JP2020534413A5 - - Google Patents
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- JP2020534413A5 JP2020534413A5 JP2020516570A JP2020516570A JP2020534413A5 JP 2020534413 A5 JP2020534413 A5 JP 2020534413A5 JP 2020516570 A JP2020516570 A JP 2020516570A JP 2020516570 A JP2020516570 A JP 2020516570A JP 2020534413 A5 JP2020534413 A5 JP 2020534413A5
- Authority
- JP
- Japan
- Prior art keywords
- bis
- group
- solution composition
- diamine
- aminophenoxy
- 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.)
- Pending
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- 239000000203 mixture Substances 0.000 claims description 20
- 150000004985 diamines Chemical class 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 17
- 229920001721 polyimide Polymers 0.000 claims description 14
- NVKGJHAQGWCWDI-UHFFFAOYSA-N 4-[4-amino-2-(trifluoromethyl)phenyl]-3-(trifluoromethyl)aniline Chemical compound FC(F)(F)C1=CC(N)=CC=C1C1=CC=C(N)C=C1C(F)(F)F NVKGJHAQGWCWDI-UHFFFAOYSA-N 0.000 claims description 12
- 125000003118 aryl group Chemical group 0.000 claims description 10
- 229920005575 poly(amic acid) Polymers 0.000 claims description 10
- 150000000000 tetracarboxylic acids Chemical class 0.000 claims description 9
- QQGYZOYWNCKGEK-UHFFFAOYSA-N 5-[(1,3-dioxo-2-benzofuran-5-yl)oxy]-2-benzofuran-1,3-dione Chemical group C1=C2C(=O)OC(=O)C2=CC(OC=2C=C3C(=O)OC(C3=CC=2)=O)=C1 QQGYZOYWNCKGEK-UHFFFAOYSA-N 0.000 claims description 8
- GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 claims description 8
- 125000000962 organic group Chemical group 0.000 claims description 8
- 239000000758 substrate Substances 0.000 claims description 8
- -1 Tetracarboxylic acid dianhydride Chemical class 0.000 claims description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 6
- 239000011521 glass Substances 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 6
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 claims description 4
- 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 claims description 4
- HLBLWEWZXPIGSM-UHFFFAOYSA-N 4-Aminophenyl ether Chemical compound C1=CC(N)=CC=C1OC1=CC=C(N)C=C1 HLBLWEWZXPIGSM-UHFFFAOYSA-N 0.000 claims description 4
- MQJKPEGWNLWLTK-UHFFFAOYSA-N Dapsone Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=C1 MQJKPEGWNLWLTK-UHFFFAOYSA-N 0.000 claims description 4
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 150000008064 anhydrides Chemical class 0.000 claims description 4
- 150000004984 aromatic diamines Chemical class 0.000 claims description 4
- 125000006159 dianhydride group Chemical group 0.000 claims description 4
