JP2016037604A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2016037604A5 JP2016037604A5 JP2015148813A JP2015148813A JP2016037604A5 JP 2016037604 A5 JP2016037604 A5 JP 2016037604A5 JP 2015148813 A JP2015148813 A JP 2015148813A JP 2015148813 A JP2015148813 A JP 2015148813A JP 2016037604 A5 JP2016037604 A5 JP 2016037604A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- dichloride
- organic solvent
- substituted
- polyamide
- 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
Links
- 238000004519 manufacturing process Methods 0.000 claims description 14
- 239000004952 Polyamide Substances 0.000 claims description 11
- 229920002647 polyamide Polymers 0.000 claims description 11
- 239000003960 organic solvent Substances 0.000 claims description 10
- 150000004985 diamines Chemical class 0.000 claims description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 6
- GHLZUHZBBNDWHW-UHFFFAOYSA-N nonanamide Chemical compound CCCCCCCCC(N)=O GHLZUHZBBNDWHW-UHFFFAOYSA-N 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 4
- 150000001408 amides Chemical class 0.000 claims description 4
- 239000003153 chemical reaction reagent Substances 0.000 claims description 4
- 238000000034 method Methods 0.000 claims 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims 4
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims 4
- 125000003118 aryl group Chemical group 0.000 claims 4
- 229910052736 halogen Inorganic materials 0.000 claims 4
- 150000002367 halogens Chemical class 0.000 claims 4
- 238000005286 illumination Methods 0.000 claims 4
- 230000003287 optical effect Effects 0.000 claims 4
- 125000000547 substituted alkyl group Chemical group 0.000 claims 4
- 125000003107 substituted aryl group Chemical group 0.000 claims 4
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims 2
- 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 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical group CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000005907 alkyl ester group Chemical group 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 150000002431 hydrogen Chemical class 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 239000000463 material Substances 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims 2
- 125000005415 substituted alkoxy group Chemical group 0.000 claims 2
- 125000004434 sulfur atom Chemical group 0.000 claims 2
- LXEJRKJRKIFVNY-UHFFFAOYSA-N terephthaloyl chloride Chemical compound ClC(=O)C1=CC=C(C(Cl)=O)C=C1 LXEJRKJRKIFVNY-UHFFFAOYSA-N 0.000 claims 2
- 125000004001 thioalkyl group Chemical group 0.000 claims 2
- ZFPGARUNNKGOBB-UHFFFAOYSA-N 1-Ethyl-2-pyrrolidinone Chemical compound CCN1CCCC1=O ZFPGARUNNKGOBB-UHFFFAOYSA-N 0.000 claims 1
- GGYVTHJIUNGKFZ-UHFFFAOYSA-N 1-methylpiperidin-2-one Chemical compound CN1CCCCC1=O GGYVTHJIUNGKFZ-UHFFFAOYSA-N 0.000 claims 1
- UENRXLSRMCSUSN-UHFFFAOYSA-N 3,5-diaminobenzoic acid Chemical compound NC1=CC(N)=CC(C(O)=O)=C1 UENRXLSRMCSUSN-UHFFFAOYSA-N 0.000 claims 1
- LVYXPOCADCXMLP-UHFFFAOYSA-N 3-butoxy-n,n-dimethylpropanamide Chemical compound CCCCOCCC(=O)N(C)C LVYXPOCADCXMLP-UHFFFAOYSA-N 0.000 claims 1
- LBVMWHCOFMFPEG-UHFFFAOYSA-N 3-methoxy-n,n-dimethylpropanamide Chemical compound COCCC(=O)N(C)C LBVMWHCOFMFPEG-UHFFFAOYSA-N 0.000 claims 1
- QDBOAKPEXMMQFO-UHFFFAOYSA-N 4-(4-carbonochloridoylphenyl)benzoyl chloride Chemical compound C1=CC(C(=O)Cl)=CC=C1C1=CC=C(C(Cl)=O)C=C1 QDBOAKPEXMMQFO-UHFFFAOYSA-N 0.000 claims 1
