Of these, acrylic acid, methacrylic acid, maleic anhydride and the like are preferable from the viewpoint of copolymerization reactivity and the solubility of the obtained resin in an aqueous alkali solution.

(b) can be obtained, for example, by reacting a polymerizable compound having an ethylenic unsaturated bond with a cyclic ether structure having 2 to 4 carbon atoms (e.g., at least one member selected from the group consisting of oxiran ring, oxetane ring and tetrahydrofuran ring) .

(b) is preferably a monomer having a cyclic ether having 2 to 4 carbon atoms and a (meth) acryloyloxy group.

In the present specification, "(meth) acrylic acid" represents at least one kind selected from the group consisting of acrylic acid and methacrylic acid. Quot ;, " (meth) acryloyl ", and " (meth) acrylate "

(b) include a monomer having an oxiranyl group and an ethylenically unsaturated bond, a monomer having an oxetanyl group and an ethylenically unsaturated bond, a monomer having an ethylenically unsaturated bond and a tetrahydrofuryl group, and the like.

(b) is preferably a monomer having an oxiranyl group and an ethylenically unsaturated bond in that the reliability of the obtained color filter can be further improved, such as heat resistance, chemical resistance and the like.

(meth) acrylate, sec-butyl (meth) acrylate, tert-butyl (meth) acrylate, 2-ethylhexyl (Meth) acrylate, cyclohexyl (meth) acrylate, dodecyl (meth) acrylate, lauryl (meth) acrylate, stearyl (meth) acrylate, cyclopentyl (Meth) acrylate, tricyclo [5.2.1.0 ^2,6 ] decan-8-yl (meth) acrylate [referred to in the art as "dicyclopentanyl (meth) acrylate" (Also referred to as "tricyclodecyl (meth) acrylate"), tricyclo [5.2.1.0 ^2,6 ] decen-8-yl (meth) acrylate (Meth) acrylate], dicyclopentyloxyethyl (meth) acrylate, isobornyl (meth) acrylate, adamantyl (meth) acrylate, allyl (Meth) acrylate esters such as pargyl (meth) acrylate, phenyl (meth) acrylate, naphthyl (meth) acrylate and benzyl (meth) acrylate;

(Meth) acrylic acid esters having a hydroxyl group such as 2-hydroxyethyl (meth) acrylate and 2-hydroxypropyl (meth) acrylate;

Dicarboxylic acid diesters such as diethyl maleate, diethyl fumarate, and diethyl itaconate;

2-ene, 5-methylbicyclo [2.2.1] hept-2-ene, 5-ethylbicyclo [2.2.1] hept- 2.2.1] hept-2-ene, 5- (2'-hydroxyethyl) bicyclo [2.2.1] hept- 2.2.1] hept-2-ene, 5-methoxybicyclo [2.2.1] (2'-hydroxyethyl) bicyclo [2.2.1] hept-2-ene, 5,6-di (hydroxymethyl) bicyclo [2.2.1] hept- Ene, 5,6-dimethoxybicyclo [2.2.1] hept-2-ene, 5,6-diethoxybicyclo [2.2.1] hept- 2.2.1] hept-2-ene, 5-hydroxymethyl-5-methylbicyclo [2.2.1] hept- 2-ene, 5-tert-butoxycarbonylbicyclo [2.2.1] hept-2-ene, 5-cyclohexyloxycarbonylbicyclo [2.2.1] hept- Cyclohexyl [2.2.1] hept-2-ene, 5,6-bis 2,6-bis (cyclohexyloxycarbonyl) bicyclo [2.2.1] hept-2-ene and the like such as bis (tert-butoxycarbonyl) bicyclo [2.2.1] hept- Cyclo-unsaturated compounds;

N-phenylmaleimide, N-cyclohexylmaleimide, N-benzylmaleimide, N-succinimidyl-3-maleimide benzoate, N-succinimidyl-4-maleimide butyrate, N- Dicarbonylimide derivatives such as N-succinimidyl-3-maleimidepropionate and N- (9-acridinyl) maleimide;

And examples thereof include styrene,? -Methylstyrene, m-methylstyrene, p-methylstyrene, vinyltoluene, p-methoxystyrene, acrylonitrile, methacrylonitrile, vinyl chloride, vinylidene chloride, acrylamide, methacrylamide, Vinyl, 1,3-butadiene, isoprene, 2,3-dimethyl-1,3-butadiene and the like.

Of these, styrene, vinyltoluene, benzyl (meth) acrylate, tricyclo [5.2.1.0 ^2,6 ] decan-8-yl (meth) acrylate, N-phenylmaleimide, N -Cyclohexylmaleimide, N-benzylmaleimide, bicyclo [2.2.1] hept-2-ene are preferred.

Specific examples of the resin (B) include 3,4-epoxycyclohexylmethyl (meth) acrylate / (meth) acrylic acid copolymer, 3,4-epoxytricyclo [5.2.1.0 ^2.6 ] decyl (meth) A resin [K1] such as a (meth) acrylic acid copolymer; (Meth) acrylate / benzyl (meth) acrylate / (meth) acrylic acid copolymer, glycidyl (meth) acrylate / styrene / (meth) acrylic acid copolymer, 3,4-epoxytricyclo [5.2 .1.0 ^2.6] decyl (meth) acrylate / (meth) acrylic acid / N- cyclohexyl maleimide copolymer, the resin composition comprising 3,4-tricyclo [5.2.1.0 ^2.6] decyl (meth) acrylate / (meth) acrylic acid / Vinyltoluene copolymer, and a resin [K2] such as 3-methyl-3- (meth) acryloyloxymethyloxetane / (meth) acrylic acid / styrene copolymer; A resin such as benzyl (meth) acrylate / (meth) acrylic acid copolymer, styrene / (meth) acrylic acid copolymer, benzyl (meth) acrylate / tricyclodecyl (meth) acrylate / (meth) ]; A resin obtained by adding glycidyl (meth) acrylate to a benzyl (meth) acrylate / (meth) acrylic acid copolymer and a resin obtained by adding glycidyl (meth) acrylate to a tricyclodecyl (meth) acrylate / styrene / (meth) ) Resin, a resin obtained by adding glycidyl (meth) acrylate to a tricyclodecyl (meth) acrylate / benzyl (meth) acrylate / (meth) acrylic acid copolymer; A resin obtained by reacting a copolymer of tricyclodecyl (meth) acrylate / glycidyl (meth) acrylate with (meth) acrylic acid, a resin obtained by reacting tricyclodecyl (meth) acrylate / styrene / glycidyl (meth) A resin [K5] such as a resin obtained by reacting a (meth) acrylic acid with a copolymer; A resin such as a resin obtained by further reacting a resin obtained by reacting (meth) acrylic acid with a copolymer of tricyclodecyl (meth) acrylate / glycidyl (meth) acrylate and tetrahydrophthalic anhydride, and the like .

Resin [K1] can be synthesized by, for example, the method described in "Experimental Method of Polymer Synthesis" (published by Otsu Takayuki, Hot Co Joe, 1st Edition, 1st Ed., March 1, 1972) Can be prepared by reference to the literature.

The resin (B) is preferably one kind selected from the group consisting of a resin [K1], a resin [K2] and a resin [K3], more preferably a resin [K2] It is one kind selected from the group. When these resins are used, the colored curable resin composition is excellent in developing property. From the viewpoint of the adhesion between the colored pattern and the substrate, the resin [K2] is more preferable.

The weight average molecular weight of the resin (B) in terms of polystyrene is preferably 3,000 to 100,000, more preferably 5,000 to 50,000, and still more preferably 5,000 to 30,000. When the molecular weight is within the above range, the hardness of the coating film is improved and the residual film ratio is also high, the solubility of the unexposed portion in the developing solution is good, and the resolution of the coloring pattern tends to be improved.

The molecular weight distribution (weight average molecular weight (Mw) / number average molecular weight (Mn)) of the resin (B) is preferably 1.1 to 6, and more preferably 1.2 to 4.

The acid value of the resin (B) is preferably 50 to 170 mg-KOH / g, more preferably 60 to 150 mg-KOH / g, and still more preferably 70 to 135 mg-KOH / g. Here, the acid value is a value measured as the amount (mg) of potassium hydroxide necessary to neutralize 1 g of the resin (B), and can be determined by titration using, for example, an aqueous potassium hydroxide solution.

The content of the resin (B) is preferably from 7 to 65% by mass, more preferably from 13 to 60% by mass, and still more preferably from 17 to 55% by mass, based on the total solid content. When the content of the resin (B) is in the above-described range, a colored pattern can be formed, and the resolution and residual film ratio of the colored pattern tends to be improved.

