WO2013031428A1 - トリアジン側鎖を有する新規化合物、着色組成物、インクジェット用インク、インクジェット記録方法、カラーフィルター、及びカラートナー - Google Patents
トリアジン側鎖を有する新規化合物、着色組成物、インクジェット用インク、インクジェット記録方法、カラーフィルター、及びカラートナー Download PDFInfo
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- WO2013031428A1 WO2013031428A1 PCT/JP2012/068597 JP2012068597W WO2013031428A1 WO 2013031428 A1 WO2013031428 A1 WO 2013031428A1 JP 2012068597 W JP2012068597 W JP 2012068597W WO 2013031428 A1 WO2013031428 A1 WO 2013031428A1
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- QLNURPLJGQZFAA-UHFFFAOYSA-N CN(c(c(C(c1c2cccc1)=C1)c3C2=O)ccc3Nc(cc(cc2)Nc3nc(O)nc(Nc4cc(S(O)(=O)=O)ccc4S(O)(=O)=O)n3)c2S(O)(=O)=O)C1=O Chemical compound CN(c(c(C(c1c2cccc1)=C1)c3C2=O)ccc3Nc(cc(cc2)Nc3nc(O)nc(Nc4cc(S(O)(=O)=O)ccc4S(O)(=O)=O)n3)c2S(O)(=O)=O)C1=O QLNURPLJGQZFAA-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/006—Preparation of organic pigments
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41J—TYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
- B41J2/00—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed
- B41J2/005—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed characterised by bringing liquid or particles selectively into contact with a printing material
- B41J2/01—Ink jet
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B11/00—Diaryl- or thriarylmethane dyes
- C09B11/04—Diaryl- or thriarylmethane dyes derived from triarylmethanes, i.e. central C-atom is substituted by amino, cyano, alkyl
- C09B11/10—Amino derivatives of triarylmethanes
- C09B11/24—Phthaleins containing amino groups ; Phthalanes; Fluoranes; Phthalides; Rhodamine dyes; Phthaleins having heterocyclic aryl rings; Lactone or lactame forms of triarylmethane dyes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B11/00—Diaryl- or thriarylmethane dyes
- C09B11/28—Pyronines ; Xanthon, thioxanthon, selenoxanthan, telluroxanthon dyes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
- C09D11/32—Inkjet printing inks characterised by colouring agents
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
- C09D11/32—Inkjet printing inks characterised by colouring agents
- C09D11/328—Inkjet printing inks characterised by colouring agents characterised by dyes
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- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/20—Filters
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/09—Colouring agents for toner particles
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/09—Colouring agents for toner particles
- G03G9/0906—Organic dyes
- G03G9/0914—Acridine; Azine; Oxazine; Thiazine-;(Xanthene-) dyes
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/09—Colouring agents for toner particles
- G03G9/0906—Organic dyes
- G03G9/0924—Dyes characterised by specific substituents
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/20—Filters
- G02B5/22—Absorbing filters
- G02B5/223—Absorbing filters containing organic substances, e.g. dyes, inks or pigments
Definitions
- the present invention relates to a novel compound having a triazine side chain, a coloring composition containing the compound, an inkjet ink, an inkjet recording method, a color filter, and a color toner.
- the ink jet recording method is a method of printing by causing ink droplets to fly and adhere to a recording medium such as paper as is well known.
- This printing method is capable of printing high-resolution, high-quality images at high speed and easily with an inexpensive apparatus.
- technical development has recently been carried out as an image forming method that can replace photographs. .
- inkjet inks When forming a color image using an inkjet recording method, it is common to use at least yellow ink, magenta ink, cyan ink, and black ink.
- water-based inks are mainly used for these ink-jet inks from the viewpoint of safety such as odor and fire hazard.
- These inks have physical properties such as viscosity and surface tension within an appropriate range, nozzle clogging, excellent storage stability, and a high density recording image, light resistance, ozone resistance, Properties such as excellent water resistance and moisture resistance are required.
- the magenta dye has problems that fading and color tone change due to ozone and light (sunlight, fluorescent lamp, etc.) are significantly larger than other dyes (cyan dye, yellow dye). Therefore, the ozone resistance and light resistance of magenta ink are inferior to those of other inks, resulting in a change in color tone of the entire printed image due to fading of magenta ink, resulting in a loss of quality.
- an acid dye having good color development and high water solubility such as C.I. I. Acid Red 52, 249, 289, etc. are known, but when these dyes are used alone, the nozzles are not clogged due to their high water solubility, but they are resistant to ozone, light, and moisture. Was very low.
- Patent Document 1 discloses a magenta dye ink having excellent light resistance, water resistance, color tone, clogging reliability, and the like by using a magenta dye having a triazine side chain having a specific structure.
- Patent Document 2 discloses a magenta inkjet recording liquid using a xanthene derivative substituted with an amino group which may have a substituent as a dye, which is excellent in light fastness of a color image and good. It describes that it is excellent in color tone for color reproducibility.
- An object of the present invention is to provide a dye that can further improve image fastness such as ozone resistance, light resistance, and moisture resistance, and can give a printed matter with excellent print density.
- the present inventors have found that a novel compound having a specific structure derived from a xanthene skeleton, in which a triazine unit having a specific linking group is introduced into a side chain, The present inventors have found that the performance relating to image fastness such as light resistance and moisture resistance can be further improved and a printed matter having an excellent print density can be obtained, and the present invention has been completed.
- the present invention is as follows.
- R 0 to R 3 each independently represents a hydrogen atom or a substituent.
- R 0 and R 1 , R 0 and L, or R 1 and L may be bonded to each other to form a ring.
- L represents a single bond or a divalent linking group.
- D represents a residue obtained by removing n hydrogen atoms from the compound represented by the general formula (2).
- n represents an integer of 1 or more. However, when n represents an integer of 2 or more, the plurality of R 0 to R 3 and L may be the same or different.
- R 4 to R 24 each independently represents a hydrogen atom or a substituent.
- the compound represented by the general formula (1) has at least one ionic hydrophilic group.
- R 4 , R 8 , R 9 and R 13 each independently represents a hydrogen atom or an aliphatic group, and the colored composition according to [1] above.
- R 5 to R 7 , R 10 to R 12 and R 14 to R 23 represent a hydrogen atom, and the coloring composition according to the above [1] or [2].
- R 24 represents a hydrogen atom or an ionic hydrophilic group.
- D represents R 5 to R 7 , R 10 of the compound represented by the general formula (2).
- the colored composition as described in [3] above which represents a residue obtained by removing n hydrogen atoms from hydrogen atoms as R 12 and R 24 .
- N represents an integer of 1 to 7.
- a color filter comprising a compound represented by the general formula (1) according to any one of [1] to [5] above.
- the compound represented by General formula (1) each independently represents a hydrogen atom or a substituent.
- R 0 and R 1 , R 0 and L, or R 1 and L may be bonded to each other to form a ring.
- L represents a single bond or a divalent linking group.
- D represents a residue obtained by removing n hydrogen atoms from the compound represented by the general formula (2).
- n represents an integer of 1 or more.
- R 4 to R 24 each independently represents a hydrogen atom or a substituent.
- the compound represented by the general formula (1) has at least one ionic hydrophilic group.
- a specific triazine unit that provides a printed matter with improved image fastness, such as ozone resistance, light resistance, moisture resistance, etc. of the printed matter, and excellent print density.
- a novel compound having a specific structure derived from a xanthene skeleton, a coloring composition containing the compound, an inkjet ink, and an inkjet recording method. Furthermore, a color filter and a color toner containing the novel compound are provided.
- (Substituent group A) For example, halogen atom, alkyl group, aralkyl group, alkenyl group, alkynyl group, aryl group, heterocyclic group, cyano group, hydroxyl group, nitro group, alkoxy group, aryloxy group, silyloxy group, heterocyclic oxy group, acyloxy group , Carbamoyloxy group, alkoxycarbonyloxy group, aryloxycarbonyloxy group, amino group, acylamino group, aminocarbonylamino group, alkoxycarbonylamino group, aryloxycarbonylamino group, sulfamoylamino group, alkyl or arylsulfonylamino group , Mercapto group, alkylthio group, arylthio group, heterocyclic thio group, sulfamoyl group, alkyl or arylsulfinyl group, alkyl or aryl
- examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom.
- alkyl group examples include linear, branched, and cyclic substituted or unsubstituted alkyl groups, and include cycloalkyl groups, bicycloalkyl groups, and tricyclo structures having many ring structures.
- An alkyl group (for example, an alkyl group of an alkoxy group or an alkylthio group) in a substituent described below also represents such an alkyl group.
- the alkyl group is preferably an alkyl group having 1 to 30 carbon atoms, such as a methyl group, an ethyl group, an n-propyl group, an i-propyl group, a t-butyl group, an n-octyl group, an eicosyl group.
- the cycloalkyl group is preferably a substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms, such as a cyclohexyl group, A cyclopentyl group, 4-n-dodecylcyclohexyl group and the like.
- the bicycloalkyl group is preferably a substituted or unsubstituted bicycloalkyl group having 5 to 30 carbon atoms, that is, a bicycloalkane having 5 to 30 carbon atoms.
- Monovalent groups from which one hydrogen atom has been removed for example, bicyclo [1,2,2] heptan-2-yl group, bicycl [2,2,2] octan-3-yl group.
- aralkyl group examples include a substituted or unsubstituted aralkyl group, and the substituted or unsubstituted aralkyl group is preferably an aralkyl group having 7 to 30 carbon atoms. Examples thereof include a benzyl group and a 2-phenethyl group.
- alkenyl group examples include linear, branched, and cyclic substituted or unsubstituted alkenyl groups, and include cycloalkenyl groups and bicycloalkenyl groups.
- the alkenyl group is preferably a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, such as a vinyl group, an allyl group, a prenyl group, a geranyl group, an oleyl group, and the like.
- bicycloalkenyl group a substituted or unsubstituted bicycloalkenyl group, preferably a substituted or unsubstituted bicycloalkenyl group having 5 to 30 carbon atoms, That is, a monovalent group obtained by removing one hydrogen atom of a bicycloalkene having one double bond, for example, bicyclo [2 2,1] hept-2-en-1-yl group, a bicyclo [2,2,2] oct-2-en-4-yl group and the like.
- the alkynyl group is preferably a substituted or unsubstituted alkynyl group having 2 to 30 carbon atoms, such as an ethynyl group, a propargyl group, a trimethylsilylethynyl group, and the like.
