JPWO2020109187A5 - - Google Patents
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- JPWO2020109187A5 JPWO2020109187A5 JP2021531060A JP2021531060A JPWO2020109187A5 JP WO2020109187 A5 JPWO2020109187 A5 JP WO2020109187A5 JP 2021531060 A JP2021531060 A JP 2021531060A JP 2021531060 A JP2021531060 A JP 2021531060A JP WO2020109187 A5 JPWO2020109187 A5 JP WO2020109187A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- formula
- groups
- substituted
- silane
- 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.)
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- 125000000217 alkyl group Chemical group 0.000 claims 26
- 239000000203 mixture Substances 0.000 claims 21
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims 19
- -1 amino, oximino Chemical group 0.000 claims 18
- 229910000077 silane Inorganic materials 0.000 claims 18
- 125000003342 alkenyl group Chemical group 0.000 claims 17
- 125000003118 aryl group Chemical group 0.000 claims 17
- 229910052739 hydrogen Inorganic materials 0.000 claims 15
- 239000001257 hydrogen Substances 0.000 claims 15
- 125000000304 alkynyl group Chemical group 0.000 claims 14
- 125000004432 carbon atom Chemical group C* 0.000 claims 14
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 13
- 150000002431 hydrogen Chemical class 0.000 claims 13
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 12
- 125000001072 heteroaryl group Chemical group 0.000 claims 10
- 150000001875 compounds Chemical class 0.000 claims 8
- 239000002318 adhesion promoter Substances 0.000 claims 6
- 239000003054 catalyst Substances 0.000 claims 5
- 125000005842 heteroatom Chemical group 0.000 claims 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 5
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 5
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 claims 4
- 125000002252 acyl group Chemical group 0.000 claims 4
- 125000002947 alkylene group Chemical group 0.000 claims 4
- 229910052736 halogen Inorganic materials 0.000 claims 4
- 150000002367 halogens Chemical class 0.000 claims 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims 4
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 4
- 229920002554 vinyl polymer Polymers 0.000 claims 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 3
- 125000004423 acyloxy group Chemical group 0.000 claims 3
- 125000003302 alkenyloxy group Chemical group 0.000 claims 3
- 150000001412 amines Chemical class 0.000 claims 3
- 125000004104 aryloxy group Chemical group 0.000 claims 3
- 150000002148 esters Chemical class 0.000 claims 3
- CWAFVXWRGIEBPL-UHFFFAOYSA-N ethoxysilane Chemical compound CCO[SiH3] CWAFVXWRGIEBPL-UHFFFAOYSA-N 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 125000006832 (C1-C10) alkylene group Chemical group 0.000 claims 2
- 125000002030 1,2-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([*:2])C([H])=C1[H] 0.000 claims 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
- GYCKQBWUSACYIF-UHFFFAOYSA-N Ethyl salicylate Chemical compound CCOC(=O)C1=CC=CC=C1O GYCKQBWUSACYIF-UHFFFAOYSA-N 0.000 claims 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 2
- 239000000853 adhesive Substances 0.000 claims 2
- 230000001070 adhesive effect Effects 0.000 claims 2
- 150000001298 alcohols Chemical class 0.000 claims 2
- 150000001721 carbon Chemical group 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 claims 2
- 125000004122 cyclic group Chemical group 0.000 claims 2