≪ Polymerizable compound (C) >

The polymerizable compound (C) is a compound which can be polymerized by an active radical and / or an acid generated from the polymerization initiator (D), and examples thereof include a compound having a polymerizable ethylenically unsaturated bond, (Meth) acrylic acid ester compound.

Examples of the polymerizable compound having one ethylenically unsaturated bond include nonylphenylcarbitol acrylate, 2-hydroxy-3-phenoxypropyl acrylate, 2-ethylhexylcarbitol acrylate, 2-hydroxyethyl acrylate , N-vinylpyrrolidone, and the above-mentioned (a), (b) and (c).

Examples of polymerizable compounds having two ethylenically unsaturated bonds include 1,6-hexanediol di (meth) acrylate, ethylene glycol di (meth) acrylate, neopentyl glycol di (meth) acrylate, triethylene glycol di (Meth) acrylate, bis (acryloyloxyethyl) ether of bisphenol A, and 3-methylpentanediol di (meth) acrylate.

The polymerizable compound (C) is preferably a polymerizable compound having three or more ethylenic unsaturated bonds. Examples of such polymerizable compounds include trimethylolpropane tri (meth) acrylate, pentaerythritol tri (meth) acrylate, pentaerythritol tetra (meth) acrylate, dipentaerythritol penta (meth) acrylate, dipentaerythritol (Meth) acrylate, tetrapentaerythritol hexa (meth) acrylate, tripentaerythritol hexa (meth) acrylate, tripentaerythritol hexa (meth) acrylate, - (meth) acryloyloxyethyl) isocyanurate, ethylene glycol modified pentaerythritol tetra (meth) acrylate, ethylene glycol modified dipentaerythritol hexa (meth) acrylate, propylene glycol modified pentaerythritol tetra Propylene glycol-modified dipentaerythritol hexa (meth) acrylate, Caprolactone-modified tetra (meth) acrylate, caprolactone-modified dipentaerythritol hexa (meth) acrylate, and the like. Of these, dipentaerythritol penta (meth) acrylate and dipentaerythritol hexa Acrylate is preferable.

The weight average molecular weight of the polymerizable compound (C) is preferably 150 or more and 2,900 or less, and more preferably 250 to 1,500 or less.

The content of the polymerizable compound (C) is preferably from 7 to 65% by mass, more preferably from 13 to 60% by mass, and still more preferably from 17 to 55% by mass, based on the total solid content.

The content ratio of the resin (B) to the polymerizable compound (C) (resin (B): polymerizable compound (C)) is preferably 20:80 to 80:20, more preferably 35: : 65 to 80:20.

When the content of the polymerizable compound (C) is within the above range, the residual film ratio at the time of forming a color pattern and the chemical resistance of the color filter tend to be improved.

≪ Polymerization initiator (D) >

The polymerization initiator (D) is not particularly limited as long as it is a compound capable of generating an active radical or an acid by the action of light or heat and capable of initiating polymerization, and a known polymerization initiator can be used.

Examples of the polymerization initiator (D) include O-acyloxime compounds, alkylphenone compounds, imidazole compounds, triazine compounds and acylphosphine oxide compounds.

Examples of the O-acyloxime compound include N-benzoyloxy-1- (4-phenylsulfanylphenyl) butan-1-one-2-imine, N-benzoyloxy- 1-one-2-imine, N-benzoyloxy-1- (4-phenylsulfanylphenyl) -3- cyclopentylpropan- Yl] ethane-1-imine, N-acetoxy-1- [9-ethyl-6- {2-methyl-4- (3,3- Dimethyl-2,4-dioxacyclopentanylmethyloxy) benzoyl} -9H-carbazol-3-yl] ethan- 1-imine, N- acetoxy- 1- [ ) -9H-carbazol-3-yl] -3-cyclopentylpropan- 1-imine, N-benzoyloxy- Yl] -3-cyclopentylpropan-1-one-2-imine and the like. Commercially available products such as Irgacure (registered trademark) OXE01, OXE02 (manufactured by BASF) and N-1919 (manufactured by ADEKA) may be used. Among them, the O-acyloxime compound is preferably an N-benzoyloxy-1- (4-phenylsulfanylphenyl) butan- 1-one-2-imine and N-benzoyloxy-1- (4-phenylsulfanylphenyl) -3-cyclopentylpropan- , And N-benzoyloxy-1- (4-phenylsulfanylphenyl) octan-1-one-2-imine are more preferable.

Examples of the alkylphenone compound include 2-methyl-2-morpholino-1- (4-methylsulfanylphenyl) propan- (4-methylphenyl) methyl] -1- [4- (4-morpholinyl) phenyl] butan-1-one, 2-hydroxy- 2-methyl-1- [4- (2-hydroxyethoxy) phenyl] propan-1-one, 1-hydroxycyclohexylphenyl Ketone, oligomers of 2-hydroxy-2-methyl-1- (4-isopropenylphenyl) propane-1-one,?,? - diethoxyacetophenone and benzyldimethyl ketal. IRGACURE (registered trademark) 369, 907, 379 (manufactured by BASF), or the like may be used.

Examples of the imidazole compound include 2,2'-bis (2-chlorophenyl) -4,4 ', 5,5'-tetraphenylbimidazole, 2,2'-bis (2,3- -4,4 ', 5,5'-tetraphenylbiimidazole (see JP-A 6-75372, JP-A 6-75373, etc.), 2,2'-bis -Chlorophenyl) -4,4 ', 5,5'-tetraphenylbiimidazole, 2,2'-bis (2-chlorophenyl) -4,4' Imidazole, 2,2'-bis (2-chlorophenyl) -4,4 ', 5,5'-tetra (dialkoxyphenyl) , 4 ', 5,5'-tetra (trialkoxyphenyl) biimidazole (Japanese Patent Publication No. 48-38403, Japanese Patent Laid-Open No. 62-174204, Imidazole compounds in which the phenyl group in the 5'-position is substituted by a carboalkoxy group (see, for example, JP-A 7-10913).

Examples of the triazine compound include 2,4-bis (trichloromethyl) -6- (4-methoxyphenyl) -1,3,5-triazine, 2,4-bis (trichloromethyl) -6- 4-methoxynaphthyl) -1,3,5-triazine, 2,4-bis (trichloromethyl) -6-piperonyl-1,3,5-triazine, 2,4- (Trichloromethyl) -6- [2- (5-methylfuran-2-yl) 2-yl) ethenyl] -1,3,5-triazine, 2,4-bis (trichloromethyl) -6- [2- (Trichloromethyl) -6- [2- (4-diethylamino-2-methylphenyl) ethenyl] -1,3,5-triazine, 2,4- 6- [2- (3,4-dimethoxyphenyl) ethenyl] -1,3,5-triazine, and the like.

Examples of the acylphosphine oxide compound include 2,4,6-trimethylbenzoyldiphenylphosphine oxide and the like.

Examples of the polymerization initiator (D) include benzoin compounds such as benzoin, benzoin methyl ether, benzoin ethyl ether, benzoin isopropyl ether, and benzoin isobutyl ether; Benzophenone, methyl o-benzoylbenzoate, 4-phenylbenzophenone, 4-benzoyl-4'-methyldiphenylsulfide, 3,3 ', 4,4'-tetra (tert- butylperoxycarbonyl) benzophenone Benzophenone compounds such as 2,4,6-trimethylbenzophenone; Quinone compounds such as 9,10-phenanthrenequinone, 2-ethyl anthraquinone, and campquinone; Butyl-2-chloroacridone, benzyl, methyl phenylglyoxylate, and titanocene compounds.

The polymerization initiator (D) is preferably a polymerization initiator comprising at least one member selected from the group consisting of alkylphenone compounds, triazine compounds, acylphosphine oxide compounds, O-acyloxime compounds and imidazole compounds , And more preferably an O-acyloxime compound.

The content of the polymerization initiator (D) is preferably 0.1 to 40 parts by mass, and more preferably 1 to 30 parts by mass, based on 100 parts by mass of the total amount of the resin (B) and the polymerizable compound (C).

The colored curable resin composition of the present invention may further contain a solvent (E), a leveling agent (F), and the like.