- the aryl group is preferably a substituted or unsubstituted aryl group having 6 to 30 carbon atoms, such as a phenyl group, a p-tolyl group, a naphthyl group, an m-chlorophenyl group, an o-hexadecanoylaminophenyl group, and the like. Can be mentioned.
- the heterocyclic group is preferably a monovalent group obtained by removing one hydrogen atom from a 5- or 6-membered substituted or unsubstituted aromatic or non-aromatic heterocyclic compound, and more preferably a carbon number.
- Examples thereof include 3 to 30 5- or 6-membered aromatic heterocyclic groups such as a 2-furyl group, a 2-thienyl group, a 2-pyrimidinyl group, and a 2-benzothiazolyl group.
- the alkoxy group is preferably a substituted or unsubstituted alkoxy group having 1 to 30 carbon atoms, such as a methoxy group, an ethoxy group, an isopropoxy group, a t-butoxy group, an n-octyloxy group, or a 2-methoxyethoxy group. Etc.
- the aryloxy group is preferably a substituted or unsubstituted aryloxy group having 6 to 30 carbon atoms, such as a phenoxy group, 2-methylphenoxy group, 4-t-butylphenoxy group, 3-nitrophenoxy group, 2 -Tetradecanoylaminophenoxy group and the like.
- silyloxy group examples include substituted or unsubstituted silyloxy groups having 0 to 20 carbon atoms, such as trimethylsilyloxy group and diphenylmethylsilyloxy group.
- the heterocyclic oxy group is preferably a substituted or unsubstituted heterocyclic oxy group having 2 to 30 carbon atoms, such as a 1-phenyltetrazol-5-oxy group and a 2-tetrahydropyranyloxy group.
- the acyloxy group is preferably a formyloxy group, a substituted or unsubstituted alkylcarbonyloxy group having 2 to 30 carbon atoms, a substituted or unsubstituted arylcarbonyloxy group having 6 to 30 carbon atoms, such as an acetyloxy group, Examples include pivaloyloxy group, stearoyloxy group, benzoyloxy group, p-methoxyphenylcarbonyloxy group and the like.
- the carbamoyloxy group is preferably a substituted or unsubstituted carbamoyloxy group having 1 to 30 carbon atoms, such as N, N-dimethylcarbamoyloxy group, N, N-diethylcarbamoyloxy group, morpholinocarbonyloxy group, N , N-di-n-octylaminocarbonyloxy group, Nn-octylcarbamoyloxy group and the like.
- the alkoxycarbonyloxy group is preferably a substituted or unsubstituted alkoxycarbonyloxy group having 2 to 30 carbon atoms, such as a methoxycarbonyloxy group, an ethoxycarbonyloxy group, a t-butoxycarbonyloxy group, or an n-octylcarbonyloxy group. Etc.
- aryloxycarbonyloxy group a substituted or unsubstituted aryloxycarbonyloxy group having 7 to 30 carbon atoms such as phenoxycarbonyloxy group, p-methoxyphenoxycarbonyloxy group, pn-hexadecyloxy is preferable. Examples include phenoxycarbonyloxy group.
- the amino group includes an alkylamino group, an arylamino group, and a heterocyclic amino group, preferably an amino group, a substituted or unsubstituted alkylamino group having 1 to 30 carbon atoms, a substituted or unsubstituted group having 6 to 30 carbon atoms.
- the substituted anilino group include a methylamino group, a dimethylamino group, an anilino group, an N-methyl-anilino group, a diphenylamino group, and a triazinylamino group.
- the acylamino group is preferably a formylamino group, a substituted or unsubstituted alkylcarbonylamino group having 1 to 30 carbon atoms, a substituted or unsubstituted arylcarbonylamino group having 6 to 30 carbon atoms, such as an acetylamino group, Examples include pivaloylamino group, lauroylamino group, benzoylamino group, 3,4,5-tri-n-octyloxyphenylcarbonylamino group, and the like.
- the aminocarbonylamino group is preferably a substituted or unsubstituted aminocarbonylamino group having 1 to 30 carbon atoms, such as a carbamoylamino group, N, N-dimethylaminocarbonylamino group, N, N-diethylaminocarbonylamino group. And a morpholinocarbonylamino group.
- the alkoxycarbonylamino group is preferably a substituted or unsubstituted alkoxycarbonylamino group having 2 to 30 carbon atoms, such as a methoxycarbonylamino group, an ethoxycarbonylamino group, a t-butoxycarbonylamino group, or an n-octadecyloxycarbonylamino group. Group, N-methyl-methoxycarbonylamino group and the like.
- the aryloxycarbonylamino group is preferably a substituted or unsubstituted aryloxycarbonylamino group having 7 to 30 carbon atoms, such as phenoxycarbonylamino group, p-chlorophenoxycarbonylamino group, mn-octyloxyphenoxy. Examples thereof include a carbonylamino group.
- the sulfamoylamino group is preferably a substituted or unsubstituted sulfamoylamino group having 0 to 30 carbon atoms, such as a sulfamoylamino group, N, N-dimethylaminosulfonylamino group, Nn- Examples include octylaminosulfonylamino group.
- the alkyl or arylsulfonylamino group is preferably a substituted or unsubstituted alkylsulfonylamino group having 1 to 30 carbon atoms, a substituted or unsubstituted arylsulfonylamino group having 6 to 30 carbon atoms, such as a methylsulfonylamino group.
- the alkylthio group is preferably a substituted or unsubstituted alkylthio group having 1 to 30 carbon atoms, such as a methylthio group, an ethylthio group, and an n-hexadecylthio group.
- the arylthio group is preferably a substituted or unsubstituted arylthio group having 6 to 30 carbon atoms, such as a phenylthio group, a p-chlorophenylthio group, and an m-methoxyphenylthio group.
- heterocyclic thio group examples include substituted or unsubstituted heterocyclic thio groups having 2 to 30 carbon atoms, such as 2-benzothiazolylthio group and 1-phenyltetrazol-5-ylthio group.
- the sulfamoyl group is preferably a substituted or unsubstituted sulfamoyl group having 0 to 30 carbon atoms, such as N-ethylsulfamoyl group, N- (3-dodecyloxypropyl) sulfamoyl group, N, N-dimethylsulfuryl group.
- Examples include a famoyl group, an N-acetylsulfamoyl group, an N-benzoylsulfamoyl group, and an N- (N′-phenylcarbamoyl) sulfamoyl group.
- the alkyl or arylsulfinyl group is preferably a substituted or unsubstituted alkylsulfinyl group having 1 to 30 carbon atoms, a substituted or unsubstituted arylsulfinyl group having 6 to 30 carbon atoms, such as a methylsulfinyl group, an ethylsulfinyl group, phenyl. Examples thereof include a sulfinyl group and a p-methylphenylsulfinyl group.
- the alkyl or arylsulfonyl group is preferably a substituted or unsubstituted alkylsulfonyl group having 1 to 30 carbon atoms, a substituted or unsubstituted arylsulfonyl group having 6 to 30 carbon atoms, such as a methylsulfonyl group, an ethylsulfonyl group, or a phenyl group. Examples thereof include a sulfonyl group and a p-methylphenylsulfonyl group.
- the acyl group is preferably a formyl group, a substituted or unsubstituted alkylcarbonyl group having 2 to 30 carbon atoms, a substituted or unsubstituted arylcarbonyl group having 7 to 30 carbon atoms, a substituted or unsubstituted group having 2 to 30 carbon atoms.
- Heterocyclic carbonyl groups bonded to carbonyl groups at substituted carbon atoms eg, acetyl, pivaloyl, 2-chloroacetyl, stearoyl, benzoyl, pn-octyloxyphenylcarbonyl, 2-pyridyl
- Examples thereof include a carbonyl group and a 2-furylcarbonyl group.
- the aryloxycarbonyl group is preferably a substituted or unsubstituted aryloxycarbonyl group having 7 to 30 carbon atoms, such as a phenoxycarbonyl group, an o-chlorophenoxycarbonyl group, an m-nitrophenoxycarbonyl group, pt- A butylphenoxycarbonyl group etc. are mentioned.
- the alkoxycarbonyl group is preferably a substituted or unsubstituted alkoxycarbonyl group having 2 to 30 carbon atoms, such as a methoxycarbonyl group, an ethoxycarbonyl group, a t-butoxycarbonyl group, and an n-octadecyloxycarbonyl group.
- the carbamoyl group is preferably a substituted or unsubstituted carbamoyl group having 1 to 30 carbon atoms, such as a carbamoyl group, an N-methylcarbamoyl group, an N, N-dimethylcarbamoyl group, or an N, N-di-n-octyl group.
- a carbamoyl group, an N- (methylsulfonyl) carbamoyl group, and the like can be given.
- the aryl or heterocyclic azo group is preferably a substituted or unsubstituted arylazo group having 6 to 30 carbon atoms, a substituted or unsubstituted heterocyclic azo group having 3 to 30 carbon atoms, such as phenylazo, p-chlorophenylazo, 5-ethylthio-1,3,4-thiadiazol-2-ylazo and the like.
- Preferred examples of the imide group include an N-succinimide group and an N-phthalimide group.
- the phosphino group is preferably a substituted or unsubstituted phosphino group having 0 to 30 carbon atoms, such as a dimethylphosphino group, a diphenylphosphino group, a methylphenoxyphosphino group, and the like.
- the phosphinyl group is preferably a substituted or unsubstituted phosphinyl group having 0 to 30 carbon atoms, such as a phosphinyl group, a dioctyloxyphosphinyl group, a diethoxyphosphinyl group, and the like.
- the phosphinyloxy group is preferably a substituted or unsubstituted phosphinyloxy group having 0 to 30 carbon atoms, such as a diphenoxyphosphinyloxy group and a dioctyloxyphosphinyloxy group.
- the phosphinylamino group is preferably a substituted or unsubstituted phosphinylamino group having 0 to 30 carbon atoms, such as a dimethoxyphosphinylamino group or a dimethylaminophosphinylamino group.
- silyl group examples include substituted or unsubstituted silyl groups having 0 to 30 carbon atoms, such as a trimethylsilyl group, a t-butyldimethylsilyl group, and a phenyldimethylsilyl group.
- a sulfo group, a carboxyl group, a thiocarboxyl group, a sulfino group, a phosphono group, a dihydroxyphosphino group, a quaternary ammonium group and the like can be mentioned. Particularly preferred are a sulfo group and a carboxyl group.
- the carboxyl group, phosphono group and sulfo group may be in the form of a salt. Examples of counter cations that form a salt include ammonium ion, alkali metal ion (eg, lithium ion, sodium ion, potassium ion) and organic.
