JP2016531191A5 - - Google Patents
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- JP2016531191A5 JP2016531191A5 JP2016542019A JP2016542019A JP2016531191A5 JP 2016531191 A5 JP2016531191 A5 JP 2016531191A5 JP 2016542019 A JP2016542019 A JP 2016542019A JP 2016542019 A JP2016542019 A JP 2016542019A JP 2016531191 A5 JP2016531191 A5 JP 2016531191A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- formula
- ene
- hept
- branched
- 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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- 229920000642 polymer Polymers 0.000 claims 17
- 229910052739 hydrogen Inorganic materials 0.000 claims 14
- 239000001257 hydrogen Substances 0.000 claims 14
- 239000000178 monomer Substances 0.000 claims 14
- 125000000217 alkyl group Chemical group 0.000 claims 12
- 239000000203 mixture Substances 0.000 claims 12
- 150000002431 hydrogen Chemical class 0.000 claims 11
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 10
- 125000003710 aryl alkyl group Chemical group 0.000 claims 10
- 125000000753 cycloalkyl group Chemical group 0.000 claims 10
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 6
- 125000003118 aryl group Chemical group 0.000 claims 6
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 6
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
- -1 (C 1 -C 2) alkyl maleimide Chemical compound 0.000 claims 4
- 125000006545 (C1-C9) alkyl group Chemical group 0.000 claims 4
- WWUVJRULCWHUSA-UHFFFAOYSA-N 2-methyl-1-pentene Chemical compound CCCC(C)=C WWUVJRULCWHUSA-UHFFFAOYSA-N 0.000 claims 4
- 125000004104 aryloxy group Chemical group 0.000 claims 4
- 229910052736 halogen Inorganic materials 0.000 claims 4
- 150000002367 halogens Chemical class 0.000 claims 4
- 125000000466 oxiranyl group Chemical group 0.000 claims 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims 3
- 229910052799 carbon Inorganic materials 0.000 claims 3
- 150000001721 carbon Chemical group 0.000 claims 3
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims 3
- 125000000524 functional group Chemical group 0.000 claims 3
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical group C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 claims 3
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 claims 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 2
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 2
- FJLUATLTXUNBOT-UHFFFAOYSA-N 1-Hexadecylamine Chemical compound CCCCCCCCCCCCCCCCN FJLUATLTXUNBOT-UHFFFAOYSA-N 0.000 claims 2
- PEALEMBUUUVDRP-UHFFFAOYSA-N 1-[4-(5-bicyclo[2.2.1]hept-2-enyl)butyl]-3,4-dimethylpyrrole-2,5-dione Chemical compound O=C1C(C)=C(C)C(=O)N1CCCCC1C(C=C2)CC2C1 PEALEMBUUUVDRP-UHFFFAOYSA-N 0.000 claims 2
- FXNDIJDIPNCZQJ-UHFFFAOYSA-N 2,4,4-trimethylpent-1-ene Chemical compound CC(=C)CC(C)(C)C FXNDIJDIPNCZQJ-UHFFFAOYSA-N 0.000 claims 2
- LAAVYEUJEMRIGF-UHFFFAOYSA-N 2,4,4-trimethylpent-2-ene Chemical compound CC(C)=CC(C)(C)C LAAVYEUJEMRIGF-UHFFFAOYSA-N 0.000 claims 2
