TWI665514B - 負型著色組成物、著色硬化膜及顯示元件 - Google Patents
負型著色組成物、著色硬化膜及顯示元件 Download PDFInfo
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- TWI665514B TWI665514B TW103143197A TW103143197A TWI665514B TW I665514 B TWI665514 B TW I665514B TW 103143197 A TW103143197 A TW 103143197A TW 103143197 A TW103143197 A TW 103143197A TW I665514 B TWI665514 B TW I665514B
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- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
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- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
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- DQFBYFPFKXHELB-VAWYXSNFSA-N trans-chalcone Chemical compound C=1C=CC=CC=1C(=O)\C=C\C1=CC=CC=C1 DQFBYFPFKXHELB-VAWYXSNFSA-N 0.000 description 1
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 1
- DQZNLOXENNXVAD-UHFFFAOYSA-N trimethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OC)(OC)OC)CCC2OC21 DQZNLOXENNXVAD-UHFFFAOYSA-N 0.000 description 1
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- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-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
- G03F7/0045—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
- G03F7/0005—Production of optical devices or components in so far as characterised by the lithographic processes or materials used therefor
- G03F7/0007—Filters, e.g. additive colour filters; Components for display devices
-
- 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
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Materials For Photolithography (AREA)
- Optical Filters (AREA)
- Polymerisation Methods In General (AREA)
- Liquid Crystal (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Electroluminescent Light Sources (AREA)
- Graft Or Block Polymers (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2013259318 | 2013-12-16 | ||
| JP2013-259318 | 2013-12-16 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TW201530258A TW201530258A (zh) | 2015-08-01 |
| TWI665514B true TWI665514B (zh) | 2019-07-11 |
Family
ID=53413823
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW103143197A TWI665514B (zh) | 2013-12-16 | 2014-12-11 | 負型著色組成物、著色硬化膜及顯示元件 |
Country Status (4)
| Country | Link |
|---|---|
| JP (6) | JP6520091B2 (https=) |
| KR (1) | KR102435805B1 (https=) |
| CN (2) | CN104714367B (https=) |
| TW (1) | TWI665514B (https=) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI769146B (zh) * | 2016-01-08 | 2022-07-01 | 日商富士軟片股份有限公司 | 著色組成物、著色組成物的製造方法、彩色濾光片、圖案形成方法、固體攝像元件及圖像顯示裝置 |
| JP6607054B2 (ja) * | 2016-01-20 | 2019-11-20 | 三菱ケミカル株式会社 | 感光性樹脂組成物、硬化物、ブラックマトリックス及び画像表示装置 |
| KR102247840B1 (ko) | 2016-03-18 | 2021-05-03 | 제이에스알 가부시끼가이샤 | 표시 소자용 기판, 표시 소자용 기판의 제조 방법 및 표시 소자 |
| WO2022163449A1 (ja) * | 2021-01-28 | 2022-08-04 | 東レ株式会社 | 着色樹脂組成物、着色膜、加飾基板 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2003207888A (ja) * | 2002-01-11 | 2003-07-25 | Fuji Photo Film Co Ltd | 染料含有ネガ型硬化性組成物、並びにこれを含むカラーフィルタ及びその製造方法 |
| JP2011039316A (ja) * | 2009-08-12 | 2011-02-24 | Fujifilm Corp | 着色硬化性組成物、カラーフィルタ及びその製造方法、固体撮像素子、液晶ディスプレイ、有機elディスプレイ、並びに画像表示デバイス |
Family Cites Families (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0812292B2 (ja) | 1989-07-20 | 1996-02-07 | 凸版印刷株式会社 | 耐熱性カラーフィルターおよびその製造方法 |
| JP2891418B2 (ja) | 1988-11-26 | 1999-05-17 | 凸版印刷株式会社 | カラーフィルターおよびその製造方法 |
| JPH0635188A (ja) | 1992-07-15 | 1994-02-10 | Nippon Kayaku Co Ltd | カラーフィルター用光重合組成物及びカラーフィルター |
