JPS60188427A - 新規なポリイミド樹脂及びその製造方法 - Google Patents
新規なポリイミド樹脂及びその製造方法Info
- Publication number
- JPS60188427A JPS60188427A JP4616984A JP4616984A JPS60188427A JP S60188427 A JPS60188427 A JP S60188427A JP 4616984 A JP4616984 A JP 4616984A JP 4616984 A JP4616984 A JP 4616984A JP S60188427 A JPS60188427 A JP S60188427A
- Authority
- JP
- Japan
- Prior art keywords
- polyimide resin
- heat resistance
- transparency
- dianhydride
- 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
Links
- 229920001721 polyimide Polymers 0.000 title claims abstract description 40
- 239000009719 polyimide resin Substances 0.000 title claims abstract description 20
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 150000004984 aromatic diamines Chemical class 0.000 claims abstract description 17
- 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 abstract description 11
- 230000018044 dehydration Effects 0.000 claims abstract description 8
- 238000006297 dehydration reaction Methods 0.000 claims abstract description 8
- 150000004985 diamines Chemical class 0.000 claims abstract description 3
- 125000006158 tetracarboxylic acid group Chemical group 0.000 claims description 9
- 238000006798 ring closing metathesis reaction Methods 0.000 claims description 5
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims description 4
- 238000006068 polycondensation reaction Methods 0.000 claims description 4
- FYHBMPWRHCWNBC-UHFFFAOYSA-N 2-(3-bicyclo[2.2.1]heptanyl)acetic acid Chemical compound C1CC2C(CC(=O)O)CC1C2 FYHBMPWRHCWNBC-UHFFFAOYSA-N 0.000 claims 1
- 239000000470 constituent Substances 0.000 claims 1
- 239000010408 film Substances 0.000 abstract description 23
- 239000000126 substance Substances 0.000 abstract description 7
- 239000011347 resin Substances 0.000 abstract description 5
- 229920005989 resin Polymers 0.000 abstract description 5
- 125000003118 aryl group Chemical group 0.000 abstract description 4
- 239000004973 liquid crystal related substance Substances 0.000 abstract description 4
- 239000000853 adhesive Substances 0.000 abstract description 3
- 230000001070 adhesive effect Effects 0.000 abstract description 3
- 239000012769 display material Substances 0.000 abstract description 3
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 abstract description 2
- 210000003298 dental enamel Anatomy 0.000 abstract description 2
- 150000000000 tetracarboxylic acids Chemical class 0.000 abstract 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 239000012789 electroconductive film Substances 0.000 abstract 1
- 239000004642 Polyimide Substances 0.000 description 20
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 19
- 238000000034 method Methods 0.000 description 15
- 229920005575 poly(amic acid) Polymers 0.000 description 13
- 239000007788 liquid Substances 0.000 description 10
- 238000002834 transmittance Methods 0.000 description 7
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 6
- 238000005979 thermal decomposition reaction Methods 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- VLDPXPPHXDGHEW-UHFFFAOYSA-N 1-chloro-2-dichlorophosphoryloxybenzene Chemical compound ClC1=CC=CC=C1OP(Cl)(Cl)=O VLDPXPPHXDGHEW-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 238000002329 infrared spectrum Methods 0.000 description 4
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- -1 aliphatic tetracarboxylic acid Chemical class 0.000 description 3
- 238000004040 coloring Methods 0.000 description 3