≪ Solvent (E) >

The solvent (E) is not particularly limited, and a solvent commonly used in the field can be used. As the solvent, an ester solvent (a solvent containing -COO- and no -O- in the molecule), an ether solvent (a solvent containing -O- and -COO- in the molecule), an ether ester (Solvent containing -COO- and -O- in the molecule), ketone solvent (solvent containing -CO- in the molecule and not including -COO-), alcohol solvent (containing OH in the molecule, O-, -CO- and -COO-), aromatic hydrocarbon solvents, amide solvents, dimethylsulfoxide and the like.

Examples of the ester solvent include methyl lactate, ethyl lactate, butyl lactate, methyl 2-hydroxyisobutyrate, ethyl acetate, n-butyl acetate, isobutyl acetate, pentyl formate, isopentyl acetate, butyl propionate, isopropyl butyrate, ethyl butyrate , Butyl butyrate, methyl pyruvate, ethyl pyruvate, propyl pyruvate, methyl acetoacetate, ethyl acetoacetate, cyclohexanol acetate, and γ-butyrolactone.

Examples of the ether solvent include ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monopropyl ether, ethylene glycol monobutyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol monobutyl ether, Propylene glycol monopropyl ether, propylene glycol monobutyl ether, 3-methoxy-1-butanol, 3-methoxy-3-methylbutanol, tetrahydrofuran, tetrahydrofuran , 1,4-dioxane, diethylene glycol dimethyl ether, diethylene glycol diethyl ether, diethylene glycol methyl ethyl ether, diethylene glycol dipropyl ether, diethylene glycol dibutyl ether, anisole, A brush, and the like.

Examples of the ether ester solvent include methyl methoxyacetate, ethyl methoxyacetate, butyl methoxyacetate, methyl ethoxyacetate, ethyl ethoxyacetate, methyl 3-methoxypropionate, ethyl 3-methoxypropionate, Ethoxypropionate, methyl 2-ethoxypropionate, ethyl 2-ethoxypropionate, ethyl 2-ethoxypropionate, ethyl 2-methoxypropionate, ethyl 2-methoxypropionate, ethyl 2-methoxypropionate, Methyl propionate, methyl propionate, methyl 2-ethoxy-2-methyl propionate, 3-methoxybutyl acetate, 3-methyl-3-methoxybutyl acetate, propylene glycol monomethyl ether acetate, propylene glycol monoethyl ether acetate, Monopropyl ether acetate, ethylene glycol monomethyl ether acetate, ethylene glycol monoethyl ether acetate, diethylene glycol monoethyl ether acetate , Di, and the like ethylene glycol monobutyl ether acetate, dipropylene glycol methyl ether acetate.

Examples of the ketone solvent include 4-hydroxy-4-methyl-2-pentanone, acetone, 2-butanone, 2-heptanone, 3-heptanone, 4- Cyclopentanone, cyclohexanone, isophorone, and the like.

Examples of the alcohol solvent include methanol, ethanol, propanol, butanol, hexanol, cyclohexanol, ethylene glycol, propylene glycol, glycerin and the like.

Examples of the aromatic hydrocarbon solvent include benzene, toluene, xylene, and mesitylene.

Examples of the amide solvent include N, N-dimethylformamide, N, N-dimethylacetamide and N-methylpyrrolidone.

These solvents may be used alone or in combination of two or more.

Among them, propylene glycol monomethyl ether acetate, ethyl lactate, propylene glycol monomethyl ether, ethyl 3-ethoxypropionate, ethylene glycol monomethyl ether, ethylene glycol monobutyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl Methoxybutyl acetate, 3-methoxy-1-butanol, 4-hydroxy-4-methyl-2-pentanone, N, N-dimethylformamide, N-methylpyrrolidone and the like are preferable , Propylene glycol monomethyl ether acetate, propylene glycol monomethyl ether, ethylene glycol monobutyl ether, dipropylene glycol methyl ether acetate, ethyl lactate, 3-methoxybutyl acetate, 3-methoxy-1-butanol, Ethyl propionate, and N-methyl pyrrolidone are more preferred.

The content of the solvent (E) is preferably 70 to 95% by mass, and more preferably 75 to 92% by mass, based on the total amount of the colored curable resin composition. In other words, the solid content of the colored curable resin composition is preferably 5 to 30% by mass, and more preferably 8 to 25% by mass. When the content of the solvent (E) is within the above range, the flatness at the time of coating becomes good, and the color characteristic is not insufficient when the color filter is formed, and the display characteristics tend to be good.

≪ Leveling agent (F) >

The colored curable resin composition of the present invention may contain a leveling agent (F). Examples of the leveling agent (F) include a silicone surfactant, a fluorinated surfactant, and a silicon surfactant having a fluorine atom. These may have a polymerizable group in the side chain.

Examples of the silicone surfactant include a surfactant having a siloxane bond in the molecule. Specific examples thereof include TORAY silicone DC3PA, TORAY silicone SH7PA, TORAY silicone DC11PA, TORAY silicone SH21PA, TORAY silicone SH28PA, TORAY silicone SH29PA, TORAY silicone SH30PA, TORAY silicone SH8400 (trade name: Toray Dow Corning) KP322, KP323, KP324, KP326, KP340, KP341 (manufactured by Shin-Etsu Chemical Co., Ltd.), TSF400, TSF401, TSF410, TSF4300, TSF4440, TSF4445, TSF4446, TSF4452 and TSF4460 (Momentive Performance Materials Japan Height Manufactured by Kao Corporation).

Examples of the fluorine-based surfactant include a surfactant having a fluorocarbon chain in the molecule. Specific examples of the polymer include Flared (registered trademark) FC430, Florad FC431 (manufactured by Sumitomo 3M Ltd.), Megapack (registered trademark) F142D, Megapack F171, Megapack F172, Megapack F173, Megapack F177, (Trade name) manufactured by Mitsubishi Chemical Corporation, Mitsubishi Chemical Corporation, Mitsubishi Chemical Corporation, Mitsubishi Chemical Corporation, Mitsubishi Chemical Corporation, Mitsubishi Chemical Corporation, Mitsubishi Chemical Corporation, Mitsubishi Chemical Corporation, Mitsubishi Chemical Corporation, (Manufactured by Asahi Glass Co., Ltd.) and E5844 (manufactured by Daikin Fine Chemical Co., Ltd.), and the like, and the like, .

Examples of the silicon-based surfactant having a fluorine atom include a surfactant having a siloxane bond and a fluorocarbon chain in the molecule. Specific examples thereof include Megapac (registered trademark) R08, Megapac BL20, Megapac F475, Megapac F477 and Megapac F443 (manufactured by DIC Corporation).

When the leveling agent (F) is contained, the content thereof is preferably 0.001 mass% or more and 0.2 mass% or less, more preferably 0.002 mass% or more and 0.1 mass% or less, relative to the total amount of the colored curable resin composition, Preferably 0.005 mass% or more and 0.07 mass% or less. When the content of the leveling agent (F) is within the above range, the flatness of the color filter can be improved.

≪ Other components >

The colored curable resin composition of the present invention may contain additives known in the art, such as polymerization initiators, fillers, other polymer compounds, adhesion promoters, antioxidants, light stabilizers, and chain transfer agents, if necessary.

≪ Process for producing colored curable resin composition >

The colored curable resin composition of the present invention can be obtained, for example, by mixing a colorant (A), a resin (B), a polymerizable compound (C), a polymerization initiator (D), a solvent (E) It can be prepared by mixing other components.

The pigment in the case of containing the pigment (P) is preferably mixed with part or all of the solvent (E) in advance and dispersed using a bead mill or the like until the average particle diameter of the pigment becomes about 0.2 탆 or less . At this time, if necessary, a part or all of the pigment dispersant and the resin (B) may be blended. The desired coloring curable resin composition can be prepared by mixing the remaining components in the thus obtained pigment dispersion to a predetermined concentration.

The compound (II) is preferably dissolved in a part or all of the solvent (E) to prepare a solution. The solution is preferably filtered with a filter having a pore size of about 0.01 to 1 mu m.

The colored curable resin composition after mixing is preferably filtered with a filter having a pore diameter of about 0.01 to 10 mu m.

<Manufacturing Method of Color Filter>

A coating film formed using the colored curable resin composition of the present invention or a color filter formed using the colored curable resin composition also falls within the scope of the present invention.

The coating film of the present invention can be obtained by a conventionally known method. For example, the coating film of the present invention can be obtained by applying the above-mentioned colored curable resin composition to a substrate, drying it to form a colored composition layer, and further curing the colored curable resin composition layer have.

The curing can be performed by heating or exposing the colored curable resin composition layer by a conventionally known method.

The color filter of the present invention can be formed by the same process as the coating film of the present invention. The color filter of the present invention may include a coloring pattern.

