TWI502004B - 群集官能性聚有機矽氧烷之製法及其使用方法 - Google Patents
群集官能性聚有機矽氧烷之製法及其使用方法 Download PDFInfo
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- TWI502004B TWI502004B TW099136760A TW99136760A TWI502004B TW I502004 B TWI502004 B TW I502004B TW 099136760 A TW099136760 A TW 099136760A TW 99136760 A TW99136760 A TW 99136760A TW I502004 B TWI502004 B TW I502004B
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- 229960005181 morphine Drugs 0.000 description 1
- 125000001421 myristyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- GYVGXEWAOAAJEU-UHFFFAOYSA-N n,n,4-trimethylaniline Chemical compound CN(C)C1=CC=C(C)C=C1 GYVGXEWAOAAJEU-UHFFFAOYSA-N 0.000 description 1
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- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- DAHPIMYBWVSMKQ-UHFFFAOYSA-N n-hydroxy-n-phenylnitrous amide Chemical compound O=NN(O)C1=CC=CC=C1 DAHPIMYBWVSMKQ-UHFFFAOYSA-N 0.000 description 1
- YPHQUSNPXDGUHL-UHFFFAOYSA-N n-methylprop-2-enamide Chemical compound CNC(=O)C=C YPHQUSNPXDGUHL-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 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 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 229910000480 nickel oxide Inorganic materials 0.000 description 1
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- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 230000000269 nucleophilic effect Effects 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- QJAOYSPHSNGHNC-UHFFFAOYSA-N octadecane-1-thiol Chemical compound CCCCCCCCCCCCCCCCCCS QJAOYSPHSNGHNC-UHFFFAOYSA-N 0.000 description 1
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
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- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
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- JRWNODXPDGNUPO-UHFFFAOYSA-N oxolane;prop-2-enoic acid Chemical compound C1CCOC1.OC(=O)C=C JRWNODXPDGNUPO-UHFFFAOYSA-N 0.000 description 1
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
- 125000000913 palmityl 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])C([H])([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 description 1
- WPPLKRDOKPISSC-UHFFFAOYSA-N pentyl 2,2-dimethylpropaneperoxoate Chemical compound CCCCCOOC(=O)C(C)(C)C WPPLKRDOKPISSC-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
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- 229920003023 plastic Polymers 0.000 description 1
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- 150000003058 platinum compounds Chemical class 0.000 description 1
- CLSUSRZJUQMOHH-UHFFFAOYSA-L platinum dichloride Chemical compound Cl[Pt]Cl CLSUSRZJUQMOHH-UHFFFAOYSA-L 0.000 description 1
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- 229920002959 polymer blend Polymers 0.000 description 1
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- 238000012545 processing Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- BNMCQIRVFUGISV-UHFFFAOYSA-N propan-2-one;prop-2-enamide Chemical compound CC(C)=O.NC(=O)C=C BNMCQIRVFUGISV-UHFFFAOYSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
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- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
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- 239000007858 starting material Substances 0.000 description 1
- 150000003432 sterols Chemical class 0.000 description 1
- 235000003702 sterols Nutrition 0.000 description 1
- 150000003900 succinic acid esters Chemical class 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 1