- 239000001294 propane Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- HLBLWEWZXPIGSM-UHFFFAOYSA-N 4-Aminophenyl ether Chemical compound C1=CC(N)=CC=C1OC1=CC=C(N)C=C1 HLBLWEWZXPIGSM-UHFFFAOYSA-N 0.000 description 2
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- KZTYYGOKRVBIMI-UHFFFAOYSA-N diphenyl sulfone Chemical compound C=1C=CC=CC=1S(=O)(=O)C1=CC=CC=C1 KZTYYGOKRVBIMI-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000012456 homogeneous solution Substances 0.000 description 2
- 150000003949 imides Chemical class 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- FHBXQJDYHHJCIF-UHFFFAOYSA-N (2,3-diaminophenyl)-phenylmethanone Chemical compound NC1=CC=CC(C(=O)C=2C=CC=CC=2)=C1N FHBXQJDYHHJCIF-UHFFFAOYSA-N 0.000 description 1
- QIVUCLWGARAQIO-OLIXTKCUSA-N (3s)-n-[(3s,5s,6r)-6-methyl-2-oxo-1-(2,2,2-trifluoroethyl)-5-(2,3,6-trifluorophenyl)piperidin-3-yl]-2-oxospiro[1h-pyrrolo[2,3-b]pyridine-3,6'-5,7-dihydrocyclopenta[b]pyridine]-3'-carboxamide Chemical compound C1([C@H]2[C@H](N(C(=O)[C@@H](NC(=O)C=3C=C4C[C@]5(CC4=NC=3)C3=CC=CN=C3NC5=O)C2)CC(F)(F)F)C)=C(F)C=CC(F)=C1F QIVUCLWGARAQIO-OLIXTKCUSA-N 0.000 description 1
- AVQQQNCBBIEMEU-UHFFFAOYSA-N 1,1,3,3-tetramethylurea Chemical compound CN(C)C(=O)N(C)C AVQQQNCBBIEMEU-UHFFFAOYSA-N 0.000 description 1
- ISXCYFNKGRXZFQ-UHFFFAOYSA-N 1,1-diphenylpropane-2,2-diamine Chemical compound C=1C=CC=CC=1C(C(N)(N)C)C1=CC=CC=C1 ISXCYFNKGRXZFQ-UHFFFAOYSA-N 0.000 description 1
- WKFQMDFSDQFAIC-UHFFFAOYSA-N 2,4-dimethylthiolane 1,1-dioxide Chemical compound CC1CC(C)S(=O)(=O)C1 WKFQMDFSDQFAIC-UHFFFAOYSA-N 0.000 description 1
- OLQWMCSSZKNOLQ-UHFFFAOYSA-N 3-(2,5-dioxooxolan-3-yl)oxolane-2,5-dione Chemical compound O=C1OC(=O)CC1C1C(=O)OC(=O)C1 OLQWMCSSZKNOLQ-UHFFFAOYSA-N 0.000 description 1
- IOCXBXZBNOYTLQ-UHFFFAOYSA-N 3-nitrobenzene-1,2-diamine Chemical compound NC1=CC=CC([N+]([O-])=O)=C1N IOCXBXZBNOYTLQ-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
- VQVIHDPBMFABCQ-UHFFFAOYSA-N 5-(1,3-dioxo-2-benzofuran-5-carbonyl)-2-benzofuran-1,3-dione Chemical compound C1=C2C(=O)OC(=O)C2=CC(C(C=2C=C3C(=O)OC(=O)C3=CC=2)=O)=C1 VQVIHDPBMFABCQ-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 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
- 238000012695 Interfacial polymerization Methods 0.000 description 1
- 241001590997 Moolgarda engeli Species 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- ZWXPDGCFMMFNRW-UHFFFAOYSA-N N-methylcaprolactam Chemical compound CN1CCCCCC1=O ZWXPDGCFMMFNRW-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000000862 absorption spectrum Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- 229930188620 butyrolactone Natural products 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- ZZTCPWRAHWXWCH-UHFFFAOYSA-N diphenylmethanediamine Chemical compound C=1C=CC=CC=1C(N)(N)C1=CC=CC=C1 ZZTCPWRAHWXWCH-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000012776 electronic material Substances 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000000465 moulding Methods 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
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000000615 nonconductor Substances 0.000 description 1
- 239000012788 optical film Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 238000002411 thermogravimetry Methods 0.000 description 1
- 230000002747 voluntary effect Effects 0.000 description 1
Landscapes