- 239000010408 film Substances 0.000 claims description 4
- 125000003709 fluoroalkyl group Chemical group 0.000 claims description 4
- 229940018564 m-phenylenediamine Drugs 0.000 claims description 4
- CXISKMDTEFIGTG-UHFFFAOYSA-N [4-(1,3-dioxo-2-benzofuran-5-carbonyl)oxyphenyl] 1,3-dioxo-2-benzofuran-5-carboxylate Chemical compound C1=C2C(=O)OC(=O)C2=CC(C(OC=2C=CC(OC(=O)C=3C=C4C(=O)OC(=O)C4=CC=3)=CC=2)=O)=C1 CXISKMDTEFIGTG-UHFFFAOYSA-N 0.000 claims description 3
- SXGMVGOVILIERA-UHFFFAOYSA-N (2R,3S)-2,3-diaminobutanoic acid Natural products CC(N)C(N)C(O)=O SXGMVGOVILIERA-UHFFFAOYSA-N 0.000 claims description 2
- NSGXIBWMJZWTPY-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropane Chemical compound FC(F)(F)CC(F)(F)F NSGXIBWMJZWTPY-UHFFFAOYSA-N 0.000 claims description 2
- LSEWRAOHDIBHFX-UHFFFAOYSA-N 2-[(1-carboxyanthracen-2-yl)methyl]anthracene-1-carboxylic acid Chemical compound C(C1=C(C2=CC3=CC=CC=C3C=C2C=C1)C(=O)O)C1=C(C2=CC3=CC=CC=C3C=C2C=C1)C(=O)O LSEWRAOHDIBHFX-UHFFFAOYSA-N 0.000 claims description 2
- MSTZGVRUOMBULC-UHFFFAOYSA-N 2-amino-4-[2-(3-amino-4-hydroxyphenyl)-1,1,1,3,3,3-hexafluoropropan-2-yl]phenol Chemical compound C1=C(O)C(N)=CC(C(C=2C=C(N)C(O)=CC=2)(C(F)(F)F)C(F)(F)F)=C1 MSTZGVRUOMBULC-UHFFFAOYSA-N 0.000 claims description 2
- ZBMISJGHVWNWTE-UHFFFAOYSA-N 3-(4-aminophenoxy)aniline Chemical compound C1=CC(N)=CC=C1OC1=CC=CC(N)=C1 ZBMISJGHVWNWTE-UHFFFAOYSA-N 0.000 claims description 2
- XUSNPFGLKGCWGN-UHFFFAOYSA-N 3-[4-(3-aminopropyl)piperazin-1-yl]propan-1-amine Chemical compound NCCCN1CCN(CCCN)CC1 XUSNPFGLKGCWGN-UHFFFAOYSA-N 0.000 claims description 2
- ICNFHJVPAJKPHW-UHFFFAOYSA-N 4,4'-Thiodianiline Chemical compound C1=CC(N)=CC=C1SC1=CC=C(N)C=C1 ICNFHJVPAJKPHW-UHFFFAOYSA-N 0.000 claims description 2
- YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 claims description 2
- FYYYKXFEKMGYLZ-UHFFFAOYSA-N 4-(1,3-dioxo-2-benzofuran-5-yl)-2-benzofuran-1,3-dione Chemical compound C=1C=C2C(=O)OC(=O)C2=CC=1C1=CC=CC2=C1C(=O)OC2=O FYYYKXFEKMGYLZ-UHFFFAOYSA-N 0.000 claims description 2
- AVCOFPOLGHKJQB-UHFFFAOYSA-N 4-(3,4-dicarboxyphenyl)sulfonylphthalic acid Chemical compound C1=C(C(O)=O)C(C(=O)O)=CC=C1S(=O)(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 AVCOFPOLGHKJQB-UHFFFAOYSA-N 0.000 claims description 2
- BEKFRNOZJSYWKZ-UHFFFAOYSA-N 4-[2-(4-aminophenyl)-1,1,1,3,3,3-hexafluoropropan-2-yl]aniline Chemical compound C1=CC(N)=CC=C1C(C(F)(F)F)(C(F)(F)F)C1=CC=C(N)C=C1 BEKFRNOZJSYWKZ-UHFFFAOYSA-N 0.000 claims description 2
- KWOIWTRRPFHBSI-UHFFFAOYSA-N 4-[2-[3-[2-(4-aminophenyl)propan-2-yl]phenyl]propan-2-yl]aniline Chemical compound C=1C=CC(C(C)(C)C=2C=CC(N)=CC=2)=CC=1C(C)(C)C1=CC=C(N)C=C1 KWOIWTRRPFHBSI-UHFFFAOYSA-N 0.000 claims description 2
