JP2013526632A5 - - Google Patents
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- Publication number
- JP2013526632A5 JP2013526632A5 JP2013509577A JP2013509577A JP2013526632A5 JP 2013526632 A5 JP2013526632 A5 JP 2013526632A5 JP 2013509577 A JP2013509577 A JP 2013509577A JP 2013509577 A JP2013509577 A JP 2013509577A JP 2013526632 A5 JP2013526632 A5 JP 2013526632A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- alkyl
- oligomer
- polymer
- heteroaryl
- 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
- 125000000217 alkyl group Chemical group 0.000 claims 19
- 229920000642 polymer Polymers 0.000 claims 18
- 125000001072 heteroaryl group Chemical group 0.000 claims 13
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 8
- 125000003118 aryl group Chemical group 0.000 claims 7
- 229910052757 nitrogen Inorganic materials 0.000 claims 5
- 230000000269 nucleophilic effect Effects 0.000 claims 5
- 150000002903 organophosphorus compounds Chemical class 0.000 claims 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 4
- 229910052799 carbon Inorganic materials 0.000 claims 4
- 239000011203 carbon fibre reinforced carbon Substances 0.000 claims 4
- 239000003054 catalyst Substances 0.000 claims 4
- 229910052736 halogen Inorganic materials 0.000 claims 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 4
- 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
- 150000001875 compounds Chemical class 0.000 claims 3
- 238000004132 cross linking Methods 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 239000000203 mixture Substances 0.000 claims 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 3
- -1 phenylethenyl group Chemical group 0.000 claims 3
- 150000003512 tertiary amines Chemical class 0.000 claims 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 2
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 claims 2
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 claims 2
- 239000004642 Polyimide Substances 0.000 claims 2
- 150000004984 aromatic diamines Chemical class 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 150000002367 halogens Chemical class 0.000 claims 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 239000001301 oxygen Substances 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
- 229920001721 polyimide Polymers 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 2
- YWWDBCBWQNCYNR-UHFFFAOYSA-N trimethylphosphine Chemical compound CP(C)C YWWDBCBWQNCYNR-UHFFFAOYSA-N 0.000 claims 2
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 claims 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 claims 2
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 claims 1
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical group NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims 1
- MCTWTZJPVLRJOU-UHFFFAOYSA-N 1-methyl-1H-imidazole Chemical compound CN1C=CN=C1 MCTWTZJPVLRJOU-UHFFFAOYSA-N 0.000 claims 1
- GTACSIONMHMRPD-UHFFFAOYSA-N 2-[4-[2-(benzenesulfonamido)ethylsulfanyl]-2,6-difluorophenoxy]acetamide Chemical compound C1=C(F)C(OCC(=O)N)=C(F)C=C1SCCNS(=O)(=O)C1=CC=CC=C1 GTACSIONMHMRPD-UHFFFAOYSA-N 0.000 claims 1
- AXMANIZPMQZKTG-UHFFFAOYSA-N 4-(2-phenylethynyl)-2-benzofuran-1,3-dione Chemical compound O=C1OC(=O)C2=C1C=CC=C2C#CC1=CC=CC=C1 AXMANIZPMQZKTG-UHFFFAOYSA-N 0.000 claims 1
- XGZRRDYHYZLYIJ-UHFFFAOYSA-N 5-[2-(1,3-dioxo-2-benzofuran-5-yl)ethynyl]-2-benzofuran-1,3-dione Chemical compound C1=C2C(=O)OC(=O)C2=CC(C#CC=2C=C3C(=O)OC(C3=CC=2)=O)=C1 XGZRRDYHYZLYIJ-UHFFFAOYSA-N 0.000 claims 1
- LBTIDDCTPLEEAG-UHFFFAOYSA-N 5-prop-1-ynyl-2-benzofuran-1,3-dione Chemical compound CC#CC1=CC=C2C(=O)OC(=O)C2=C1 LBTIDDCTPLEEAG-UHFFFAOYSA-N 0.000 claims 1
- 101710130081 Aspergillopepsin-1 Proteins 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 102100031007 Cytosolic non-specific dipeptidase Human genes 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 101150032643 IVa2 gene Proteins 0.000 claims 1
- 239000004952 Polyamide Substances 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 150000008064 anhydrides Chemical class 0.000 claims 1
- 150000001721 carbon Chemical group 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 239000003426 co-catalyst Substances 0.000 claims 1
- 150000004985 diamines Chemical class 0.000 claims 1
- HASCQPSFPAKVEK-UHFFFAOYSA-N dimethyl(phenyl)phosphine Chemical compound CP(C)C1=CC=CC=C1 HASCQPSFPAKVEK-UHFFFAOYSA-N 0.000 claims 1
- 239000003822 epoxy resin Substances 0.000 claims 1
- 125000001033 ether 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