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4616984A JPS60188427A (ja) | 1984-03-09 | 1984-03-09 | 新規なポリイミド樹脂及びその製造方法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4616984A JPS60188427A (ja) | 1984-03-09 | 1984-03-09 | 新規なポリイミド樹脂及びその製造方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60188427A true JPS60188427A (ja) | 1985-09-25 |
| JPH0224294B2 JPH0224294B2 (enrdf_load_stackoverflow) | 1990-05-29 |
Family
ID=12739516
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4616984A Granted JPS60188427A (ja) | 1984-03-09 | 1984-03-09 | 新規なポリイミド樹脂及びその製造方法 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60188427A (enrdf_load_stackoverflow) |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01247461A (ja) * | 1988-03-30 | 1989-10-03 | Japan Synthetic Rubber Co Ltd | 着色樹脂組成物 |
| JP2009292940A (ja) * | 2008-06-05 | 2009-12-17 | Nissan Chem Ind Ltd | ポリアミック酸およびポリイミドフィルム |
| JP2010030972A (ja) * | 2008-07-31 | 2010-02-12 | Nissan Chem Ind Ltd | 脂環式テトラカルボン酸二無水物、その製造法およびポリイミド |
| US7872148B2 (en) | 2004-10-20 | 2011-01-18 | Nissan Chemical Industries, Ltd. | Cage-shaped cyclobutanoic dianhydrides and process for production thereof |
| KR20110129907A (ko) | 2009-02-23 | 2011-12-02 | 닛산 가가쿠 고교 가부시키 가이샤 | 지환식 테트라카르복실산의 제조 방법 |
| TWI401279B (zh) * | 2005-03-29 | 2013-07-11 | Nissan Chemical Ind Ltd | Polyamic acid, polyimide and a method for producing the same |
| KR20160138980A (ko) | 2014-03-31 | 2016-12-06 | 닛산 가가쿠 고교 가부시키 가이샤 | 수지 박막의 제조방법 및 수지 박막형성용 조성물 |
| KR20170131514A (ko) | 2015-03-25 | 2017-11-29 | 닛산 가가쿠 고교 가부시키 가이샤 | 디아민 및 그의 이용 |
| KR20180063137A (ko) | 2015-09-30 | 2018-06-11 | 닛산 가가쿠 고교 가부시키 가이샤 | 수지박막형성용 조성물 |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI415876B (zh) | 2006-07-10 | 2013-11-21 | Nissan Chemical Ind Ltd | Polyacidic acid and polyimide |
| KR101674594B1 (ko) | 2009-04-10 | 2016-11-09 | 닛산 가가쿠 고교 가부시키 가이샤 | 케이지상 시클로펜탄산 2무수물 화합물, 그 제조법 및 폴리이미드 |
| KR101595614B1 (ko) | 2013-05-16 | 2016-02-18 | 코오롱인더스트리 주식회사 | 신규 산 이무수물, 이의 제조방법 및 이로부터 제조된 폴리이미드 |
| KR101548044B1 (ko) | 2013-05-16 | 2015-08-27 | 코오롱인더스트리 주식회사 | 신규 산 이무수물, 이의 제조방법 및 이로부터 제조된 폴리이미드 |
| JP6565687B2 (ja) | 2014-01-17 | 2019-08-28 | 日産化学株式会社 | シクロブタンテトラカルボン酸誘導体の製造方法 |
| KR102653978B1 (ko) | 2014-01-17 | 2024-04-02 | 닛산 가가쿠 가부시키가이샤 | 시클로부탄테트라카르복실산 유도체의 제조 방법 |
| WO2015111982A1 (ko) | 2014-01-27 | 2015-07-30 | 코오롱인더스트리 주식회사 | 폴리이미드 및 이를 이용한 필름 |
-
1984
- 1984-03-09 JP JP4616984A patent/JPS60188427A/ja active Granted
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01247461A (ja) * | 1988-03-30 | 1989-10-03 | Japan Synthetic Rubber Co Ltd | 着色樹脂組成物 |
| US7872148B2 (en) | 2004-10-20 | 2011-01-18 | Nissan Chemical Industries, Ltd. | Cage-shaped cyclobutanoic dianhydrides and process for production thereof |
| TWI401279B (zh) * | 2005-03-29 | 2013-07-11 | Nissan Chemical Ind Ltd | Polyamic acid, polyimide and a method for producing the same |
| JP2009292940A (ja) * | 2008-06-05 | 2009-12-17 | Nissan Chem Ind Ltd | ポリアミック酸およびポリイミドフィルム |
| JP2010030972A (ja) * | 2008-07-31 | 2010-02-12 | Nissan Chem Ind Ltd | 脂環式テトラカルボン酸二無水物、その製造法およびポリイミド |
| KR20110129907A (ko) | 2009-02-23 | 2011-12-02 | 닛산 가가쿠 고교 가부시키 가이샤 | 지환식 테트라카르복실산의 제조 방법 |
| KR20160138980A (ko) | 2014-03-31 | 2016-12-06 | 닛산 가가쿠 고교 가부시키 가이샤 | 수지 박막의 제조방법 및 수지 박막형성용 조성물 |
| KR20170131514A (ko) | 2015-03-25 | 2017-11-29 | 닛산 가가쿠 고교 가부시키 가이샤 | 디아민 및 그의 이용 |
| KR20180063137A (ko) | 2015-09-30 | 2018-06-11 | 닛산 가가쿠 고교 가부시키 가이샤 | 수지박막형성용 조성물 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0224294B2 (enrdf_load_stackoverflow) | 1990-05-29 |
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