JP2010047748A5 - - Google Patents
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- Publication number
- JP2010047748A5 JP2010047748A5 JP2009160981A JP2009160981A JP2010047748A5 JP 2010047748 A5 JP2010047748 A5 JP 2010047748A5 JP 2009160981 A JP2009160981 A JP 2009160981A JP 2009160981 A JP2009160981 A JP 2009160981A JP 2010047748 A5 JP2010047748 A5 JP 2010047748A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- pigment
- aromatic
- group
- rings
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 239000000049 pigment Substances 0.000 claims description 48
- 229910052739 hydrogen Inorganic materials 0.000 claims description 24
- 239000001257 hydrogen Substances 0.000 claims description 22
- 125000003118 aryl group Chemical group 0.000 claims description 20
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 17
- 229910052794 bromium Inorganic materials 0.000 claims description 10
- 229910052801 chlorine Inorganic materials 0.000 claims description 10
- 229910052731 fluorine Inorganic materials 0.000 claims description 10
- 125000001424 substituent group Chemical group 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 8
- 229910052757 nitrogen Inorganic materials 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 229910052717 sulfur Inorganic materials 0.000 claims description 8
- 125000005842 heteroatom Chemical group 0.000 claims description 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical class [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 5
- 239000002270 dispersing agent Substances 0.000 claims description 5
- 239000012860 organic pigment Substances 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 229910004013 NO 2 Inorganic materials 0.000 claims description 4
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- 239000002245 particle Substances 0.000 claims description 4
- FYNROBRQIVCIQF-UHFFFAOYSA-N pyrrolo[3,2-b]pyrrole-5,6-dione Chemical compound C1=CN=C2C(=O)C(=O)N=C21 FYNROBRQIVCIQF-UHFFFAOYSA-N 0.000 claims description 4
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims description 3
- 235000000177 Indigofera tinctoria Nutrition 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 229940097275 indigo Drugs 0.000 claims description 3
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 claims description 3
- 229910052744 lithium Inorganic materials 0.000 claims description 3
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 claims description 3
- 230000000737 periodic effect Effects 0.000 claims description 3
- 229910052700 potassium Inorganic materials 0.000 claims description 3
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- 239000011734 sodium Chemical group 0.000 claims description 3
- 125000006832 (C1-C10) alkylene group Chemical group 0.000 claims description 2
- KSLLMGLKCVSKFF-UHFFFAOYSA-N 5,12-dihydroquinolino[2,3-b]acridine-6,7,13,14-tetrone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C(=O)C(C(=O)C1=CC=CC=C1N1)=C1C2=O KSLLMGLKCVSKFF-UHFFFAOYSA-N 0.000 claims description 2
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical group [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 2
- 125000004429 atom Chemical group 0.000 claims description 2
