JP2019174801A5 - - Google Patents
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- Publication number
- JP2019174801A5 JP2019174801A5 JP2019048368A JP2019048368A JP2019174801A5 JP 2019174801 A5 JP2019174801 A5 JP 2019174801A5 JP 2019048368 A JP2019048368 A JP 2019048368A JP 2019048368 A JP2019048368 A JP 2019048368A JP 2019174801 A5 JP2019174801 A5 JP 2019174801A5
- Authority
- JP
- Japan
- Prior art keywords
- bis
- optical film
- less
- transparent polyimide
- polyimide
- Prior art date
- Legal status (The legal status 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 status listed.)
- Granted
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- 229920001721 polyimide Polymers 0.000 description 13
- 239000012788 optical film Substances 0.000 description 12
- 239000010408 film Substances 0.000 description 5
- 238000005160 1H NMR spectroscopy Methods 0.000 description 4
- 239000004642 Polyimide Substances 0.000 description 4
- 150000004984 aromatic diamines Chemical class 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- NVKGJHAQGWCWDI-UHFFFAOYSA-N 4-[4-amino-2-(trifluoromethyl)phenyl]-3-(trifluoromethyl)aniline Chemical class FC(F)(F)C1=CC(N)=CC=C1C1=CC=C(N)C=C1C(F)(F)F NVKGJHAQGWCWDI-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000002966 varnish Substances 0.000 description 3
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 125000005462 imide group Chemical group 0.000 description 2
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 1
- LXJLFVRAWOOQDR-UHFFFAOYSA-N 3-(3-aminophenoxy)aniline Chemical compound NC1=CC=CC(OC=2C=C(N)C=CC=2)=C1 LXJLFVRAWOOQDR-UHFFFAOYSA-N 0.000 description 1
- LJGHYPLBDBRCRZ-UHFFFAOYSA-N 3-(3-aminophenyl)sulfonylaniline Chemical compound NC1=CC=CC(S(=O)(=O)C=2C=C(N)C=CC=2)=C1 LJGHYPLBDBRCRZ-UHFFFAOYSA-N 0.000 description 1
- ZBMISJGHVWNWTE-UHFFFAOYSA-N 3-(4-aminophenoxy)aniline Chemical compound C1=CC(N)=CC=C1OC1=CC=CC(N)=C1 ZBMISJGHVWNWTE-UHFFFAOYSA-N 0.000 description 1
- ZMPZWXKBGSQATE-UHFFFAOYSA-N 3-(4-aminophenyl)sulfonylaniline Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=CC(N)=C1 ZMPZWXKBGSQATE-UHFFFAOYSA-N 0.000 description 1
- NYRFBMFAUFUULG-UHFFFAOYSA-N 3-[4-[2-[4-(3-aminophenoxy)phenyl]propan-2-yl]phenoxy]aniline Chemical compound C=1C=C(OC=2C=C(N)C=CC=2)C=CC=1C(C)(C)C(C=C1)=CC=C1OC1=CC=CC(N)=C1 NYRFBMFAUFUULG-UHFFFAOYSA-N 0.000 description 1
- WCXGOVYROJJXHA-UHFFFAOYSA-N 3-[4-[4-(3-aminophenoxy)phenyl]sulfonylphenoxy]aniline Chemical compound NC1=CC=CC(OC=2C=CC(=CC=2)S(=O)(=O)C=2C=CC(OC=3C=C(N)C=CC=3)=CC=2)=C1 WCXGOVYROJJXHA-UHFFFAOYSA-N 0.000 description 1
- YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 1
- QYIMZXITLDTULQ-UHFFFAOYSA-N 4-(4-amino-2-methylphenyl)-3-methylaniline Chemical compound CC1=CC(N)=CC=C1C1=CC=C(N)C=C1C QYIMZXITLDTULQ-UHFFFAOYSA-N 0.000 description 1
