CN101523289A - 包含苯甲酰甲酸酯型光引发剂的可光固化组合物 - Google Patents
包含苯甲酰甲酸酯型光引发剂的可光固化组合物 Download PDFInfo
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- CN101523289A CN101523289A CNA2007800368558A CN200780036855A CN101523289A CN 101523289 A CN101523289 A CN 101523289A CN A2007800368558 A CNA2007800368558 A CN A2007800368558A CN 200780036855 A CN200780036855 A CN 200780036855A CN 101523289 A CN101523289 A CN 101523289A
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- alkyl
- phenyl
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- compound
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- 150000001875 compounds Chemical class 0.000 claims abstract description 99
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- 125000000217 alkyl group Chemical group 0.000 claims description 22
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- IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 description 1
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- 230000003068 static effect Effects 0.000 description 1
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- 239000000454 talc Substances 0.000 description 1
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- MDDUHVRJJAFRAU-YZNNVMRBSA-N tert-butyl-[(1r,3s,5z)-3-[tert-butyl(dimethyl)silyl]oxy-5-(2-diphenylphosphorylethylidene)-4-methylidenecyclohexyl]oxy-dimethylsilane Chemical compound C1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)C(=C)\C1=C/CP(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 MDDUHVRJJAFRAU-YZNNVMRBSA-N 0.000 description 1
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- CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical compound CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 230000005144 thermotropism Effects 0.000 description 1
- CBDKQYKMCICBOF-UHFFFAOYSA-N thiazoline Chemical compound C1CN=CS1 CBDKQYKMCICBOF-UHFFFAOYSA-N 0.000 description 1
- 125000002769 thiazolinyl group Chemical group 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 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 description 1
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- 125000005208 trialkylammonium group Chemical group 0.000 description 1
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- KKFOMYPMTJLQGA-UHFFFAOYSA-N tribenzyl phosphite Chemical compound C=1C=CC=CC=1COP(OCC=1C=CC=CC=1)OCC1=CC=CC=C1 KKFOMYPMTJLQGA-UHFFFAOYSA-N 0.000 description 1
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 1
- 229960001124 trientine Drugs 0.000 description 1
- BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- 235000013976 turmeric Nutrition 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
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- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
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- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
- G03F7/028—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with photosensitivity-increasing substances, e.g. photoinitiators
- G03F7/031—Organic compounds not covered by group G03F7/029
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/76—Unsaturated compounds containing keto groups
- C07C59/90—Unsaturated compounds containing keto groups containing singly bound oxygen-containing groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/73—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids
- C07C69/738—Esters of keto-carboxylic acids or aldehydo-carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/46—Polymerisation initiated by wave energy or particle radiation
- C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
- C08F2/50—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light with sensitising agents
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/0045—Photosensitive materials with organic non-macromolecular light-sensitive compounds not otherwise provided for, e.g. dissolution inhibitors