Examples of the method for producing a colored pattern from the colored curable resin composition of the present invention include a photolithographic method, an inkjet method, a printing method and the like. Among them, a photolithographic method is preferable. The photolithographic method is a method in which the above-mentioned colored curable resin composition is applied to a substrate, followed by drying to form a colored composition layer, and the colored composition layer is exposed through a photomask and developed. In the photolithographic method, a colored coating film which is a cured product of the colored composition layer can be formed by not using a photomask at the time of exposure and / or by not developing it. The coloring pattern or colored coating film thus formed is the color filter of the present invention.

The film thickness of the color filter to be produced is not particularly limited and may be appropriately adjusted depending on the purpose and application, and is, for example, from 0.1 to 30 탆, preferably from 0.1 to 20 탆, more preferably from 0.5 to 6 탆.

Examples of the substrate include glass plates such as quartz glass, borosilicate glass, alumina silicate glass and soda lime glass whose surface is coated with silica, resin plates such as polycarbonate, polymethylmethacrylate, and polyethylene terephthalate, silicon, Aluminum, silver, silver / copper / palladium alloy thin film, or the like is formed. A separate color filter layer, a resin layer, a transistor, a circuit, and the like may be formed on these substrates.

The formation of each color pixel by the photolithographic method can be performed by a known apparatus or condition. For example, it can be produced as follows.

First, a colored curable resin composition is coated on a substrate and heated and dried (pre-baked) and / or reduced-pressure drying to remove volatile components such as a solvent and dried to obtain a smooth colored composition layer.

Examples of the application method include a spin coat method, a slit coat method, and a slit and spin coat method.

The temperature for heating and drying is preferably 30 to 120 占 폚, more preferably 50 to 110 占 폚. The heating time is preferably 10 seconds to 60 minutes, more preferably 30 seconds to 30 minutes.

In the case of performing the reduced-pressure drying, it is preferable that the drying is carried out at a temperature of 20 to 25 캜 under a pressure of 50 to 150 Pa.

The film thickness of the coloring composition layer is not particularly limited and may be suitably selected in accordance with the intended thickness of the color filter.

Next, the coloring composition layer is exposed through a photomask for forming a desired coloring pattern. The pattern on the photomask is not particularly limited and a pattern according to the intended use is used.

As a light source used for exposure, a light source that generates light having a wavelength of 250 to 450 nm is preferable. For example, light having a wavelength of less than 350 nm is cut using a filter that cuts the wavelength region, or light having wavelengths around 436 nm, 408 nm, and 365 nm is extracted using a bandpass filter Or may be selectively extracted. Specifically, examples of the light source include a mercury lamp, a light emitting diode, a metal halide lamp, and a halogen lamp.

It is preferable to use an exposure apparatus such as a mask aligner and a stepper because it is possible to uniformly irradiate the entire exposure surface with a parallel light beam or accurately align the photomask with the substrate on which the coloring composition layer is formed.

The colored composition layer after exposure is brought into contact with a developing solution to develop a colored pattern on the substrate. By the development, the unexposed portion of the colored composition layer is dissolved and removed in the developer. As the developing solution, for example, an aqueous solution of an alkaline compound such as potassium hydroxide, sodium hydrogen carbonate, sodium carbonate, tetramethylammonium hydroxide or the like is preferable. The concentration of these alkaline compounds in the aqueous solution is preferably 0.01 to 10% by mass, and more preferably 0.03 to 5% by mass. In addition, the developer may contain a surfactant.

The developing method may be any of a puddle method, a dipping method and a spraying method. Further, the substrate may be inclined at an arbitrary angle during development. After development, it is preferable to wash with water.

Further, post-baking is preferably performed on the obtained coloring pattern. The post bake temperature is preferably 150 ° C to 250 ° C, more preferably 160 ° C to 235 ° C. The post baking time is preferably 1 to 120 minutes, more preferably 10 to 60 minutes.

Example

Hereinafter, the present invention will be described more specifically by way of examples. In the examples,% and parts representing the content or amount are based on mass unless otherwise specified.

In the following examples, the structure of the compound was confirmed by mass spectrometry (LC: Agilent 1200 type, MASS; manufactured by Agilent LC / MSD type).

[Example 1]

40.6 parts of compound (VI) and 8 parts of diethylamine (compound of formula (III), manufactured by Tokyo Kasei Kogyo K.K.) were mixed under light shielding conditions in the presence of 50 parts of 1-methyl-2-pyrrolidone, And stirred for 3 hours. The obtained reaction solution was cooled to room temperature, added to a mixed solution of 400 parts of water and 20 parts of 35% hydrochloric acid, and stirred at room temperature for 1 hour to precipitate crystals. The precipitated crystals were collected as a residue of suction filtration and dried to obtain 44 parts of a compound represented by the formula (I-1-A).

Subsequently, 44 parts of the compound represented by the formula (I-1-A) and 21.4 parts of trimethoxy [3- (methylamino) propyl] silane (manufactured by Tokyo Kasei Kogyo Co., Was heated in the presence of 50 parts of money at 100 DEG C for 5 hours. The obtained reaction solution was cooled to room temperature, filtered, washed with 100 parts of water, and the obtained crystals were dried to obtain 52 parts of a compound represented by the formula (I-1).

Identification of the compound represented by the formula (I-1)

(Mass analysis) Ionization mode = ESI +: m / z = [M + H] ⁺ 599.2

                        Exact Mass: 598.1

0.35 g of a compound represented by the formula (I-1) was dissolved in chloroform to make a volume of 250 cm 3, and 2 cm 3 of the solution was diluted with ion-exchanged water to make a volume of 100 cm 3 (concentration: 0.028 g / Absorption spectra were measured using a spectrophotometer (quartz cell, optical path length: 1 cm). This compound had? Max = 558 nm.

[Example 2]

In the presence of 44 parts of the compound represented by the formula (I-1-A), 180.0 parts of 2- (ethylamino) ethanol (manufactured by Tokyo Kasei Kogyo Co., Ltd.) and 50 parts of 1- Lt; / RTI &gt; for 5 hours. The obtained reaction solution was cooled to room temperature, filtered, washed with 100 parts of water, and the obtained crystals were dried to obtain 24.7 parts of a compound represented by the formula (I-93-A).

Subsequently, 49.4 parts of the compound represented by the formula (I-93-A) and 49.5 parts of 3- (triethoxysilyl) propyl isocyanate (manufactured by Tokyo Kasei Kogyo Co., Ltd.) were refluxed in 200 parts of chloroform After cooling to room temperature, 200 parts of hexane was added to precipitate crystals. The obtained crude crystals were washed twice with 100 parts of hexane and dried to obtain 28.5 parts of the compound represented by the formula (I-93).

Identification of the compound represented by the formula (I-93)

(Mass analysis) Ionization mode = ESI +: m / z = [M + H] ⁺ 714.2

                        Exact Mass: 713.3

0.35 g of the compound represented by the formula (I-93) was dissolved in chloroform to make a volume of 250 cm 3, and 2 cm 3 of the solution was diluted with ion-exchanged water to make a volume of 100 cm 3 (concentration: 0.028 g / Absorption spectra were measured using a spectrophotometer (quartz cell, optical path length: 1 cm). This compound had? Max = 561 nm.

[Example 3]

44 parts of the compound represented by the formula (I-1-A) and 80.1 parts of methylaminoacetic acid (manufactured by Tokyo Kasei Kogyo Co., Ltd.) were heated under reflux conditions for 2 hours in the presence of 100 parts of methanol. The obtained reaction solution was cooled to room temperature and then filtered to obtain 23.7 parts of crude crystals represented by the formula (I-55-A).

Subsequently, 4.9 parts of the compound represented by the formula (I-55-A), 3 parts of 2- (trimethylsilyl) ethanol (manufactured by Tokyo Kasei Kogyo Co., 1.6 parts of carbodiimide were stirred in 50 parts of chloroform at 20 ° C to 30 ° C for 2 hours. After completion of the reaction, the organic layer was extracted three times with 50 parts of water and the organic layer was separated. The chloroform was distilled off to obtain 4.8 parts of the compound represented by the formula (I-55).

Identification of the compound represented by the formula (I-55)

(Mass analysis) Ionization mode = ESI +: m / z = [M + H] ⁺ 595.3

                        Exact Mass: 594.2

0.35 g of the compound represented by the formula (I-55) was dissolved in chloroform to make a volume of 250 cm 3, 2 cm 3 of the solution was diluted with ion-exchanged water to make a volume of 100 cm 3 (concentration: 0.028 g / Absorption spectra were measured using a spectrophotometer (quartz cell, optical path length: 1 cm). This compound had? Max = 556 nm.

