JP2013528573A5 - - Google Patents
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- Publication number
- JP2013528573A5 JP2013528573A5 JP2013504288A JP2013504288A JP2013528573A5 JP 2013528573 A5 JP2013528573 A5 JP 2013528573A5 JP 2013504288 A JP2013504288 A JP 2013504288A JP 2013504288 A JP2013504288 A JP 2013504288A JP 2013528573 A5 JP2013528573 A5 JP 2013528573A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- formula
- polyimide
- compound
- oligoimide
- 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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- 150000001875 compounds Chemical class 0.000 claims 16
- 239000004642 Polyimide Substances 0.000 claims 15
- 229920001721 polyimide Polymers 0.000 claims 15
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 6
- 125000003118 aryl group Chemical group 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 4
- 229910052760 oxygen Inorganic materials 0.000 claims 4
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 3
- -1 3,3', 4,4'-tetracarboxybiphenyl dianhydride Chemical compound 0.000 claims 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 3
- 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 3
- 150000004984 aromatic diamines Chemical class 0.000 claims 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 3
- 229910052799 carbon Inorganic materials 0.000 claims 3
- 125000004432 carbon atom Chemical group C* 0.000 claims 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims 3
- 229910052736 halogen Inorganic materials 0.000 claims 3
- 150000002367 halogens Chemical class 0.000 claims 3
- 125000001072 heteroaryl group Chemical group 0.000 claims 3
- 239000001301 oxygen Substances 0.000 claims 3
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims 2
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 claims 2
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims 2
- HLBLWEWZXPIGSM-UHFFFAOYSA-N 4-Aminophenyl ether Chemical compound C1=CC(N)=CC=C1OC1=CC=C(N)C=C1 HLBLWEWZXPIGSM-UHFFFAOYSA-N 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- LGRFSURHDFAFJT-UHFFFAOYSA-N phthalic anhydride Chemical compound C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 claims 2
- VLDPXPPHXDGHEW-UHFFFAOYSA-N 1-chloro-2-dichlorophosphoryloxybenzene Chemical compound ClC1=CC=CC=C1OP(Cl)(Cl)=O VLDPXPPHXDGHEW-UHFFFAOYSA-N 0.000 claims 1
- DKKYOQYISDAQER-UHFFFAOYSA-N 3-[3-(3-aminophenoxy)phenoxy]aniline Chemical compound NC1=CC=CC(OC=2C=C(OC=3C=C(N)C=CC=3)C=CC=2)=C1 DKKYOQYISDAQER-UHFFFAOYSA-N 0.000 claims 1
- YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 claims 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 claims 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 claims 1
- QQGYZOYWNCKGEK-UHFFFAOYSA-N 5-[(1,3-dioxo-2-benzofuran-5-yl)oxy]-2-benzofuran-1,3-dione Chemical compound C1=C2C(=O)OC(=O)C2=CC(OC=2C=C3C(=O)OC(C3=CC=2)=O)=C1 QQGYZOYWNCKGEK-UHFFFAOYSA-N 0.000 claims 1
- 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 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 238000007334 copolymerization reaction Methods 0.000 claims 1
- 125000001033 ether group Chemical group 0.000 claims 1
- 239000000945 filler Substances 0.000 claims 1
- 125000002541 furyl group Chemical group 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- 125000000654 isopropylidene group Chemical group C(C)(C)=* 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims 1
- 125000001624 naphthyl group Chemical group 0.000 claims 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 239000000049 pigment Substances 0.000 claims 1
- 239000004014 plasticizer Substances 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 125000006160 pyromellitic dianhydride group Chemical group 0.000 claims 1
- 230000002787 reinforcement Effects 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 125000001174 sulfone group Chemical group 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- 125000000101 thioether group Chemical group 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- NJMOHBDCGXJLNJ-UHFFFAOYSA-N trimellitic anhydride chloride Chemical compound ClC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 NJMOHBDCGXJLNJ-UHFFFAOYSA-N 0.000 claims 1
- DWMRKSPJCFARBH-UHFFFAOYSA-N OC(c1c2ccc(CNCc(cc3C(O4)=O)ccc3C4=O)c1)OC2=O Chemical compound OC(c1c2ccc(CNCc(cc3C(O4)=O)ccc3C4=O)c1)OC2=O DWMRKSPJCFARBH-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP10160198.7 | 2010-04-16 | ||
| EP10160198A EP2380867A1 (en) | 2010-04-16 | 2010-04-16 | Novel cross-linker |
| EP10193811 | 2010-12-06 | ||
| EP10193811.6 | 2010-12-06 | ||
| PCT/EP2011/055992 WO2011128431A1 (en) | 2010-04-16 | 2011-04-15 | Novel cross-linker |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013528573A JP2013528573A (ja) | 2013-07-11 |