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/038—Macromolecular compounds which are rendered insoluble or differentially wettable
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
- C07C2601/10—Systems containing only non-condensed rings with a five-membered ring the ring being unsaturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- General Physics & Mathematics (AREA)
- Polymers & Plastics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Paints Or Removers (AREA)
- Polymerisation Methods In General (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Detergent Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP06121655.2 | 2006-10-03 | ||
| EP06121655 | 2006-10-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN101523289A true CN101523289A (zh) | 2009-09-02 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNA2007800368558A Pending CN101523289A (zh) | 2006-10-03 | 2007-09-24 | 包含苯甲酰甲酸酯型光引发剂的可光固化组合物 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US20100022676A1 (https=) |
| EP (1) | EP2069866A2 (https=) |
| JP (1) | JP2010505977A (https=) |
| CN (1) | CN101523289A (https=) |
| WO (1) | WO2008040650A2 (https=) |
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| CN102002022A (zh) * | 2010-10-29 | 2011-04-06 | 苏州凯康化工科技有限公司 | 一种月桂酸改性环氧丙烯酸酯及其制备方法和应用 |
| WO2011160262A1 (zh) * | 2010-06-25 | 2011-12-29 | 北京英力科技发展有限公司 | 低挥发性苯甲酰基甲酸酯 |
| CN102442909A (zh) * | 2010-06-25 | 2012-05-09 | 北京英力科技发展有限公司 | 低挥发低迁移性苯甲酰基甲酸酯 |
| CN102746785A (zh) * | 2011-04-19 | 2012-10-24 | 比亚迪股份有限公司 | 一种双重固化涂料组合物及其固化方法 |
| CN104423156A (zh) * | 2013-09-05 | 2015-03-18 | 东友精细化工有限公司 | 非显示部遮光图案形成用感光性树脂组合物 |
| CN104755507A (zh) * | 2012-10-22 | 2015-07-01 | 蓝宝迪有限公司 | 用于led光固化的3-酮香豆素 |
| CN106957618A (zh) * | 2015-12-10 | 2017-07-18 | 科络普拉斯特弗里茨米勒有限公司 | 耐高温的彩色特别是橙色胶粘带以及用于制备其的方法和载体及具有此类胶粘带的电缆束 |
| CN107239002A (zh) * | 2017-07-07 | 2017-10-10 | 深圳市华星光电技术有限公司 | Uv固化粉末光阻组合物及其制作方法、彩膜基板的制作方法 |
| CN109503735A (zh) * | 2017-09-15 | 2019-03-22 | 常州强力先端电子材料有限公司 | 光引发剂、包含其的光固化组合物及其应用 |
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| WO2025228451A1 (zh) * | 2024-04-30 | 2025-11-06 | 常州强力先端电子材料有限公司 | 一种光引发剂及其制备方法和应用 |
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| CN109456242B (zh) * | 2017-09-06 | 2021-02-12 | 常州强力电子新材料股份有限公司 | 硫鎓盐光引发剂、其制备方法、包含其的光固化组合物及其应用 |
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| CN110804337A (zh) * | 2019-11-06 | 2020-02-18 | 甘肃天后光学科技有限公司 | 隐形眼镜彩色油墨、所用光亮剂及其制备方法 |
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Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0576837A (ja) * | 1991-09-25 | 1993-03-30 | Sekisui Chem Co Ltd | 光硬化型樹脂組成物の硬化方法 |
| CN1244190A (zh) * | 1997-01-30 | 2000-02-09 | 西巴特殊化学品控股有限公司 | 非挥发性苯基乙醛酸酯 |
| US6562464B1 (en) * | 1999-03-24 | 2003-05-13 | Basf Aktiengesellschaft | Utilization of phenylglyoxalic acid esters as photoinitiators |
| CN1447844A (zh) * | 2000-08-14 | 2003-10-08 | 西巴特殊化学品控股有限公司 | 采用表面活性的光致引发剂的涂料的制备方法 |
| CN1649905A (zh) * | 2002-04-26 | 2005-08-03 | 西巴特殊化学品控股有限公司 | 可引入的光敏引发剂 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3856529A (en) * | 1967-05-26 | 1974-12-24 | Kalle Ag | Method and materials for making half tone prints |
| US4014844A (en) * | 1970-06-26 | 1977-03-29 | Agence Nationale De Valorisation De La Recherche (Anvar) | Process for grafting polymers on carbon black through free radical mechanism |
| US3930868A (en) * | 1973-05-23 | 1976-01-06 | The Richardson Company | Light sensitive arylglyoxyacrylate compositions |
| US4038164A (en) * | 1975-09-18 | 1977-07-26 | Stauffer Chemical Company | Photopolymerizable aryl and heterocyclic glyoxylate compositions and process |
| US4024296A (en) * | 1976-02-02 | 1977-05-17 | Ppg Industries, Inc. | Photocatalyst system and pigmented actinic light polymerizable coating compositions containing the same |
