Coloring composition, ink for inkjet recording and inkjet recording method

US9023139B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9023139-B2
Application numberUS-201414472775-A
CountryUS
Kind codeB2
Filing dateAug 29, 2014
Priority dateFeb 29, 2012
Publication dateMay 5, 2015
Grant dateMay 5, 2015

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

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There is provided a coloring composition including the compound represented by Formula (1) described in the specification and the compound selected from (A) to (C) described in the specification.

First claim

Opening claim text (preview).

What is claimed is: 1. A coloring composition comprising: a compound represented by the following Formula (1); and a compound selected from the group consisting of (A) to (C), wherein (A) is a compound represented by the following Formula (A4), (B) is at least one selected from the group consisting of a compound represented by the following Formula (B4) and a compound represented by the following Formula (B5), and (C) is a compound selected from the group consisting of compounds represented by the following Formula (C4): wherein, in Formula (1), L represents a linking group represented by Formula (V1), (V2), (V3) or (V4), D represents a residue in which 1 to 5 hydrogen atoms are removed from a compound represented by Formula (2), wherein in Formula (2), R 4 , R 8 , R 9 and R 13 each independently represent a hydrogen atom or an alkyl group, and R 5 to R 7 , R 10 to R 12 and R 14 to R 24 represent a hydrogen atom or a substituent, provided that at least one ionic hydrophilic groups are possessed, m represents an integer of 1 to 10, provided that a plurality of L's is optionally the same or different, and n represents an integer from 2 to 10, provided that a plurality of D's is optionally the same or different: wherein, in Formula (VI), R 101 and R 102 each independently represent a hydrogen B atom or a substituent, in Formula (V2), R 201 and R 202 each independently represent a hydrogen atom or a substituent, L 201 represents a divalent linking group, and R 201 and R 202 are optionally combined with each other to form a ring, in Formula (V3), R 301 , R 302 and R 303 each independently represent a hydrogen atom or a substituent, X represents an alkylene group having 2 to 20 carbon atoms, which may have a substituent, and L 301 represents a single bond or a divalent linking group, and in Formula (V4), R 401 and R 402 each independently represent a hydrogen atom or a substituent: wherein, in Formula (A4), R 21 , R 22 and R 23 each independently represent a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 9 carbon atoms, an alkoxy group having 1 to 9 carbon atoms, a halogen atom, a hydroxyl group, a substituted or unsubstituted carbamoyl group, a substituted or unsubstituted sulfamoyl group, a substituted or unsubstituted amino group, a nitro group, a sulfonic acid ester group, a substituted or unsubstituted alkylsulfonyl group having 1 to 9 carbon atoms, an arylsulfonyl group having 6 to 15 carbon atoms, a carboxyl group or a carboxylic acid ester group, R 27 represents a substituted or unsubstituted amino group, or —OR 26 , m represents 0, 1 or 2, R 24 , R 25 and R 26 each independently represent a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 18 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 18 carbon atoms, a substituted or unsubstituted aryl group, a substituted or unsubstituted aralkyl group or a substituted or unsubstituted heterocyclic group, M 4 represents a hydrogen atom or a counter cation, and M 4 's are optionally the same or different: wherein, R 21 and R 22 each independently represent a hydrogen atom or a substituted or unsubstituted alkyl group, Y 21 and Y 22 each independently represent a chlorine atom, a hydroxyl group, a substituted or unsubstituted amino group, an alkoxy group and a substituted or unsubstituted phenoxy group, X represents a divalent linking group, and M 4 represents a hydrogen atom or a counter cation, and M 4 's are optionally the same or different: wherein, in Formula (B5), R 31 represents a hydrogen atom or a substituted or unsubstituted alkyl group, Y 31 represents a chlorine atom, a hydroxyl group, a substituted or unsubstituted amino group or a morpholino group, M 5 represents a hydrogen atom or a counter cation, and M 5 's are optionally the same or different, and X 31 represents a group represented by the following Formula (B5-1): wherein, in Formula (B5-1), R 32 , R 33 , R 34 , R 35 and R 36 each independently represent a hydrogen atom, an alkyl group having 1 to 8 carbon atoms or —COOM′ wherein M′ represents a hydrogen atom or a counter cation, provided that at least one of R 32 , R 33 , R 34 , R 35 and R 36 represents an alkyl group having 1 to 8 carbon atoms or —COOM′: wherein, in Formula (C4), Z 1 represents an electron-withdrawing group having a Hammett's substituent constant σp value of 0.20 or more, Z 2 represents a hydrogen atom, an aliphatic group, an aromatic group, an acyl group or a heterocyclic group, R 23 and R 24 each independently represent a hydrogen atom, an aliphatic group, an aromatic group, a heterocyclic group, an acyl group, an alkoxycarbonyl group, an aryloxycarbonyl group, a carbamoyl group, an alkylsulfonyl group, an arylsulfonyl group or a sulfamoyl group, provided that there is no case where both R 23 and R 24 are a hydrogen atom at the same time, R 21 and R 22 each independently represent a hydrogen atom, a halogen atom, an aliphatic group, an aromatic group, a heterocyclic group, a cyano group, a carboxyl group, a carbamoyl group, an alkoxycarbonyl group, an aryloxycarbonyl group, an acyl group, a hydroxyl group, an alkoxy group, an aryloxy group, a silyloxy group, an acyloxy group, a carbamoyloxy group, a heterocyclic oxy group, an alkoxycarbonyloxy group, an aryloxycarbonyloxy group, an alkylamino group, an arylamino group, a heterocyclic amino group, an acylamino group, a ureido group, a sulfamoylamino group, an alkoxycarbonylamino group, an aryloxycarbonylamino group, an alkyl or arylsulfonylamino group, an aryloxycarbonylamino group, a nitro group, an alkyl or arylthio group, an alkyl or arylsulfonyl group, an alkyl or arylsulfinyl group, a sulfamoyl group, a sulfo group or a heterocyclic thio group, and R 21 and R 23 or R 23 and R 24 optionally combine with each other to form a 5- or 6-membered ring, R 25 and R 29 each independently represent an alkyl group, an alkoxy group or a halogen atom, provided that when both R 25 and R 29 are an alkyl group at the same time, a sum of the number of carbon atoms constituting the alkyl group is 3 or more, and these groups are optionally substituted, R 26 , R 27 and R 28 each independently have the same meaning as R 21 and R 22 , and R 25 and R 26 , or R 28 and R 29 are optionally condensed with each other to form a ring, Q represents a hydrogen atom, an aliphatic group, an aromatic group or a heterocyclic group, each group of Z 1 , Z 2 , R 21 , R 22 , R 23 , R 24 and Q optionally further has a substituent, and Formula (C4) has at least one ionic hydrophilic group. 2. The coloring composition of claim 1 , wherein in Formula (2), R 5 to R 7 , R 10 to R 12 and R 14 to R 23 represent a hydrogen atom. 3. The coloring composition of claim 1 , wherein in Formula (1), D represen

Assignees

Inventors

Classifications

  • Six-membered rings · CPC title

  • with aromatically bound amino groups · CPC title

  • C09D11/328Primary

    characterised by dyes · CPC title

  • also containing heterocyclic groups other than triazine groups · CPC title

  • Triazines · CPC title

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Frequently asked questions

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What does patent US9023139B2 cover?
There is provided a coloring composition including the compound represented by Formula (1) described in the specification and the compound selected from (A) to (C) described in the specification.
Who is the assignee on this patent?
Fujifilm Corp
What technology area does this patent fall under?
Primary CPC classification C09D11/328. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue May 05 2015 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).