- 239000004205 dimethyl polysiloxane Substances 0.000 claims 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 2
- 229940005667 ethyl salicylate Drugs 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 2
- BVBBZEKOMUDXMZ-UHFFFAOYSA-N n,n-diethyl-3-triethoxysilylpropan-1-amine Chemical compound CCO[Si](OCC)(OCC)CCCN(CC)CC BVBBZEKOMUDXMZ-UHFFFAOYSA-N 0.000 claims 2
- WYMSENKWVCCQGJ-UHFFFAOYSA-N n,n-dimethyl-1-triethoxysilylmethanamine Chemical compound CCO[Si](CN(C)C)(OCC)OCC WYMSENKWVCCQGJ-UHFFFAOYSA-N 0.000 claims 2
- AQIQPUUNTCVHBS-UHFFFAOYSA-N n,n-dimethyl-3-triethoxysilylpropan-1-amine Chemical compound CCO[Si](OCC)(OCC)CCCN(C)C AQIQPUUNTCVHBS-UHFFFAOYSA-N 0.000 claims 2
- UMXXGDJOCQSQBV-UHFFFAOYSA-N n-ethyl-n-(triethoxysilylmethyl)ethanamine Chemical compound CCO[Si](OCC)(OCC)CN(CC)CC UMXXGDJOCQSQBV-UHFFFAOYSA-N 0.000 claims 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 2
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 claims 2
- 229910052710 silicon Inorganic materials 0.000 claims 2
- ROWWCTUMLAVVQB-UHFFFAOYSA-N triethoxysilylmethanamine Chemical compound CCO[Si](CN)(OCC)OCC ROWWCTUMLAVVQB-UHFFFAOYSA-N 0.000 claims 2
- HXLAEGYMDGUSBD-UHFFFAOYSA-N 3-[diethoxy(methyl)silyl]propan-1-amine Chemical compound CCO[Si](C)(OCC)CCCN HXLAEGYMDGUSBD-UHFFFAOYSA-N 0.000 claims 1
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 claims 1
- NSYVWNZRHYLPDY-UHFFFAOYSA-N 6-[dimethoxy(methyl)silyl]-1-n,1-n-dimethylhexane-1,4-diamine Chemical compound CO[Si](C)(OC)CCC(N)CCCN(C)C NSYVWNZRHYLPDY-UHFFFAOYSA-N 0.000 claims 1
- 229910003849 O-Si Inorganic materials 0.000 claims 1
- 229910003872 O—Si Inorganic materials 0.000 claims 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 125000000732 arylene group Chemical group 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 235000013877 carbamide Nutrition 0.000 claims 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims 1
- 239000011248 coating agent Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- ZWTJVXCCMKLQKS-UHFFFAOYSA-N diethoxy(ethyl)silicon Chemical compound CCO[Si](CC)OCC ZWTJVXCCMKLQKS-UHFFFAOYSA-N 0.000 claims 1
- GAURFLBIDLSLQU-UHFFFAOYSA-N diethoxy(methyl)silicon Chemical compound CCO[Si](C)OCC GAURFLBIDLSLQU-UHFFFAOYSA-N 0.000 claims 1
- BODAWKLCLUZBEZ-UHFFFAOYSA-N diethoxy(phenyl)silicon Chemical compound CCO[Si](OCC)C1=CC=CC=C1 BODAWKLCLUZBEZ-UHFFFAOYSA-N 0.000 claims 1
- CTLDFURRFMJGON-UHFFFAOYSA-N dimethoxy-methyl-(3-piperazin-1-ylpropyl)silane Chemical compound CO[Si](C)(OC)CCCN1CCNCC1 CTLDFURRFMJGON-UHFFFAOYSA-N 0.000 claims 1
- XMKVMJPCDLDMTQ-UHFFFAOYSA-N ethenyl(diethoxy)silane Chemical compound CCO[SiH](C=C)OCC XMKVMJPCDLDMTQ-UHFFFAOYSA-N 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 claims 1
- 239000000945 filler Substances 0.000 claims 1
- 125000005553 heteroaryloxy group Chemical group 0.000 claims 1
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 230000007062 hydrolysis Effects 0.000 claims 1
- 238000006460 hydrolysis reaction Methods 0.000 claims 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 1
- 150000003949 imides Chemical class 0.000 claims 1
- 239000004615 ingredient Substances 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
- 125000005647 linker group Chemical group 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- INJVFBCDVXYHGQ-UHFFFAOYSA-N n'-(3-triethoxysilylpropyl)ethane-1,2-diamine Chemical compound CCO[Si](OCC)(OCC)CCCNCCN INJVFBCDVXYHGQ-UHFFFAOYSA-N 0.000 claims 1