- Cation eg, tetramethylammonium ion, tetramethylguanidinium ion, tetramethylphosphonium
- lithium salt, sodium salt, potassium salt, ammonium salt is preferable
- lithium salt or mixed salt containing lithium salt as a main component Are more preferred, and lithium salts are most preferred.
- the salt when the compound is a salt, the salt is dissociated into ions in the ink, but is expressed as “contains a salt” for convenience.
- the compound represented by General formula (1) of this invention is demonstrated in detail.
- the compound (pigment) represented by the general formula (1) of the present invention includes a compound, a salt thereof, and a hydrate thereof.
- the compound of the present invention has a relatively high color development and high fastness. I.
- Acid Red 289 is used as a base and a triazine unit having a specific linking group containing a sulfamoyl group is introduced, the sulfamoyl group of the linking group suppresses oxidative degradation of the dye, and images such as ozone resistance and light resistance It is a highly colored dye with outstanding fastness, and the formation of intermolecular hydrogen bonds between the dyes by the introduced triazine unit suppresses the movement of the dyes and is also excellent in moisture resistance (color transfer due to humidity). There is an effect.
- R 0 to R 3 each independently represents a hydrogen atom or a substituent.
- R 0 and R 1 , R 0 and L, or R 1 and L may be bonded to each other to form a ring.
- L represents a single bond or a divalent linking group.
- D represents a residue obtained by removing n hydrogen atoms from the compound represented by the general formula (2).
- n represents an integer of 1 or more. However, when n represents an integer of 2 or more, the plurality of R 0 to R 3 and L may be the same or different.
- R 4 to R 24 each independently represents a hydrogen atom or a substituent.
- the compound represented by the general formula (1) has at least one ionic hydrophilic group.
- R 0 to R 3 each independently represents a hydrogen atom or a substituent.
- substituents include the above-described substituent group A.
- R 0 and R 1 each independently represent a hydrogen atom or a substituent, and are a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted aralkyl group, substituted or An unsubstituted aryl group, a substituted or unsubstituted heterocyclic group, and a substituted or unsubstituted alkenyl group are preferred, a hydrogen atom, a substituted or unsubstituted alkyl group is more preferred, and a hydrogen atom is most preferred.
- R 2 and R 3 each independently represent a hydrogen atom or a substituent, preferably a hydrogen atom or the above substituent group A, and preferably a hydrogen atom, a substituted or unsubstituted amino group, a hydroxyl group, a substituted or unsubstituted alkoxy.
- a group, a substituted or unsubstituted aryloxy group, a substituted or unsubstituted alkylthio group, a substituted or unsubstituted arylthio group, and a substituted or unsubstituted heterocyclic thio group are preferred, and a substituted or unsubstituted amino group is more preferred.
- Examples of the substituent when the substituent represented by R 2 and R 3 further has a substituent include the substituent group A, and an alkyl group, an aryl group, or a heterocyclic group is preferable. These may be further substituted with the substituent group A, and more preferably substituted with an ionic hydrophilic group.
- At least one of R 0 to R 3 is preferably a group having a sulfonic acid group, a carboxyl group, or an ionic hydrophilic group as a substituent.
- the ionic hydrophilic group include a sulfo group, a carboxyl group, a phosphono group, and a quaternary ammonium group.
- a carboxyl group, a phosphono group, and a sulfo group are preferable, and a carboxyl group and a sulfo group are particularly preferable.
- the carboxyl group, phosphono group and sulfo group may be in the form of a salt.
- Examples of the counter ion forming the salt include ammonium ion, alkali metal ion (eg, lithium ion, sodium ion, potassium ion) and organic cation. (Eg, tetramethylammonium ion, tetramethylguanidinium ion, tetramethylphosphonium).
- alkali metal salts are preferable, and lithium ions are particularly preferable because they increase the solubility of the compound and improve the ink stability.
- ionic hydrophilic groups those having at least two in one molecule of the compound represented by the general formula (1) are preferable, and in particular, at least two ionic hydrophilic groups selected from a sulfo group and a carboxyl group are included. Those having ⁇ 8 are preferred, and those having 2 ⁇ 4 are particularly preferred.
- R 0 and R 1 , R 0 and L, or R 1 and L may be bonded to each other to form a ring.
- the ring formed by combining R 0 and R 1 , R 0 and L, or R 1 and L is preferably a 5- to 10-membered ring, more preferably a 5- or 6-membered ring.
- R 0 and R 1 , R 0 and L, or R 1 and L are bonded to each other to form a ring
- R 0 and R 1 are preferably alkylene groups.
- the ring formed may have a substituent, and examples of the substituent include the substituent group A, and an alkyl group is preferable.
- L is a trivalent linking group
- the trivalent linking group is a divalent linking as L described later.
- L represents a single bond or a divalent linking group.
- divalent linking groups include oxy group (—O—), thio group (—S—), carbonyl group (—CO—), sulfonyl group (—SO 2 —), imino group (—NH—), alkylene A group (preferably an alkylene group having 1 to 10 carbon atoms, more preferably an alkylene group having 2 to 6 carbon atoms), an arylene group (preferably an arylene group having 6 to 20 carbon atoms, more preferably an arylene group having 6 to 10 carbon atoms).
- a cycloalkylene group (preferably a cycloalkylene group having 3 to 15 carbon atoms, more preferably a cycloalkylene group having 5 to 10 carbon atoms), and a group formed by a combination thereof.
- substituent groups may have a substituent, and examples of the substituent include the substituent group A, and an alkyl group is preferable.
- L is preferably an alkylene group having 1 to 10 carbon atoms which may have a substituent, or an arylene group having 6 to 10 carbon atoms which may have a substituent, more preferably a substituent.
- D represents a residue obtained by removing n hydrogen atoms from the compound represented by the general formula (2).
- n represents an integer of 1 or more.
- n is preferably an integer of 1 to 7, more preferably an integer of 1 to 4, still more preferably an integer of 1 to 3, and particularly preferably 1 or 2.
- R 4 to R 24 each independently represents a hydrogen atom or a substituent.
- substituent include the above-described substituent group A.
- R 4 , R 8 , R 9 and R 13 preferably each independently represent a hydrogen atom or an aliphatic group.
- the aliphatic group may be unsubstituted or substituted, may be saturated or unsaturated, is preferably an aliphatic group having 1 to 20 carbon atoms, and is an alkyl group having 1 to 20 carbon atoms. Is more preferable, and an alkyl group having 1 to 10 carbon atoms is more preferable.
- R 4 , R 8 , R 9 and R 13 each independently preferably represent an aliphatic group from the viewpoint of hue.
- R 5 to R 7 , R 10 to R 12 and R 14 to R 23 preferably represent a hydrogen atom from the viewpoint of ease of synthesis.
- R 24 preferably represents a hydrogen atom or an ionic hydrophilic group.
- D is a residue obtained by removing n hydrogen atoms from the hydrogen atoms as R 5 to R 7 , R 10 to R 12 and R 24 of the compound represented by the general formula (2). It is preferable to represent a group from the viewpoint of ease of synthesis and hue.
- n represents an integer of 1 to 7.
- n is preferably an integer of 1 to 4, more preferably an integer of 1 to 3, and particularly preferably 1 or 2. When n is 1 or more, the moisture resistance is improved.
- D is preferably a residue obtained by removing at least one hydrogen atom from hydrogen atoms as R 10 to R 12 and R 24 of the compound represented by the general formula (2).
- R 24 is not a hydrogen atom for removing a hydrogen atom from a compound represented by the general formula (2) to form a residue, it is more preferably an ionic hydrophilic group.
- a, b and c each represent the ratio of each substituent introduced as the substituent R in the compound of the present invention represented by the general formula (1) obtained.
- the method for synthesizing the compound of the present invention is not particularly limited, and for example, the methods described in [0154] to [0169] of JP-A No. 2010-254964 can be used.
- the coloring composition of the present invention contains at least one compound represented by the above general formula (1) of the present invention.
- the coloring composition of the present invention can contain a medium, but is particularly suitable as an inkjet ink when a solvent is used as the medium.
- the coloring composition of the present invention can be prepared by dissolving and / or dispersing the compound of the present invention in a lipophilic medium or an aqueous medium as a medium. Preferably, an aqueous medium is used.
- the coloring composition of the present invention includes an ink composition excluding a medium.
- the content of the compound of the present invention contained in the colored composition is determined by the type of substituent in the general formula (1) used, the type of solvent component used for producing the colored composition, and the like.
- the content of the compound represented by the general formula (1) or the salt thereof in the colored composition is preferably 1 to 10% by mass with respect to the total mass of the colored composition, and is preferably 2 to 6% by mass. % Is more preferable.
- the content of the compound represented by the general formula (1) contained in the coloring composition 1% by mass or more, it is possible to improve the color developability of the ink on the recording medium when printed, and it is necessary. Image density can be ensured.
- the total amount of the compounds represented by the general formula (1) contained in the coloring composition is 10% by mass or less, the discharging property of the coloring composition can be improved when used in the ink jet recording method. In addition, it is possible to obtain an effect such that the inkjet nozzle is not easily clogged.
- the coloring composition of the present invention may contain other additives as necessary within a range that does not impair the effects of the present invention.
- other additives include additives that can be used in the inkjet ink described below.
- the present invention also relates to an inkjet ink (more specifically, an inkjet recording ink) containing the coloring composition of the present invention.
- the inkjet ink can be prepared by dissolving and / or dispersing the compound (mixture) of the present invention in a lipophilic medium or an aqueous medium.
- the ink uses an aqueous medium. If necessary, other additives are contained within a range that does not impair the effects of the present invention.
- additives include, for example, anti-drying agents (wetting agents), anti-fading agents, emulsion stabilizers, penetration enhancers, ultraviolet absorbers, preservatives, anti-fungal agents, pH adjusters, surface tension adjusters, Well-known additives, such as a foaming agent, a viscosity modifier, a dispersing agent, a dispersion stabilizer, a rust preventive agent, a chelating agent, are mentioned. These various additives are directly added to the ink liquid in the case of water-soluble ink. When an oil-soluble dye is used in the form of a dispersion, it is generally added to the dispersion after the preparation of the dye dispersion, but it may be added to the oil phase or the aqueous phase at the time of preparation.
- the anti-drying agent is preferably used for the purpose of preventing clogging due to drying of the ink-jet ink at the ink jet port of the nozzle used in the ink-jet recording method.
- a water-soluble organic solvent having a vapor pressure lower than that of water is preferable.
- Specific examples include ethylene glycol, propylene glycol, diethylene glycol, polyethylene glycol, thiodiglycol, dithiodiglycol, 2-methyl-1,3-propanediol, 1,2,6-hexanetriol, acetylene glycol derivatives, glycerin.
