TW201638153A - 聚醯亞胺系光學薄膜、其製造方法及有機電致發光顯示器 - Google Patents

聚醯亞胺系光學薄膜、其製造方法及有機電致發光顯示器 Download PDF

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Publication number: TW201638153A
Authority: TW; Taiwan
Prior art keywords: film; polyimine; group; optical film; formula
Prior art date: 2015-03-24

Application number

TW105108668A

Other languages

English (en)

Chinese (zh)

Inventor

Kenta Mashima

Hiroki Umeda

Yasutoshi Ito

Naoya Iwagami

Original Assignee

Konica Minolta Inc

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.)

2015-03-24

Filing date

2016-03-21

Publication date

2016-11-01

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=56978015&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=TW201638153(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

2016-03-21 Application filed by Konica Minolta Inc filed Critical Konica Minolta Inc

2016-11-01 Publication of TW201638153A publication Critical patent/TW201638153A/zh

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WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical group CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 1
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LJZVDOUZSMHXJH-UHFFFAOYSA-K ruthenium(3+);triiodide Chemical compound [Ru+3].[I-].[I-].[I-] LJZVDOUZSMHXJH-UHFFFAOYSA-K 0.000 description 1
238000000926 separation method Methods 0.000 description 1
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239000006104 solid solution Substances 0.000 description 1
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239000011593 sulfur Substances 0.000 description 1
ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
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YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
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Classifications

- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- 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
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C41/00—Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor
- B29C41/24—Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor for making articles of indefinite length
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L79/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen or carbon only, not provided for in groups C08L61/00 - C08L77/00
- C08L79/04—Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
- C08L79/08—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/02—Details

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Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Manufacturing & Machinery (AREA)
Health & Medical Sciences (AREA)
Physics & Mathematics (AREA)
Materials Engineering (AREA)
Mechanical Engineering (AREA)
General Physics & Mathematics (AREA)
Optics & Photonics (AREA)
Electroluminescent Light Sources (AREA)
Manufacture Of Macromolecular Shaped Articles (AREA)
Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Devices For Indicating Variable Information By Combining Individual Elements (AREA)

TW105108668A 2015-03-24 2016-03-21 聚醯亞胺系光學薄膜、其製造方法及有機電致發光顯示器 TW201638153A (zh)

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JP6541856B1 (ja)	2018-10-02	2019-07-10	住友化学株式会社	光学フィルム、フレキシブル表示装置及び光学フィルムの製造方法
JP6556317B1 (ja)	2018-11-27	2019-08-07	住友化学株式会社	光学積層体、フレキシブル表示装置及び光学積層体の製造方法
JP2021063212A (ja) *	2019-10-15	2021-04-22	住友化学株式会社	光学フィルム
WO2021085283A1 (ja) *	2019-10-31	2021-05-06	住友化学株式会社	ポリアミドイミド樹脂
CN114599739A (zh)	2019-10-31	2022-06-07	住友化学株式会社	光学膜和柔性显示装置
JP2021075700A (ja) *	2019-10-31	2021-05-20	住友化学株式会社	ポリアミドイミド樹脂
KR102686387B1 (ko)	2019-11-01	2024-07-22	삼성디스플레이 주식회사	표시 장치 및 표시 장치 제조 방법
CN114967321B (zh) *	2022-06-21	2023-03-07	广东工业大学	一种光敏聚酰亚胺衍生氮掺杂碳图案及其制备方法和应用

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4222884A (en)	1978-12-04	1980-09-16	Ethyl Corporation	Antioxidant
JPS60139413A (ja) *	1983-12-27	1985-07-24	Mitsubishi Plastics Ind Ltd	ポリエ−テルイミド粗面フイルムの製法
JP2000169579A (ja) *	1998-12-02	2000-06-20	Teijin Ltd	有機溶剤可溶性ポリイミドおよびその製造方法
JP2001302913A (ja) *	2000-04-21	2001-10-31	Unitika Ltd	ポリイミド前駆体溶液及びそれから得られるポリイミド被膜
US20060084741A1 (en) *	2004-10-19	2006-04-20	Sapna Blackburn	Polyetherimide composition, film, process, and article
JP5167059B2 (ja) *	2007-10-02	2013-03-21	日東電工株式会社	偏光板、光学フィルムおよび画像表示装置
KR102198316B1 (ko) *	2012-06-19	2021-01-04	닛테츠 케미컬 앤드 머티리얼 가부시키가이샤	표시장치 및 그 제조방법, 그리고 표시장치 지지기재용 폴리이미드 필름 및 그 제조방법
JP6457168B2 (ja) *	2012-06-19	2019-01-23	日鉄ケミカル＆マテリアル株式会社	表示装置支持基材用ポリイミドフィルム、及びその積層体、並びその製造方法
KR20150136097A (ko) *	2013-04-26	2015-12-04	코니카 미놀타 가부시키가이샤	편광판, 그 제조 방법 및 액정 표시 장치
JP6350523B2 (ja) *	2013-05-28	2018-07-04	旭硝子株式会社	フレキシブル基材およびその製造方法、ガラス積層体およびその製造方法、電子デバイスの製造方法

2016
- 2016-03-04 WO PCT/JP2016/056756 patent/WO2016152459A1/ja active Application Filing
- 2016-03-04 JP JP2017508162A patent/JP6635110B2/ja active Active
- 2016-03-04 KR KR1020177024910A patent/KR102046699B1/ko active IP Right Grant
- 2016-03-21 TW TW105108668A patent/TW201638153A/zh unknown

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
TWI752146B (zh) *	2017-01-09	2022-01-11	美商克萊譚克公司	在晶圓幾何系統中透明薄膜誤差校正型態
CN110199210A (zh) *	2017-01-20	2019-09-03	住友化学株式会社	光学膜及光学膜的制造方法
TWI758399B (zh) *	2017-01-20	2022-03-21	日商住友化學股份有限公司	光學膜及光學膜之製造方法

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