- GBNPJBBNCBLPQT-UHFFFAOYSA-N 2-(5-bicyclo[2.2.1]hept-2-enylmethoxymethyl)oxirane Chemical compound C1C(C=C2)CC2C1COCC1CO1 GBNPJBBNCBLPQT-UHFFFAOYSA-N 0.000 claims 2
- AOBIOSPNXBMOAT-UHFFFAOYSA-N 2-[2-(oxiran-2-ylmethoxy)ethoxymethyl]oxirane Chemical compound C1OC1COCCOCC1CO1 AOBIOSPNXBMOAT-UHFFFAOYSA-N 0.000 claims 2
- BEHBBKCBARHMJQ-UHFFFAOYSA-N 5-(2-phenylethyl)bicyclo[2.2.1]hept-2-ene Chemical compound C1C(C=C2)CC2C1CCC1=CC=CC=C1 BEHBBKCBARHMJQ-UHFFFAOYSA-N 0.000 claims 2
- VCOXSVQMANZZDY-UHFFFAOYSA-N 5-[2-(2-methoxyethoxy)ethoxymethyl]bicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(COCCOCCOC)CC1C=C2 VCOXSVQMANZZDY-UHFFFAOYSA-N 0.000 claims 2
- VTWPBVSOSWNXAX-UHFFFAOYSA-N 5-decylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(CCCCCCCCCC)CC1C=C2 VTWPBVSOSWNXAX-UHFFFAOYSA-N 0.000 claims 2
- QHJIJNGGGLNBNJ-UHFFFAOYSA-N 5-ethylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(CC)CC1C=C2 QHJIJNGGGLNBNJ-UHFFFAOYSA-N 0.000 claims 2
- WMWDGZLDLRCDRG-UHFFFAOYSA-N 5-hexylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(CCCCCC)CC1C=C2 WMWDGZLDLRCDRG-UHFFFAOYSA-N 0.000 claims 2
- PCBPVYHMZBWMAZ-UHFFFAOYSA-N 5-methylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(C)CC1C=C2 PCBPVYHMZBWMAZ-UHFFFAOYSA-N 0.000 claims 2
- GOLQZWYZZWIBCA-UHFFFAOYSA-N 5-octylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(CCCCCCCC)CC1C=C2 GOLQZWYZZWIBCA-UHFFFAOYSA-N 0.000 claims 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims 2
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 claims 2
- 229920001774 Perfluoroether Polymers 0.000 claims 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims 2
- 125000004423 acyloxy group Chemical group 0.000 claims 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 claims 2
- 150000001602 bicycloalkyls Chemical group 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- 229920001577 copolymer Polymers 0.000 claims 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 claims 2
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 claims 2
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 claims 2
- GCSJLQSCSDMKTP-UHFFFAOYSA-N ethenyl(trimethyl)silane Chemical compound C[Si](C)(C)C=C GCSJLQSCSDMKTP-UHFFFAOYSA-N 0.000 claims 2
- 125000005553 heteroaryloxy group Chemical group 0.000 claims 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical group O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims 2
- 238000004377 microelectronic Methods 0.000 claims 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 claims 2
- 230000005693 optoelectronics Effects 0.000 claims 2
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims 2
- 239000002904 solvent Substances 0.000 claims 2
- 125000006529 (C3-C6) alkyl group Chemical group 0.000 claims 1
- QECCQGLIYMMHCR-UHFFFAOYSA-N 2-({2,2-Bis[(2-oxiranylmethoxy)methyl]butoxy}methyl)oxirane Chemical compound C1OC1COCC(COCC1OC1)(CC)COCC1CO1 QECCQGLIYMMHCR-UHFFFAOYSA-N 0.000 claims 1
- WJQOZHYUIDYNHM-UHFFFAOYSA-N 2-tert-Butylphenol Chemical compound CC(C)(C)C1=CC=CC=C1O WJQOZHYUIDYNHM-UHFFFAOYSA-N 0.000 claims 1