- Polyhydric alcohols typified by trimethylolpropane, etc., lower alkyl ethers of polyhydric alcohols such as ethylene glycol monomethyl (or ethyl) ether, diethylene glycol monomethyl (or ethyl) ether, triethylene glycol monoethyl (or butyl) ether 2-pyrrolidone, N-methyl-2-pyrrolidone, 1,3-dimethyl-2-imidazolidinone, heterocyclic rings such as N-ethylmorpholine, sulfolane, dimethyl sulfoxide, 3 Sulfur-containing compounds such as sulfolane, diacetone alcohol, polyfunctional compounds such as diethanolamine, and urea derivatives.
- lower alkyl ethers of polyhydric alcohols such as ethylene glycol monomethyl (or ethyl) ether, diethylene glycol monomethyl (or ethyl) ether, triethylene glycol monoethyl (or butyl)
- polyhydric alcohols such as glycerin and diethylene glycol are more preferred.
- said anti-drying agent may be used independently and may be used together 2 or more types. These drying inhibitors are preferably contained in the ink in an amount of 10 to 50% by mass.
- the penetration accelerator is preferably used for the purpose of allowing the ink for inkjet to penetrate better into the paper.
- penetration enhancers alcohols such as ethanol, isopropanol, butanol, di (tri) ethylene glycol monobutyl ether, 1,2-hexanediol, sodium lauryl sulfate, sodium oleate, nonionic surfactants, etc. can be used. . If these are contained in the ink in an amount of 5 to 30% by mass, they usually have a sufficient effect, and it is preferable to use them in an additive amount range that does not cause printing bleeding or paper loss (print-through).
- UV absorbers are used for the purpose of improving image storage stability.
- examples of the ultraviolet absorber include benzotriazoles described in JP-A Nos. 58-185677, 61-190537, JP-A-2-782, JP-A-5-97075, JP-A-9-34057, and the like.
- the anti-fading agent is used for the purpose of improving image storage stability.
- various organic and metal complex anti-fading agents can be used.
- Organic anti-fading agents include hydroquinones, alkoxyphenols, dialkoxyphenols, phenols, anilines, amines, indanes, chromans, alkoxyanilines, heterocycles, etc. Complex, zinc complex and the like. More specifically, Research Disclosure No. No. 17643, No. VII, I to J, ibid. 15162, ibid. No. 18716, page 650, left column, ibid. No. 36544, page 527, ibid. No. 307105, page 872, ibid. The compounds described in the patent cited in Japanese Patent No. 15162 and the compounds represented by the general formulas and compound examples of the representative compounds described on pages 127 to 137 of JP-A-62-215272 can be used.
- antifungal agent examples include sodium dehydroacetate, sodium benzoate, sodium pyridinethione-1-oxide, ethyl p-hydroxybenzoate, 1,2-benzisothiazolin-3-one and salts thereof. These are preferably used in an amount of 0.02 to 1.00% by mass in the ink.
- the neutralizing agent organic base, inorganic alkali
- the pH adjuster is preferably added so that the inkjet ink has a pH of 6 to 10, and more preferably added to have a pH of 7 to 10.
- the surface tension adjusting agent includes nonionic, cationic or anionic surfactants.
- the surface tension of the inkjet ink of the present invention is preferably 25 to 70 mN / m. Further, 25 to 60 mN / m is preferable.
- the viscosity of the inkjet ink of the present invention is preferably 30 mPa ⁇ s or less. Furthermore, it is more preferable to adjust to 20 mPa ⁇ s or less.
- surfactants include fatty acid salts, alkyl sulfate esters, alkyl benzene sulfonates, alkyl naphthalene sulfonates, dialkyl sulfosuccinates, alkyl phosphate ester salts, naphthalene sulfonate formalin condensates, polyoxyethylene alkyl sulfates.
- Anionic surfactants such as ester salts, polyoxyethylene alkyl ether, polyoxyethylene alkyl allyl ether, polyoxyethylene fatty acid ester, sorbitan fatty acid ester, polyoxyethylene sorbitan fatty acid ester, polyoxyethylene alkylamine, glycerin fatty acid ester
- Nonionic surfactants such as oxyethyleneoxypropylene block copolymers are preferred.
- SURFYNOLS Air Products & Chemicals
- An amine oxide type amphoteric surfactant such as N, N-dimethyl-N-alkylamine oxide is also preferred.
- fluorine-based, silicone-based compounds, chelating agents represented by EDTA, and the like can be used as necessary.
- the compound of the present invention is dispersed in an aqueous medium, as described in JP-A Nos. 11-286637, 2000-78491, 2000-80259, 2000-62370, etc.
- Colored fine particles containing a compound and an oil-soluble polymer are dispersed in an aqueous medium, or as described in Japanese Patent Application Nos. 2000-78454, 2000-78491, 2000-203856, and 2000-203857.
- the compound of the present invention dissolved in a high boiling point organic solvent is dispersed in an aqueous medium.
- the specific method for dispersing the compound of the present invention in an aqueous medium, the oil-soluble polymer to be used, the high-boiling organic solvent, the additive, and the amount used thereof are preferably those described in the above-mentioned patent publications. be able to.
- the compound of the present invention may be dispersed in a fine particle state as a solid. At the time of dispersion, a dispersant or a surfactant can be used.
- Dispersing devices include simple stirrer, impeller stirring method, in-line stirring method, mill method (for example, colloid mill, ball mill, sand mill, attritor, roll mill, agitator mill, etc.), ultrasonic method, high pressure emulsification dispersion method (high pressure homogenizer)
- mill method for example, colloid mill, ball mill, sand mill, attritor, roll mill, agitator mill, etc.
- ultrasonic method for example, colloid mill, ball mill, sand mill, attritor, roll mill, agitator mill, etc.
- ultrasonic method for example, colloid mill, ball mill, sand mill, attritor, roll mill, agitator mill, etc.
- ultrasonic method for example, colloid mill, ball mill, sand mill, attritor, roll mill, agitator mill, etc.
- high pressure homogenizer high pressure homogenizer
- Specific examples of commercially available devices include gorin homogenizers, microfluid
- a mixture containing water as a main component and optionally adding a water-miscible organic solvent can be used.
- the water-miscible organic solvent include alcohol (eg, methanol, ethanol, propanol, isopropanol, butanol, isobutanol, sec-butanol, t-butanol, pentanol, hexanol, cyclohexanol, benzyl alcohol), polyvalent Alcohols (eg, ethylene glycol, diethylene glycol, triethylene glycol, polyethylene glycol, propylene glycol, dipropylene glycol, polypropylene glycol, butylene glycol, hexanediol, pentanediol, glycerin, hexanetriol, thiodiglycol), glycol derivatives (eg , Ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene
- the compound of the present invention is preferably contained in an amount of 0.2 parts by mass or more and 10 parts by mass or less, more preferably 1 part by mass or more and 6 parts by mass or less.
- other pigments may be used in combination with the compound of the present invention.
- the total content of the dyes is preferably within the above range.
- the inkjet ink of the present invention preferably has a viscosity of 30 mPa ⁇ s or less.
- the surface tension is preferably 25 mN / m or more and 70 mN / m or less.
- Viscosity and surface tension are various additives such as viscosity modifiers, surface tension modifiers, specific resistance modifiers, film modifiers, UV absorbers, antioxidants, antifading agents, antifungal agents, and rust inhibitors. It can be adjusted by adding a dispersant and a surfactant.
- the ink-jet ink of the present invention can be used not only for forming a single color image but also for forming a full color image.
- a magenta color ink, a cyan color ink, and a yellow color ink can be used, and a black color ink may be further used to adjust the color tone.
- Any applicable yellow dye can be used.
- coupler components as coupling components (hereinafter referred to as coupler components); for example, coupler components Azomethine dyes having open-chain type active methylene compounds as examples; methine dyes such as benzylidene dyes and monomethine oxonol dyes; quinone dyes such as naphthoquinone dyes and anthraquinone dyes, and other dyes Examples of the species include quinophthalone dyes, nitro / nitroso dyes, acridine dyes, and acridinone dyes.
- coupler components Azomethine dyes having open-chain type active methylene compounds as examples; methine dyes such as benzylidene dyes and monomethine oxonol dyes; quinone dyes such as naphthoquinone dyes and anthraquinone dyes, and other dyes Examples of the species include quinophthalone dyes, nitro / nitroso dyes, acri
- magenta dye Any applicable magenta dye can be used.
- aryl or heteryl azo dyes having phenols, naphthols, anilines, etc. as coupler components for example, azomethine dyes having pyrazolones, pyrazolotriazoles, etc.
- coupler components for example arylidene dyes, styryl dyes, merocyanine dyes, cyanine dyes, Methine dyes such as oxonol dyes; Carbonium dyes such as diphenylmethane dyes, triphenylmethane dyes, xanthene dyes, etc., quinone dyes such as naphthoquinone, anthraquinone, anthrapyridone, etc., condensed polycycles such as dioxazine dyes, etc. And dyes.
- arylidene dyes for example arylidene dyes, styryl dyes, merocyanine dyes, cyanine dyes, Methine dyes such as oxonol dyes; Carbonium dyes such as diphenylmethane dyes, triphenylmethane dyes, xanthene dyes, etc., quinone dyes such as naphthoquinone, an
- cyan dye can be used.
- aryl or heteryl azo dyes having phenols, naphthols, anilines and the like as coupler components for example, azomethine dyes having phenols, naphthols, heterocyclic rings such as pyrrolotriazole as coupler components; cyanine dyes, oxonol dyes, Polymethine dyes such as merocyanine dyes; carbonium dyes such as diphenylmethane dyes, triphenylmethane dyes, xanthene dyes; phthalocyanine dyes; anthraquinone dyes; indigo / thioindigo dyes.
- each of the above dyes may exhibit yellow, magenta, and cyan colors only after a part of the chromophore is dissociated.
- the counter cation is an alkali metal or an inorganic cation such as ammonium.
- it may be an organic cation such as pyridinium or a quaternary ammonium salt, and may further be a polymer cation having these in a partial structure.
- Applicable black materials include disazo, trisazo, tetraazo dyes, and carbon black dispersions.
- the ink composition of the present invention can be used for recording methods such as printing, copying, marking, writing, drawing, stamping and the like, and is particularly suitable for use in an ink jet recording method.
- the present invention also relates to an inkjet recording method for forming an image using the colored composition or the inkjet ink of the present invention.
