JP2012515240A5 - - Google Patents
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- Publication number
- JP2012515240A5 JP2012515240A5 JP2011545713A JP2011545713A JP2012515240A5 JP 2012515240 A5 JP2012515240 A5 JP 2012515240A5 JP 2011545713 A JP2011545713 A JP 2011545713A JP 2011545713 A JP2011545713 A JP 2011545713A JP 2012515240 A5 JP2012515240 A5 JP 2012515240A5
- Authority
- JP
- Japan
- Prior art keywords
- formula
- alkyl
- group
- unsubstituted
- dispersion
- 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
Links
- 239000006185 dispersion Substances 0.000 claims description 13
- 229910052760 oxygen Inorganic materials 0.000 claims description 10
- 229920000642 polymer Polymers 0.000 claims description 10
- 239000003086 colorant Substances 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 150000003839 salts Chemical class 0.000 claims description 8
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims description 8
- 239000002270 dispersing agent Substances 0.000 claims description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims description 6
- 239000000178 monomer Substances 0.000 claims description 6
- 239000001301 oxygen Substances 0.000 claims description 6
- 125000001424 substituent group Chemical group 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- 101100240519 Caenorhabditis elegans nhr-13 gene Proteins 0.000 claims description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- ODUCDPQEXGNKDN-UHFFFAOYSA-N nitroxyl Chemical compound O=N ODUCDPQEXGNKDN-UHFFFAOYSA-N 0.000 claims description 4
- 230000000379 polymerizing effect Effects 0.000 claims description 4
- 229920000193 polymethacrylate Polymers 0.000 claims description 4
- 150000003254 radicals Chemical class 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 230000009435 amidation Effects 0.000 claims description 2
- 238000007112 amidation reaction Methods 0.000 claims description 2
- 125000004429 atom Chemical group 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 229920001577 copolymer Polymers 0.000 claims description 2
- 239000012634 fragment Substances 0.000 claims description 2
- 230000007062 hydrolysis Effects 0.000 claims description 2
- 238000006460 hydrolysis reaction Methods 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 239000003999 initiator Substances 0.000 claims description 2
- 230000000977 initiatory effect Effects 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- 230000004048 modification Effects 0.000 claims description 2
- 238000012986 modification Methods 0.000 claims description 2
- 239000002245 particle Substances 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 238000006116 polymerization reaction Methods 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- 238000005809 transesterification reaction Methods 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims 3
- DYLIWHYUXAJDOJ-OWOJBTEDSA-N (e)-4-(6-aminopurin-9-yl)but-2-en-1-ol Chemical compound NC1=NC=NC2=C1N=CN2C\C=C\CO DYLIWHYUXAJDOJ-OWOJBTEDSA-N 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000004815 dispersion polymer Substances 0.000 claims 1