[Example 4]

6 parts of the compound represented by the formula (I-1-A) and 60 parts of dehydrated chloroform (manufactured by Kanto Kagaku Co., Ltd.) were mixed at room temperature. 5.3 parts of trimethoxy [3- (methylamino) propyl] silane (manufactured by Tokyo Kasei Kogyo Co., Ltd.) was added dropwise to the obtained mixture at a temperature not exceeding 40 캜, and the mixture was stirred at 70 캜 for 8 hours. The resulting reaction mixture was cooled to room temperature. The resulting mixture was added to 196 parts of n-hexane to precipitate a solid. The resulting precipitate was filtered, and the obtained solid was washed with propylene glycol monomethyl ether acetate, followed by n-hexane, and dried to obtain 6.2 parts of a compound represented by the formula (I-1). The yield was 76%.

[Example 5]

3 parts of the compound represented by the formula (I-1-A) and 30 parts of dehydrated chloroform (manufactured by Kanto Kagaku Co., Ltd.) were mixed at room temperature. 3.2 parts of trimethoxy [3- (butylamino) propyl] silane (manufactured by Tokyo Kasei Kogyo Co., Ltd.) was added dropwise at a temperature not exceeding 40 占 폚, and the mixture was stirred at 80 占 폚 for 23 hours. The resulting reaction mixture was cooled to room temperature. The obtained mixture was added to 98 parts of n-hexane to precipitate a solid. The obtained precipitate was filtered, and the resulting solid was washed with n-hexane and then dried to obtain 2.0 parts of a compound represented by the formula (I-117). The yield was 45%.

Identification of the compound represented by the formula (I-117)

(Mass analysis) Ionization mode = ESI +: m / z = [M + H] ⁺ 641.3

                        Exact Mass: 640.3

0.35 g of the compound represented by the formula (I-117) was dissolved in chloroform to make a volume of 250 cm 3, and 2 cm 3 of the solution was diluted with ion-exchanged water to make a volume of 100 cm 3 (concentration: 0.028 g / Absorption spectra were measured using a spectrophotometer (quartz cell, optical path length: 1 cm). This compound had? Max = 551 nm.

[Example 6]

5 parts of the compound represented by the formula (I-1-A) and 25 parts of dehydrated chloroform (manufactured by Kanto Kagaku Co., Ltd.) were mixed at room temperature. To the obtained mixture, 14.5 parts of trimethoxy [3- (phenylamino) propyl] silane (manufactured by Tokyo Kasei Kogyo Co., Ltd.) was added dropwise at a temperature not exceeding 40 캜, and the mixture was stirred at 80 캜 for 12 hours. The resulting reaction mixture was cooled to room temperature. The resulting mixture was added to 100 parts of toluene to precipitate a solid. The resulting precipitate was filtered, and the resulting solid was washed with n-heptane and dried to obtain 3.2 parts of the compound represented by the formula (I-118). The yield was 43%.

Identification of the compound represented by the formula (I-118)

(Mass analysis) Ionization mode = ESI +: m / z = [M + H] ⁺ 661.2

                        Exact Mass: 660.2

0.35 g of the compound represented by the formula (I-118) was dissolved in chloroform to make a volume of 250 cm 3, and 2 cm 3 of the solution was diluted with ion-exchanged water to make a volume of 100 cm 3 (concentration: 0.028 g / Absorption spectra were measured using a spectrophotometer (quartz cell, optical path length: 1 cm). This compound had? Max = 550 nm.

[Example 7]

5 parts of the compound represented by the formula (I-1-A) and 25 parts of dehydrated chloroform (manufactured by Kanto Kagaku Co., Ltd.) were mixed at room temperature. To the resulting mixture, 11.6 parts of bis [3- (trimethoxysilyl) propyl] amine (manufactured by Tokyo Kasei Kogyo Co., Ltd.) was added dropwise at a temperature not exceeding 40 캜, and the mixture was stirred at 60 캜 for 12 hours. The resulting reaction mixture was cooled to room temperature. The obtained mixture was added to 90 parts of a mixed solution of ethyl acetate / n-hexane (8/2) to precipitate a solid. The resulting precipitate was collected by filtration, washed with 50 parts of a mixed solution of ethyl acetate / n-hexane (8/2) and dried to obtain 6.7 parts of a compound represented by the formula (I-119). The yield was 79%.

Identification of the compound represented by the formula (I-119)

(Mass analysis) Ionization mode = ESI +: m / z = [M + H] ⁺ 747.3

                        Exact Mass: 746.3

0.35 g of the compound represented by the formula (I-119) was dissolved in chloroform to make a volume of 250 cm 3, and 2 cm 3 of the solution was diluted with ion-exchanged water to make a volume of 100 cm 3 (concentration: 0.028 g / Absorption spectra were measured using a spectrophotometer (quartz cell, optical path length: 1 cm). This compound had? Max = 549 nm.

[Example 8]

4 parts of the compound represented by the formula (I-1-A) and 42 parts of dehydrated chloroform (manufactured by Kanto Kagaku) were mixed at room temperature. To the obtained mixture, 3.5 parts of 3-aminopropyltrimethoxysilane (manufactured by Tokyo Kasei Kogyo Co., Ltd.) was added dropwise at a temperature not exceeding 40 ° C, and the mixture was stirred at 30 ° C for 5 hours. The resulting reaction mixture was cooled to room temperature. The resulting mixture was poured into 150 parts of n-hexane. The obtained precipitate was filtered, and the obtained solid was washed with n-hexane and dried to obtain 2.8 parts of a compound represented by the formula (I-37). The yield was 52%.

Identification of the compound represented by the formula (I-37)

(Mass analysis) Ionization mode = ESI +: m / z = [M + H] ⁺ 585.2

                        Exact Mass: 584.2

0.35 g of the compound represented by the formula (I-37) was dissolved in chloroform to make a volume of 250 cm 3, and 2 cm 3 of the solution was diluted with ion-exchanged water to make a volume of 100 cm 3 (concentration: 0.028 g / Absorption spectra were measured using a spectrophotometer (quartz cell, optical path length: 1 cm). This compound had? Max = 536 nm.

[Example 9]

3 parts of the compound represented by the formula (I-1-A) and 15 parts of dehydrated chloroform (manufactured by Kanto Kagaku Co., Ltd.) were mixed at room temperature. 3 parts of trimethoxy [3- (ethylamino) isobutyl] silane (manufactured by Gelest) was added dropwise at a temperature not exceeding 40 캜, and the mixture was stirred at 80 캜 for 12 hours. The resulting reaction mixture was cooled to room temperature. The obtained mixture was added to 90 parts of propylene glycol monomethyl ether acetate to precipitate a solid. The obtained precipitate was filtered, and the resulting solid was washed with n-hexane and dried to obtain 3.9 parts of a compound represented by the formula (I-120). The yield was 91%.

Identification of the compound represented by the formula (I-120)

(Mass analysis) Ionization mode = ESI +: m / z = [M + H] ⁺ 626.4

                        Exact Mass: 626.3

0.35 g of the compound represented by the formula (I-120) was dissolved in chloroform to make a volume of 250 cm 3, and 2 cm 3 of the solution was diluted with ion-exchanged water to make a volume of 100 cm 3 (concentration: 0.028 g / Absorption spectra were measured using a spectrophotometer (quartz cell, optical path length: 1 cm). This compound had? Max = 549 nm.

[Example 10]

3 parts of the compound of the formula (VI) having the following structure and 15 parts of dehydrated chloroform [manufactured by Kanto Kagaku Co., Ltd.] were mixed at room temperature. To the obtained mixture, 7 parts of trimethoxy [3- (butylamino) propyl] silane (manufactured by Tokyo Kasei Kogyo Co., Ltd.) was added dropwise at a temperature not exceeding 40 캜, and the mixture was stirred at 80 캜 for 12 hours. The resulting reaction mixture was cooled to room temperature. The resultant mixture was added to 50 parts of a mixed solution of ethyl acetate / n-hexane (9/1) to precipitate a solid. The resulting precipitate was filtered, and the resulting solid was washed with a mixed solution of ethyl acetate / n-hexane (9/1) and dried to obtain 1.1 parts of a compound represented by the formula (I-121). The yield was 36%.