- VMHKBUVJDUPCDZ-UHFFFAOYSA-N 4-[2-[4-amino-2-(trifluoromethyl)phenoxy]phenoxy]-3-(trifluoromethyl)aniline Chemical compound FC(F)(F)C1=CC(N)=CC=C1OC1=CC=CC=C1OC1=CC=C(N)C=C1C(F)(F)F VMHKBUVJDUPCDZ-UHFFFAOYSA-N 0.000 claims 1
- BUDGDBNWOFUGQK-UHFFFAOYSA-N 4-[4,4-diamino-2-(trifluoromethyl)cyclohexa-2,5-dien-1-ylidene]-3-(trifluoromethyl)cyclohexa-2,5-diene-1,1-diamine Chemical group NC1(C=C(C(C=C1)=C1C(=CC(N)(C=C1)N)C(F)(F)F)C(F)(F)F)N BUDGDBNWOFUGQK-UHFFFAOYSA-N 0.000 claims 1
- 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 1
- NZOHUOCKJIYPKT-UHFFFAOYSA-N 4-[4-amino-2-(trifluoromethoxy)phenyl]-3-(trifluoromethoxy)aniline Chemical compound FC(F)(F)OC1=CC(N)=CC=C1C1=CC=C(N)C=C1OC(F)(F)F NZOHUOCKJIYPKT-UHFFFAOYSA-N 0.000 claims 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 claims 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 claims 1
- QGLBZNZGBLRJGS-UHFFFAOYSA-N Dihydro-3-methyl-2(3H)-furanone Chemical compound CC1CCOC1=O QGLBZNZGBLRJGS-UHFFFAOYSA-N 0.000 claims 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 1
- 239000000010 aprotic solvent Substances 0.000 claims 1
- FDQSRULYDNDXQB-UHFFFAOYSA-N benzene-1,3-dicarbonyl chloride Chemical compound ClC(=O)C1=CC=CC(C(Cl)=O)=C1 FDQSRULYDNDXQB-UHFFFAOYSA-N 0.000 claims 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 claims 1
- 239000011521 glass Substances 0.000 claims 1
- 150000002596 lactones Chemical class 0.000 claims 1
- AJFDBNQQDYLMJN-UHFFFAOYSA-N n,n-diethylacetamide Chemical compound CCN(CC)C(C)=O AJFDBNQQDYLMJN-UHFFFAOYSA-N 0.000 claims 1
- YKOQQFDCCBKROY-UHFFFAOYSA-N n,n-diethylpropanamide Chemical compound CCN(CC)C(=O)CC YKOQQFDCCBKROY-UHFFFAOYSA-N 0.000 claims 1
- VIJUZNJJLALGNJ-UHFFFAOYSA-N n,n-dimethylbutanamide Chemical compound CCCC(=O)N(C)C VIJUZNJJLALGNJ-UHFFFAOYSA-N 0.000 claims 1
- MBHINSULENHCMF-UHFFFAOYSA-N n,n-dimethylpropanamide Chemical compound CCC(=O)N(C)C MBHINSULENHCMF-UHFFFAOYSA-N 0.000 claims 1
- 229910052710 silicon Inorganic materials 0.000 claims 1
- 239000010703 silicon Substances 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 0 C**(C=CC=C1)C=C1N Chemical compound C**(C=CC=C1)C=C1N 0.000 description 2
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462034399P | 2014-08-07 | 2014-08-07 | |
| US62/034,399 | 2014-08-07 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016037604A JP2016037604A (ja) | 2016-03-22 |
| JP2016037604A5 true JP2016037604A5 (https=) | 2016-12-28 |
| JP6153571B2 JP6153571B2 (ja) | 2017-06-28 |
Family
ID=55266933
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015148813A Active JP6153571B2 (ja) | 2014-08-07 | 2015-07-28 | ポリアミドの製造方法 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US20160039974A1 (https=) |
| JP (1) | JP6153571B2 (https=) |
| KR (1) | KR20160018418A (https=) |
| CN (1) | CN105367783A (https=) |
| TW (1) | TW201609862A (https=) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105491839A (zh) * | 2014-10-02 | 2016-04-13 | 亚克朗聚合物系统公司 | 盖构件和电子器件 |
| US9696199B2 (en) * | 2015-02-13 | 2017-07-04 | Taiwan Biophotonic Corporation | Optical sensor |
| JP6798154B2 (ja) * | 2016-06-15 | 2020-12-09 | 富士ゼロックス株式会社 | 無端ベルト、画像形成装置、及び無端ベルトユニット |
| KR102376154B1 (ko) * | 2016-08-03 | 2022-03-18 | 닛산 가가쿠 가부시키가이샤 | 박리층 형성용 조성물 |
| KR102117151B1 (ko) | 2017-09-29 | 2020-05-29 | 주식회사 엘지화학 | 폴리이미드 전구체 용액 및 이를 이용하여 제조된 폴리이미드 필름 |
