CN109791357B - 感光性树脂组合物、固化物及图像显示装置 - Google Patents
感光性树脂组合物、固化物及图像显示装置 Download PDFInfo
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- CN109791357B CN109791357B CN201780056225.0A CN201780056225A CN109791357B CN 109791357 B CN109791357 B CN 109791357B CN 201780056225 A CN201780056225 A CN 201780056225A CN 109791357 B CN109791357 B CN 109791357B
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- 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
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- G—PHYSICS
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- 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
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- G03F7/028—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with photosensitivity-increasing substances, e.g. photoinitiators
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- 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
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- 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
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- 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
- G03F7/09—Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers
- G03F7/105—Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers having substances, e.g. indicators, for forming visible images
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
- C07D209/80—[b, c]- or [b, d]-condensed
- C07D209/82—Carbazoles; Hydrogenated carbazoles
- C07D209/88—Carbazoles; Hydrogenated carbazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the ring system
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/79—Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
- C07D307/80—Radicals substituted by oxygen atoms
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- Optics & Photonics (AREA)
- Materials For Photolithography (AREA)
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KR101848567B1 (ko) * | 2016-11-18 | 2018-04-12 | 롬엔드하스전자재료코리아유한회사 | 착색 감광성 수지 조성물 및 이로부터 제조된 차광성 스페이서 |
KR102400347B1 (ko) * | 2017-09-26 | 2022-05-20 | 후지필름 가부시키가이샤 | 경화성 조성물, 경화막, 고체 촬상 장치, 및 경화막의 제조 방법 |
CN111095104B (zh) * | 2017-09-27 | 2024-01-16 | 三菱化学株式会社 | 感光性着色组合物、固化物、黑色矩阵及图像显示装置 |
WO2020196139A1 (ja) * | 2019-03-27 | 2020-10-01 | 東レ株式会社 | 感光性樹脂組成物、感光性樹脂シート、中空構造の製造方法および電子部品 |
WO2021006315A1 (ja) | 2019-07-10 | 2021-01-14 | 東レ株式会社 | ネガ型感光性樹脂組成物、硬化膜、有機elディスプレイ及び硬化膜の製造方法 |
JP7382768B2 (ja) * | 2019-09-06 | 2023-11-17 | 日鉄ケミカル&マテリアル株式会社 | ブラックレジスト用感光性樹脂組成物及びその硬化塗膜、並びにカラーフィルター遮光膜の製造方法 |
JP7453023B2 (ja) | 2020-03-12 | 2024-03-19 | 東京応化工業株式会社 | 着色感光性組成物、着色膜及び着色膜の製造方法 |
WO2024004732A1 (ja) * | 2022-06-29 | 2024-01-04 | 富士フイルム株式会社 | 感光性組成物、膜、光学フィルタ、固体撮像素子および画像表示装置 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010204174A (ja) * | 2009-02-27 | 2010-09-16 | Fujifilm Corp | 感光性積層体及び感光性フィルム、並びに、プリント基板の製造方法 |