- HESXPOICBNWMPI-UHFFFAOYSA-N 4-[2-[4-[2-(4-aminophenyl)propan-2-yl]phenyl]propan-2-yl]aniline Chemical compound C=1C=C(C(C)(C)C=2C=CC(N)=CC=2)C=CC=1C(C)(C)C1=CC=C(N)C=C1 HESXPOICBNWMPI-UHFFFAOYSA-N 0.000 claims description 2
- KMKWGXGSGPYISJ-UHFFFAOYSA-N 4-[4-[2-[4-(4-aminophenoxy)phenyl]propan-2-yl]phenoxy]aniline Chemical group C=1C=C(OC=2C=CC(N)=CC=2)C=CC=1C(C)(C)C(C=C1)=CC=C1OC1=CC=C(N)C=C1 KMKWGXGSGPYISJ-UHFFFAOYSA-N 0.000 claims description 2
- 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 claims description 2
- 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 claims description 2
- IWFSADBGACLBMH-UHFFFAOYSA-N 4-[4-[4-[4-amino-2-(trifluoromethyl)phenoxy]phenyl]phenoxy]-3-(trifluoromethyl)aniline Chemical group FC(F)(F)C1=CC(N)=CC=C1OC1=CC=C(C=2C=CC(OC=3C(=CC(N)=CC=3)C(F)(F)F)=CC=2)C=C1 IWFSADBGACLBMH-UHFFFAOYSA-N 0.000 claims description 2
- SLHXQWDUYXSTPA-UHFFFAOYSA-N 4-[5-(4-aminophenoxy)pentoxy]aniline Chemical compound C1=CC(N)=CC=C1OCCCCCOC1=CC=C(N)C=C1 SLHXQWDUYXSTPA-UHFFFAOYSA-N 0.000 claims description 2
- ZHBXLZQQVCDGPA-UHFFFAOYSA-N 5-[(1,3-dioxo-2-benzofuran-5-yl)sulfonyl]-2-benzofuran-1,3-dione Chemical compound C1=C2C(=O)OC(=O)C2=CC(S(=O)(=O)C=2C=C3C(=O)OC(C3=CC=2)=O)=C1 ZHBXLZQQVCDGPA-UHFFFAOYSA-N 0.000 claims description 2
- HJSYPLCSZPEDCQ-UHFFFAOYSA-N 5-[2-(3-amino-4-methylphenyl)-1,1,1,3,3,3-hexafluoropropan-2-yl]-2-methylaniline Chemical compound C1=C(N)C(C)=CC=C1C(C(F)(F)F)(C(F)(F)F)C1=CC=C(C)C(N)=C1 HJSYPLCSZPEDCQ-UHFFFAOYSA-N 0.000 claims description 2
- MQAHXEQUBNDFGI-UHFFFAOYSA-N 5-[4-[2-[4-[(1,3-dioxo-2-benzofuran-5-yl)oxy]phenyl]propan-2-yl]phenoxy]-2-benzofuran-1,3-dione Chemical compound C1=C2C(=O)OC(=O)C2=CC(OC2=CC=C(C=C2)C(C)(C=2C=CC(OC=3C=C4C(=O)OC(=O)C4=CC=3)=CC=2)C)=C1 MQAHXEQUBNDFGI-UHFFFAOYSA-N 0.000 claims description 2
- 102100024089 Aldo-keto reductase family 1 member C2 Human genes 0.000 claims description 2
- NEENBBXMGIEAEK-UHFFFAOYSA-N C1(=C(C(=CC=C1)C=O)C=O)C1=CC(=C(C=C1)C=O)C=O Chemical compound C1(=C(C(=CC=C1)C=O)C=O)C1=CC(=C(C=C1)C=O)C=O NEENBBXMGIEAEK-UHFFFAOYSA-N 0.000 claims description 2
- 101000690303 Homo sapiens Aldo-keto reductase family 1 member C2 Proteins 0.000 claims description 2
- AMNPXXIGUOKIPP-UHFFFAOYSA-N [4-(carbamothioylamino)phenyl]thiourea Chemical compound NC(=S)NC1=CC=C(NC(N)=S)C=C1 AMNPXXIGUOKIPP-UHFFFAOYSA-N 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- 239000000010 aprotic solvent Substances 0.000 claims description 2
- 239000012965 benzophenone Substances 0.000 claims description 2