- PHQOGHDTIVQXHL-UHFFFAOYSA-N n'-(3-trimethoxysilylpropyl)ethane-1,2-diamine Chemical compound CO[Si](OC)(OC)CCCNCCN PHQOGHDTIVQXHL-UHFFFAOYSA-N 0.000 claims 1
- NHBRUUFBSBSTHM-UHFFFAOYSA-N n'-[2-(3-trimethoxysilylpropylamino)ethyl]ethane-1,2-diamine Chemical compound CO[Si](OC)(OC)CCCNCCNCCN NHBRUUFBSBSTHM-UHFFFAOYSA-N 0.000 claims 1
- MQWFLKHKWJMCEN-UHFFFAOYSA-N n'-[3-[dimethoxy(methyl)silyl]propyl]ethane-1,2-diamine Chemical compound CO[Si](C)(OC)CCCNCCN MQWFLKHKWJMCEN-UHFFFAOYSA-N 0.000 claims 1
- ZLDHYRXZZNDOKU-UHFFFAOYSA-N n,n-diethyl-3-trimethoxysilylpropan-1-amine Chemical compound CCN(CC)CCC[Si](OC)(OC)OC ZLDHYRXZZNDOKU-UHFFFAOYSA-N 0.000 claims 1
- DFVIRQNGJPSMQP-UHFFFAOYSA-N n,n-dimethyl-1-trimethoxysilylmethanamine Chemical compound CO[Si](OC)(OC)CN(C)C DFVIRQNGJPSMQP-UHFFFAOYSA-N 0.000 claims 1
- QIOYHIUHPGORLS-UHFFFAOYSA-N n,n-dimethyl-3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN(C)C QIOYHIUHPGORLS-UHFFFAOYSA-N 0.000 claims 1
- KBJFYLLAMSZSOG-UHFFFAOYSA-N n-(3-trimethoxysilylpropyl)aniline Chemical compound CO[Si](OC)(OC)CCCNC1=CC=CC=C1 KBJFYLLAMSZSOG-UHFFFAOYSA-N 0.000 claims 1
- VNBLTKHUCJLFSB-UHFFFAOYSA-N n-(trimethoxysilylmethyl)aniline Chemical compound CO[Si](OC)(OC)CNC1=CC=CC=C1 VNBLTKHUCJLFSB-UHFFFAOYSA-N 0.000 claims 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- KPIIDEIURMTGCD-UHFFFAOYSA-N n-ethyl-n-(trimethoxysilylmethyl)ethanamine Chemical compound CCN(CC)C[Si](OC)(OC)OC KPIIDEIURMTGCD-UHFFFAOYSA-N 0.000 claims 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 230000000269 nucleophilic effect Effects 0.000 claims 1
- 125000005702 oxyalkylene group Chemical group 0.000 claims 1
- 239000004014 plasticizer Substances 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 125000006413 ring segment Chemical group 0.000 claims 1
- 229920006395 saturated elastomer Polymers 0.000 claims 1
- 238000007789 sealing Methods 0.000 claims 1
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical class [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 claims 1
- 150000003568 thioethers Chemical class 0.000 claims 1
- 150000003606 tin compounds Chemical class 0.000 claims 1
- QQQSFSZALRVCSZ-UHFFFAOYSA-N triethoxysilane Chemical compound CCO[SiH](OCC)OCC QQQSFSZALRVCSZ-UHFFFAOYSA-N 0.000 claims 1
- PZJJKWKADRNWSW-UHFFFAOYSA-N trimethoxysilicon Chemical group CO[Si](OC)OC PZJJKWKADRNWSW-UHFFFAOYSA-N 0.000 claims 1
- ARKBFSWVHXKMSD-UHFFFAOYSA-N trimethoxysilylmethanamine Chemical compound CO[Si](CN)(OC)OC ARKBFSWVHXKMSD-UHFFFAOYSA-N 0.000 claims 1
- 150000003672 ureas Chemical class 0.000 claims 1
- 150000003673 urethanes Chemical class 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP18209567.9A EP3660116B1 (en) | 2018-11-30 | 2018-11-30 | Endcapped curable polyorganosiloxanes |
| EP18209567.9 | 2018-11-30 | ||
| PCT/EP2019/082324 WO2020109187A1 (en) | 2018-11-30 | 2019-11-22 | Endcapped curable polyorganosiloxanes |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2022509300A JP2022509300A (ja) | 2022-01-20 |
| JPWO2020109187A5 true JPWO2020109187A5 (https=) | 2022-11-30 |
| JP2022509300A5 JP2022509300A5 (https=) | 2022-11-30 |
Family
ID=64745861
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021531060A Pending JP2022509300A (ja) | 2018-11-30 | 2019-11-22 | エンドキャップされた硬化性ポリオルガノシロキサン |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US12037461B2 (https=) |