Identification of the compound represented by the formula (I-121)

(Mass analysis) Ionization mode = ESI +: m / z = [M + H] ⁺ 803.3

                        Exact Mass: 802.3

0.35 g of the compound represented by the formula (I-121) was dissolved in chloroform to make a volume of 250 cm 3, and 2 cm 3 of the solution was diluted with ion-exchanged water to make a volume of 100 cm 3 (concentration: 0.028 g / Absorption spectra were measured using a spectrophotometer (quartz cell, optical path length: 1 cm). This compound had? Max = 549 nm.

[Example 11]

3 parts of the compound of the formula (VI) having the following structure and 15 parts of dehydrated chloroform [manufactured by Kanto Kagaku Co., Ltd.] were mixed at room temperature. 4.9 parts of trimethoxy [3- (ethylamino) isobutyl] silane (manufactured by Gelest) was added dropwise to the resulting mixture at a temperature not exceeding 40 캜, and the mixture was stirred at 80 캜 for 14 hours. The resulting reaction mixture was cooled to room temperature. The obtained reaction mixture was added to 30 parts of n-hexane to precipitate a solid. The obtained precipitate was filtered, and the obtained solid was washed with n-hexane and dried to obtain 1.9 parts of a compound represented by the formula (I-122). The yield was 33%.

Identification of the compound represented by the formula (I-122)

(Mass analysis) Ionization mode = ESI +: m / z = [M + H] ⁺ 775.3

                        Exact Mass: 774.3

0.35 g of the compound represented by the formula (I-122) was dissolved in chloroform to make a volume of 250 cm 3, and 2 cm 3 of the solution was diluted with ion-exchanged water to make a volume of 100 cm 3 (concentration: 0.028 g / Absorption spectra were measured using a spectrophotometer (quartz cell, optical path length: 1 cm). This compound had? Max = 549 nm.

[Example 12]

6 parts of the compound of the formula (VI) having the following structure and 30 parts of dehydrated chloroform [manufactured by Kanto Kagaku Co., Ltd.] were mixed at room temperature. To the obtained mixture, 15.2 parts of bis [3- (trimethoxysilyl) propyl] amine (manufactured by Tokyo Kasei Kogyo Co., Ltd.) was added dropwise at a temperature not exceeding 40 캜, and the mixture was stirred at 80 캜 for 11 hours. The resulting reaction mixture was cooled to room temperature. The obtained reaction mixture was added to 90 parts of n-hexane to precipitate a solid. The obtained precipitate was filtered, washed with n-hexane and dried to obtain 4.5 parts of a compound represented by the formula (I-123). The yield was 30%.

Identification of the compound represented by the formula (I-123)

(Mass analysis) Ionization mode = ESI +: m / z = [M + H] ⁺ 1015.4

                        Exact Mass: 1014.4

0.35 g of the compound represented by the formula (I-123) was dissolved in chloroform to make a volume of 250 cm 3, and 2 cm 3 of the solution was diluted with ion-exchanged water to make a volume of 100 cm 3 (concentration: 0.028 g / Absorption spectra were measured using a spectrophotometer (quartz cell, optical path length: 1 cm). This compound had? Max = 552 nm.

[Synthesis of resin]

In a flask equipped with a reflux condenser, a dropping funnel and a stirrer, nitrogen was appropriately flowed to make a nitrogen atmosphere, and 100 parts of propylene glycol monomethyl ether acetate was added and heated to 85 DEG C with stirring. Subsequently, 19 parts of methacrylic acid, 3,4-epoxytricyclo [5.2.1.0 ^2,6 ] decan-8-yl acrylate and 3,4-epoxytricyclo [5.2.1.0 ^2,6 ] Decane-9-yl acrylate (content ratio: 50:50 in molar ratio) (trade name "E-DCPA", manufactured by Daicel Chemical Industries, Ltd.) in 40 parts of propylene glycol monomethyl ether acetate, Was added dropwise over about 5 hours. On the other hand, a solution prepared by dissolving 26 parts of polymerization initiator 2,2'-azobis (2,4-dimethylvaleronitrile) in 120 parts of propylene glycol monomethyl ether acetate was dropped into a flask over about 5 hours using another dropping pump Respectively. After the dropping of the polymerization initiator was completed, the temperature was maintained at the same temperature for about 3 hours and then cooled to room temperature to obtain a copolymer and resin (B-1) solution having a solid content of 43.5%. The obtained resin (B-1) had a weight average molecular weight of 8000, a molecular weight distribution of 1.98, and an acid value in terms of solid content of 53 mg-KOH / g.

The weight average molecular weight (Mw) and the number average molecular weight (Mn) of the resin in terms of polystyrene were measured by the GPC method under the following conditions.

Device ; HLC-8120GPC (manufactured by Tosoh Corporation)

column ; TSK-GELG2000HXL

Column temperature; 40 ℃

Solvent; Tetrahydrofuran [THF]

Flow rate; 1.0 ml / min

Solid concentration of the test solution; 0.001 to 0.01 mass%

Dose; 50 μl

Detector; RI

Calibration standards; TSK STANDARD POLYSTYRENE

                   F-40, F-4, F-288, A-2500 and A-500 (manufactured by Tosoh Corporation)

The ratio (Mw / Mn) of the weight average molecular weight and the number average molecular weight in terms of polystyrene obtained as described above was defined as a molecular weight distribution.

[Preparation of colored curable resin composition]

Example 13

Dye (A1): A dye represented by the formula (I-1) 2.6 parts;

Alkali-soluble resin (B): Resin (B-1) (in terms of solid content) 53 parts;

Polymerizable compound (C): dipentaerythritol hexaacrylate [KAYARAD (R) DPHA; Manufactured by Nippon Kayaku Co., Ltd.] 50 parts;

Polymerization initiator (D): N-benzoyloxy-1- (4-phenylsulfanylphenyl) octan-1-one-2-imine [Irgacure (registered trademark) OXE-01; Manufactured by BASF; O-acyloxime compound] 10 parts;

Solvent (E): Propylene glycol monomethyl ether acetate 700 parts;

Solvent (E): Propylene glycol monomethyl ether 80 parts;

And

Leveling agent (F): Megapack (registered trademark) F554 (manufactured by DIC Corporation) 0.1 part

Were mixed to obtain a colored curable resin composition.

Example 14

Dye (A1): A dye represented by the formula (I-93) Part 2;

Alkali-soluble resin (B): Resin (B-1) (in terms of solid content) 53 parts;

Polymerizable compound (C): dipentaerythritol hexaacrylate [KAYARAD (R) DPHA; Manufactured by Nippon Kayaku Co., Ltd.] 50 parts;

Polymerization initiator (D): N-benzoyloxy-1- (4-phenylsulfanylphenyl) octan-1-one-2-imine [Irgacure (registered trademark) OXE-01; Manufactured by BASF; O-acyloxime compound] 10 parts;

Solvent (E): Propylene glycol monomethyl ether acetate 700 parts;

Solvent (E): Propylene glycol monomethyl ether 80 parts;

And

Leveling agent (F): Megapack (registered trademark) F554 (manufactured by DIC Corporation) 0.1 part

Were mixed to obtain a colored curable resin composition.

Example 15

Dye (A1): A dye represented by the formula (I-55) 2.9 parts;

Alkali-soluble resin (B): Resin (B-1) (in terms of solid content) 53 parts;

Polymerizable compound (C): dipentaerythritol hexaacrylate [KAYARAD (R) DPHA; Manufactured by Nippon Kayaku Co., Ltd.] 50 parts;

Polymerization initiator (D): N-benzoyloxy-1- (4-phenylsulfanylphenyl) octan-1-one-2-imine [Irgacure (registered trademark) OXE-01; Manufactured by BASF; O-acyloxime compound] 10 parts;

Solvent (E): Propylene glycol monomethyl ether acetate 700 parts;

Solvent (E): Propylene glycol monomethyl ether 80 parts;

And

Leveling agent (F): Megapack (registered trademark) F554 (manufactured by DIC Corporation) 0.1 part

Were mixed to obtain a colored curable resin composition.

Comparative Example 1

Rhodamine B (manufactured by Tokyo Kasei Kogyo Co., Ltd.) 4 parts;

Alkali-soluble resin (B): Resin (B-1) (in terms of solid content) 31 parts;

Polymerizable compound (C): dipentaerythritol hexaacrylate [KAYARAD (R) DPHA; Manufactured by Nippon Kayaku Co., Ltd.] 30 parts;

Polymerization initiator (D): N-benzoyloxy-1- (4-phenylsulfanylphenyl) octan-1-one-2-imine [Irgacure (registered trademark) OXE-01; Manufactured by BASF; O-acyloxime compound] 8.3 parts;

Solvent (E): Ethyl lactate 50 parts;

Solvent (E): Dimethylformamide 150 parts;

Were mixed to obtain a colored curable resin composition.