- energy is supplied to the ink jet ink, and a known image receiving material, that is, plain paper, resin coated paper, such as JP-A-8-169172, JP-A-8-27693, -276670, 7-276789, 9-323475, JP-A-62-238783, JP-A-10-153789, JP-A-10-217473, JP-A-10-235995, Form images on dedicated inkjet paper, film, electrophotographic co-paper, fabric, glass, metal, ceramics, etc. described in JP-A-10-337947, JP-A-10-217597, JP-A-10-337947, etc. .
- a polymer fine particle dispersion (also referred to as polymer latex) may be used in combination for the purpose of imparting glossiness or water resistance or improving weather resistance.
- the timing of applying the polymer latex to the image receiving material may be before, after, or simultaneously with the application of the colorant, and therefore the addition place may be in the image receiving paper. It may be in ink or may be used as a liquid material of polymer latex alone.
- the method described in the specification can be preferably used.
- the support in recording paper and recording film is made of chemical pulp such as LBKP and NBKP, mechanical pulp such as GP, PGW, RMP, TMP, CTMP, CMPMP, CGP, and waste paper pulp such as DIP.
- Additives such as known pigments, binders, sizing agents, fixing agents, cationic agents, paper strength enhancers, etc. can be mixed and manufactured using various devices such as long net paper machines and circular net paper machines. is there.
- either synthetic paper or plastic film sheets may be used.
- the thickness of the support is preferably 10 to 250 ⁇ m and the basis weight is preferably 10 to 250 g / m 2 .
- the support may be provided with an ink receiving layer and a backcoat layer as they are, or after a size press or anchor coat layer is provided with starch, polyvinyl alcohol or the like, an ink receiving layer and a backcoat layer may be provided. Further, the support may be flattened by a calendar device such as a machine calendar, a TG calendar, or a soft calendar.
- a calendar device such as a machine calendar, a TG calendar, or a soft calendar.
- paper and plastic films laminated on both sides with polyolefin for example, polyethylene, polystyrene, polyethylene terephthalate, polybutene and copolymers thereof
- a white pigment for example, titanium oxide or zinc oxide
- a tinting dye for example, cobalt blue, ultramarine blue, or neodymium oxide
- the ink receiving layer provided on the support contains a pigment and an aqueous binder.
- a white pigment is preferable, and as the white pigment, calcium carbonate, kaolin, talc, clay, diatomaceous earth, synthetic amorphous silica, aluminum silicate, magnesium silicate, calcium silicate, aluminum hydroxide, alumina, lithopone, zeolite, Examples thereof include white inorganic pigments such as barium sulfate, calcium sulfate, titanium dioxide, zinc sulfide and zinc carbonate, and organic pigments such as styrene pigments, acrylic pigments, urea resins and melamine resins.
- porous inorganic pigments are preferable, and synthetic amorphous silica having a large pore area is particularly preferable.
- synthetic amorphous silica either anhydrous silicic acid obtained by a dry production method or hydrous silicic acid obtained by a wet production method can be used, but it is particularly desirable to use hydrous silicic acid.
- aqueous binder contained in the ink receiving layer examples include water-soluble polyvinyl alcohol, silanol-modified polyvinyl alcohol, starch, cationized starch, casein, gelatin, carboxymethylcellulose, hydroxyethylcellulose, polyvinylpyrrolidone, polyalkylene oxide, polyalkylene oxide derivatives, and the like.
- Water-dispersible polymers such as water-soluble polymers, styrene butadiene latexes, and acrylic emulsions. These aqueous binders can be used alone or in combination of two or more.
- polyvinyl alcohol and silanol-modified polyvinyl alcohol are particularly preferable in terms of adhesion to the pigment and resistance to peeling of the ink receiving layer.
- the ink receiving layer can contain a mordant, a water resistance agent, a light resistance improver, a surfactant, and other additives in addition to the pigment and the aqueous binder.
- the mordant added to the ink receiving layer is preferably immobilized.
- a polymer mordant is preferably used.
- the polymer mordant JP-A-48-28325, JP-A-54-74430, JP-A-54-124726, JP-A-55-22766, JP-A-55-142339, JP-A-60-23850, JP-A-60-23851, 60-23852, 60-23835, 60-57836, 60-60643, 60-118834, 60-122940, 60-122941, 60-122942, 60- No. 235134, JP-A-1-161236, U.S. Pat.Nos.
- the water-proofing agent is effective for making the image water-resistant.
- cationic resins are particularly desirable.
- examples of such cationic resins include polyamide polyamine epichlorohydrin, polyethyleneimine, polyamine sulfone, dimethyl diallyl ammonium chloride polymer, cationic polyacrylamide, colloidal silica, etc.
- polyamide polyamine epichlorohydrin is particularly preferable. is there.
- the content of these cationic resins is preferably 1 to 15% by mass, particularly 3 to 10% by mass, based on the total solid content of the ink receiving layer.
- the light resistance improver examples include zinc sulfate, zinc oxide, hindered amine antioxidants, and benzotriazole ultraviolet absorbers such as benzophenone. Of these, zinc sulfate is particularly preferred.
- the surfactant functions as a coating aid, a peelability improver, a slippage improver or an antistatic agent.
- Surfactants are described in JP-A Nos. 62-173463 and 62-183457.
- An organic fluoro compound may be used in place of the surfactant.
- the organic fluoro compound is preferably hydrophobic.
- Examples of the organic fluoro compound include a fluorine-based surfactant, an oily fluorine-based compound (for example, fluorine oil), and a solid fluorine compound resin (for example, tetrafluoroethylene resin).
- the organic fluoro compounds are described in JP-B-57-9053 (columns 8 to 17), JP-A-61-2994 and JP-A-62-135826.
- the ink receiving layer may be one layer or two layers.
- Recording paper and recording film can be provided with a backcoat layer, and examples of components that can be added to this layer include white pigments, aqueous binders, and other components.
- white pigments contained in the backcoat layer include light calcium carbonate, heavy calcium carbonate, kaolin, talc, calcium sulfate, barium sulfate, titanium dioxide, zinc oxide, zinc sulfide, zinc carbonate, satin white, and aluminum silicate.
- White inorganic pigments such as diatomaceous earth, calcium silicate, magnesium silicate, synthetic amorphous silica, colloidal silica, colloidal alumina, pseudoboehmite, aluminum hydroxide, alumina, lithopone, zeolite, hydrous halloysite, magnesium carbonate, magnesium hydroxide
- organic pigments such as styrene plastic pigment, acrylic plastic pigment, polyethylene, microcapsule, urea resin and melamine resin.
- aqueous binder contained in the backcoat layer As the aqueous binder contained in the backcoat layer, styrene / maleate copolymer, styrene / acrylate copolymer, polyvinyl alcohol, silanol modified polyvinyl alcohol, starch, cationized starch, casein, gelatin, carboxymethylcellulose Water-soluble polymers such as hydroxyethyl cellulose and polyvinyl pyrrolidone, and water-dispersible polymers such as styrene butadiene latex and acrylic emulsion. Examples of other components contained in the backcoat layer include an antifoaming agent, an antifoaming agent, a dye, a fluorescent brightening agent, a preservative, and a water-proofing agent.
- Polymer latex may be added to the constituent layers (including the backcoat layer) of the inkjet recording paper and recording film.
- the polymer latex is used for the purpose of improving film physical properties such as dimensional stabilization, curling prevention, adhesion prevention, and film cracking prevention.
- the polymer latex is described in JP-A Nos. 62-245258, 62-136648, and 62-110066.
- a polymer latex having a low glass transition temperature 40 ° C. or lower
- cracking and curling of the layer can be prevented.
- curling can be prevented by adding a polymer latex having a high glass transition temperature to the backcoat layer.
- the ink of the present invention is not limited to an ink jet recording system, and is a known system, for example, a charge control system that discharges ink using electrostatic attraction, a drop-on-demand system (pressure) that uses the vibration pressure of a piezo element.
- Pulse method acoustic ink jet method that converts electrical signal into acoustic beam and irradiates ink and uses ink to discharge ink
- thermal ink jet that heats ink to form bubbles and uses generated pressure Used for systems.
- Inkjet recording methods use a method of ejecting a large number of low-density inks called photo inks in a small volume, a method of improving image quality using a plurality of inks having substantially the same hue and different concentrations, and colorless and transparent inks. The method is included.
- the present invention also relates to a color filter containing the compound represented by the general formula (1).
- a method for forming a color filter a pattern is first formed with a photoresist and then dyed, or disclosed in JP-A-4-163552, JP-A-4-128703, and JP-A-4-175653.
- a method of forming a pattern with a photoresist to which a dye is added Any of these methods may be used as a method used for introducing the compound of the present invention into a color filter. Preferred methods are described in JP-A-4-175753 and JP-A-6-35182.
- the positive resist composition comprising a thermosetting resin, a quinonediazide compound, a cross-linking agent, a dye and a solvent, and after coating on a substrate, exposing through a mask and developing the exposed portion. Then, a positive resist pattern is formed, the positive resist pattern is exposed on the entire surface, and then the exposed positive resist pattern is cured, and a color filter forming method can be mentioned.
- a black matrix is formed according to a conventional method, and an RGB primary color system or Y, M, C complementary color system color filter can be obtained.
- the amount of the compound of the present invention is not limited but is preferably 0.1 to 50% by mass.
- thermosetting resin quinonediazide compound, cross-linking agent, and solvent used in this case and the amounts used thereof are preferably those described in the above-mentioned patent documents.
- the present invention also relates to a color toner containing the compound represented by the general formula (1).
- the content of the compound of the present invention in 100 parts by weight of the color toner is not particularly limited, but it is preferably 0.1 parts by weight or more, more preferably 1 to 20 parts by weight, and 2 to 10 parts by weight. Is most preferred.
- the binder resin for a color toner into which the compound of the present invention is introduced all commonly used binders can be used. Examples thereof include styrene resin, acrylic resin, styrene / acrylic resin, and polyester resin. Inorganic fine powders and organic fine particles may be externally added to the toner for the purpose of improving fluidity and controlling charging.
- Silica fine particles and titania fine particles whose surface is treated with an alkyl group-containing coupling agent or the like are preferably used. These have a number average primary particle size of preferably 10 to 500 nm, and more preferably 0.1 to 20% by mass in the toner.
- release agent all conventionally used release agents can be used. Specific examples include olefins such as low molecular weight polypropylene, low molecular weight polyethylene, and ethylene-propylene copolymer, microcrystalline wax, carnauba wax, sazole wax, and paraffin wax. These addition amounts are preferably 1 to 5% by mass in the toner.
- the charge control agent may be added as necessary, but is preferably colorless from the viewpoint of color development. Examples thereof include those having a quaternary ammonium salt structure and those having a calixarene structure.