- BBRLKRNNIMVXOD-UHFFFAOYSA-N bis[4-(3-aminophenoxy)phenyl]methanone Chemical compound NC1=CC=CC(OC=2C=CC(=CC=2)C(=O)C=2C=CC(OC=3C=C(N)C=CC=3)=CC=2)=C1 BBRLKRNNIMVXOD-UHFFFAOYSA-N 0.000 claims description 2
- 238000009835 boiling Methods 0.000 claims description 2
- 239000011248 coating agent Substances 0.000 claims description 2
- 238000000576 coating method Methods 0.000 claims description 2
- 239000013039 cover film Substances 0.000 claims description 2
- 230000009477 glass transition Effects 0.000 claims description 2
- 238000002834 transmittance Methods 0.000 claims description 2
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 claims description 2
- 230000004580 weight loss Effects 0.000 claims description 2
- 125000006158 tetracarboxylic acid group Chemical group 0.000 description 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2022179489A JP7623334B2 (ja) | 2017-09-19 | 2022-11-09 | 電子デバイスで使用するためのロ－カラーポリマー |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201762560274P | 2017-09-19 | 2017-09-19 | |
| US62/560,274 | 2017-09-19 | ||
| PCT/US2018/050388 WO2019060169A1 (en) | 2017-09-19 | 2018-09-11 | LOW-COLORED POLYMERS FOR USE IN ELECTRONIC DEVICES |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2022179489A Division JP7623334B2 (ja) | 2017-09-19 | 2022-11-09 | 電子デバイスで使用するためのロ－カラーポリマー |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2020534413A JP2020534413A (ja) | 2020-11-26 |
| JP2020534413A5 true JP2020534413A5 (enExample) | 2021-09-24 |
Family
ID=65810483
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020516570A Pending JP2020534413A (ja) | 2017-09-19 | 2018-09-11 | 電子デバイスで使用するためのロ−カラーポリマー |
| JP2022179489A Active JP7623334B2 (ja) | 2017-09-19 | 2022-11-09 | 電子デバイスで使用するためのロ－カラーポリマー |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2022179489A Active JP7623334B2 (ja) | 2017-09-19 | 2022-11-09 | 電子デバイスで使用するためのロ－カラーポリマー |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US20200216614A1 (enExample) |
| JP (2) | JP2020534413A (enExample) |
| KR (1) | KR102746213B1 (enExample) |
| CN (1) | CN111386299A (enExample) |
| TW (1) | TWI808096B (enExample) |
| WO (1) | WO2019060169A1 (enExample) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2020110948A1 (ja) * | 2018-11-28 | 2020-06-04 | 三菱瓦斯化学株式会社 | ポリイミド樹脂、ポリイミドワニス及びポリイミドフィルム |
| CN112521603B (zh) | 2019-09-19 | 2023-06-02 | 臻鼎科技股份有限公司 | 聚酰胺酸嵌段共聚物及其制备方法、聚酰亚胺覆铜板及电路板 |
| TWI764046B (zh) * | 2019-09-19 | 2022-05-11 | 臻鼎科技股份有限公司 | 聚醯胺酸嵌段共聚物及其製備方法、聚醯亞胺覆銅板及電路板 |
| KR102147367B1 (ko) | 2019-09-30 | 2020-08-24 | 에스케이이노베이션 주식회사 | 윈도우 커버 필름 및 이를 포함하는 플렉서블 디스플레이 패널 |