[Formation of pattern]

The colored curable composition was coated on a square glass substrate (Eagle XG; Corning) having a side of 2 inches by one side by a spin coat method, and then prebaked at 100 캜 for 3 minutes to obtain a composition layer.

After cooling, the distance between the glass substrate on which the composition layer was formed and the quartz glass photomask was set to 100 mu m, and exposure was performed with an exposure machine (TME-150 RSK; (Manufactured by Topcon Co., Ltd.) at an exposure amount of 150 mJ / cm 2 (based on 365 nm) in an air atmosphere. As the photomask, a photomask having a 100 μm line and space pattern was used.

After the light irradiation, the coating film was immersed in an aqueous developing solution containing 0.12% of a nonionic surfactant and 0.04% of potassium hydroxide at 23 DEG C for 80 seconds, washed with water, and postbaked in an oven at 220 DEG C for 20 minutes , And a coloring pattern was obtained.

[Heat resistance evaluation]

The coating film of the colored curable resin composition was heated at 230 占 폚 for 20 minutes and the color difference? Eab * before and after heating of the coated film was measured using a colorimeter (OSP-SP-200; OLYMPUS). The coating films obtained in Example 13, Example 14 and Example 15 were each evaluated for heat resistance as above, and as a result, the color differences (ΔEab *) were 10.6, 9.2 and 11.3.

As a result of evaluating the heat resistance in the same manner as in Comparative Example 1, the color difference (? Eab *) was 80.1, and it was found that the coating film obtained from the composition of the present invention had excellent heat resistance.

When a colored curable resin composition containing a dye having a silicon atom and having a maximum absorption wavelength in chloroform of 500 nm to 600 nm is used, a color filter excellent in heat resistance can be provided. This color filter is useful as a color filter used in display devices (liquid crystal display devices, organic EL devices, electronic paper, etc.) and solid-state image pickup devices.

Claims (18)

A colorant (A) comprising a dye (A1) having a silicon atom and having a maximum absorption wavelength in chloroform of 500 nm to 600 nm,
The resin (B)
The polymerizable compound (C)
The polymerization initiator (D)
And a coloring curable resin. A dye according to claim 1, wherein the dye (A1) is a dye having a xanthene skeleton having a substituent,
Wherein the substituent comprises an organic silicon group. The colored curable resin composition according to claim 2, wherein the organosilicon group has a silyloxy group. The colored curable resin composition according to claim 1, wherein the dye (A1) is a compound represented by the formula (II).

[In the formula (II), R ²¹ to R ²⁴ each independently represent a hydrogen atom, a monovalent saturated hydrocarbon group having 1 to 10 carbon atoms, a phenyl group which may have a substituent, or a group represented by the formula (ii). Provided that at least one of R ²¹ to R ²⁴ is a group represented by the formula (ii).
-R ⁵⁰ -Si (R ²⁹ ) ₃ (ii)
(R ²⁹ represents an alkoxy group having 1 to 4 carbon atoms or a hydrogen atom, a hydroxyl group, having 1 to 4 carbon atoms, * represents a bonding number (結合手) with a nitrogen atom. A plurality of R ²⁹ may be the same respectively Or may be different.
R ⁵⁰ represents an alkanediyl group having 1 to 10 carbon atoms, and -CH ₂ - which constitutes the alkanediyl group is -O-, -CO-, -NR ¹¹ -, -OCO-, -COO-, -OCONH- , -CONH-, or -NHCO-).
In R ²¹ to R ²⁴ , a hydrogen atom contained in a monovalent saturated hydrocarbon group having 1 to 10 carbon atoms may be substituted with a halogen atom, and -CH ₂ - included in the saturated hydrocarbon group may be -O-, -CO-, NR ¹¹ -, -OCO-, -COO-, -OCONH-, -CONH- or -NHCO-.
R ²⁵ and R ²⁶ each independently represent a hydrogen atom or an alkyl group having 1 to 6 carbon atoms.
R ²⁷ and R ²⁸ are each independently selected from _{^{-OH, -SO 3 -, -SO 3}} H, -SO 3 - Z +, -CO 2 -, -CO 2 H, -CO 2 - Z +, -CO 2 R ¹⁴ shows a -SO ₃ R ¹⁵ or -SO ₂ NR ¹² R ^13.
R ¹⁴ and R ¹⁵ each independently represent a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a halogen atom.
Z ⁺ represents ⁺ N (R ¹⁶ ) ₄ , Na ⁺ or K ⁺ .
R ¹¹ , R ¹² and R ¹³ each independently represent a hydrogen atom or a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms.
R ¹⁶ each independently represents a hydrogen atom or a monovalent saturated hydrocarbon group of 1 to 20 carbon atoms.
and p represents an integer of 0 to 4.] The alkanediyl group having 1 to 10 carbon atoms as represented by R ⁵⁰ in claim 4, wherein -CH ₂ - is -O-, -CO-, -NR ¹¹ -, -OCO-, -COO-, -OCONH- , -CONH-, or -NHCO-. The colored curable resin composition according to claim 4, wherein in the formula (ii), R ⁵⁰ is an alkanediyl group having 1 to 8 carbon atoms and R ²⁹ is a hydroxy group or an alkoxy group having 1 to 4 carbon atoms. The monovalent saturated hydrocarbon group having 1 to 10 carbon atoms represented by R ²¹ to R ²⁴ in claim 4, wherein -CH ₂ - is -OCO-, -COO-, -OCONH-, -CONH- and -NHCO- And R &lt; 2 &gt; is a compound which may be substituted with at least one group selected from the group consisting of R &lt; 1 &gt; A coated film formed using the colored curable resin composition according to claim 1 or 2. A color filter formed using the colored curable resin composition according to claim 1 or 2. A display device comprising the color filter according to claim 9. A compound represented by the formula (II).

[In the formula (II), R ²¹ to R ²⁴ each independently represent a hydrogen atom, a monovalent saturated hydrocarbon group having 1 to 10 carbon atoms, a phenyl group which may have a substituent, or a group represented by the formula (ii). Provided that at least one of R ²¹ to R ²⁴ is a group represented by the formula (ii).
-R ⁵⁰ -Si (R ²⁹ ) ₃ (ii)
(Wherein R ²⁹ represents a hydrogen atom, a hydroxy group, an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms, and * indicates the number of bonds with a nitrogen atom. The plurality of R ^{29 s} may be the same or different .
R ⁵⁰ represents an alkanediyl group having 1 to 10 carbon atoms, and -CH ₂ - which constitutes the alkanediyl group is -O-, -CO-, -NR ¹¹ -, -OCO-, -COO-, -OCONH- , -CONH-, or -NHCO-).
In R ²¹ to R ²⁴ , a hydrogen atom contained in a monovalent saturated hydrocarbon group having 1 to 10 carbon atoms may be substituted with a halogen atom, and -CH ₂ - included in the saturated hydrocarbon group may be -O-, -CO-, NR ¹¹ -, -OCO-, -COO-, -OCONH-, -CONH- or -NHCO-.
R ²⁵ and R ²⁶ each independently represent a hydrogen atom or an alkyl group having 1 to 6 carbon atoms.
R ²⁷ and R ²⁸ are each independently selected from _{^{-OH, -SO 3 -, -SO 3}} H, -SO 3 - Z +, -CO 2 -, -CO 2 H, -CO 2 - Z +, -CO 2 R ¹⁴ shows a -SO ₃ R ¹⁵ or -SO ₂ NR ¹² R ^13.
R ¹⁴ and R ¹⁵ each independently represent a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a halogen atom.
Z ⁺ represents ⁺ N (R ¹⁶ ) ₄ , Na ⁺ or K ⁺ .
R ¹¹ , R ¹² and R ¹³ each independently represent a hydrogen atom or a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms.
R ¹⁶ each independently represents a hydrogen atom or a monovalent saturated hydrocarbon group of 1 to 20 carbon atoms.
and p represents an integer of 0 to 4.] 12. The method of claim 11, Al of 1 to 10 carbon atoms represented by R ⁵⁰ is alkanediyl group, -CH ₂ - is ^{-O-, -CO-, -NR 11 -,} -OCO-, -COO-, -OCONH- , -CONH-, or -NHCO-. The compound according to claim 11, wherein in the formula (ii), R ⁵⁰ is an alkanediyl group having 1 to 8 carbon atoms and R ²⁹ is a hydroxy group or an alkoxy group having 1 to 4 carbon atoms. A process for producing a compound represented by the formula (II) comprising a step of reacting a compound represented by the formula (IV) with a compound represented by the formula (V).