- HLBLWEWZXPIGSM-UHFFFAOYSA-N 4-Aminophenyl ether Chemical compound C1=CC(N)=CC=C1OC1=CC=C(N)C=C1 HLBLWEWZXPIGSM-UHFFFAOYSA-N 0.000 description 1
- WUPRYUDHUFLKFL-UHFFFAOYSA-N 4-[3-(4-aminophenoxy)phenoxy]aniline Chemical compound C1=CC(N)=CC=C1OC1=CC=CC(OC=2C=CC(N)=CC=2)=C1 WUPRYUDHUFLKFL-UHFFFAOYSA-N 0.000 description 1
- JCRRFJIVUPSNTA-UHFFFAOYSA-N 4-[4-(4-aminophenoxy)phenoxy]aniline Chemical compound C1=CC(N)=CC=C1OC(C=C1)=CC=C1OC1=CC=C(N)C=C1 JCRRFJIVUPSNTA-UHFFFAOYSA-N 0.000 description 1
- HYDATEKARGDBKU-UHFFFAOYSA-N 4-[4-[4-(4-aminophenoxy)phenyl]phenoxy]aniline Chemical group C1=CC(N)=CC=C1OC1=CC=C(C=2C=CC(OC=3C=CC(N)=CC=3)=CC=2)C=C1 HYDATEKARGDBKU-UHFFFAOYSA-N 0.000 description 1
- UTDAGHZGKXPRQI-UHFFFAOYSA-N 4-[4-[4-(4-aminophenoxy)phenyl]sulfonylphenoxy]aniline Chemical compound C1=CC(N)=CC=C1OC1=CC=C(S(=O)(=O)C=2C=CC(OC=3C=CC(N)=CC=3)=CC=2)C=C1 UTDAGHZGKXPRQI-UHFFFAOYSA-N 0.000 description 1
- CIZUMWWHWPJAAK-UHFFFAOYSA-N 4-[9-(4-amino-3-chlorophenyl)fluoren-9-yl]-2-chloroaniline Chemical compound C1=C(Cl)C(N)=CC=C1C1(C=2C=C(Cl)C(N)=CC=2)C2=CC=CC=C2C2=CC=CC=C21 CIZUMWWHWPJAAK-UHFFFAOYSA-N 0.000 description 1
- RXNKCIBVUNMMAD-UHFFFAOYSA-N 4-[9-(4-amino-3-fluorophenyl)fluoren-9-yl]-2-fluoroaniline Chemical compound C1=C(F)C(N)=CC=C1C1(C=2C=C(F)C(N)=CC=2)C2=CC=CC=C2C2=CC=CC=C21 RXNKCIBVUNMMAD-UHFFFAOYSA-N 0.000 description 1
- YRKVLGUIGNRYJX-UHFFFAOYSA-N 4-[9-(4-amino-3-methylphenyl)fluoren-9-yl]-2-methylaniline Chemical compound C1=C(N)C(C)=CC(C2(C3=CC=CC=C3C3=CC=CC=C32)C=2C=C(C)C(N)=CC=2)=C1 YRKVLGUIGNRYJX-UHFFFAOYSA-N 0.000 description 1
- KIFDSGGWDIVQGN-UHFFFAOYSA-N 4-[9-(4-aminophenyl)fluoren-9-yl]aniline Chemical compound C1=CC(N)=CC=C1C1(C=2C=CC(N)=CC=2)C2=CC=CC=C2C2=CC=CC=C21 KIFDSGGWDIVQGN-UHFFFAOYSA-N 0.000 description 1
- MQJKPEGWNLWLTK-UHFFFAOYSA-N Dapsone Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=C1 MQJKPEGWNLWLTK-UHFFFAOYSA-N 0.000 description 1
- 206010039424 Salivary hypersecretion Diseases 0.000 description 1
- FDLQZKYLHJJBHD-UHFFFAOYSA-N [3-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC(CN)=C1 FDLQZKYLHJJBHD-UHFFFAOYSA-N 0.000 description 1
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- JBTWLSYIZRCDFO-UHFFFAOYSA-N ethyl methyl carbonate Chemical compound CCOC(=O)OC JBTWLSYIZRCDFO-UHFFFAOYSA-N 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 229940018564 m-phenylenediamine Drugs 0.000 description 1
- NTNWKDHZTDQSST-UHFFFAOYSA-N naphthalene-1,2-diamine Chemical compound C1=CC=CC2=C(N)C(N)=CC=C21 NTNWKDHZTDQSST-UHFFFAOYSA-N 0.000 description 1
- KQSABULTKYLFEV-UHFFFAOYSA-N naphthalene-1,5-diamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1N KQSABULTKYLFEV-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- -1 polyethylene terephthalate Polymers 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 208000026451 salivation Diseases 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2018063083 | 2018-03-28 | ||