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims 1
- 239000002202 Polyethylene glycol Substances 0.000 claims 1
- XUCHXOAWJMEFLF-UHFFFAOYSA-N bisphenol F diglycidyl ether Chemical compound C1OC1COC(C=C1)=CC=C1CC(C=C1)=CC=C1OCC1CO1 XUCHXOAWJMEFLF-UHFFFAOYSA-N 0.000 claims 1
- 239000003431 cross linking reagent Substances 0.000 claims 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 claims 1
- BDJSOPWXYLFTNW-UHFFFAOYSA-N methyl 3-methoxypropanoate Chemical compound COCCC(=O)OC BDJSOPWXYLFTNW-UHFFFAOYSA-N 0.000 claims 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 238000000059 patterning Methods 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 229920001223 polyethylene glycol Polymers 0.000 claims 1
- 229920001451 polypropylene glycol Polymers 0.000 claims 1
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 claims 1
- 230000005855 radiation Effects 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361878263P | 2013-09-16 | 2013-09-16 | |
| US61/878,263 | 2013-09-16 | ||
| PCT/US2014/054181 WO2015038411A2 (en) | 2013-09-16 | 2014-09-05 | Amine treated maleic anhydride polymers, compositions and applications thereof |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016531191A JP2016531191A (ja) | 2016-10-06 |
| JP2016531191A5 true JP2016531191A5 (enExample) | 2017-07-20 |
| JP6321811B2 JP6321811B2 (ja) | 2018-05-09 |
Family
ID=51541388
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016542019A Active JP6321811B2 (ja) | 2013-09-16 | 2014-09-05 | アミン処理無水マレイン酸ポリマー、組成物およびそれらの利用 |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US9422376B2 (enExample) |
| JP (1) | JP6321811B2 (enExample) |
| TW (1) | TWI627217B (enExample) |
| WO (1) | WO2015038411A2 (enExample) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI659046B (zh) * | 2015-05-06 | 2019-05-11 | Sumitomo Bakelite Co., Ltd. | 作爲永久介電材料的順丁烯二醯亞胺及環烯烴單體之聚合物 |
| TWI692674B (zh) | 2015-12-31 | 2020-05-01 | 日商住友電木股份有限公司 | 衍生自降莰二烯和馬來酸酐之聚合物及其用途 |
| JP6707741B2 (ja) * | 2016-05-09 | 2020-06-10 | 学校法人早稲田大学 | イミド架橋型樹脂、透明フィルム及び表面保護フィルム |
| TWI732111B (zh) | 2017-03-28 | 2021-07-01 | 日商住友電木股份有限公司 | 感光性組成物、彩色濾光片及由其衍生之微透鏡 |
| WO2018179807A1 (ja) * | 2017-03-30 | 2018-10-04 | 日本ゼオン株式会社 | 感放射線樹脂組成物および電子部品 |
| CN109991813B (zh) | 2017-12-29 | 2022-06-21 | 财团法人工业技术研究院 | 感光型复合材料及使用其形成复合薄膜的方法 |
| CN110007558A (zh) | 2017-12-29 | 2019-07-12 | 财团法人工业技术研究院 | 组合物、包含其的绝缘材料及其制法 |
| JP6958402B2 (ja) * | 2018-02-09 | 2021-11-02 | 住友ベークライト株式会社 | ポリマー、感光性樹脂組成物、感光性樹脂膜、パターン、有機エレクトロルミネッセンス素子、パターンを備えた基板の製造方法およびポリマーの製造方法 |
| JP7115120B2 (ja) * | 2018-07-31 | 2022-08-09 | 住友ベークライト株式会社 | 感光性接着材組成物、および構造体 |
| EP3842863A4 (en) * | 2018-08-20 | 2021-11-03 | Mitsubishi Gas Chemical Company, Inc. | FILM EDUCATION MATERIAL FOR LITHOGRAPHY, COMPOSITION FOR FILM FORMATION FOR LITHOGRAPHY, LAYER FILM FOR LITHOGRAPHY AND PATTERN GENERATION PROCESS |
| KR20210049870A (ko) * | 2018-08-28 | 2021-05-06 | 스미또모 베이크라이트 가부시키가이샤 | 네거티브형 감광성 수지 조성물, 및 그것을 이용한 반도체 장치 |
| TW202030227A (zh) * | 2018-11-21 | 2020-08-16 | 日商三菱瓦斯化學股份有限公司 | 微影用膜形成材料、微影用膜形成用組成物、微影用下層膜及圖型形成方法 |
