TWI612103B - 著色組成物、著色硬化膜、顯示元件及固態攝影元件 - Google Patents

著色組成物、著色硬化膜、顯示元件及固態攝影元件 Download PDF

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Publication number: TWI612103B
Authority: TW; Taiwan
Prior art keywords: mass; parts; coloring; pigment; red
Prior art date: 2013-02-12

Application number

TW103104345A

Other languages

English (en)

Chinese (zh)

Other versions

TW201434997A (zh

Inventor

Jung Wan Ryu

Akihiro Takemura

Kouji Itano

Hiroyuki Komatsu

Original Assignee

Jsr Corp

Priority date (The priority date 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 date listed.)

2013-02-12

Filing date

2014-02-11

Publication date

2018-01-21

2014-02-11 Application filed by Jsr Corp filed Critical Jsr Corp

2014-09-16 Publication of TW201434997A publication Critical patent/TW201434997A/zh

2018-01-21 Application granted granted Critical

2018-01-21 Publication of TWI612103B publication Critical patent/TWI612103B/zh

Links

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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
- G03F7/09—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
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B57/00—Other synthetic dyes of known constitution
- C09B57/04—Isoindoline dyes
- 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
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F39/00—Integrated devices, or assemblies of multiple devices, comprising at least one element covered by group H10F30/00, e.g. radiation detectors comprising photodiode arrays
- H10F39/80—Constructional details of image sensors
- H10F39/805—Coatings
- H10F39/8053—Colour filters
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10H—INORGANIC LIGHT-EMITTING SEMICONDUCTOR DEVICES HAVING POTENTIAL BARRIERS
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Publication number	Priority date	Publication date	Assignee	Title
KR101943340B1 (ko)	2014-12-25	2019-01-29	후지필름 가부시키가이샤	착색 조성물, 착색 조성물의 제조 방법, 컬러 필터, 패턴 형성 방법, 컬러 필터의 제조 방법, 고체 촬상 소자, 및 화상 표시 장치
KR20180034525A (ko) *	2015-08-31	2018-04-04	후지필름 가부시키가이샤	착색 감광성 조성물, 경화막, 컬러 필터, 차광막, 고체 촬상 소자, 화상 표시 장치, 및 경화막의 제조 방법
KR101895911B1 (ko) *	2016-01-11	2018-09-07	삼성에스디아이 주식회사	감광성 수지 조성물, 이를 이용한 감광성 수지막 및 컬러 필터
KR101895310B1 (ko) *	2016-01-25	2018-09-05	삼성에스디아이 주식회사	감광성 수지 조성물, 감광성 수지막 및 이를 이용한 컬러필터
JP2018168266A (ja) *	2017-03-29	2018-11-01	株式会社日本触媒	硬化性樹脂組成物及びその用途
JP6954077B2 (ja) *	2017-12-13	2021-10-27	東洋インキＳｃホールディングス株式会社	カラーフィルタ用着色組成物およびその製造方法
JP7605652B2 (ja)	2020-03-31	2024-12-24	サカタインクス株式会社	カラーフィルター用赤色顔料分散組成物
KR102762228B1 (ko) *	2021-02-26	2025-02-07	동우 화인켐 주식회사	감광성 수지 조성물, 이를 이용하여 제조된 컬러필터 및 이를 포함하는 표시장치
CN118742581A (zh) *	2022-02-25	2024-10-01	株式会社日本触媒	聚合物及其感光性树脂组合物
JP7605255B1 (ja)	2023-07-10	2024-12-24	ａｒｔｉｅｎｃｅ株式会社	赤色感光性組成物、膜、カラーフィルタ、固体撮像素子、及び画像表示装置

Citations (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH10300920A (ja) *	1997-04-28	1998-11-13	Sumitomo Chem Co Ltd	カラーフィルター用着色組成物およびカラーフィルター

Family Cites Families (14)

* Cited by examiner, † Cited by third party
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
JP2003057425A (ja) *	2001-08-08	2003-02-26	Toyo Ink Mfg Co Ltd	カラーフィルタ用顔料、その製造方法、およびそれを用いたカラーフィルタ用着色組成物
JP2003057434A (ja) *	2001-08-08	2003-02-26	Toyo Ink Mfg Co Ltd	カラーフィルタ
EP2196505B1 (en) *	2007-08-22	2014-03-05	Toyo Ink Mfg. Co. Ltd.	Pigment composition for color filter and coloring composition for color filter
JP5523677B2 (ja) *	2007-09-26	2014-06-18	富士フイルム株式会社	顔料分散組成物、光硬化性組成物、およびカラーフィルタ
US9442372B2 (en) *	2007-09-26	2016-09-13	Fujifilm Corporation	Pigment dispersion composition, photocurable composition and color filter
JP5348522B2 (ja) *	2008-06-27	2013-11-20	大日本印刷株式会社	着色組成物およびカラーフィルタ
JP2010223987A (ja) *	2009-03-19	2010-10-07	Dnp Fine Chemicals Co Ltd	カラーフィルター用赤色組成物及びそれを有するカラーフィルター
JP5377021B2 (ja) *	2009-03-23	2013-12-25	太陽ホールディングス株式会社	硬化性樹脂組成物、それを用いたドライフィルム及びプリント配線板
JP5707105B2 (ja) *	2010-11-19	2015-04-22	東洋インキＳｃホールディングス株式会社	カラーフィルタ用黄色着色組成物及びカラーフィルタ
TWI476273B (zh) *	2012-12-04	2015-03-11	迪愛生股份有限公司	Liquid crystal display device

2014
- 2014-02-05 JP JP2014019903A patent/JP6281305B2/ja active Active
- 2014-02-07 KR KR1020140013934A patent/KR102164864B1/ko active Active
- 2014-02-11 TW TW103104345A patent/TWI612103B/zh active

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH10300920A (ja) *	1997-04-28	1998-11-13	Sumitomo Chem Co Ltd	カラーフィルター用着色組成物およびカラーフィルター

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JP2014178676A (ja)	2014-09-25
TW201434997A (zh)	2014-09-16
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TWI612103B (zh)	2018-01-21	著色組成物、著色硬化膜、顯示元件及固態攝影元件
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TWI651371B (zh)	2019-02-21	著色組成物、著色硬化膜、以及顯示元件及固態攝影元件
TWI627233B (zh)	2018-06-21	著色組成物、著色硬化膜及顯示元件
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