- the carrier either an uncoated carrier composed only of magnetic material particles such as iron or ferrite, or a resin-coated carrier in which the magnetic material particle surface is coated with a resin or the like may be used.
- the average particle diameter of this carrier is preferably 30 to 150 ⁇ m in terms of volume average particle diameter.
- the image forming method to which the toner is applied is not particularly limited.
- a method of forming a color image by repeatedly forming a color image on a photoconductor to form an image, or an image formed on a photoconductor For example, a method of sequentially transferring to an intermediate transfer member or the like and forming a color image on the intermediate transfer member or the like and then transferring it to an image forming member such as paper to form a color image, or the like.
- the reaction solution was allowed to react at room temperature for 2 hours while maintaining the pH at 4.5 using an aqueous 2N sodium hydroxide solution. Insoluble matters were removed with a Whatman GF / F filter, and then 16.8 g of dimethylamine was added, followed by stirring overnight at room temperature. The reaction solution was heated to an internal temperature of 40 ° C., 90 g of dimethylamine was added thereto, and the mixture was reacted at 60 ° C. for 30 minutes. Sodium chloride corresponding to 10% of the total mass was added, and the pH was adjusted to 1 using concentrated hydrochloric acid.
- reaction solution was cooled to room temperature, slowly dropped into 250 g of ice water in which 25 g of sodium chloride was dissolved, and the precipitated crystals were collected by filtration and washed with cold saturated brine to obtain a wet cake of intermediate B.
- intermediate A 2.56 g was dispersed in 100 mL of water in a 500 mL flask, adjusted to pH 8.5 with 2N sodium hydroxide, and dissolved. The whole amount of the intermediate B wet cake was added thereto.
- the pH was adjusted to 9.0 using sodium hydroxide, then the internal temperature was raised to 50 ° C. and the mixture was stirred for 90 minutes while maintaining the pH at 9.0, then adjusted to pH 12 and stirred overnight.
- the internal temperature was cooled to 30 ° C.
- insoluble matter was removed with a Whatman qualitative filter paper, and the pH of the resulting aqueous solution was adjusted to 8.0 using hydrochloric acid water.
- salting out was performed by adding sodium chloride having a weight corresponding to 20% of the volume.
- the precipitated crystals are separated by filtration, redissolved in 250 mL of water, and the resulting aqueous solution is purified by dialysis until the electric conductivity is 10 ⁇ S or less. Thereafter, the aqueous solution is passed through a Whatman GF / F filter, and then 60 The oven moisture at 0 ° C.
- Example 1 Deionized water was added to the following ingredients to make 100 g, followed by stirring for 1 hour while heating at 30 to 40 ° C. Thereafter, the pH was adjusted to 9 with KOH 10 mol / L, and the mixture was filtered under reduced pressure through a microfilter having an average pore size of 0.25 ⁇ m to prepare a magenta ink liquid.
- the ink liquids B to E and the ink liquids F to I were used as the ink liquids for comparison using the following compounds in the same manner as the preparation of the ink liquid A. It was adjusted.
- the dyes used in ink liquids B to E are sodium salts of exemplary compounds described in Table 11 below.
- ⁇ Ozone resistance> While passing dry air through the double glass tube of the Siemens type ozonizer, an AC voltage of 5 kV was applied, and using this, the ozone gas concentration was 0.5 ⁇ 0.1 ppm, the room temperature was set in a dark place, The photo glossy paper on which the image was formed was allowed to stand for 7 days, and the image density before and after being left under ozone gas was measured using a reflection densitometer (X-Rite 310TR) and evaluated as a dye residual ratio. The reflection density was measured at three points of 1, 1.5 and 2.0.
- the ozone gas concentration in the box was set using an ozone gas monitor (model: OZG-EM-01) manufactured by APPLICS. The evaluation was made in three stages, with A being a dye residual ratio of 70% or more at any concentration, A being 1 or 2 points being less than 70% B, and C being less than 70% at all concentrations.
- ⁇ Moisture resistance> During inkjet recording, a check pattern (a pattern in which squares having a 1.5 mm square with a density of 100% and 0% were alternately combined) was created to obtain a magenta-white check pattern print with high contrast. . After printing, the printed matter with the check pattern dried for 24 hours is allowed to stand for 3 days under the condition of 80 ° C. and 70% RH, and the degree of bleeding from the colored portion to the white portion is visually evaluated. Evaluation was made in three stages, where B was slightly blurred and C was clearly blurred.
- ⁇ Print density> The print density at a print density of 100% is measured using a reflection densitometer (X-Rite 310TR), and when the print density is 2.2 or more, A, when 2.0 or less and less than 2.2, B.2. A case of less than 0 was evaluated as C, and evaluated in three stages.
- the inks of the examples using the dyes of the present invention have excellent ozone resistance, light resistance, moisture resistance, and print density performance, and are compared with other comparative examples. Thus, it can be seen that it has extremely high performance.
- the present invention it is possible to provide a dye that can further improve image fastness such as ozone resistance, light resistance and moisture resistance, and can give a printed matter having an excellent print density.
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Abstract
Description