- 229910052792 caesium Inorganic materials 0.000 claims description 2
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 150000001768 cations Chemical class 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 2
- 235000019239 indanthrene blue RS Nutrition 0.000 claims description 2
- UHOKSCJSTAHBSO-UHFFFAOYSA-N indanthrone blue Chemical compound C1=CC=C2C(=O)C3=CC=C4NC5=C6C(=O)C7=CC=CC=C7C(=O)C6=CC=C5NC4=C3C(=O)C2=C1 UHOKSCJSTAHBSO-UHFFFAOYSA-N 0.000 claims description 2
- PXZQEOJJUGGUIB-UHFFFAOYSA-N isoindolin-1-one Chemical compound C1=CC=C2C(=O)NCC2=C1 PXZQEOJJUGGUIB-UHFFFAOYSA-N 0.000 claims description 2
- GWVMLCQWXVFZCN-UHFFFAOYSA-N isoindoline Chemical compound C1=CC=C2CNCC2=C1 GWVMLCQWXVFZCN-UHFFFAOYSA-N 0.000 claims description 2
- BSIHWSXXPBAGTC-UHFFFAOYSA-N isoviolanthrone Chemical compound C12=CC=CC=C2C(=O)C2=CC=C3C(C4=C56)=CC=C5C5=CC=CC=C5C(=O)C6=CC=C4C4=C3C2=C1C=C4 BSIHWSXXPBAGTC-UHFFFAOYSA-N 0.000 claims description 2
- 229910052751 metal Inorganic materials 0.000 claims description 2
- 239000002184 metal Substances 0.000 claims description 2
- OBJNZHVOCNPSCS-UHFFFAOYSA-N naphtho[2,3-f]quinazoline Chemical compound C1=NC=C2C3=CC4=CC=CC=C4C=C3C=CC2=N1 OBJNZHVOCNPSCS-UHFFFAOYSA-N 0.000 claims description 2
- DGBWPZSGHAXYGK-UHFFFAOYSA-N perinone Chemical group C12=NC3=CC=CC=C3N2C(=O)C2=CC=C3C4=C2C1=CC=C4C(=O)N1C2=CC=CC=C2N=C13 DGBWPZSGHAXYGK-UHFFFAOYSA-N 0.000 claims description 2
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 2
- 239000011591 potassium Chemical group 0.000 claims description 2
- LLBIOIRWAYBCKK-UHFFFAOYSA-N pyranthrene-8,16-dione Chemical compound C12=CC=CC=C2C(=O)C2=CC=C3C=C4C5=CC=CC=C5C(=O)C5=C4C4=C3C2=C1C=C4C=C5 LLBIOIRWAYBCKK-UHFFFAOYSA-N 0.000 claims description 2
- 229910052701 rubidium Inorganic materials 0.000 claims description 2
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 claims description 2
- 230000007704 transition Effects 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 7
- 239000000975 dye Substances 0.000 claims 2
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims 2
- -1 C 1 -C 8 -alkoxy Chemical group 0.000 claims 1
- 150000003863 ammonium salts Chemical class 0.000 claims 1
- 150000002500 ions Chemical class 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 description 11
- AGIJRRREJXSQJR-UHFFFAOYSA-N 2h-thiazine Chemical compound N1SC=CC=C1 AGIJRRREJXSQJR-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102008032092.7 | 2008-07-08 | ||
| DE200810032092 DE102008032092A1 (de) | 2008-07-08 | 2008-07-08 | Binäre Diketopyrrolopyrrol-Pigmentzusammensetzung zur Verwendung in Colorfiltern |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010047748A JP2010047748A (ja) | 2010-03-04 |
| JP2010047748A5 true JP2010047748A5 (https=) | 2012-07-26 |
| JP5717230B2 JP5717230B2 (ja) | 2015-05-13 |
Family
ID=41258097
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009160981A Expired - Fee Related JP5717230B2 (ja) | 2008-07-08 | 2009-07-07 | カラーフィルターにおいて使用するための２成分ジケトピロロピロール系顔料組成物 |
Country Status (3)
| Country | Link |
|---|---|
| EP (1) | EP2146230B1 (https=) |
| JP (1) | JP5717230B2 (https=) |
| DE (1) | DE102008032092A1 (https=) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI431071B (zh) | 2007-10-17 | 2014-03-21 | Clariant Finance Bvi Ltd | 用於彩色濾光片中的二酮基吡咯并吡咯顏料組成物 |