| JPWO2021112092A1 (enExample) * | 2019-12-06 | 2021-06-10 | ||
| US11998330B2 (en) * | 2021-01-29 | 2024-06-04 | Medtronic Minimed, Inc. | Interference rejection membranes useful with analyte sensors |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3370047A (en) * | 1964-09-03 | 1968-02-20 | Union Carbide Corp | Pour point depressants and lubricating compositions thereof |
| JPS5165214A (ja) | 1974-11-29 | 1976-06-05 | Emu Betsukaa Reimondo | Rootariienjin |
| JPS52132091A (en) * | 1976-04-28 | 1977-11-05 | Kansai Paint Co Ltd | Polymerizable solid resin compositions |
| US4397995A (en) * | 1980-12-29 | 1983-08-09 | Monsanto Company | Polymeric anti-tumor agent and method of preparation |
| US4740561A (en) * | 1985-12-25 | 1988-04-26 | Ube Industries, Ltd. | Process for the preparation of N-(hydroxyphenyl)malemide copolymer |
| JPH02146045A (ja) * | 1988-02-17 | 1990-06-05 | Tosoh Corp | フォトレジスト組成物 |
| EP0380676B1 (en) * | 1988-02-17 | 1994-05-04 | Tosoh Corporation | Photoresist composition |
| FR2699540B1 (fr) * | 1992-12-23 | 1995-02-24 | Atochem Elf Sa | Polymère thermoplastique transparent ayant une température de transition vitreuse élevée et une stabilité thermique améliorée. |
| US6407197B1 (en) * | 1998-03-04 | 2002-06-18 | Dsm N.V. | Aqueous dispersion of a polymer |
| NL1008469C2 (nl) * | 1998-03-04 | 1999-09-07 | Dsm Nv | Waterige dispersies van een polymeer. |
| US5886194A (en) * | 1998-03-04 | 1999-03-23 | Isp Investments Inc. | Hydroxyamino-derivatized polymers of olefin-maleic anhydride in the form of their maleimide maleamic acid and α- olefin-maleic anhydride half-acid/half ester or full acid repeat units process for making same |
| JP3262108B2 (ja) | 1998-09-09 | 2002-03-04 | 東レ株式会社 | ポジ型感光性樹脂組成物 |
| JP2001242616A (ja) * | 2000-02-29 | 2001-09-07 | Fujifilm Arch Co Ltd | ポジ型感光性樹脂組成物 |
| JP3952756B2 (ja) | 2001-11-29 | 2007-08-01 | 日本ゼオン株式会社 | 感放射線性樹脂組成物及びその利用 |
| US7524594B2 (en) | 2004-07-07 | 2009-04-28 | Promerus Llc | Photosensitive dielectric resin compositions, films formed therefrom and semiconductor and display devices encompassing such films |
| TWI505046B (zh) * | 2008-01-24 | 2015-10-21 | Jsr Corp | 光阻圖型之形成方法及微細化光阻圖型之樹脂組成物 |
| DE102008021511A1 (de) * | 2008-04-30 | 2009-11-05 | Clariant International Limited | Pigmentdispergatoren und leicht dispergierbare feste Pigmentzubereitungen |
| EP2643371B1 (en) * | 2010-11-24 | 2014-04-02 | Promerus, LLC | A self-imageable film forming polymer, compositions thereof and devices and structures made therefrom |
| KR101496976B1 (ko) | 2011-07-14 | 2015-03-02 | 스미토모 베이클리트 컴퍼니 리미티드 | 화학 방사선에 대한 이미지-와이즈 노광 후에 패턴화된 층을 형성하는 중합체 및 이의 조성물 |
-
2014
- 2014-09-05 JP JP2016542019A patent/JP6321811B2/ja active Active
- 2014-09-05 TW TW103130741A patent/TWI627217B/zh not_active IP Right Cessation
- 2014-09-05 US US14/477,928 patent/US9422376B2/en active Active
- 2014-09-05 WO PCT/US2014/054181 patent/WO2015038411A2/en not_active Ceased
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