- SNRUBQQJIBEYMU-NJFSPNSNSA-N dodecane Chemical group CCCCCCCCCCC[14CH3] SNRUBQQJIBEYMU-NJFSPNSNSA-N 0.000 claims 1
- 239000000049 pigment Substances 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 description 2
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP09150843 | 2009-01-19 | ||
| EP09150843.2 | 2009-01-19 | ||
| PCT/EP2010/050089 WO2010081756A1 (en) | 2009-01-19 | 2010-01-07 | Black pigment dispersion |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2012515240A JP2012515240A (ja) | 2012-07-05 |
| JP2012515240A5 true JP2012515240A5 (enExample) | 2013-02-21 |
| JP5683491B2 JP5683491B2 (ja) | 2015-03-11 |
Family
ID=40911912
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011545713A Expired - Fee Related JP5683491B2 (ja) | 2009-01-19 | 2010-01-07 | 黒色顔料分散液 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US8674006B2 (enExample) |
| EP (1) | EP2387599B1 (enExample) |
| JP (1) | JP5683491B2 (enExample) |
| KR (1) | KR101704076B1 (enExample) |
| CN (1) | CN102282216B (enExample) |
| CA (1) | CA2749240A1 (enExample) |
| MX (1) | MX2011007484A (enExample) |
| RU (1) | RU2541013C2 (enExample) |
| TW (1) | TWI478986B (enExample) |
| WO (1) | WO2010081756A1 (enExample) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5675647B2 (ja) * | 2009-01-19 | 2015-02-25 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | 有機黒色顔料およびその製造 |
| KR101342538B1 (ko) | 2011-11-01 | 2013-12-17 | (주) 디에이치홀딩스 | 공기차단밸브 및 이를 이용한 재시동안정화방법 |
| KR102112041B1 (ko) * | 2012-06-01 | 2020-05-18 | 바스프 에스이 | 흑색 착색제 혼합물 |
| JP6170673B2 (ja) | 2012-12-27 | 2017-07-26 | 富士フイルム株式会社 | カラーフィルタ用組成物、赤外線透過フィルタ及びその製造方法、並びに赤外線センサー |
| JP6489008B2 (ja) | 2013-09-25 | 2019-03-27 | 三菱ケミカル株式会社 | 感光性着色組成物、着色スペーサー及び画像表示装置 |
| JP6547931B2 (ja) * | 2014-10-27 | 2019-07-24 | 花王株式会社 | 着色硬化性樹脂組成物 |
| CN107001497A (zh) * | 2014-12-18 | 2017-08-01 | 花王株式会社 | 着色固化性树脂组合物 |
| CN109642089B (zh) * | 2016-08-24 | 2020-12-01 | 东丽株式会社 | 黑色颜料及其制造方法、颜料分散液、感光性组合物及其固化物 |
| JP2017116955A (ja) * | 2017-03-03 | 2017-06-29 | 富士フイルム株式会社 | 赤外線透過フィルタ用組成物、赤外線透過フィルタ、赤外線透過フィルタの製造方法、及び、赤外線センサー |
| KR102174436B1 (ko) | 2017-08-17 | 2020-11-04 | 주식회사 엘지화학 | 불용성 안료 화합물의 정성분석방법 |
| JP6764894B2 (ja) * | 2018-04-19 | 2020-10-07 | 富士フイルム株式会社 | 赤外線透過フィルタ用組成物、赤外線透過フィルタ、赤外線透過フィルタの製造方法、及び、赤外線センサー |
| US20200197240A1 (en) | 2018-12-19 | 2020-06-25 | The Procter & Gamble Company | Absorbent article comprising printed region |
| JP2019049759A (ja) * | 2018-12-26 | 2019-03-28 | 富士フイルム株式会社 | 赤外線透過フィルタ用組成物、赤外線透過組成物層、赤外線透過フィルタ、赤外線透過フィルタの製造方法、及び、赤外線センサー |
| US20230192962A1 (en) * | 2020-04-14 | 2023-06-22 | Basf Se | An amine-modified polymer, a controlled free radical polymerization for preparing the same and implementations thereof |
| JP7625243B2 (ja) | 2020-10-16 | 2025-02-03 | 山陽色素株式会社 | 黒色顔料分散体 |
| JP2023004245A (ja) | 2021-06-25 | 2023-01-17 | 山陽色素株式会社 | 黒色顔料分散体及び有彩色顔料分散体 |
| JPWO2023054116A1 (enExample) | 2021-09-29 | 2023-04-06 | ||
| JPWO2024171841A1 (enExample) * | 2023-02-16 | 2024-08-22 | ||