- SJMYWORNLPSJQO-UHFFFAOYSA-N tert-butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)(C)C SJMYWORNLPSJQO-UHFFFAOYSA-N 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- SWAXTRYEYUTSAP-UHFFFAOYSA-N tert-butyl ethaneperoxoate Chemical compound CC(=O)OOC(C)(C)C SWAXTRYEYUTSAP-UHFFFAOYSA-N 0.000 description 1
- DLSMLZRPNPCXGY-UHFFFAOYSA-N tert-butylperoxy 2-ethylhexyl carbonate Chemical compound CCCCC(CC)COC(=O)OOOC(C)(C)C DLSMLZRPNPCXGY-UHFFFAOYSA-N 0.000 description 1
- CSKKAINPUYTTRW-UHFFFAOYSA-N tetradecoxycarbonyloxy tetradecyl carbonate Chemical compound CCCCCCCCCCCCCCOC(=O)OOC(=O)OCCCCCCCCCCCCCC CSKKAINPUYTTRW-UHFFFAOYSA-N 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- XDLNRRRJZOJTRW-UHFFFAOYSA-N thiohypochlorous acid Chemical compound ClS XDLNRRRJZOJTRW-UHFFFAOYSA-N 0.000 description 1
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- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- CMHHITPYCHHOGT-UHFFFAOYSA-N tributylborane Chemical compound CCCCB(CCCC)CCCC CMHHITPYCHHOGT-UHFFFAOYSA-N 0.000 description 1
- VYDLWQPLCBCJGV-UHFFFAOYSA-N tridodecylborane Chemical compound CCCCCCCCCCCCB(CCCCCCCCCCCC)CCCCCCCCCCCC VYDLWQPLCBCJGV-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- WXRGABKACDFXMG-UHFFFAOYSA-N trimethylborane Chemical compound CB(C)C WXRGABKACDFXMG-UHFFFAOYSA-N 0.000 description 1
- 239000005051 trimethylchlorosilane Substances 0.000 description 1
- OGJDNTCMTVTFAS-UHFFFAOYSA-N trioctylborane Chemical compound CCCCCCCCB(CCCCCCCC)CCCCCCCC OGJDNTCMTVTFAS-UHFFFAOYSA-N 0.000 description 1
- KQBSGRWMSNFIPG-UHFFFAOYSA-N trioxane Chemical compound C1COOOC1 KQBSGRWMSNFIPG-UHFFFAOYSA-N 0.000 description 1
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- NQPDZGIKBAWPEJ-UHFFFAOYSA-M valerate Chemical compound CCCCC([O-])=O NQPDZGIKBAWPEJ-UHFFFAOYSA-M 0.000 description 1
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- 150000003755 zirconium compounds Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/48—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms
- C08G77/50—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms by carbon linkages
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/14—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- General Chemical & Material Sciences (AREA)
- Silicon Polymers (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Epoxy Resins (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Sealing Material Composition (AREA)
Applications Claiming Priority (1)
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| US25928209P | 2009-11-09 | 2009-11-09 |
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| TW201134857A TW201134857A (en) | 2011-10-16 |
| TWI502004B true TWI502004B (zh) | 2015-10-01 |
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| TW099136760A TWI502004B (zh) | 2009-11-09 | 2010-10-27 | 群集官能性聚有機矽氧烷之製法及其使用方法 |
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| JP (3) | JP5559345B2 (enExample) |
| KR (1) | KR101650474B1 (enExample) |
| CN (1) | CN102597065B (enExample) |
| TW (1) | TWI502004B (enExample) |
| WO (1) | WO2011056832A1 (enExample) |
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| TWI502004B (zh) * | 2009-11-09 | 2015-10-01 | Dow Corning | 群集官能性聚有機矽氧烷之製法及其使用方法 |
| WO2013037105A1 (en) * | 2011-09-13 | 2013-03-21 | Dow Corning (China) Holding Co., Ltd. | Filled silicone composition, preparation and uses thereof |
| JP2013092633A (ja) * | 2011-10-25 | 2013-05-16 | Adeka Corp | ポジ型感光性組成物 |
| CN108686203A (zh) * | 2012-04-04 | 2018-10-23 | 哈洛齐梅公司 | 使用抗透明质酸剂和肿瘤靶向紫杉烷的组合疗法 |