また特許文献2には、置換基を有していてもよいアミノ基で置換されたキサンテン誘導体を色素とするマゼンタ色のインクジェット記録液が開示されており、色画像の耐光性に優れ、良好な色再現性のための色調に優れることが記載されている。
本発明は、耐オゾン性、耐光性、耐湿性をはじめとする画像堅牢性が更に改良され、更に印画濃度に優れた印画物を与える色素を提供することを目的とする。
一般式(1)で表される化合物を含有する、着色組成物。
Lは、単結合又は2価の連結基を表す。
Dは、一般式(2)で表される化合物から水素原子をn個取り除いた残基を表す。
nは、1以上の整数を表す。但し、nが2以上の整数を表す場合、複数のR0~R3及びLは、それぞれ同一でも異なっていてもよい。
一般式(2)中、R4~R24はそれぞれ独立に、水素原子又は置換基を表す。
但し、一般式(1)で表される化合物は、少なくとも1個のイオン性親水性基を有する。
〔2〕
一般式(2)中、R4、R8、R9及びR13はそれぞれ独立に、水素原子又は脂肪族基を表す、上記〔1〕に記載の着色組成物。
〔3〕
一般式(2)中、R5~R7、R10~R12及びR14~R23は水素原子を表す、上記〔1〕又は〔2〕に記載の着色組成物。
〔4〕
一般式(2)中、R24は、水素原子又はイオン性親水性基を表し、一般式(1)中、Dは一般式(2)で表される化合物のR5~R7、R10~R12及びR24としての水素原子から、水素原子をn個取り除いた残基を表す、上記〔3〕に記載の着色組成物。但し、nは1~7の整数を表す。
〔5〕
一般式(1)中、Lは、置換基を有していてもよい炭素数1~10のアルキレン基を表す、上記〔1〕~〔4〕のいずれか1項に記載の着色組成物。
〔6〕
上記〔1〕~〔5〕のいずれか1項に記載の着色組成物を含有するインクジェット用インク。
〔7〕
上記〔1〕~〔5〕のいずれか1項に記載の着色組成物又は上記〔6〕に記載のインクジェット用インクを用いて、画像形成するインクジェット記録方法。
〔8〕
上記〔1〕~〔5〕のいずれか1項に記載の一般式(1)で表される化合物を含有するカラーフィルター。
〔9〕
上記〔1〕~〔5〕のいずれか1項に記載の一般式(1)で表される化合物を含有するカラートナー。
〔10〕
一般式(1)で表される化合物。
Lは、単結合又は2価の連結基を表す。
Dは、一般式(2)で表される化合物から水素原子をn個取り除いた残基を表す。
nは、1以上の整数を表す。但し、nが2以上の整数を表す場合、複数のR0~R3及びLは、それぞれ同一でも異なっていてもよい。
一般式(2)中、R4~R24はそれぞれ独立に、水素原子又は置換基を表す。
但し、一般式(1)で表される化合物は、少なくとも1個のイオン性親水性基を有する。
更に、該新規化合物を含有するカラーフィルター、及びカラートナーが提供される。
まず、本発明において、置換基群A、イオン性親水性基について定義する。
例えば、ハロゲン原子、アルキル基、アラルキル基、アルケニル基、アルキニル基、アリール基、ヘテロ環基、シアノ基、ヒドロキシル基、ニトロ基、アルコキシ基、アリールオキシ基、シリルオキシ基、ヘテロ環オキシ基、アシルオキシ基、カルバモイルオキシ基、アルコキシカルボニルオキシ基、アリールオキシカルボニルオキシ基、アミノ基、アシルアミノ基、アミノカルボニルアミノ基、アルコキシカルボニルアミノ基、アリールオキシカルボニルアミノ基、スルファモイルアミノ基、アルキル又はアリールスルホニルアミノ基、メルカプト基、アルキルチオ基、アリールチオ基、ヘテロ環チオ基、スルファモイル基、アルキル又はアリールスルフィニル基、アルキル又はアリールスルホニル基、アシル基、アリールオキシカルボニル基、アルコキシカルボニル基、カルバモイル基、アリール又はヘテロ環アゾ基、イミド基、ホスフィノ基、ホスフィニル基、ホスフィニルオキシ基、ホスフィニルアミノ基、シリル基、イオン性親水性基が例として挙げられる。これらの置換基は更に置換されてもよく、更なる置換基としては、以上に説明した置換基群Aから選択される基を挙げることができる。
アルキルチオ基としては、好ましくは、炭素数1から30の置換若しくは無置換のアルキルチオ基、例えば、メチルチオ基、エチルチオ基、n-ヘキサデシルチオ基等が挙げられる。
スルホ基、カルボキシル基、チオカルボキシル基、スルフィノ基、ホスホノ基、ジヒドロキシホスフィノ基、4級アンモニウム基などが挙げられる。特に好ましくはスルホ基、カルボキシル基である。またカルボキシル基、ホスホノ基及びスルホ基は塩の状態であってもよく、塩を形成する対カチオンの例には、アンモニウムイオン、アルカリ金属イオン(例、リチウムイオン、ナトリウムイオン、カリウムイオン)及び有機カチオン(例、テトラメチルアンモニウムイオン、テトラメチルグアニジウムイオン、テトラメチルホスホニウム)が含まれ、リチウム塩、ナトリウム塩、カリウム塩、アンモニウム塩が好ましく、リチウム塩又はリチウム塩を主成分とする混合塩が更に好ましく、リチウム塩が最も好ましい。
以下に、本発明の一般式(1)で表される化合物について詳細に説明する。
本発明の一般式(1)で表される化合物(色素)は、化合物とその塩及びこれらの水和物を含む。
本発明の化合物は、キサンテン系化合物の中でも、比較的高発色かつ高堅牢なC.I.アシッドレッド289を母体とし、スルファモイル基を含む特定の連結基を有するトリアジンユニットが導入されているため、連結基のスルファモイル基により色素の酸化分解が抑制され、耐オゾン性、耐光性、などの画像堅牢性が格段に優れる高発色な染料となり、また、導入されたトリアジンユニットによる色素同士の分子間水素結合の形成により、色素の移動が抑制され、耐湿性(湿度による色移り)にも優れるという効果を奏する。
Lは、単結合又は2価の連結基を表す。
Dは、一般式(2)で表される化合物から水素原子をn個取り除いた残基を表す。
nは、1以上の整数を表す。但し、nが2以上の整数を表す場合、複数のR0~R3及びLは、それぞれ同一でも異なっていてもよい。
一般式(2)中、R4~R24はそれぞれ独立に、水素原子又は置換基を表す。
但し、一般式(1)で表される化合物は、少なくとも1個のイオン性親水性基を有する。
R2及びR3が表す置換基が更に置換基を有する場合の置換基としては、前記置換基群Aを挙げることができ、アルキル基、アリール基、又はヘテロ環基が好ましい。これらは更に前記置換基群Aにより置換されていてもよく、イオン性親水性基により置換されていることがより好ましい。
なお、R0とL、又は、R1とLとが互いに結合して環を形成する場合、Lは3価の連結基となり、3価の連結基としては後述のLとしての2価の連結基から任意の一つの水素原子を除してなる3価の連結基が挙げられる。
Lは、置換基を有していてもよい炭素数1~10のアルキレン基、置換基を有していてもよい炭素数6~10のアリーレン基であることが好ましく、より好ましくは置換基を有していてもよい炭素数1~10のアルキレン基であり、更に好ましくは置換基を有していてもよい炭素数2~6のアルキレン基である。
nは、1以上の整数を表す。
nは、1~7の整数であることが好ましく、より好ましくは1~4の整数であり、更に好ましくは1~3の整数であり、特に好ましくは1又は2である。
一般式(2)中、R4、R8、R9及びR13はそれぞれ独立に、水素原子又は脂肪族基を表すことが好ましい。脂肪族基は、無置換でも置換基を有していてもよく、飽和でも不飽和であってもよく、総炭素数1~20の脂肪族基が好ましく、総炭素数1~20のアルキル基がより好ましく、総炭素数1~10のアルキル基がより好ましい。例えば、メチル基、エチル基、ビニル基、アリル基、エチニル基、イソプロペニル基、2-エチルヘキシル基が挙げられる。R4、R8、R9及びR13はそれぞれ独立に、脂肪族基を表すことが色相の観点で好ましい。
一般式(2)中、R5~R7、R10~R12及びR14~R23は水素原子を表すことが、合成の容易性の観点で好ましい。
本発明の着色組成物は、少なくとも一種の本発明の上記一般式(1)で表される化合物を含有する。本発明の着色組成物は、媒体を含有させることができるが、媒体として溶媒を用いた場合は特にインクジェット用インクとして好適である。本発明の着色組成物は、媒体として、親油性媒体や水性媒体を用いて、それらの中に、本発明の化合物を溶解及び/又は分散させることによって作製することができる。好ましくは、水性媒体を用いる場合である。本発明の着色組成物には、媒体を除いたインク用組成物も含まれる。
次に本発明のインクジェット用インクについて説明する。
本発明は、本発明の着色組成物を含有するインクジェット用インク(より具体的にはインクジェット記録用インク)にも関する。
インクジェット用インクは、親油性媒体や水性媒体中に前記本発明の化合物(混合物)を溶解及び/又は分散させることによって作製することができる。好ましくは、水性媒体を用いたインクである。
必要に応じてその他の添加剤を、本発明の効果を害しない範囲内において含有される。その他の添加剤としては、例えば、乾燥防止剤(湿潤剤)、褪色防止剤、乳化安定剤、浸透促進剤、紫外線吸収剤、防腐剤、防黴剤、pH調整剤、表面張力調整剤、消泡剤、粘度調整剤、分散剤、分散安定剤、防錆剤、キレート剤等の公知の添加剤が挙げられる。これらの各種添加剤は、水溶性インクの場合にはインク液に直接添加する。油溶性染料を分散物の形で用いる場合には、染料分散物の調製後分散物に添加するのが一般的であるが、調製時に油相又は水相に添加してもよい。
適用できる黒色材としては、ジスアゾ、トリスアゾ、テトラアゾ染料のほか、カーボンブラックの分散体を挙げることができる。
本発明は、本発明の着色組成物又はインクジェット用インクを用いて、画像形成するインクジェット記録方法にも関する。
本発明のインクジェット記録方法は、前記インクジェット用インクにエネルギーを供与して、公知の受像材料、即ち普通紙、樹脂コート紙、例えば特開平8-169172号公報、同8-27693号公報、同2-276670号公報、同7-276789号公報、同9-323475号公報、特開昭62-238783号公報、特開平10-153989号公報、同10-217473号公報、同10-235995号公報、同10-337947号公報、同10-217597号公報、同10-337947号公報等に記載されているインクジェット専用紙、フイルム、電子写真共用紙、布帛、ガラス、金属、陶磁器等に画像を形成する。
記録紙及び記録フィルムにおける支持体は、LBKP、NBKP等の化学パルプ、GP、PGW、RMP、TMP、CTMP、CMP、CGP等の機械パルプ、DIP等の古紙パルプ等からなり、必要に応じて従来公知の顔料、バインダー、サイズ剤、定着剤、カチオン剤、紙力増強剤等の添加剤を混合し、長網抄紙機、円網抄紙機等の各種装置で製造されたもの等が使用可能である。これらの支持体の他に合成紙、プラスチックフィルムシートのいずれであってもよく、支持体の厚みは10~250μm、坪量は10~250g/m2が望ましい。
支持体には、そのままインク受容層及びバックコート層を設けてもよいし、デンプン、ポリビニルアルコール等でサイズプレスやアンカーコート層を設けた後、インク受容層及びバックコー卜層を設けてもよい。更に支持体には、マシンカレンダー、TGカレンダー、ソフトカレンダー等のカレンダー装置により平坦化処理を行ってもよい。本発明では支持体として、両面をポリオレフィン(例えば、ポリエチレン、ポリスチレン、ポリエチレンテレフタレート、ポリブテン及びそれらのコポリマー)でラミネートした紙及びプラスチックフィルムがより好ましく用いられる。
ポリオレフィン中に、白色顔料(例えば、酸化チタン、酸化亜鉛)又は色味付け染料(例えば、コバルトブルー、群青、酸化ネオジウム)を添加することが好ましい。
インク受容層は、顔料及び水性結着剤の他に媒染剤、耐水化剤、耐光性向上剤、界面活性剤、その他の添加剤を含有することができる。
ポリマー媒染剤については、特開昭48-28325号、同54-74430号、同54-124726号、同55-22766号、同55-142339号、同60-23850号、同60-23851号、同60-23852号、同60-23853号、同60-57836号、同60-60643号、同60-118834号、同60-122940号、同60-122941号、同60-122942号、同60-235134号、特開平1-161236号の各公報、米国特許2484430号、同2548564号、同3148061号、同3309690号、同4115124号、同4124386号、同4193800号、同4273853号、同4282305号、同4450224号の各明細書に記載がある。特開平1-161236号公報の212~215頁に記載のポリマー媒染剤を含有する受像材料が特に好ましい。同公報記載のポリマー媒染剤を用いると、優れた画質の画像が得られ、かつ画像の耐光性が改善される。
本発明は、前記一般式(1)で表される化合物を含有するカラーフィルターにも関する。