| CN118956180A (zh) * | 2024-07-31 | 2024-11-15 | 山东凯瑞尔光电科技有限公司 | 一种低反射率黑色分散液及制备方法 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1568231A (en) * | 1976-03-10 | 1980-05-29 | Ici Ltd | Substituted 2,6-dioxo-2,6-dihydrobenzo (1:2-b; 4:5-6')-difuran or dipyrrole dyestuffs |
| JPH0848893A (ja) | 1994-08-09 | 1996-02-20 | Sumitomo Chem Co Ltd | 新規ベンゾジフラノン化合物およびそれを用いる疎水性繊維材料の染色または捺染方法 |
| JP3572774B2 (ja) * | 1996-01-19 | 2004-10-06 | 三菱化学株式会社 | 光学的記録媒体及び情報記録方法 |
| US6503937B1 (en) | 1998-10-22 | 2003-01-07 | Ciba Specialty Chemicals Corporation | Oxobenzofuranylide-dihydroindolone |
| WO2001032577A1 (en) | 1999-11-03 | 2001-05-10 | Ciba Specialty Chemicals Holding Inc. | Pigmented vitreous material its precursor glass items coated therewith and method of its preparation |
| TWI236482B (en) * | 2000-11-13 | 2005-07-21 | Ciba Sc Holding Ag | Process for the (co)polymerization of vinyl chloride in the presence of a stable free nitroxyl radical |
| US6849679B2 (en) | 2001-05-21 | 2005-02-01 | Ciba Specialty Chemicals Corporation | Pigment compositions with modified block copolymer dispersants |
| CN100577692C (zh) * | 2005-01-11 | 2010-01-06 | 西巴特殊化学品控股有限公司 | 用受控自由基聚合方法制备的均聚物和共聚物的后改性方法 |
| EP1948738B1 (en) | 2005-10-26 | 2018-02-28 | Basf Se | Coloured particles for electrophoretic displays |
| JP2007266411A (ja) | 2006-03-29 | 2007-10-11 | Nippon Kayaku Co Ltd | 電界効果トランジスタ |
| WO2008003604A2 (en) | 2006-07-05 | 2008-01-10 | Ciba Holding Inc. | Coloured organic electrophoretic particles |
| JP5431150B2 (ja) | 2006-07-06 | 2014-03-05 | チバ ホールディング インコーポレーテッド | 電気泳動移動性有機着色剤を含むカプセル化分散剤 |
| JP5554058B2 (ja) * | 2006-07-11 | 2014-07-23 | コーニンクレッカ フィリップス エヌ ヴェ | 電気泳動デバイス及び電気泳動デバイスを制御する方法 |
| WO2008052592A1 (en) * | 2006-10-30 | 2008-05-08 | Telecom Italia S.P.A. | High security use of bank cards and system therefore |
| JP4549363B2 (ja) * | 2007-05-18 | 2010-09-22 | 株式会社リコー | 電気泳動粒子及びこれを利用した画像表示装置 |
| WO2009010521A2 (en) * | 2007-07-19 | 2009-01-22 | Basf Se | Nir-inert substrates comprising bis-oxodihydroindolylen-benzodifuranones |
| US8270063B2 (en) | 2007-09-07 | 2012-09-18 | Basf Se | Encapsulated dispersions comprising electrophoretically mobile organic colorants |
| JP5675647B2 (ja) | 2009-01-19 | 2015-02-25 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | 有機黒色顔料およびその製造 |
-
2010
- 2010-01-07 CA CA2749240A patent/CA2749240A1/en not_active Abandoned
- 2010-01-07 RU RU2011134468/05A patent/RU2541013C2/ru not_active IP Right Cessation
- 2010-01-07 CN CN201080004855.1A patent/CN102282216B/zh not_active Expired - Fee Related
- 2010-01-07 EP EP10700968A patent/EP2387599B1/en not_active Not-in-force
- 2010-01-07 WO PCT/EP2010/050089 patent/WO2010081756A1/en not_active Ceased
- 2010-01-07 US US13/144,106 patent/US8674006B2/en not_active Expired - Fee Related
- 2010-01-07 MX MX2011007484A patent/MX2011007484A/es not_active Application Discontinuation
- 2010-01-07 KR KR1020117019154A patent/KR101704076B1/ko not_active Expired - Fee Related
- 2010-01-07 JP JP2011545713A patent/JP5683491B2/ja not_active Expired - Fee Related
- 2010-01-18 TW TW099101243A patent/TWI478986B/zh not_active IP Right Cessation
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