JP2011525480A5 - - Google Patents
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- Publication number
- JP2011525480A5 JP2011525480A5 JP2011512067A JP2011512067A JP2011525480A5 JP 2011525480 A5 JP2011525480 A5 JP 2011525480A5 JP 2011512067 A JP2011512067 A JP 2011512067A JP 2011512067 A JP2011512067 A JP 2011512067A JP 2011525480 A5 JP2011525480 A5 JP 2011525480A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- phenyl
- substituted
- halogen
- unsubstituted
- 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
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 107
- 125000000217 alkyl group Chemical group 0.000 claims description 102
- 229910052736 halogen Inorganic materials 0.000 claims description 74
- 150000002367 halogens Chemical class 0.000 claims description 74
- 229910052760 oxygen Inorganic materials 0.000 claims description 37
- 125000001072 heteroaryl group Chemical group 0.000 claims description 28
- 229910052739 hydrogen Inorganic materials 0.000 claims description 28
- 239000001257 hydrogen Substances 0.000 claims description 28
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 25
- 150000002431 hydrogen Chemical class 0.000 claims description 25
- 229910052717 sulfur Inorganic materials 0.000 claims description 24
- 125000001624 naphthyl group Chemical group 0.000 claims description 20
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 16
- -1 OR 3 Chemical group 0.000 claims description 15
- 125000006832 (C1-C10) alkylene group Chemical group 0.000 claims description 12
- 125000001589 carboacyl group Chemical group 0.000 claims description 12
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 12
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 11
- 125000006710 (C2-C12) alkenyl group Chemical group 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 9
- 125000002947 alkylene group Chemical group 0.000 claims description 8
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 8
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 8
- 125000006678 phenoxycarbonyl group Chemical group 0.000 claims description 8
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims description 6
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 6
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 6
- 125000004957 naphthylene group Chemical group 0.000 claims description 6
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 6
- 229920006395 saturated elastomer Polymers 0.000 claims description 5
- 125000006729 (C2-C5) alkenyl group Chemical group 0.000 claims description 4
- 125000003860 C1-C20 alkoxy group Chemical group 0.000 claims description 4
- 125000004414 alkyl thio group Chemical group 0.000 claims description 4
- 235000010290 biphenyl Nutrition 0.000 claims description 4
- 239000004305 biphenyl Substances 0.000 claims description 4
- 125000000332 coumarinyl group Chemical group O1C(=O)C(=CC2=CC=CC=C12)* 0.000 claims description 4
- 125000004956 cyclohexylene group Chemical group 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims description 4
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 125000004641 (C1-C12) haloalkyl group Chemical group 0.000 claims description 2