| US4279720A (en) * | 1978-07-13 | 1981-07-21 | Ciba-Geigy Corporation | Photocurable composition |
| US4475999A (en) * | 1983-06-06 | 1984-10-09 | Stauffer Chemical Company | Sensitization of glyoxylate photoinitiators |
| TW369554B (en) * | 1995-10-19 | 1999-09-11 | Three Bond Co Ltd | Photocurable composition |
| JP3425311B2 (ja) * | 1996-03-04 | 2003-07-14 | 株式会社東芝 | ネガ型感光性ポリマー樹脂組成物、これを用いたパターン形成方法、および電子部品 |
| US8414982B2 (en) * | 2004-12-22 | 2013-04-09 | Basf Se | Process for the production of strongly adherent coatings |
-
2007
- 2007-09-24 US US12/442,779 patent/US20100022676A1/en not_active Abandoned
- 2007-09-24 EP EP07820500A patent/EP2069866A2/en not_active Withdrawn
- 2007-09-24 WO PCT/EP2007/060093 patent/WO2008040650A2/en not_active Ceased
- 2007-09-24 JP JP2009530842A patent/JP2010505977A/ja active Pending
- 2007-09-24 CN CNA2007800368558A patent/CN101523289A/zh active Pending
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0576837A (ja) * | 1991-09-25 | 1993-03-30 | Sekisui Chem Co Ltd | 光硬化型樹脂組成物の硬化方法 |
| CN1244190A (zh) * | 1997-01-30 | 2000-02-09 | 西巴特殊化学品控股有限公司 | 非挥发性苯基乙醛酸酯 |
| US6562464B1 (en) * | 1999-03-24 | 2003-05-13 | Basf Aktiengesellschaft | Utilization of phenylglyoxalic acid esters as photoinitiators |
| CN1447844A (zh) * | 2000-08-14 | 2003-10-08 | 西巴特殊化学品控股有限公司 | 采用表面活性的光致引发剂的涂料的制备方法 |
| CN1649905A (zh) * | 2002-04-26 | 2005-08-03 | 西巴特殊化学品控股有限公司 | 可引入的光敏引发剂 |
Cited By (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2011160262A1 (zh) * | 2010-06-25 | 2011-12-29 | 北京英力科技发展有限公司 | 低挥发性苯甲酰基甲酸酯 |
| CN102442909A (zh) * | 2010-06-25 | 2012-05-09 | 北京英力科技发展有限公司 | 低挥发低迁移性苯甲酰基甲酸酯 |
| CN102442909B (zh) * | 2010-06-25 | 2013-10-30 | 北京英力科技发展有限公司 | 低挥发低迁移性苯甲酰基甲酸酯 |
| CN102002022A (zh) * | 2010-10-29 | 2011-04-06 | 苏州凯康化工科技有限公司 | 一种月桂酸改性环氧丙烯酸酯及其制备方法和应用 |
| CN102002022B (zh) * | 2010-10-29 | 2013-05-08 | 苏州凯康化工科技有限公司 | 一种月桂酸改性环氧丙烯酸酯及其制备方法和应用 |
| CN102746785A (zh) * | 2011-04-19 | 2012-10-24 | 比亚迪股份有限公司 | 一种双重固化涂料组合物及其固化方法 |
| CN102746785B (zh) * | 2011-04-19 | 2014-12-17 | 比亚迪股份有限公司 | 一种双重固化涂料组合物及其固化方法 |
| CN104755507B (zh) * | 2012-10-22 | 2017-10-03 | 意大利艾坚蒙树脂有限公司 | 用于led光固化的3‑酮香豆素 |
| CN104755507A (zh) * | 2012-10-22 | 2015-07-01 | 蓝宝迪有限公司 | 用于led光固化的3-酮香豆素 |
| CN104423156B (zh) * | 2013-09-05 | 2019-04-26 | 东友精细化工有限公司 | 非显示部遮光图案形成用感光性树脂组合物 |
| CN104423156A (zh) * | 2013-09-05 | 2015-03-18 | 东友精细化工有限公司 | 非显示部遮光图案形成用感光性树脂组合物 |
| CN106957618A (zh) * | 2015-12-10 | 2017-07-18 | 科络普拉斯特弗里茨米勒有限公司 | 耐高温的彩色特别是橙色胶粘带以及用于制备其的方法和载体及具有此类胶粘带的电缆束 |
| CN107239002B (zh) * | 2017-07-07 | 2019-12-06 | 深圳市华星光电技术有限公司 | Uv固化粉末光阻组合物及其制作方法、彩膜基板的制作方法 |
| CN107239002A (zh) * | 2017-07-07 | 2017-10-10 | 深圳市华星光电技术有限公司 | Uv固化粉末光阻组合物及其制作方法、彩膜基板的制作方法 |
| CN110658679A (zh) * | 2017-07-07 | 2020-01-07 | 深圳市华星光电技术有限公司 | Uv固化粉末光阻组合物及其制作方法、彩膜基板的制作方法 |
| CN110673439A (zh) * | 2017-07-07 | 2020-01-10 | 深圳市华星光电技术有限公司 | Uv固化粉末光阻组合物及其制作方法、彩膜基板的制作方法 |
| CN110737172A (zh) * | 2017-07-07 | 2020-01-31 | 深圳市华星光电技术有限公司 | Uv固化粉末光阻组合物及其制作方法、彩膜基板的制作方法 |
| CN110673439B (zh) * | 2017-07-07 | 2023-05-02 | Tcl华星光电技术有限公司 | Uv固化粉末光阻组合物及其制作方法、彩膜基板的制作方法 |
| CN110658679B (zh) * | 2017-07-07 | 2023-05-02 | Tcl华星光电技术有限公司 | Uv固化粉末光阻组合物及其制作方法、彩膜基板的制作方法 |
| CN109503735A (zh) * | 2017-09-15 | 2019-03-22 | 常州强力先端电子材料有限公司 | 光引发剂、包含其的光固化组合物及其应用 |
| CN117865923A (zh) * | 2024-01-08 | 2024-04-12 | 湖北固润科技股份有限公司 | 甲酰甲酸香豆素化合物、其制备方法和用途以及包含其的光引发剂组合物和可光固化组合物 |
| WO2025228451A1 (zh) * | 2024-04-30 | 2025-11-06 | 常州强力先端电子材料有限公司 | 一种光引发剂及其制备方法和应用 |
| WO2025228453A1 (zh) * | 2024-04-30 | 2025-11-06 | 常州强力先端电子材料有限公司 | 一种光固化组合物及其应用 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2008040650A3 (en) | 2009-01-08 |
| WO2008040650A2 (en) | 2008-04-10 |
| US20100022676A1 (en) | 2010-01-28 |
| EP2069866A2 (en) | 2009-06-17 |
| JP2010505977A (ja) | 2010-02-25 |
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