CN102015633A (zh) * | 2008-04-25 | 2011-04-13 | 三菱化学株式会社 | 酮肟酯类化合物及其应用 |
JP2011105713A (ja) * | 2009-10-23 | 2011-06-02 | Mitsubishi Chemicals Corp | ケトオキシムエステル系化合物及びその利用 |
CN105531260A (zh) * | 2013-09-10 | 2016-04-27 | 巴斯夫欧洲公司 | 肟酯光引发剂 |
CN105556390A (zh) * | 2013-09-25 | 2016-05-04 | 三菱化学株式会社 | 感光性着色组合物、黑色矩阵、着色间隔物、图像显示装置及颜料分散液 |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100796517B1 (ko) | 2006-07-18 | 2008-01-21 | 제일모직주식회사 | 컬러필터용 감광성 수지 조성물 및 이를 이용한 이미지센서컬러필터 |
CN101528694B (zh) | 2006-12-27 | 2012-03-07 | 株式会社艾迪科 | 肟酯化合物和含有该化合物的光聚合引发剂 |
KR101472869B1 (ko) * | 2008-04-28 | 2014-12-15 | 후지필름 가부시키가이샤 | 광중합성 조성물, 컬러필터용 광중합성 조성물, 컬러필터와 그 제조 방법, 고체촬상소자, 및 평판 인쇄판 원판 |
KR20100109860A (ko) * | 2009-04-01 | 2010-10-11 | 도요 잉키 세이조 가부시끼가이샤 | 감광성 착색 조성물 및 컬러 필터 |
JP5535814B2 (ja) * | 2009-09-14 | 2014-07-02 | 富士フイルム株式会社 | 光重合性組成物、カラーフィルタ、及びその製造方法、固体撮像素子、液晶表示装置、平版印刷版原版、並びに、新規化合物 |
KR101469519B1 (ko) * | 2011-10-07 | 2014-12-08 | (주)경인양행 | 옥심 에스테르 화합물 및 그것을 포함하는 광중합 개시제 |
WO2014069197A1 (ja) * | 2012-11-01 | 2014-05-08 | 株式会社Adeka | アルカリ現像性感光性組成物 |
JP6252039B2 (ja) * | 2013-08-27 | 2017-12-27 | 凸版印刷株式会社 | カラーフィルタ及び液晶表示装置 |
KR101988696B1 (ko) * | 2014-03-11 | 2019-06-12 | 동우 화인켐 주식회사 | 청색 감광성 수지 조성물, 이를 포함하는 청색 컬러필터 및 표시장치 |
KR101917406B1 (ko) * | 2014-03-21 | 2018-11-09 | 동우 화인켐 주식회사 | 고색재현이 가능한 착색 광경화성 수지조성물, 컬러필터 및 이를 구비한 액정표시장치 |
CN106488941B (zh) * | 2014-07-04 | 2019-12-10 | 三菱化学株式会社 | 树脂、感光性树脂组合物、固化物、滤色片及图像显示装置 |
JP6254280B2 (ja) * | 2014-07-15 | 2017-12-27 | 東京応化工業株式会社 | 化合物 |
JP6088105B1 (ja) * | 2015-08-27 | 2017-03-01 | 東京応化工業株式会社 | 感光性組成物、パターン形成方法、硬化物、及び表示装置 |
JP6692184B2 (ja) * | 2016-03-01 | 2020-05-13 | 株式会社Dnpファインケミカル | カラーフィルタ用感光性着色樹脂組成物、カラーフィルタ、表示装置 |
JP7091039B2 (ja) * | 2017-09-05 | 2022-06-27 | 東洋インキScホールディングス株式会社 | 有機el表示装置用赤色着色組成物、カラーフィルタ及び有機el表示装置 |
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Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102015633A (zh) * | 2008-04-25 | 2011-04-13 | 三菱化学株式会社 | 酮肟酯类化合物及其应用 |
JP2010204174A (ja) * | 2009-02-27 | 2010-09-16 | Fujifilm Corp | 感光性積層体及び感光性フィルム、並びに、プリント基板の製造方法 |
JP2011105713A (ja) * | 2009-10-23 | 2011-06-02 | Mitsubishi Chemicals Corp | ケトオキシムエステル系化合物及びその利用 |
CN105531260A (zh) * | 2013-09-10 | 2016-04-27 | 巴斯夫欧洲公司 | 肟酯光引发剂 |
CN105556390A (zh) * | 2013-09-25 | 2016-05-04 | 三菱化学株式会社 | 感光性着色组合物、黑色矩阵、着色间隔物、图像显示装置及颜料分散液 |
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TWI745431B (zh) | 2021-11-11 |
TW201818152A (zh) | 2018-05-16 |
KR102402726B1 (ko) | 2022-05-27 |
KR20190051976A (ko) | 2019-05-15 |
JP2022028782A (ja) | 2022-02-16 |
JP7283519B2 (ja) | 2023-05-30 |
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