- 238000000034 method Methods 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000002950 monocyclic group Chemical group 0.000 claims 1
- 229920006122 polyamide resin Polymers 0.000 claims 1
- 229920000647 polyepoxide Polymers 0.000 claims 1
- 125000006160 pyromellitic dianhydride group Chemical group 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 125000001174 sulfone group Chemical group 0.000 claims 1
- 125000000101 thioether group Chemical group 0.000 claims 1
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 claims 1
- HEMCGZPSGYRIOL-UHFFFAOYSA-N C(C1)C11CCCC1 Chemical compound C(C1)C11CCCC1 HEMCGZPSGYRIOL-UHFFFAOYSA-N 0.000 description 1
- 0 C*Cc(cc(cc1)C(C#*C)=O)c1C(*)=O Chemical compound C*Cc(cc(cc1)C(C#*C)=O)c1C(*)=O 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE1050475 | 2010-05-14 | ||
| SE1050475-1 | 2010-05-14 | ||
| SE1050631-9 | 2010-06-18 | ||
| SE1050631 | 2010-06-18 | ||
| PCT/EP2011/057864 WO2011141578A1 (en) | 2010-05-14 | 2011-05-16 | Catalysis of cross-linking |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013526632A JP2013526632A (ja) | 2013-06-24 |
| JP2013526632A5 true JP2013526632A5 (cg-RX-API-DMAC7.html) | 2014-03-27 |
| JP5792800B2 JP5792800B2 (ja) | 2015-10-14 |
Family
ID=44343180
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013509577A Active JP5792800B2 (ja) | 2010-05-14 | 2011-05-16 | 架橋の触媒反応 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US8697823B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP2569343B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP5792800B2 (cg-RX-API-DMAC7.html) |
| CN (1) | CN102892800B (cg-RX-API-DMAC7.html) |
| WO (1) | WO2011141578A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102844291B (zh) * | 2010-04-16 | 2015-06-17 | 聂克斯姆化学有限公司 | 新型交联剂 |
| WO2012131063A1 (en) | 2011-04-01 | 2012-10-04 | Nexam Chemical Ab | Improved oligo- and polyimides |
| JP5834251B2 (ja) * | 2011-11-22 | 2015-12-16 | パナソニックＩｐマネジメント株式会社 | フレキシブル金属張基材、フレキシブル金属張基材の製造方法、プリント配線板、多層フレキシブルプリント配線板、及びフレックスリジッドプリント配線板 |
| JP2013173820A (ja) * | 2012-02-23 | 2013-09-05 | Pi R & D Co Ltd | 新規ポリイミド及びそれを含む印刷用組成物 |
| EP2653467B1 (en) * | 2012-04-20 | 2014-09-03 | Nexam Chemical AB | Process for producing (ethyne-1,2-diyl)bis(isobenzofuran-1,3- dione) |
| EP2899179A1 (en) | 2014-01-24 | 2015-07-29 | Nexam Chemical AB | Combination of cross-linkers including carbon-carbon triple bonds |
| JP6750146B2 (ja) * | 2015-10-13 | 2020-09-02 | 株式会社ピーアイ技術研究所 | 電着用ポリイミド及びそれを含む電着塗料組成物 |
| WO2017123948A1 (en) | 2016-01-13 | 2017-07-20 | Martin Weinberg | Polyamide electrical insulation for use in liquid filled transformers |
| 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 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| DE19532316C1 (de) | 1995-09-01 | 1997-05-22 | Bayer Ag | Vernetzbare Polysiloxan-Mischungen, ein Verfahren zur Herstellung und deren Verwendung |
| AUPO549397A0 (en) * | 1997-03-07 | 1997-03-27 | Commonwealth Scientific And Industrial Research Organisation | Reduced temperature curing of acetylenic polymers |
| US20030064235A1 (en) * | 2000-08-09 | 2003-04-03 | Yuichi Okawa | Optical members made of polymide resins |
| RU2276159C2 (ru) | 2001-07-12 | 2006-05-10 | Асахи Гласс Компани, Лимитед | Фторированный ароматический полимер и его применение |
| JP4513956B2 (ja) * | 2003-07-30 | 2010-07-28 | 日本電気株式会社 | 有機高分子膜及びその製造方法 |
| JP4501391B2 (ja) | 2003-09-30 | 2010-07-14 | 旭硝子株式会社 | 架橋性含フッ素芳香族プレポリマー及びその用途 |
| EP1995635A4 (en) | 2006-03-16 | 2011-03-30 | Asahi Glass Co Ltd | NEGATIVE LIGHT-SENSITIVE FLUORATED AROMATIC RESIN COMPOSITION |
| WO2007142124A1 (ja) | 2006-06-02 | 2007-12-13 | Asahi Glass Company, Limited | 架橋性プレポリマーならびにその製造方法および用途 |
| US20100062273A1 (en) | 2007-02-19 | 2010-03-11 | Sumitomo Bakelite Co., Ltd | Photosensitive resin composition, cured film, protective film, insulating film, semiconductor device and display device using the same |
| JP2010077192A (ja) * | 2008-09-24 | 2010-04-08 | Fujifilm Corp | 樹脂組成物、該樹脂組成物を用いた硬化物、フレキシブル銅張り積層板及びフレキシブルプリント基板 |
-
2011
- 2011-05-16 EP EP11721287.8A patent/EP2569343B1/en not_active Not-in-force
- 2011-05-16 WO PCT/EP2011/057864 patent/WO2011141578A1/en not_active Ceased
- 2011-05-16 JP JP2013509577A patent/JP5792800B2/ja active Active
- 2011-05-16 CN CN201180024067.3A patent/CN102892800B/zh not_active Expired - Fee Related
- 2011-05-16 US US13/697,583 patent/US8697823B2/en active Active
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