Compound, coloring composition, ink jet recording ink, ink jet recording method, ink jet printer cartridge, ink jet recording material, color filter, color toner, and transfer ink
US-2016312032-A1 · Oct 27, 2016 · US
US9963605B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9963605-B2 |
| Application number | US-201715464821-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 21, 2017 |
| Priority date | Sep 30, 2014 |
| Publication date | May 8, 2018 |
| Grant date | May 8, 2018 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Provided are a coloring composition, an ink jet recording ink, and an ink jet recording method, the coloring composition including a betaine compound and at least one xanthene compound of a compound represented by Formula (1), a compound represented by Formula (2), a compound having a repeating unit represented by Formula (3), or a compound represented by Formula (4).
Opening claim text (preview).
What is claimed is: 1. A coloring composition comprising a betaine compound represented by Formula (A2), and at least one of a compound represented by Formula (1), a compound represented by Formula (2), a compound having a repeating unit represented by Formula (3), or a compound represented by Formula (4), wherein in Formula (A2), R a1 , R a2 , and R a3 each independently represents an alkyl group, an aryl group, or a heterocyclic group, and may be linked to each other to form a cyclic structure, and L a represents a divalent linking group, in Formula (1) and Formula (2), R 1 , R 3 , R 4 , R 5 , R 6 , R 8 , R 9 , R 10 , R 11 , R 12 , R 13 , R 14 , R 15 , R 16 , R 17 , R 18 , R 19 , R 20 , R 31 , R 32 , R 34 , R 35 ,R 36 , R 37 , R 39 , and R 40 each independently represents a hydrogen atom or a substituent, and X 1 , X 2 , X 3 , and X 4 each independently represents a hydroxyl group, a substituted or unsubstituted alkoxy group, a substituted or unsubstituted aryloxy group, a substituted or unsubstituted heterocyclic oxy group, a substituted or unsubstituted alkylamino group, a substituted or unsubstituted arylamino group, a substituted or unsubstituted heterylamino group, a substituted or unsubstituted carbonylamino group, a substituted or unsubstituted acyloxy group, a substituted or unsubstituted aminocarbonyloxy group, a substituted or unsubstituted sulfonylamino group, a substituted or unsubstituted alkoxycarbonylamino group, a substituted or unsubstituted aryloxycarbonylamino group, a substituted or unsubstituted ureido group, a substituted or unsubstituted alkylthio group, or a substituted or unsubstituted arylthio group, in Formula (3), L 1 represents a divalent linking group, D 1 represents a partial structure obtained by removing two hydrogen atoms from the compound represented by Formula (1) or (2), n 1 represents 2 to 100, and a plurality of L 1 's and a plurality of D 1 's may be the same as or different from each other, and in Formula (4), L 2 represents a n 2 -valent linking group, D 2 represents a partial structure obtained by removing one hydrogen atom from the compound represented by Formula (1) or (2), n 2 represents an integer of 2 to 6, and a plurality of D 2 's may be the same as or different from each other. 2. The coloring composition according to claim 1 , wherein the compound represented by Formula (1) or Formula (2) is a compound represented by the following Formula (1-1) or Formula (2-1), in Formula (1-1) and Formula (2-1), R 1 , R 3 , R 4 , R 5 , R 6 , R 8 , R 9 , R 10 , R 11 , R 12 , R 13 , R 14 , R 15 , R 16 , R 17 , R 18 , R 19 , R 20 , R 31 , R 32 , R 34 , R 35 , R 36 , R 37 , R 39 , and R 40 each independently represents a hydrogen atom or a substituent, and R 101 , R 102 , R 103 , and R 104 each independently represents a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, a substituted or unsubstituted heterocyclic group, a substituted or unsubstituted carbonyl group, a substituted or unsubstituted sulfonyl group, a substituted or unsubstituted alkoxycarbonyl group, a substituted or unsubstituted aryloxycarbonyl group, a carbamoyl group, a substituted or unsubstituted monoalkylaminocarbonyl group, a substituted or unsubstituted dialkylaminocarbonyl group, a substituted or unsubstituted monoarylaminocarbonyl group, a substituted or unsubstituted diarylaminocarbonyl group, or a substituted or unsubstituted alkylarylaminocarbonyl group. 3. The coloring composition according to claim 2 , wherein R 101 , R 102 , R 103 , and R 104 each independently represents a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, a substituted or unsubstituted heterocyclic group, a substituted or unsubstituted sulfonyl group, a substituted or unsubstituted alkoxycarbonyl group, a substituted or unsubstituted aryloxycarbonyl group, a carbamoyl group, a substituted or unsubstituted monoalkylaminocarbonyl group, a substituted or unsubstituted dialkylaminocarbonyl group, a substituted or unsubstituted monoarylaminocarbonyl group, a substituted or unsubstituted diarylaminocarbonyl group, or a substituted or unsubstituted alkylarylaminocarbonyl group. 4. The coloring composition according to claim 1 , wherein R 1 , R 5 , R 6 , R 10 , R 31 , R 35 , R 36 , and R 40 in Formula (1), or Formula (2) each independently represents an alkyl group having 1 to 6 carbon atoms. 5. The coloring composition according to claim 1 , wherein R 4 and R 9 in Formula (1) each independently represents a sulfo group. 6. The coloring composition according to claim 1 , wherein R 12 and R 15 in Formula (1) each independently represents a sulfo group. 7. The coloring composition according to claim 1 , wherein the content of at least one of the compound represented by Formula (1), the compound represented by Formula (2), the compound having the repeating unit represented by Formula (3), or the compound represented by Formula (4) is 1 to 20 mass %. 8. The coloring composition according to claim 1 , wherein the content of the betaine compound is 0.01 to 20 mass %. 9. An ink jet recording ink comprising the coloring composition according to claim 1 . 10. The ink jet recording ink according to claim 9 comprising a betaine compound, water, and at least one of a compound represented by Formula (1), a compound represented by Formula (2), a compound having a repeating unit represented by Formula (3), or a compound represented by Formula (4), wherein the total mass of inorganic ions in the ink jet recording ink is 2 mass % or lower with respect to the mass of the ink jet recording ink. 11. An ink jet recording method comprising forming an image using the ink jet recording ink according to claim 9 . 12. An ink jet recording method comprising forming an image using the coloring composition according to claim 1 . 13. The coloring composition according to claim 1 , wherein, in Formula (1) and Formula (2), X 1 and X 2 each independently represents a hydroxyl group, a substituted or unsubstituted alkoxy group, a substituted or unsubstituted aryloxy group, a substituted or unsubstituted heterocyclic oxy group, a substituted or unsubstituted alkylamino group, a substituted or unsubstituted arylamino group, a substituted or unsubstituted heterylamino group, a substituted or unsubstituted acyloxy group, a substituted or unsubstituted aminocarbonyloxy group, a substituted or unsubstituted sulfonylamino group, a substituted or unsubstituted alkoxycarbonylamino group, a substituted or unsubstituted aryloxycarbonylamino group, a substituted or unsubstituted ureido group, a substituted or unsubstituted alkylthio group, or a substituted or unsubstituted arylthio group.
characterised by dyes · CPC title
Pyronines {; Xanthon, thioxanthon, selenoxanthan, telluroxanthon dyes} · CPC title
Ink jet · CPC title
containing a diaryl- or triarylmethane dye · CPC title
Phthaleins containing amino groups {; Phthalanes; Fluoranes; Phthalides; Rhodamine dyes; Phthaleins having heterocyclic aryl rings; Lactone or lactame forms of triarylmethane dyes} · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.