- 125000003358 C2-C20 alkenyl group Chemical group 0.000 claims description 2
- VWBYXJRDIQCSLW-UHFFFAOYSA-N O=[P](c1ccccc1)c1ccccc1 Chemical group O=[P](c1ccccc1)c1ccccc1 VWBYXJRDIQCSLW-UHFFFAOYSA-N 0.000 claims description 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 2
- 125000003118 aryl group 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
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 2
- 125000005226 heteroaryloxycarbonyl group Chemical group 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims 17
- 239000000463 material Substances 0.000 claims 8
- 239000000654 additive Substances 0.000 claims 4
- 238000004519 manufacturing process Methods 0.000 claims 4
- 230000000996 additive effect Effects 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- 239000003973 paint Substances 0.000 claims 3
- 229920002120 photoresistant polymer Polymers 0.000 claims 3
- 239000000049 pigment Substances 0.000 claims 3
- 229920005989 resin Polymers 0.000 claims 3
- 239000011347 resin Substances 0.000 claims 3
- 239000000758 substrate Substances 0.000 claims 3
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 claims 2
- 238000004042 decolorization Methods 0.000 claims 2
- 239000002270 dispersing agent Substances 0.000 claims 2
- 238000005530 etching Methods 0.000 claims 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims 1
- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims 1
- 150000008065 acid anhydrides Chemical class 0.000 claims 1
- 150000001266 acyl halides Chemical class 0.000 claims 1
- 239000000853 adhesive Substances 0.000 claims 1
- 230000001070 adhesive effect Effects 0.000 claims 1
- 150000008064 anhydrides Chemical class 0.000 claims 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims 1
- 150000004056 anthraquinones Chemical class 0.000 claims 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims 1
- 239000012965 benzophenone Substances 0.000 claims 1
- 239000011230 binding agent Substances 0.000 claims 1
- 239000007795 chemical reaction product Substances 0.000 claims 1
- 229920001577 copolymer Polymers 0.000 claims 1
- 229960000956 coumarin Drugs 0.000 claims 1
- 235000001671 coumarin Nutrition 0.000 claims 1
- 238000013500 data storage Methods 0.000 claims 1
- 230000005670 electromagnetic radiation Effects 0.000 claims 1
- 238000010894 electron beam technology Methods 0.000 claims 1
- 238000009713 electroplating Methods 0.000 claims 1
- 239000003822 epoxy resin Substances 0.000 claims 1
- 239000003365 glass fiber Substances 0.000 claims 1
- 238000003384 imaging method Methods 0.000 claims 1
- 239000000976 ink Substances 0.000 claims 1
- 230000001678 irradiating effect Effects 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 239000011159 matrix material Substances 0.000 claims 1
- 239000003094 microcapsule Substances 0.000 claims 1
- 238000004377 microelectronic Methods 0.000 claims 1
- 150000002763 monocarboxylic acids Chemical class 0.000 claims 1
- 239000000178 monomer Substances 0.000 claims 1
- 230000003287 optical effect Effects 0.000 claims 1
- 229920000620 organic polymer Polymers 0.000 claims 1
- 239000003504 photosensitizing agent Substances 0.000 claims 1
- 238000007747 plating Methods 0.000 claims 1