| JP2018063083 | 2018-03-28 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2019174801A JP2019174801A (ja) | 2019-10-10 |
| JP2019174801A5 true JP2019174801A5 (enExample) | 2022-03-18 |
| JP7361479B2 JP7361479B2 (ja) | 2023-10-16 |
Family
ID=68113104
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019048368A Active JP7361479B2 (ja) | 2018-03-28 | 2019-03-15 | 透明ポリイミド系高分子を含む光学フィルム |
Country Status (4)
| Country | Link |
|---|---|
| JP (1) | JP7361479B2 (enExample) |
| KR (1) | KR102769184B1 (enExample) |
| CN (1) | CN110317353A (enExample) |
| TW (1) | TWI821262B (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW202208512A (zh) * | 2020-07-02 | 2022-03-01 | 日商住友化學股份有限公司 | 光學膜及柔性顯示裝置 |
| US12384886B2 (en) | 2022-03-03 | 2025-08-12 | Asahi Kasei Kabushiki Kaisha | Porous polyimide composition and polyamide acid composition |
| CN116693927B (zh) * | 2022-03-03 | 2024-09-27 | 旭化成株式会社 | 多孔质聚酰亚胺组合物和聚酰胺酸组合物 |
| KR20230134903A (ko) * | 2022-03-15 | 2023-09-22 | 주식회사 엘지화학 | 고분자 수지 조성물, 고분자 수지 필름의 제조방법, 고분자 수지 필름 및 이를 이용한 디스플레이 장치용 기판, 및 광학 장치 |
| WO2023249022A1 (ja) * | 2022-06-24 | 2023-12-28 | 三菱瓦斯化学株式会社 | ポリイミドワニスの製造方法 |
| DE112023000118T5 (de) | 2022-07-28 | 2024-08-22 | Murata Manufacturing Co., Ltd. | Elektrooptisches polymer |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3735361B2 (ja) * | 2003-08-07 | 2006-01-18 | 日東電工株式会社 | 光学フィルムの製造方法、それにより得られた光学フィルム、液晶パネルおよび液晶表示装置 |
| JP2011222779A (ja) * | 2010-04-09 | 2011-11-04 | Dainippon Printing Co Ltd | 薄膜素子用基板の製造方法、薄膜素子の製造方法および薄膜トランジスタの製造方法 |
| JP5862674B2 (ja) * | 2011-09-29 | 2016-02-16 | Jsr株式会社 | 樹脂組成物およびそれを用いた膜形成方法 |
| KR101646283B1 (ko) * | 2011-12-27 | 2016-08-08 | 코오롱인더스트리 주식회사 | 폴리아믹산 용액 |
| JP2013227500A (ja) * | 2012-03-30 | 2013-11-07 | New Japan Chem Co Ltd | 溶剤可溶性ポリイミド樹脂 |
| KR101692648B1 (ko) * | 2012-09-14 | 2017-01-03 | 미쓰이 가가쿠 가부시키가이샤 | 투명 폴리이미드 적층체 및 그의 제조 방법 |
| KR101387031B1 (ko) * | 2013-02-28 | 2014-04-18 | 한국과학기술원 | 유리섬유직물이 매립된 플렉시블 디스플레이용 무색투명 폴리이미드 필름 제조방법 |
| MX382575B (es) * | 2013-10-18 | 2025-03-13 | Toray Industries | Composición de resina de poliamida, método de fabricación y producto moldeado. |
| JP2015174905A (ja) | 2014-03-14 | 2015-10-05 | Dic株式会社 | 硬化性アミドイミド樹脂、硬化性樹脂組成物及びその硬化物 |
| WO2017014286A1 (ja) * | 2015-07-22 | 2017-01-26 | 住友化学株式会社 | ポリイミド系ワニス、それを用いたポリイミド系フィルムの製造方法、及び、ポリイミド系フィルム |
| JP6917187B2 (ja) * | 2016-05-10 | 2021-08-11 | 住友化学株式会社 | 光学フィルム、及びこれを用いたフレキシブルデバイス |
-
2019
- 2019-03-15 JP JP2019048368A patent/JP7361479B2/ja active Active
- 2019-03-26 TW TW108110475A patent/TWI821262B/zh active
- 2019-03-27 KR KR1020190035358A patent/KR102769184B1/ko active Active
- 2019-03-27 CN CN201910241912.0A patent/CN110317353A/zh active Pending
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