| DE102008032090A1 (de) | 2008-07-08 | 2010-01-14 | Clariant International Ltd. | PR 254-Pigmentzubereitung zur Verwendung in Colorfiltern |
| TW201111447A (en) * | 2009-07-14 | 2011-04-01 | Sumitomo Chemical Co | Production method of pigment dispersion solution |
| JP5615131B2 (ja) * | 2010-10-28 | 2014-10-29 | 三菱鉛筆株式会社 | 筆記具用油性インク組成物 |
| US8933239B1 (en) | 2013-07-16 | 2015-01-13 | Dow Global Technologies Llc | Bis(aryl)acetal compounds |
| US9063420B2 (en) | 2013-07-16 | 2015-06-23 | Rohm And Haas Electronic Materials Llc | Photoresist composition, coated substrate, and method of forming electronic device |
| US8962779B2 (en) | 2013-07-16 | 2015-02-24 | Dow Global Technologies Llc | Method of forming polyaryl polymers |
| US9410016B2 (en) | 2013-07-16 | 2016-08-09 | Dow Global Technologies Llc | Aromatic polyacetals and articles comprising them |
| JP7233831B2 (ja) * | 2017-07-27 | 2023-03-07 | 東友ファインケム株式会社 | 着色硬化性樹脂組成物、カラーフィルタ、及び表示装置 |
| CN108949155B (zh) * | 2018-08-29 | 2020-02-18 | 济南大学 | 一种检测细胞内连二亚硫酸钠的荧光探针及其应用 |
| KR102850555B1 (ko) * | 2019-01-11 | 2025-08-25 | 산요 시키소 가부시키가이샤 | 아조 안료 조성물 및 그의 제조 방법 |
| JP6729776B1 (ja) * | 2019-04-25 | 2020-07-22 | 東洋インキＳｃホールディングス株式会社 | 紫外線吸収材料、およびその組成物 |
| EP4063426B1 (en) | 2019-11-18 | 2025-06-18 | Sekisui Chemical Co., Ltd. | Black particles, black coating material, coating film, and black matrix for color filters |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS56118462A (en) | 1980-02-25 | 1981-09-17 | Toyo Ink Mfg Co Ltd | Pigment composition |
| EP0184982B1 (de) | 1984-11-07 | 1991-01-23 | Ciba-Geigy Ag | Verfahren zur Herstellung von Pyrrolo-[3,4-c]-pyrrolen und neue Pyrrolo-[3,4-c]-pyrrole |
| US4632704A (en) | 1985-02-06 | 1986-12-30 | Ciba-Geigy Corporation | Process for the preparation of high yield pigments |
| US4791204A (en) * | 1985-11-26 | 1988-12-13 | Ciba-Geigy Corporation | 1,4-diketopyrrolo[3,4-c]pyrrole pigments |
| ES2370485T3 (es) | 1999-07-09 | 2011-12-16 | Basf Se | C.i. pigmento red 254 con propiedades colorantes mejoradas. |
| DE19958181A1 (de) | 1999-12-02 | 2001-06-07 | Clariant Gmbh | Pigmentdispergatoren auf Basis von Diketopyrrolopyrrolverbindungen und Pigmentzubereitungen |
| DE10106147A1 (de) | 2001-02-10 | 2002-08-14 | Clariant Gmbh | Saure Pigmentdispergatoren und Pigmentzubereitungen |
| KR100932089B1 (ko) * | 2001-04-24 | 2009-12-16 | 시바 홀딩 인크 | 안료 조성물 및 착색된 수계 피복 물질 |
| DE10235573A1 (de) * | 2002-08-03 | 2004-02-12 | Clariant Gmbh | Pigmentzubereitungen auf Basis von Diketopyrrolopyrrolpigmenten zum verzugsfreien Pigmentieren von teilkristallinen Kunststoffen |
| ES2342078T3 (es) * | 2005-11-28 | 2010-07-01 | Agfa Graphics N.V. | Dispersiones del pigmento dicetopirrolo-pirrol no acuosas usando sinergistas de dispersion. |
| CN101918497B (zh) * | 2007-12-26 | 2014-05-28 | 东洋油墨制造股份有限公司 | 红色滤色器用颜料组合物、该颜料组合物的制造方法、使用该颜料组合物的着色组合物和滤色器 |
-
2008
- 2008-07-08 DE DE200810032092 patent/DE102008032092A1/de not_active Withdrawn
-
2009
- 2009-06-09 EP EP20090007596 patent/EP2146230B1/de not_active Not-in-force
- 2009-07-07 JP JP2009160981A patent/JP5717230B2/ja not_active Expired - Fee Related
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