- 229920000647 polyepoxide Polymers 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 239000002491 polymer binding agent Substances 0.000 claims 1
- 150000007519 polyprotic acids Polymers 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 229910000679 solder Inorganic materials 0.000 claims 1
- 125000006850 spacer group Chemical group 0.000 claims 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 claims 1
- 239000002966 varnish Substances 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP08157706 | 2008-06-06 | ||
| EP08157706.6 | 2008-06-06 | ||
| PCT/EP2009/056397 WO2009147031A2 (en) | 2008-06-06 | 2009-05-27 | Oxime ester photoinitiators |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011525480A JP2011525480A (ja) | 2011-09-22 |
| JP2011525480A5 true JP2011525480A5 (enExample) | 2012-07-19 |
| JP5566378B2 JP5566378B2 (ja) | 2014-08-06 |
Family
ID=40042788
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011512067A Expired - Fee Related JP5566378B2 (ja) | 2008-06-06 | 2009-05-27 | オキシムエステル光開始剤 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US8507725B2 (enExample) |
| EP (1) | EP2303833B1 (enExample) |
| JP (1) | JP5566378B2 (enExample) |
| KR (1) | KR101626172B1 (enExample) |
| CN (1) | CN102112438B (enExample) |
| TW (1) | TWI466853B (enExample) |
| WO (1) | WO2009147031A2 (enExample) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE541865T1 (de) * | 2008-06-06 | 2012-02-15 | Basf Se | Fotoinitiatormischungen |
| KR101648996B1 (ko) * | 2008-11-03 | 2016-08-17 | 바스프 에스이 | 광개시제 혼합물 |
| CN103064254B (zh) * | 2011-10-20 | 2017-11-17 | 日立化成株式会社 | 感光性树脂组合物、感光性元件、抗蚀图形的形成方法以及印刷电路板的制造方法 |
| JP5799799B2 (ja) * | 2011-10-20 | 2015-10-28 | 日立化成株式会社 | 感光性樹脂組成物、感光性エレメント、レジストパターンの形成方法及びプリント配線板の製造方法 |
| WO2013083505A1 (en) | 2011-12-07 | 2013-06-13 | Basf Se | Oxime ester photoinitiators |
| CN103698976A (zh) * | 2012-09-27 | 2014-04-02 | 李妤 | 新型激光数字全息高密度存储显示材料的制备 |
| WO2014097595A1 (ja) * | 2012-12-21 | 2014-06-26 | 日立化成デュポンマイクロシステムズ株式会社 | 感光性樹脂組成物、それを用いたパターン硬化膜の製造方法及び半導体装置 |
| CN105531260B (zh) * | 2013-09-10 | 2019-05-31 | 巴斯夫欧洲公司 | 肟酯光引发剂 |
| CN103819583B (zh) * | 2014-03-18 | 2016-05-18 | 常州强力电子新材料股份有限公司 | 一种含硝基双肟酯类光引发剂及其制备方法和应用 |
| CN104672354A (zh) * | 2015-02-04 | 2015-06-03 | 天津墨森科技有限公司 | 一种双肟酯类光引发剂及其制备方法和应用 |
| CN107614485A (zh) * | 2015-08-24 | 2018-01-19 | 株式会社艾迪科 | 肟酯化合物及含有该化合物的聚合引发剂 |
| JP6713112B2 (ja) * | 2016-04-27 | 2020-06-24 | 東京応化工業株式会社 | 化合物及びその製造方法 |
| TWI664500B (zh) * | 2016-06-30 | 2019-07-01 | 奇美實業股份有限公司 | 黑色感光性樹脂組成物及其應用 |
| CN110023307B (zh) * | 2017-03-16 | 2024-01-02 | 株式会社艾迪科 | 肟酯化合物及含有该化合物的光聚合引发剂 |
| CN109134710B (zh) * | 2017-06-15 | 2021-08-03 | 常州强力电子新材料股份有限公司 | 一种芳基硫鎓盐肟酯类光引发剂及其合成与应用 |
| CN109134711B (zh) * | 2017-06-15 | 2021-08-03 | 常州强力电子新材料股份有限公司 | 一种硫鎓盐光引发剂及其制备与应用 |
| KR102355406B1 (ko) * | 2017-06-29 | 2022-01-25 | 스미또모 가가꾸 가부시키가이샤 | 착색 경화성 수지 조성물, 컬러 필터 및 표시 장치 |
| JP2020200272A (ja) * | 2019-06-11 | 2020-12-17 | 株式会社Adeka | カルバモイルオキシム化合物並びに該化合物を含有する重合開始剤及び重合性組成物 |
| WO2025225376A1 (ja) * | 2024-04-23 | 2025-10-30 | 富士フイルム株式会社 | 光硬化性組成物、画素の製造方法、膜、光学フィルタ、固体撮像素子、画像表示装置および光重合開始剤 |