カラーフィルターの形成方法としては、初めにフォトレジストによりパターンを形成し、次いで染色する方法、或いは特開平4-163552号、特開平4-128703号、特開平4-175753号公報で開示されているように色素を添加したフォトレジストによりパターンを形成する方法がある。本発明の化合物をカラーフィルターに導入する場合に用いられる方法としては、これらのいずれの方法を用いても良いが、好ましい方法としては、特開平4-175753号や特開平6-35182号に記載されたところの、熱硬化性樹脂、キノンジアジド化合物、架橋剤、色素及び溶剤を含有してなるポジ型レジスト組成物、並びに、それを基体上に塗布後、マスクを通して露光し、該露光部を現像してポジ型レジストパターンを形成させ、上記ポジ型レジストパターンを全面露光し、次いで露光後のポジ型レジストパターンを硬化させることからなるカラーフィルターの形成方法を挙げる事ができる。又、常法に従いブラックマトリックスを形成させ、RGB原色系あるいはY、M、C補色系カラーフィルターを得ることができる。カラーフィルターの場合も本発明の化合物の使用量の制限はないが0.1~50質量%が好ましい。
本発明は、前記一般式(1)で表される化合物を含有するカラートナーにも関する。
カラートナー100質量部中の本発明の化合物の含有量は特に制限がないが、0.1質量部以上含有するのが好ましく、1~20質量部がより好ましく、2~10質量部含有するのが最も好ましい。本発明の化合物を導入するカラートナー用バインダー樹脂としては一般に使用される全てのバインダーが使用出来る。例えば、スチレン系樹脂・アクリル系樹脂・スチレン/アクリル系樹脂・ポリエステル樹脂等が挙げられる。
トナーに対して流動性向上、帯電制御等を目的として無機微粉末、有機微粒子を外部添加しても良い。表面をアルキル基含有のカップリング剤等で処理したシリカ微粒子、チタニア微粒子が好ましく用いられる。なお、これらは数平均一次粒子径が10~500nmのものが好ましく、更にはトナー中に0.1~20質量%添加するのが好ましい。
合成例1:例示化合物1(b=0.5、c=1.5)の合成
(中間体Aの合成)
1000mLフラスコに、塩化シアヌル27.6g、氷水100g、カルソレン油5滴を混合し撹拌した。別途、アニリン-2,5-ジスルホン酸モノナトリウム42.1gを水150gに分散させ、2N水酸化ナトリウム水溶液を用いてpH6に調整して溶解させた溶液を、内温5度以下に保ちながらゆっくりと添加した。2N水酸化ナトリウム水溶液を用いて反応液をpH4.5に保ちながら室温で2時間反応させた。ワットマン製GF/Fフィルタで不溶物を除去し、その後ジメチルアミン16.8gを加え、室温にて終夜攪拌した。反応液を内温40度に加温し、ここへジメチルアミン90gを加え、60度で30分間反応させた。全体質量の10%に相当する塩化ナトリウムを加え、濃塩酸を用いてpHを1に調整した。内温を室温まで冷却し、析出している結晶をろ過し、飽和食塩水、続いてアセトンで十分に洗浄した後に、60度の送風乾燥器で終夜乾燥させ中間体Aの白色結晶を得た。この化合物は元素分析結果を元に純度82%(残りは塩化ナトリウム及び水と推定)であることがわかった。
100mLフラスコに塩化チオニル40mLを加え室温で撹拌した。ここへC.I.アシッドレッド289(中外化成(株)製、商品名CHUGAI AMINOL FAST PINK)3.4gを注意深くゆっくりと加え、その後DMF 4mLを加え、内温を55℃まで昇温し90分間撹拌した。反応液を室温まで冷却し、塩化ナトリウム25gを溶解させた氷水250gへゆっくりと滴下し、析出した結晶をろ別し、冷飽和食塩水で洗浄し、中間体Bのウエットケーキを得た。
別途500mLフラスコに、中間体A2.56gを水100mLに分散させ、2N水酸化ナトリウムを用いてpH8.5に調整し溶解させた。ここに上記中間体Bのウエットケーキ全量を加えた。水酸化ナトリウムを用いてpHを9.0に調整し、その後内温を50度に加温しpHを9.0に保ちながら90分撹拌し、その後pH12に調整し終夜撹拌した。反応液がほぼ溶解したことを確認し、内温を30度に冷却し、ワットマン製定性ろ紙にて不溶物を除去し、得られた水溶液のpHを塩酸水を用いてpHを8.0に調整し、体積の20%に相当する重さの塩化ナトリウムを加えて塩析した。析出した結晶をろ別し、水250mLに再溶解させ、得られた水溶液を透析により電気伝導度が10μS以下になるまで精製し、その後、水溶液をワットマン製GF/Fフィルタを通した後に、60℃のオーブン水分を除去し完固させ、例示化合物1の金属光沢結晶を得た。収量3.4g。
MSスペクトル(m/z、nega)により、c=2、b=0に相当する1483(M-H)、741(M-2H/2、100%)と、c=1、b=1に相当する1068(M-H)と533(M-2H/2)が観測された。また1H NMR(DMSO‐d6)による積分比の解析から、トリアジン側鎖は、アシッドレッド289の色素部位に対して約1.5個導入されていると推定した。
このことから、本例示化合物はbとcの割合がb=0.5、c=1.5となるような下記例示化合物1a~1fの混合物であると推定している。
下記の成分に脱イオン水を加え100gとした後、30~40℃で加熱しながら1時間撹拌した。その後KOH 10mol/LにてpH=9に調製し、平均孔径0.25μmのミクロフィルターで減圧濾過しマゼンタ用インク液を調製した。
本発明の色素(例示化合物1(b=0.5、c=1.5))3.50g
ジエチレングリコール 10.65g
グリセリン 14.70g
ジエチレングリコールモノブチルエーテル 12.70g
トリエタノールアミン 0.65g
オルフィンE1010(日信化学工業(株)製) 0.9g
以上の各実施例(インク液A~E)及び比較例(インク液F~I)のインクジェット用インクについて、下記評価を行った。その結果を表11に示した。
なお、表11において、耐オゾン性、耐光性、耐湿性は、各インクジェット用インクを、インクジェットプリンター(EPSON(株)社製;PM-700C)でフォト光沢紙(EPSON社製PM写真紙<光沢>(KA420PSK、EPSON))に画像を記録した後で評価したものである。印画濃度は各インクジェット記録用インクを、インクジェットプリンター(EPSON(株)社製;PM-700C)で普通紙(Canon社製普通紙(GF500、Canon)に画像を記録した後で評価したものである。
シーメンス型オゾナイザーの二重ガラス管内に乾燥空気を通しながら、5kV交流電圧を印加し、これを用いてオゾンガス濃度が0.5±0.1ppm、室温、暗所に設定されたボックス内に、前記画像を形成したフォト光沢紙を7日間放置し、オゾンガス下放置前後の画像濃度を反射濃度計(X-Rite310TR)を用いて測定し、色素残存率として評価した。なお、前記反射濃度は、1、1.5及び2.0の3点で測定した。ボックス内のオゾンガス濃度は、APPLICS製オゾンガスモニター(モデル:OZG-EM-01)を用いて設定した。
何れの濃度でも色素残存率が70%以上の場合をA、1又は2点が70%未満をB、全ての濃度で70%未満の場合をCとして、三段階で評価した。
記録した直後の画像濃度Ciを測定した後、ウェザーメーター(アトラスC.165)を用いて、画像にキセノン光(8万5千ルクス)を7日間照射した後、再び画像濃度Cfを測定し、キセノン光照射前後の画像濃度の差から色素残存率({(Ci-Cf)/Ci}×100%)を算出し評価した。画像濃度は反射濃度計(X-Rite310TR)を用いて測定した。
色素残存率は、反射濃度が1、1.5及び2.0の3点で測定した。いずれの濃度においても色素残存率が80%以上の場合をA、1又は2点が80%未満の場合をB、すべての濃度で80%未満の場合をCとして三段階で評価した。
インクジェット記録の際、チェック柄のパターン(濃度100%と0%の1.5mm角を有する正方形を交互に組み合わせたパターン)を作成し、コントラストの高いマゼンタ-ホワイトのチェック柄の印画物を得た。印画後、24時間乾燥を行ったチェック柄の印画物を80℃70%RHの条件で3日間放置し、着色部分からホワイト部分へのにじみの程度を目視で評価し、ほとんどにじまない場合をA、ややにじむ場合をB、明らかににじむ場合をCとして、三段階で評価した。
印画濃度100%における印画濃度を、反射濃度計(X-Rite310TR)を用いて測定し、印画濃度が2.2以上の場合をA、2.0以上2.2未満の場合をB、2.0未満の場合をCとして、三段階で評価した。
<カラートナーの作製>
本発明の色素(例示化合物1(b=0.5、c=1.5))3質量部、トナー用樹脂〔スチレン-アクリル酸エステル共重合体;ハイマーTB-1000F(商品名、三洋化成(株)製)〕100質量部をボールミルで混合粉砕後、150℃に加熱して熔融混和を行い、冷却後ハンマーミルを用いて粗粉砕し、次いでエアージェット方式による微粉砕機で微粉砕した。更に分級して1~20μmの粒子を選択し、トナーとした。
このトナー10質量部に対しキャリヤ鉄粉(EFV250/400、商品名、日本鉄粉(株)製)900質量部を均一に混合し現像剤とした。この現像剤を用いて乾式普通紙電子写真複写機〔NP-5000、商品名、キャノン(株)製〕で複写を行ったところ、優れた分光特性を有し、トナーとして優れた性質を示すことがわかった。
<カラーフィルターの作製>
(ポジ型レジスト組成物の調製)
m-クレゾール/p-クレゾール/ホルムアルデヒド(反応モル比=5/5/7.5)混合物から得たクレゾールノボラック樹脂(ポリスチレン換算質量平均分子量4300)3.4質量部、下式のフェノール化合物を用いて製造したo-ナフトキノンジアジド-5-スルホン酸エステル(平均2個の水酸基がエステル化されている)1.8質量部、ヘキサメトキシメチロール化メラミン0.8質量部、乳酸エチル20質量部、及び例示化合物1(b=0.5、c=1.5)を1質量部混合してポジ型レジスト組成物を得た。
得られたポジ型レジスト組成物をシリコンウエハにスピンコートした後、溶剤を蒸発させた。次いで、マスクを通してシリコンウエハを露光し、キノンジアジド化合物を分解させた。その後100℃で加熱し、次いでアルカリ現像により露光部を除去して0.8μmの解像度を有するポジ型着色パターンを得た。これを全面露光後、150℃、15分加熱してマゼンタの補色系カラーフィルターを得た。露光は、i線露光ステッパーHITACHI LD-5010-i(商品名、(株)日立製作所製、NA=0.40)により行った。また、現像液は、SOPD又はSOPD-B(いずれも商品名、住友化学工業(株)製)を用いた。
得られたカラーフィルターは色純度が良好でかつ透明度が高く、良好な性能を示した。
本出願は、2011年8月30日出願の日本特許出願(特願2011-188043)に基づくものであり、その内容はここに参照として取り込まれる。
Claims (10)
- 一般式(2)中、R4、R8、R9及びR13はそれぞれ独立に、水素原子又は脂肪族基を表す、請求項1に記載の着色組成物。
- 一般式(2)中、R5~R7、R10~R12及びR14~R23は水素原子を表す、請求項1又は2に記載の着色組成物。
- 一般式(2)中、R24は、水素原子又はイオン性親水性基を表し、一般式(1)中、Dは一般式(2)で表される化合物のR5~R7、R10~R12及びR24としての水素原子から、水素原子をn個取り除いた残基を表す、請求項3に記載の着色組成物。但し、nは1~7の整数を表す。
- 一般式(1)中、Lは、置換基を有していてもよい炭素数1~10のアルキレン基を表す、請求項1~4のいずれか1項に記載の着色組成物。
- 請求項1~5のいずれか1項に記載の着色組成物を含有するインクジェット用インク。
- 請求項1~5のいずれか1項に記載の着色組成物又は請求項6に記載のインクジェット用インクを用いて、画像形成するインクジェット記録方法。
- 請求項1~5のいずれか1項に記載の一般式(1)で表される化合物を含有するカラーフィルター。
- 請求項1~5のいずれか1項に記載の一般式(1)で表される化合物を含有するカラートナー。
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CN104144986A (zh) * | 2012-02-29 | 2014-11-12 | 富士胶片株式会社 | 着色组合物、喷墨记录用油墨及喷墨记录方法 |
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TWI570192B (zh) | 2017-02-11 |
KR101689135B1 (ko) | 2016-12-23 |
AU2012303205B2 (en) | 2017-01-05 |
US20140170538A1 (en) | 2014-06-19 |
KR20140059209A (ko) | 2014-05-15 |
EP2752465B1 (en) | 2018-04-04 |
EP2752465A1 (en) | 2014-07-09 |
JP2013049776A (ja) | 2013-03-14 |
US8852293B2 (en) | 2014-10-07 |
CN103814089B (zh) | 2016-04-27 |
EP2752465A4 (en) | 2015-06-17 |
CA2846116A1 (en) | 2013-03-07 |
TW201309763A (zh) | 2013-03-01 |
JP5696004B2 (ja) | 2015-04-08 |
CN103814089A (zh) | 2014-05-21 |
AU2012303205A1 (en) | 2014-03-13 |
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