| KR102230059B1 (ko) | 2018-01-11 | 2021-03-18 | 주식회사 엘지화학 | 폴리아미드이미드 수지 필름 |
| KR20190115282A (ko) * | 2018-04-02 | 2019-10-11 | 주식회사 엘지화학 | 폴리아미드 블록 공중합체 및 이를 포함하는 폴리아미드 필름 |
| KR102718970B1 (ko) * | 2019-01-25 | 2024-10-16 | 주식회사 엘지화학 | 폴리아미드계 (공)중합체의 제조방법, 및 이를 이용한 폴리아미드계 (공)중합 수지 조성물, 고분자 필름 |
| KR102798816B1 (ko) * | 2020-03-23 | 2025-04-18 | 주식회사 엘지화학 | 폴리아미드 수지 조성물, 이의 제조방법, 및 이를 이용한 고분자 필름 및 수지 적층체 |
| KR102713248B1 (ko) * | 2020-12-31 | 2024-10-02 | 코오롱인더스트리 주식회사 | 낮은 색변환 지수를 갖는 광학 필름 및 이를 포함하는 표시장치 |
| KR102711953B1 (ko) * | 2020-12-31 | 2024-09-27 | 코오롱인더스트리 주식회사 | 우수한 광학 특성을 갖는 광학 필름 및 이를 포함하는 표시장치 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3696076A (en) * | 1970-05-22 | 1972-10-03 | Celanese Corp | Formation of cast films of aromatic polyamides |
| US4962181A (en) * | 1989-05-08 | 1990-10-09 | Hoechst Celanese Corp. | Polyamide polymer having 12-F fluorine-containing linking groups |
| JPH06157747A (ja) * | 1992-11-27 | 1994-06-07 | Hitachi Chem Co Ltd | 精製されたポリシロキサン構造を有するポリアミド共重合体の製造方法 |
| JP3246793B2 (ja) * | 1993-04-28 | 2002-01-15 | 日本油脂株式会社 | 高酸素透過性コンタクトレンズ |
| KR100994399B1 (ko) * | 2002-10-31 | 2010-11-16 | 도레이 카부시키가이샤 | 폴리아미드 및 폴리아미드 필름 |
| JP5347528B2 (ja) * | 2009-01-26 | 2013-11-20 | 三菱瓦斯化学株式会社 | ポリアミド |
| US9457496B2 (en) * | 2011-03-23 | 2016-10-04 | Akron Polymer Systems, Inc. | Aromatic polyamide films for transparent flexible substrates |
| US9856376B2 (en) * | 2011-07-05 | 2018-01-02 | Akron Polymer Systems, Inc. | Aromatic polyamide films for solvent resistant flexible substrates |
| JP6204478B2 (ja) * | 2012-09-24 | 2017-09-27 | アクロン ポリマー システムズ，インク． | ポリアミド溶液、ディスプレイ用素子、光学用素子、又は照明用素子の製造方法、およびポリアミド溶液の製造方法 |
-
2015
- 2015-07-28 JP JP2015148813A patent/JP6153571B2/ja active Active
- 2015-08-03 TW TW104125045A patent/TW201609862A/zh unknown
- 2015-08-05 US US14/818,431 patent/US20160039974A1/en not_active Abandoned
- 2015-08-06 KR KR1020150111112A patent/KR20160018418A/ko not_active Ceased
- 2015-08-07 CN CN201510483841.7A patent/CN105367783A/zh active Pending
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2016037604A5 (https=) | ||
| JP2014522894A5 (https=) | ||
| JP2013155329A5 (https=) | ||
| CN102449031B (zh) | 含有聚酰胺酸烷基酯的聚酰亚胺前体组合物 | |
| CN104837809B (zh) | 包含六氟异丙醇基的二胺、使用其的聚酰亚胺和聚酰胺、其环化物、及其制造方法 | |
| JP6849173B2 (ja) | ポリイミド前駆体溶液及びそれを用いて製造されたポリイミドフィルム | |
| JP4679328B2 (ja) | 含フッ素重合性単量体及びそれを用いた高分子化合物 | |
| JP2018119141A5 (https=) | ||
| ATE516319T1 (de) | Verfahren zur herstellung von polyamiden in extrudern | |
| JP2005232024A (ja) | シルセスキオキサン骨格を有するジアミン及びそれを用いた重合体 | |
| KR20120095347A (ko) | Ｐｍｄａ, ｄａｄｅ, ｂｐｄａ 및 9,9-비스(4-아미노페닐)플루오렌 성분을 함유하는 유기 용매에 가용인 폴리이미드 조성물 및 그 제조 방법 | |
| JP2014125455A (ja) | 含フッ素非対称ジアミン化合物を用いた高分子化合物とその製造方法 | |
| JP2000290374A (ja) | 含フッ素ポリベンゾオキサゾール | |
| JP2008150534A (ja) | 含フッ素ジアミンおよびそれを用いた高分子化合物 | |
| JP2009280571A5 (https=) | ||
| JP2016056357A5 (https=) | ||
| JP2016503075A5 (https=) | ||
| RU2011111081A (ru) | Способ получения микробусин и микробусины | |
| JP2012530167A5 (https=) | ||
| JPH0527649B2 (https=) | ||
| CN115803364A (zh) | 聚酰胺、聚酰胺酰亚胺和它们的衍生物、光学薄膜和显示装置以及它们的制造方法 | |
| JPWO2020235601A5 (ja) | ポリアミド酸溶液の製造方法、および積層体の製造方法 | |
| JP2016098260A (ja) | ポリアミド溶液 | |
| JP6268959B2 (ja) | 含フッ素重合性単量体およびそれを用いた高分子化合物 | |
| JP5523456B2 (ja) | 有機溶媒に可溶な、ｐｍｄａ、ｄａｄｅ、ｄａ、ビス（アミノ−４−ヒドロキシフェニル）スルホン成分を含むポリイミドおよびその製造方法 |