| TWI708802B (zh) * | 2019-10-03 | 2020-11-01 | 達邁科技股份有限公司 | 顯示器用之連續式透明聚醯亞胺膜製造方法 |
| JP7359662B2 (ja) * | 2019-11-26 | 2023-10-11 | 株式会社カネカ | ポリイミド樹脂、ポリイミド溶液、ポリイミドフィルム |
| KR102280933B1 (ko) * | 2020-04-14 | 2021-07-23 | 에스케이이노베이션 주식회사 | 윈도우 커버 필름 및 이를 포함하는 플렉서블 디스플레이 패널 |
| CN111690135B (zh) * | 2020-07-21 | 2022-04-29 | 中国科学院宁波材料技术与工程研究所 | 含金刚烷结构的二胺单体、聚酰亚胺薄膜、其制法与应用 |
| KR20220032905A (ko) * | 2020-09-08 | 2022-03-15 | 주식회사 엘지화학 | 폴리이미드계 수지 필름 및 이를 이용한 디스플레이 장치용 기판, 및 광학 장치 |
| CN114456378B (zh) * | 2020-11-09 | 2024-02-27 | 江苏三月科技股份有限公司 | 一种用于液晶取向剂的聚酰亚胺及其制备的液晶取向膜 |
| CN117460762A (zh) | 2021-06-07 | 2024-01-26 | 杜邦电子公司 | 用于电子装置的聚合物 |
| KR20230066952A (ko) * | 2021-11-08 | 2023-05-16 | 주식회사 엘지화학 | 폴리이미드계 수지 필름 및 이를 이용한 디스플레이 장치용 기판, 및 광학 장치 |
| CN114920932B (zh) * | 2022-06-06 | 2023-08-22 | 黑龙江省科学院石油化学研究院 | 一种稳定性良好、耐高温热固性聚酰亚胺前驱体溶液及制备方法 |
| CN116162244B (zh) * | 2023-03-03 | 2024-02-27 | 四川大学 | 一种耐弯折聚酰亚胺薄膜及其制备方法 |
| KR20250055093A (ko) * | 2023-10-17 | 2025-04-24 | 피아이첨단소재 주식회사 | 가용 특성을 갖는 폴리이미드 및 그의 제조방법 |
| KR102727806B1 (ko) * | 2023-10-24 | 2024-11-08 | 피아이첨단소재 주식회사 | 폴리이미드 필름 및 이의 제조방법 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2883196B2 (ja) * | 1990-11-22 | 1999-04-19 | 東邦レーヨン株式会社 | 高性能ポリイミド成形体及びその製造方法 |
| JPH07173287A (ja) * | 1993-12-17 | 1995-07-11 | Toyobo Co Ltd | 有機溶媒可溶性ポリイミド |
| KR101225842B1 (ko) * | 2007-08-27 | 2013-01-23 | 코오롱인더스트리 주식회사 | 무색투명한 폴리이미드 필름 |
| JP5469578B2 (ja) * | 2010-10-01 | 2014-04-16 | 日本化薬株式会社 | プライマー層を有する銅張積層板及びそれを用いた配線基板 |
| CN105637016B (zh) * | 2014-05-30 | 2017-11-07 | 株式会社Lg化学 | 聚酰亚胺基液体和使用其制备的聚酰亚胺基膜 |
| KR102181466B1 (ko) * | 2015-03-31 | 2020-11-23 | 아사히 가세이 가부시키가이샤 | 폴리이미드 필름, 폴리이미드 바니시, 폴리이미드 필름을 이용한 제품 및 적층체 |
| CN113292853B (zh) * | 2015-04-17 | 2024-04-05 | 旭化成株式会社 | 树脂组合物、聚酰亚胺树脂膜及其制造方法 |
| EP3290461B1 (en) * | 2015-04-28 | 2024-01-17 | Kolon Industries, Inc. | Polyimide resin and film using same |
| KR20170007227A (ko) * | 2016-12-28 | 2017-01-18 | 김석진 | 폴리이미드 수지의 제조방법 및 이로써 제조된 폴리이미드 필름 |
-
2018
- 2018-09-11 US US16/648,183 patent/US20200216614A1/en not_active Abandoned
- 2018-09-11 JP JP2020516570A patent/JP2020534413A/ja active Pending
- 2018-09-11 CN CN201880071412.0A patent/CN111386299A/zh active Pending
- 2018-09-11 KR KR1020207011023A patent/KR102746213B1/ko active Active
- 2018-09-11 WO PCT/US2018/050388 patent/WO2019060169A1/en not_active Ceased
- 2018-09-14 TW TW107132399A patent/TWI808096B/zh active
-
2022
- 2022-11-07 US US17/982,217 patent/US20230074583A1/en not_active Abandoned
- 2022-11-09 JP JP2022179489A patent/JP7623334B2/ja active Active
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