[In the formulas, X ² represents a halogen atom or a trifluoromethylsulfonyloxy group.
R ²¹ , R ²² , R ²³ and R ²⁴ each independently represent a hydrogen atom, a monovalent saturated hydrocarbon group having 1 to 10 carbon atoms, a phenyl group which may have a substituent, or a group represented by the formula (ii). Provided that at least one of R ²¹ , R ²² , R ²³ or R ²⁴ is a group represented by the formula (ii).
-R ⁵⁰ -Si (R ²⁹ ) ₃ (ii)
(Wherein R ²⁹ represents a hydrogen atom, a hydroxy group, an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms, and * indicates the number of bonds with a nitrogen atom. The plurality of R ^{29 s} may be the same or different .
R ⁵⁰ represents an alkanediyl group having 1 to 10 carbon atoms, and -CH ₂ - which constitutes the alkanediyl group is -O-, -CO-, -NR ¹¹ -, -OCO-, -COO-, -OCONH- , -CONH-, or -NHCO-).
In R ²¹ , R ²² , R ²³ and R ²⁴ , the hydrogen atom contained in the monovalent saturated hydrocarbon group having 1 to 10 carbon atoms may be substituted with a halogen atom, and -CH ₂ - included in the saturated hydrocarbon group may be replaced by -O- , -CO-, -NR ¹¹ -, -OCO-, -COO-, -OCONH-, -CONH- or -NHCO-.
R ²⁵ and R ²⁶ each independently represent a hydrogen atom or an alkyl group having 1 to 6 carbon atoms.
R ²⁷ and R ²⁸ are each independently selected from _{^{-OH, -SO 3 -, -SO 3}} H, -SO 3 - Z +, -CO 2 -, -CO 2 H, -CO 2 - Z +, -CO 2 R ¹⁴ shows a -SO ₃ R ¹⁵ or -SO ₂ NR ¹² R ^13.
R ¹⁴ and R ¹⁵ each independently represent a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a halogen atom.
Z ⁺ represents ⁺ N (R ¹⁶ ) ₄ , Na ⁺ or K ⁺ .
R ¹¹ , R ¹² and R ¹³ each independently represent a hydrogen atom or a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms.
R ¹⁶ each independently represents a hydrogen atom or a monovalent saturated hydrocarbon group of 1 to 20 carbon atoms.
and p represents an integer of 0 to 4.] The process according to claim 14, wherein the compound represented by the formula (IV) is reacted with the compound represented by the formula (V) in an organic solvent having a solubility in water at 20 캜 of not more than 200 g / ℓ. A process for producing a compound represented by the formula (II-1), comprising a step of reacting a compound represented by the formula (VI), a compound represented by the formula (III) and a compound represented by the formula (V).

[In the formulas, X ¹ and X ² each independently represent a halogen atom or a trifluoromethylsulfonyloxy group.
R ²⁵ and R ²⁶ each independently represent a hydrogen atom or an alkyl group having 1 to 6 carbon atoms.
R ²⁸ is _{^{-OH, -SO 3 -, -SO 3}} H, -SO 3 - Z +, -CO 2 -, -CO 2 H, -CO 2 - Z +, -CO 2 R 14, -SO 3 R ¹⁵ or -SO ₂ represents a NR ¹² R ^13.
R ¹² and R ¹³ each independently represent a hydrogen atom or a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms.
R ¹⁴ and R ¹⁵ each independently represent a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a halogen atom.
Z ⁺ represents ⁺ N (R ¹⁶ ) ₄ , Na ⁺ or K ⁺ .
R ¹⁶ each independently represents a hydrogen atom or a monovalent saturated hydrocarbon group of 1 to 20 carbon atoms.
p represents an integer of 0 to 4;
R ³⁰ represents -SO ₂ - or -CO-.
R ²¹ , R ²² , R ²³ and R ²⁴ each independently represent a hydrogen atom, a monovalent saturated hydrocarbon group having 1 to 10 carbon atoms, a phenyl group which may have a substituent, or a group represented by the formula (ii). Provided that at least one of R ²¹ , R ²² , R ²³ or R ²⁴ is a group represented by the formula (ii).
-R ⁵⁰ -Si (R ²⁹ ) ₃ (ii)
(Wherein R ²⁹ represents a hydrogen atom, a hydroxy group, an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms, and * indicates the number of bonds with a nitrogen atom. The plurality of R ^{29 s} may be the same or different .
R ⁵⁰ represents an alkanediyl group having 1 to 10 carbon atoms, and -CH ₂ - which constitutes the alkanediyl group is -O-, -CO-, -NR ¹¹ -, -OCO-, -COO-, -OCONH- , -CONH-, or -NHCO-).
In R ²¹ , R ²² , R ²³ and R ²⁴ , the hydrogen atom contained in the monovalent saturated hydrocarbon group having 1 to 10 carbon atoms may be substituted with a halogen atom, and -CH ₂ - included in the saturated hydrocarbon group may be replaced by -O- , -CO-, -NR ¹¹ -, -OCO-, -COO-, -OCONH-, -CONH- or -NHCO-.
R ¹¹ each independently represents a hydrogen atom or a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms.
And R ³¹ represents -SO ₃ ^- or -CO ₂ ^- . The organic electroluminescent device according to claim 16, wherein the compound represented by the formula (VI), the compound represented by the formula (III) and the compound represented by the formula (V) in an organic solvent having a solubility in water at 20 캜 of 200 g / &Lt; / RTI &gt; The compound represented by the formula (VII) can be obtained by reacting the compound represented by the formula (VI) with the compound represented by the formula (III) to obtain the compound represented by the formula (VII) (II-1). &Lt; / RTI &gt;

In the formulas (VI), (III), (VII), (V) and (II-1)
X ¹ and X ² each independently represent a halogen atom or a trifluoromethylsulfonyloxy group.
R ²⁵ and R ²⁶ each independently represent a hydrogen atom or an alkyl group having 1 to 6 carbon atoms.
R ²⁸ is _{^{-OH, -SO 3 -, -SO 3}} H, -SO 3 - Z +, -CO 2 -, -CO 2 H, -CO 2 - Z +, -CO 2 R 14, -SO 3 R ¹⁵ or -SO ₂ represents a NR ¹² R ^13.
R ¹² and R ¹³ each independently represent a hydrogen atom or a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms.
R ¹⁴ and R ¹⁵ each independently represent a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a halogen atom.
Z ⁺ represents ⁺ N (R ¹⁶ ) ₄ , Na ⁺ or K ⁺ .
R ¹⁶ each independently represents a hydrogen atom or a monovalent saturated hydrocarbon group of 1 to 20 carbon atoms.
p represents an integer of 0 to 4;
R ³⁰ represents -SO ₂ - or -CO-.
R ²¹ , R ²² , R ²³ and R ²⁴ each independently represent a hydrogen atom, a monovalent saturated hydrocarbon group having 1 to 10 carbon atoms, a phenyl group which may have a substituent, or a group represented by the formula (ii). Provided that at least one of R ²¹ , R ²² , R ²³ or R ²⁴ is a group represented by the formula (ii).
-R ⁵⁰ -Si (R ²⁹ ) ₃ (ii)
(Wherein R ²⁹ represents a hydrogen atom, a hydroxy group, an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms, and * indicates the number of bonds with a nitrogen atom. The plurality of R ^{29 s} may be the same or different .
R ⁵⁰ represents an alkanediyl group having 1 to 10 carbon atoms, and -CH ₂ - which constitutes the alkanediyl group is -O-, -CO-, -NR ¹¹ -, -OCO-, -COO-, -OCONH- , -CONH-, or -NHCO-).
In R ²¹ , R ²² , R ²³ and R ²⁴ , the hydrogen atom contained in the monovalent saturated hydrocarbon group having 1 to 10 carbon atoms may be substituted with a halogen atom, and -CH ₂ - contained in the saturated hydrocarbon may be replaced by -O- , -CO-, -NR ¹¹ -, -OCO-, -COO-, -OCONH-, -CONH- or -NHCO-.
R ¹¹ each independently represents a hydrogen atom or a monovalent saturated hydrocarbon group having 1 to 20 carbon atoms.
And R ³¹ represents -SO ₃ ^- or -CO ₂ ^- .