CN111566560A - 感光性树脂组合物、间隔壁、有机场致发光元件、图像显示装置及照明 - Google Patents
感光性树脂组合物、间隔壁、有机场致发光元件、图像显示装置及照明 Download PDFInfo
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- CN111566560A CN111566560A CN201980007829.5A CN201980007829A CN111566560A CN 111566560 A CN111566560 A CN 111566560A CN 201980007829 A CN201980007829 A CN 201980007829A CN 111566560 A CN111566560 A CN 111566560A
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Classifications
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- H10K59/00—Integrated devices, or assemblies of multiple devices, comprising at least one organic light-emitting element covered by group H10K50/00
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- C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
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- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
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- C08F220/301—Esters containing oxygen in addition to the carboxy oxygen containing aromatic rings in the alcohol moiety and one oxygen in the alcohol moiety
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
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- C08F220/32—Esters containing oxygen in addition to the carboxy oxygen containing epoxy radicals
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
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- 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
- G03F7/029—Inorganic compounds; Onium compounds; Organic compounds having hetero atoms other than oxygen, nitrogen or sulfur
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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
- G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
- G03F7/032—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with binders
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- 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
- G03F7/032—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with binders
- G03F7/033—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with binders the binders being polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. vinyl polymers
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- G—PHYSICS
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- 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
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- 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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- 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
- G03F7/20—Exposure; Apparatus therefor
- G03F7/2002—Exposure; Apparatus therefor with visible light or UV light, through an original having an opaque pattern on a transparent support, e.g. film printing, projection printing; by reflection of visible or UV light from an original such as a printed image
- G03F7/2004—Exposure; Apparatus therefor with visible light or UV light, through an original having an opaque pattern on a transparent support, e.g. film printing, projection printing; by reflection of visible or UV light from an original such as a printed image characterised by the use of a particular light source, e.g. fluorescent lamps or deep UV light
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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
- G03F7/26—Processing photosensitive materials; Apparatus therefor
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- G—PHYSICS
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- G09F—DISPLAYING; ADVERTISING; SIGNS; LABELS OR NAME-PLATES; SEALS
- G09F9/00—Indicating arrangements for variable information in which the information is built-up on a support by selection or combination of individual elements
- G09F9/30—Indicating arrangements for variable information in which the information is built-up on a support by selection or combination of individual elements in which the desired character or characters are formed by combining individual elements
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- H05B33/00—Electroluminescent light sources
- H05B33/12—Light sources with substantially two-dimensional radiating surfaces
- H05B33/22—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of auxiliary dielectric or reflective layers
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- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K59/00—Integrated devices, or assemblies of multiple devices, comprising at least one organic light-emitting element covered by group H10K50/00
- H10K59/10—OLED displays
- H10K59/12—Active-matrix OLED [AMOLED] displays
- H10K59/122—Pixel-defining structures or layers, e.g. banks
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WO2022163682A1 (ja) | 2021-01-29 | 2022-08-04 | 三菱ケミカル株式会社 | 感光性樹脂組成物、硬化物、隔壁、有機電界発光素子、カラーフィルタ及び画像表示装置 |
TW202323307A (zh) | 2021-10-01 | 2023-06-16 | 日商三菱化學股份有限公司 | 感光性樹脂組合物、硬化物、阻隔壁、有機電致發光元件、及圖像顯示裝置 |
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012176816A1 (ja) * | 2011-06-21 | 2012-12-27 | 旭硝子株式会社 | ネガ型感光性樹脂組成物、隔壁、ブラックマトリックス、カラーフィルタおよび液晶表示素子 |
JP2013050549A (ja) * | 2011-08-30 | 2013-03-14 | Asahi Glass Co Ltd | ネガ型感光性樹脂組成物、隔壁、光学素子 |
CN104684994A (zh) * | 2012-09-24 | 2015-06-03 | 旭硝子株式会社 | 拒墨性组合物、负型感光性树脂组合物、固化膜、分隔壁以及光学元件 |
JP2017227771A (ja) * | 2016-06-22 | 2017-12-28 | 三菱ケミカル株式会社 | 隔壁形成用感光性樹脂組成物、隔壁、有機電界発光素子、画像表示装置及び照明 |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004151618A (ja) * | 2002-11-01 | 2004-05-27 | Asahi Glass Co Ltd | 感光性樹脂およびネガ型感光性樹脂組成物 |
JP5346509B2 (ja) * | 2007-07-10 | 2013-11-20 | 新日鉄住金化学株式会社 | カラーフィルター隔壁形成用感光性樹脂組成物及びこれを用いて形成した遮光性カラーフィルター隔壁並びにカラーフィルター |
JP5446317B2 (ja) * | 2009-02-26 | 2014-03-19 | セイコーエプソン株式会社 | 光硬化型インク組成物、インクジェット記録方法、記録物、インクセット、インクカートリッジ、及び記録装置 |
KR101768929B1 (ko) | 2010-09-30 | 2017-08-17 | 디아이씨 가부시끼가이샤 | 함불소 중합성 수지, 그것을 사용한 활성 에너지선 경화형 조성물 및 그 경화물 |
CN102746457A (zh) * | 2011-04-19 | 2012-10-24 | 住友化学株式会社 | 树脂和包含其的光刻胶组合物 |
JP2013228705A (ja) * | 2012-03-30 | 2013-11-07 | Fujifilm Corp | カラーフィルタ基板の製造方法、カラーフィルタ基板、及び、表示装置 |
KR102021745B1 (ko) | 2012-04-27 | 2019-09-17 | 에이지씨 가부시키가이샤 | 부분 가수 분해 축합물, 발잉크제, 네거티브형 감광성 수지 조성물, 경화막, 격벽 및 광학 소자 |
JP6286118B2 (ja) * | 2012-09-27 | 2018-02-28 | 東京応化工業株式会社 | レジスト組成物、レジストパターン形成方法、高分子化合物、化合物 |
KR101511476B1 (ko) | 2014-02-28 | 2015-04-10 | 스미또모 가가꾸 가부시키가이샤 | 감광성 수지 조성물 |
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Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012176816A1 (ja) * | 2011-06-21 | 2012-12-27 | 旭硝子株式会社 | ネガ型感光性樹脂組成物、隔壁、ブラックマトリックス、カラーフィルタおよび液晶表示素子 |
JP2013050549A (ja) * | 2011-08-30 | 2013-03-14 | Asahi Glass Co Ltd | ネガ型感光性樹脂組成物、隔壁、光学素子 |
CN104684994A (zh) * | 2012-09-24 | 2015-06-03 | 旭硝子株式会社 | 拒墨性组合物、负型感光性树脂组合物、固化膜、分隔壁以及光学元件 |
JP2017227771A (ja) * | 2016-06-22 | 2017-12-28 | 三菱ケミカル株式会社 | 隔壁形成用感光性樹脂組成物、隔壁、有機電界発光素子、画像表示装置及び照明 |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114901715A (zh) * | 2019-12-26 | 2022-08-12 | 住友化学株式会社 | 固化性树脂组合物和显示装置 |
CN114901715B (zh) * | 2019-12-26 | 2024-07-19 | 住友化学株式会社 | 固化性树脂组合物和显示装置 |
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JPWO2019146680A1 (ja) | 2021-01-14 |
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KR20200115465A (ko) | 2020-10-07 |
KR102636177B1 (ko) | 2024-02-14 |
WO2019146680A1 (ja) | 2019-08-01 |
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