Family Cites Families (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1180846A (en) | 1967-08-08 | 1970-02-11 | Agfa Gevaert Nv | Photopolymerisation of Ethylenically Unsaturated Organic Compounds |
| DE1908346A1 (de) * | 1968-02-20 | 1969-11-13 | Eastman Kodak Co | Substituierte Triarylamine |
| FR2393345A1 (fr) | 1977-06-01 | 1978-12-29 | Agfa Gevaert Nv | Fabrication d'elements modifies sous forme d'images |
| GB2029423A (en) | 1978-08-25 | 1980-03-19 | Agfa Gevaert Nv | Photo-polymerisable materials and recording method |
| US4590145A (en) | 1985-06-28 | 1986-05-20 | Daicel Chemical Industries, Ltd. | Photopolymerization initiator comprised of thioxanthones and oxime esters |
| US5019482A (en) | 1987-08-12 | 1991-05-28 | Asahi Kasei Kogyo Kabushiki Kaisha | Polymer/oxime ester/coumarin compound photosensitive composition |
| JPS6443562A (en) * | 1987-08-12 | 1989-02-15 | Asahi Chemical Ind | Photosensitive composition |
| JPH07271020A (ja) | 1994-03-18 | 1995-10-20 | Internatl Business Mach Corp <Ibm> | ブラックマトリックス形成用感光性組成物、カラーフィルター基板及びそれを用いた液晶表示装置 |
| SG77689A1 (en) | 1998-06-26 | 2001-01-16 | Ciba Sc Holding Ag | New o-acyloxime photoinitiators |
| NL1016815C2 (nl) * | 1999-12-15 | 2002-05-14 | Ciba Sc Holding Ag | Oximester-fotoinitiatoren. |
| WO2002100903A1 (en) | 2001-06-11 | 2002-12-19 | Ciba Specialty Chemicals Holding Inc. | Oxime ester photoinitiators having a combined structure |
| CA2505893A1 (en) | 2002-12-03 | 2004-06-17 | Ciba Specialty Chemicals Holding Inc. | Oxime ester photoinitiators with heteroaromatic groups |
| JP3754065B2 (ja) | 2003-06-10 | 2006-03-08 | 三菱化学株式会社 | 光重合性組成物及びこれを用いたカラーフィルター |
| WO2006018405A1 (en) | 2004-08-18 | 2006-02-23 | Ciba Specialty Chemicals Holding Inc. | Oxime ester photoinitiators |
| CN101321727B (zh) | 2005-12-01 | 2013-03-27 | 西巴控股有限公司 | 肟酯光敏引发剂 |
| US8586268B2 (en) | 2005-12-20 | 2013-11-19 | Basf Se | Oxime ester photoinitiators |
| CN101370772B (zh) * | 2006-01-13 | 2012-10-17 | 东洋油墨制造株式会社 | 二酮肟酯化合物及其用途 |
| JP4874659B2 (ja) * | 2006-01-24 | 2012-02-15 | 富士フイルム株式会社 | アニリン化合物及びその製造方法、並びに、感光性組成物 |
| KR20090052858A (ko) * | 2006-08-11 | 2009-05-26 | 닛폰 바루카 고교 가부시키가이샤 | 밸브 장치 |
| WO2008138724A1 (en) | 2007-05-11 | 2008-11-20 | Basf Se | Oxime ester photoinitiators |
| JP5535064B2 (ja) | 2007-05-11 | 2014-07-02 | ビーエーエスエフ ソシエタス・ヨーロピア | オキシムエステル光重合開始剤 |
| CN101687846B (zh) | 2007-05-11 | 2015-12-02 | 巴斯夫欧洲公司 | 肟酯光引发剂 |
| JP2009040762A (ja) | 2007-08-09 | 2009-02-26 | Ciba Holding Inc | オキシムエステル光開始剤 |
| ATE541865T1 (de) | 2008-06-06 | 2012-02-15 | Basf Se | Fotoinitiatormischungen |
| KR101648996B1 (ko) * | 2008-11-03 | 2016-08-17 | 바스프 에스이 | 광개시제 혼합물 |
-
2009
- 2009-05-27 CN CN200980130100.3A patent/CN102112438B/zh not_active Expired - Fee Related
- 2009-05-27 WO PCT/EP2009/056397 patent/WO2009147031A2/en not_active Ceased
- 2009-05-27 JP JP2011512067A patent/JP5566378B2/ja not_active Expired - Fee Related
- 2009-05-27 US US12/995,697 patent/US8507725B2/en not_active Expired - Fee Related
- 2009-05-27 KR KR1020117000212A patent/KR101626172B1/ko not_active Expired - Fee Related
- 2009-05-27 EP EP09757414.9A patent/EP2303833B1/en not_active Not-in-force
- 2009-06-05 TW TW098118754A patent/TWI466853B/zh not_active IP Right Cessation
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