| JP3940523B2 (ja) | 1999-04-27 | 2007-07-04 | セイコーエプソン株式会社 | インクジェット方式カラーフィルタ用樹脂組成物、カラーフィルタおよびカラーフィルタの製造方法 |
| JP3929653B2 (ja) * | 1999-08-11 | 2007-06-13 | 富士フイルム株式会社 | ネガ型レジスト組成物 |
| JP2002311586A (ja) * | 2001-04-18 | 2002-10-23 | Fuji Photo Film Co Ltd | 電子線又はx線用ネガ型レジスト組成物 |
| KR100933735B1 (ko) * | 2001-12-25 | 2009-12-24 | 후지필름 가부시키가이샤 | 염료함유 네가티브 경화성 조성물, 및 이것을 사용한 컬러 필터 및 그 제조방법 |
| JP2005266673A (ja) * | 2004-03-22 | 2005-09-29 | Kyocera Chemical Corp | カラーフィルター、液晶表示装置、ポジ型感光性樹脂組成物及びスペーサーの製造方法 |
| WO2006098261A1 (ja) * | 2005-03-14 | 2006-09-21 | Sakata Inx Corp. | 処理顔料及びその用途 |
| WO2006098291A1 (ja) * | 2005-03-15 | 2006-09-21 | Toray Industries, Inc. | 感光性樹脂組成物 |
| JP5235408B2 (ja) * | 2005-03-31 | 2013-07-10 | 富士フイルム株式会社 | 染料含有硬化性組成物、並びに、カラーフィルタおよびその製造方法 |
| JP5211438B2 (ja) * | 2005-06-09 | 2013-06-12 | 東レ株式会社 | 樹脂組成物およびそれを用いた表示装置 |
| CN101024624B (zh) * | 2006-02-24 | 2013-09-11 | 富士胶片株式会社 | 肟衍生物、可光聚合的组合物、滤色片及其制造方法 |
| JP5193446B2 (ja) * | 2006-08-31 | 2013-05-08 | 旭化成イーマテリアルズ株式会社 | ポジ型感光性樹脂組成物 |
| JP5157522B2 (ja) | 2008-02-28 | 2013-03-06 | Jsr株式会社 | 着色層形成用感放射線性組成物、カラーフィルタおよびカラー液晶表示素子 |
| JP5254650B2 (ja) * | 2008-03-28 | 2013-08-07 | 富士フイルム株式会社 | 感光性樹脂組成物、遮光性カラーフィルター及びその製造方法、並びに、固体撮像素子 |
| JPWO2010087232A1 (ja) * | 2009-01-29 | 2012-08-02 | 日本電気株式会社 | ネガ型感光性絶縁樹脂組成物及びそれを用いたパターン形成方法 |
| SG173468A1 (en) * | 2009-01-29 | 2011-09-29 | Toray Industries | Resin composition and display device formed using same |
| JP5353415B2 (ja) * | 2009-04-27 | 2013-11-27 | Jsr株式会社 | 着色組成物、カラーフィルタおよびカラー液晶表示素子 |
| JP5235966B2 (ja) * | 2010-10-18 | 2013-07-10 | 富士フイルム株式会社 | 染料含有ネガ型硬化性組成物、カラーフィルタおよびその製造方法 |
| JP5358630B2 (ja) * | 2011-08-17 | 2013-12-04 | 富士フイルム株式会社 | レジストパターン形成方法、ナノインプリント用モールドの製造方法、及びフォトマスクの製造方法 |
| JP5941635B2 (ja) * | 2011-08-31 | 2016-06-29 | 富士フイルム株式会社 | 着色組成物、並びに、これを用いたカラーフィルタの製造方法、カラーフィルタ、及び、固体撮像素子 |
| JPWO2013084932A1 (ja) * | 2011-12-09 | 2015-04-27 | Jsr株式会社 | 着色剤、着色組成物、カラーフィルタ及び表示素子 |
| TWI568802B (zh) * | 2012-04-13 | 2017-02-01 | Jsr股份有限公司 | 著色組成物、彩色濾光片及顯示元件 |
| JP2013231897A (ja) * | 2012-05-01 | 2013-11-14 | Fujifilm Corp | 感光性樹脂組成物、感光性積層体、フレキシブル回路基板、及び永久パターン形成方法 |
| JP6105858B2 (ja) * | 2012-05-17 | 2017-03-29 | 太陽インキ製造株式会社 | パターン形成方法、アルカリ現像型の熱硬化性樹脂組成物、及びプリント配線板 |
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Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2003207888A (ja) * | 2002-01-11 | 2003-07-25 | Fuji Photo Film Co Ltd | 染料含有ネガ型硬化性組成物、並びにこれを含むカラーフィルタ及びその製造方法 |
| JP2011039316A (ja) * | 2009-08-12 | 2011-02-24 | Fujifilm Corp | 着色硬化性組成物、カラーフィルタ及びその製造方法、固体撮像素子、液晶ディスプレイ、有機elディスプレイ、並びに画像表示デバイス |
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| JP2022141747A (ja) | 2022-09-29 |
| CN111176071A (zh) | 2020-05-19 |
| JP6520091B2 (ja) | 2019-05-29 |
| KR20150070017A (ko) | 2015-06-24 |
| JP7136268B2 (ja) | 2022-09-13 |
| CN111176071B (zh) | 2024-10-29 |
| JP2024109711A (ja) | 2024-08-14 |
| JP7703077B2 (ja) | 2025-07-04 |
| JP2015135476A (ja) | 2015-07-27 |
| CN104714367A (zh) | 2015-06-17 |
| JP2019095797A (ja) | 2019-06-20 |
| JP7616162B2 (ja) | 2025-01-17 |
| TW201530258A (zh) | 2015-08-01 |
| JP6911971B2 (ja) | 2021-07-28 |
| JP2020126265A (ja) | 2020-08-20 |
| KR102435805B1 (ko) | 2022-08-25 |
| JP6699717B2 (ja) | 2020-05-27 |
| JP2021157181A (ja) | 2021-10-07 |
| CN104714367B (zh) | 2020-03-13 |
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