| CN104968751B (zh) * | 2013-02-11 | 2017-04-19 | 道康宁公司 | 包含簇合官能化聚有机硅氧烷和有机硅反应性稀释剂的可固化有机硅组合物 |
| WO2014124388A1 (en) | 2013-02-11 | 2014-08-14 | Dow Corning Corporation | Alkoxy-functional organopolysiloxane resin and polymer and related methods for forming same |
| WO2014124389A1 (en) | 2013-02-11 | 2014-08-14 | Dow Corning Corporation | Moisture-curable hot melt silicone adhesive compositions including an alkoxy-functional siloxane reactive resin |
| WO2014124382A1 (en) * | 2013-02-11 | 2014-08-14 | Dow Corning Corporation | In situ method for forming thermally conductive thermal radical cure silicone composition |
| CN104968750B (zh) * | 2013-02-11 | 2017-04-19 | 道康宁公司 | 簇合官能化聚有机硅氧烷、形成所述簇合官能化聚有机硅氧烷的工艺及其使用方法 |
| CN105189685B (zh) * | 2013-02-11 | 2017-08-08 | 道康宁公司 | 用于形成导热热自由基固化有机硅组合物的方法 |
| KR102206708B1 (ko) * | 2013-02-11 | 2021-01-25 | 다우 실리콘즈 코포레이션 | 안정한 열 라디칼 경화성 실리콘 접착제 조성물 |
| GB201308072D0 (en) | 2013-05-03 | 2013-06-12 | Ramlat Ltd | Compositions and methods |
| KR102175447B1 (ko) * | 2013-07-11 | 2020-11-06 | 세메다인 가부시키 가이샤 | 도전성 경화물의 제조 방법 및 펄스광 경화성 조성물의 경화 방법 |
| US20170313591A1 (en) * | 2014-11-04 | 2017-11-02 | Thin Film Electronics Asa | Polymerization Inhibitor for Silane |
| JP2016186996A (ja) * | 2015-03-27 | 2016-10-27 | 三菱電機株式会社 | 固定抵抗器の耐硫化性評価方法および固定抵抗器の耐硫化性評価装置 |
| CN104875557A (zh) * | 2015-05-29 | 2015-09-02 | 重庆工商职业学院 | 一种汽车轮胎 |
| EP3196229B1 (en) * | 2015-11-05 | 2018-09-26 | Dow Silicones Corporation | Branched polyorganosiloxanes and related curable compositions, methods, uses and devices |
| WO2017094618A1 (ja) * | 2015-11-30 | 2017-06-08 | 東レ株式会社 | 樹脂組成物、そのシート状成型物、ならびにそれを用いた発光装置およびその製造方法 |
| WO2018056297A1 (ja) | 2016-09-26 | 2018-03-29 | 東レ・ダウコーニング株式会社 | 硬化反応性シリコーンゲルおよびその用途 |
| WO2018106011A1 (ko) * | 2016-12-09 | 2018-06-14 | 모멘티브퍼포먼스머티리얼스코리아 주식회사 | 유기 전자 소자 봉지재용 조성물 및 이를 이용하여 형성된 봉지재 |
| KR102478213B1 (ko) | 2017-04-06 | 2022-12-19 | 다우 도레이 캄파니 리미티드 | 액상 경화성 실리콘 접착제 조성물, 그 경화물 및 그 용도 |
| JP7252207B2 (ja) * | 2017-08-22 | 2023-04-04 | ダウ シリコーンズ コーポレーション | 二重硬化接着剤組成物並びにその調製及び使用方法 |
| CN111417671B (zh) * | 2017-09-29 | 2022-08-16 | 美国圣戈班性能塑料公司 | 有机硅组合物 |
| TW201917148A (zh) * | 2017-10-27 | 2019-05-01 | 美商陶氏有機矽公司 | 可固化矽氧烷黏著劑 |
| TWI801443B (zh) * | 2017-10-27 | 2023-05-11 | 美商陶氏有機矽公司 | 可固化聚有機矽氧烷組成物、藉由固化該等組成物獲得之固化體、及包含其之電子裝置 |
| JP7058106B2 (ja) * | 2017-11-01 | 2022-04-21 | 日東電工株式会社 | 粘着シート |
| CN109054730B (zh) * | 2018-07-23 | 2021-06-22 | 深圳天鼎新材料有限公司 | 一种加成型灌封胶及其制备方法和使用方法 |
| CN109266201B (zh) * | 2018-09-26 | 2020-10-20 | 南京林业大学 | 一种有机硅改性自清洁聚氨酯油性涂料及其制备方法 |
| JP7555925B2 (ja) * | 2018-12-21 | 2024-09-25 | ダウ シリコーンズ コーポレーション | 多官能性オルガノシロキサン、それを含有する組成物、及びその調製方法 |
| EP3898777B1 (en) * | 2018-12-21 | 2023-04-19 | Dow Silicones Corporation | Methods for making polyfunctional organosiloxanes and compositions containing same |
| JP7499250B2 (ja) * | 2018-12-21 | 2024-06-13 | ダウ シリコーンズ コーポレーション | 多官能性オルガノシロキサン、それを含有する組成物、及びその調製方法 |
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| JP6285283B2 (ja) | 2018-02-28 |
| EP2499185B1 (en) | 2018-07-04 |
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| JP2014208826A (ja) | 2014-11-06 |
| JP2016153512A (ja) | 2016-08-25 |
| EP2499185A1 (en) | 2012-09-19 |
| CN102597065B (zh) | 2015-07-22 |
| KR101650474B1 (ko) | 2016-08-23 |
| KR20120106744A (ko) | 2012-09-26 |
| WO2011056832A1 (en) | 2011-05-12 |
| JP2013510227A (ja) | 2013-03-21 |
| TW201134857A (en) | 2011-10-16 |
| EP2499185B8 (en) | 2018-08-15 |
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