| JP2013528573A5 true JP2013528573A5 (enExample) | 2014-03-13 |
| JP5746320B2 JP5746320B2 (ja) | 2015-07-08 |
Family
ID=44144728
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013504288A Active JP5746320B2 (ja) | 2010-04-16 | 2011-04-15 | 新規な架橋剤 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8815999B2 (enExample) |
| EP (1) | EP2558434B1 (enExample) |
| JP (1) | JP5746320B2 (enExample) |
| CN (1) | CN102844291B (enExample) |
| BR (1) | BR112012026376B1 (enExample) |
| ES (1) | ES2436892T3 (enExample) |
| TW (1) | TWI468384B (enExample) |
| WO (1) | WO2011128431A1 (enExample) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102159622A (zh) | 2008-09-23 | 2011-08-17 | 聂克斯姆化学有限公司 | 炔属聚酰胺 |
| EP2694572A1 (en) | 2011-04-01 | 2014-02-12 | Nexam Chemical AB | Improved oligo- and polyimides |
| ES2523824T3 (es) | 2012-04-20 | 2014-12-01 | Nexam Chemical Ab | Proceso para la producción de (etino-1,2-diil)bis(isobenzofuran-1,3-diona) |
| JP6175032B2 (ja) * | 2013-10-10 | 2017-08-02 | Ｊｆｅケミカル株式会社 | ベンゾフラン誘導体組成物、ポリイミド前駆体組成物およびポリイミド樹脂の製造方法 |
| EP2899179A1 (en) | 2014-01-24 | 2015-07-29 | Nexam Chemical AB | Combination of cross-linkers including carbon-carbon triple bonds |
| US20160208097A1 (en) | 2015-01-15 | 2016-07-21 | Rohm And Haas Electronic Materials Llc | Polyimide compositions and methods |
| US9892845B2 (en) | 2016-01-13 | 2018-02-13 | Martin Weinberg | Polyamide electrical insulation for use in liquid filled transformers |
| EP3246349A1 (en) | 2017-05-24 | 2017-11-22 | Nexam Chemical AB | Process for increasing the melt strength of a thermoplastic polymer |
| KR102010209B1 (ko) * | 2017-08-23 | 2019-08-12 | 우베 고산 가부시키가이샤 | 전극용 바인더 수지, 전극 합제 페이스트, 전극 및 전극의 제조 방법 |
| CN109021234B (zh) * | 2018-07-12 | 2020-12-29 | 浙江福斯特新材料研究院有限公司 | 一种高玻璃化转变温度与高耐热的热固型聚酰亚胺及制备方法 |
| CN109337101A (zh) * | 2018-08-06 | 2019-02-15 | 安徽国风塑业股份有限公司 | 一种聚酰亚胺薄膜的制备方法 |
| US11577448B1 (en) * | 2019-09-30 | 2023-02-14 | United States Of America As Represented By The Secretary Of The Air Force | Method for fabricating multiphenylethynyl-containing and lightly crosslinked polyimides capable of memorizing shapes and augmenting thermomechanical stability |
| US11504899B1 (en) * | 2019-09-30 | 2022-11-22 | United States Of America As Represented By The Secretary Of The Air Force | Method for fabricating lightly crosslinked polyimides with phenylethynyl pendants for shape-memory effect and programmed enhancement in Tg and modulus |
| CN113603662B (zh) * | 2021-06-15 | 2023-06-06 | 陕西泰合利华工业有限公司 | 一种制备4-(1-酮-2-炔苯丙烷)苯酐的方法 |
| CN115160977B (zh) * | 2022-08-17 | 2023-07-18 | 中国地质大学（北京） | 聚酰亚胺纤维膜胶粘剂及其制备方法和应用 |
| CN115232310B (zh) * | 2022-08-31 | 2024-04-09 | 中国科学院宁波材料技术与工程研究所 | 一种耐高温韧性双马来酰亚胺树脂及其制备方法与应用 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5559214A (en) * | 1993-05-28 | 1996-09-24 | Sterling Winthrop Inc. | Unsymmetrical complexing agents and targeting immunoreagents useful in thearpeutic and diagnostic compositions and methods |
| US5567800A (en) * | 1994-10-28 | 1996-10-22 | The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration | Imide oligomers endcapped with phenylethynyl phthalic anhydrides and polymers therefrom |
| AUPO549397A0 (en) * | 1997-03-07 | 1997-03-27 | Commonwealth Scientific And Industrial Research Organisation | Reduced temperature curing of acetylenic polymers |
| US6136949A (en) * | 1998-09-03 | 2000-10-24 | The Dow Chemical Company | Resins containing phenylethynl-terminated compounds |
| JP3891441B2 (ja) * | 2004-10-21 | 2007-03-14 | 独立行政法人 宇宙航空研究開発機構 | 繊維強化ポリイミド複合材料の製造方法 |
| US20080146692A1 (en) * | 2004-12-16 | 2008-06-19 | Ryuji Uehara | Unsaturated Group-Containing Polyimide Resin, Photosensitive Resin Composition Containing Same, And Cured Product Thereof |
| WO2010013620A1 (ja) * | 2008-07-31 | 2010-02-04 | マナック株式会社 | 無水フタル酸誘導体の製造方法 |
| WO2010030216A1 (en) * | 2008-09-09 | 2010-03-18 | Nexam Chemical Ab | Acetylenic poly(alkylene phthalate) |
| JP5792800B2 (ja) * | 2010-05-14 | 2015-10-14 | ネクサム ケミカル エイビー | 架橋の触媒反応 |
| JP2012221898A (ja) * | 2011-04-13 | 2012-11-12 | Sony Corp | 非水電解質電池および非水電解質、並びに電池パック、電子機器、電動車両、蓄電装置および電力システム |
-
2011
- 2011-04-15 US US13/641,470 patent/US8815999B2/en active Active
- 2011-04-15 CN CN201180019446.3A patent/CN102844291B/zh active Active
- 2011-04-15 EP EP11714980.7A patent/EP2558434B1/en active Active
- 2011-04-15 WO PCT/EP2011/055992 patent/WO2011128431A1/en not_active Ceased
- 2011-04-15 BR BR112012026376-5A patent/BR112012026376B1/pt not_active IP Right Cessation
- 2011-04-15 JP JP2013504288A patent/JP5746320B2/ja active Active
- 2011-04-15 ES ES11714980.7T patent/ES2436892T3/es active Active
- 2011-04-18 TW TW100113321A patent/TWI468384B/zh active
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