| EP (1) | EP3660116B1 (https=) |
| JP (1) | JP2022509300A (https=) |
| KR (1) | KR20210096610A (https=) |
| CA (1) | CA3120914A1 (https=) |
| ES (1) | ES2955777T3 (https=) |
| MX (1) | MX2021006105A (https=) |
| PL (1) | PL3660116T3 (https=) |
| WO (1) | WO2020109187A1 (https=) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2020012307A (es) | 2018-05-18 | 2021-01-29 | Henkel Ag & Co Kgaa | Composiciones curables que comprenden promotores de adhesion. |
| JP7424369B2 (ja) * | 2019-04-03 | 2024-01-30 | 信越化学工業株式会社 | 両末端ラクタートシリル変性オルガノポリシロキサン及びその製造方法 |
| EP3967730B1 (en) * | 2019-05-09 | 2023-12-06 | Shin-Etsu Chemical Co., Ltd. | Room-temperature-vulcanizing organopolysiloxane composition, silicone rubber, and article |
| EP4204479B1 (en) * | 2020-08-27 | 2024-07-03 | Evonik Operations GmbH | Siloxane compound and formulations comprising said compound |
| TWI807540B (zh) * | 2021-12-16 | 2023-07-01 | 臺灣塑膠工業股份有限公司 | 纖維複合材料及其製造方法 |
| PL4332109T3 (pl) * | 2022-08-31 | 2026-01-26 | Henkel Ag & Co. Kgaa | Silany i utwardzalne kompozycje je zawierające |
| TWI904506B (zh) * | 2022-12-02 | 2025-11-11 | 美商蓋列斯特股份有限公司 | 柔性皮膚黏著劑組成物 |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3627836A (en) * | 1968-11-15 | 1971-12-14 | Stauffer Wacker Silicone Corp | Modified organopolysiloxanes with mono and polyolefinic cross-linked particles generated in situ |
| DE2929635A1 (de) * | 1979-07-21 | 1981-02-12 | Bayer Ag | Polysiloxanformmassen |
| DE3210337A1 (de) | 1982-03-20 | 1983-09-22 | Consortium für elektrochemische Industrie GmbH, 8000 München | Silane, verfahren zu ihrer herstellung und massen, die unter verwendung der silane bereitet worden sind |
| DE3683086D1 (de) | 1985-06-06 | 1992-02-06 | Remet Corp | Giessen von reaktionsfaehigen metallen in keramische formen. |
| FR2603893B1 (fr) * | 1986-09-11 | 1988-12-09 | Rhone Poulenc Chimie | Composition diorganopolysiloxane durcissable en elastomere autoadherent |
| JPH051225A (ja) | 1991-06-25 | 1993-01-08 | Kanegafuchi Chem Ind Co Ltd | 硬化性組成物 |
| US5300608A (en) | 1992-03-31 | 1994-04-05 | Loctite Corporation | Process for preparing alkoxy-terminated organosiloxane fluids using organo-lithium reagents |
| JP2966257B2 (ja) | 1993-10-25 | 1999-10-25 | 信越化学工業株式会社 | 室温速硬化性オルガノポリシロキサン組成物 |
| DE60012248T2 (de) | 1999-02-26 | 2005-07-28 | Shin-Etsu Chemical Co., Ltd. | Bei Raumtemperatur schnell härtende Siliconzusammensetzung |
| JP2003342547A (ja) * | 2002-05-24 | 2003-12-03 | Sekisui Chem Co Ltd | 室温硬化性接着剤組成物 |
| PL2030976T3 (pl) * | 2007-08-31 | 2013-11-29 | Nitrochemie Gmbh | Utwardzacz do mas z kauczuku silikonowego |
| EP2774672A1 (de) * | 2013-03-04 | 2014-09-10 | Nitrochemie Aschau GmbH | Katalysator für die Vernetzung von Siliconkautschukmassen |
| JP2015098557A (ja) | 2013-11-20 | 2015-05-28 | 信越化学工業株式会社 | 多成分型オルガノポリシロキサン組成物 |
| DE202015009134U1 (de) * | 2015-03-17 | 2016-10-24 | Henkel Ag & Co. Kgaa | Härtbare Silikonzusammensetzungen |
| DE102015204788A1 (de) * | 2015-03-17 | 2016-09-22 | Henkel Ag & Co. Kgaa | Silane und härtbare Zusammensetzungen, die diese Silane als Vernetzer enthalten |
| EP3269723A1 (de) | 2016-07-13 | 2018-01-17 | Nitrochemie Aschau GmbH | Härter für silikonkautschukmassen |
| EP3269785A1 (de) | 2016-07-13 | 2018-01-17 | Nitrochemie Aschau GmbH | Zusammensetzung für silikonkautschukmassen |
| EP3392313A1 (de) | 2017-04-21 | 2018-10-24 | Nitrochemie Aschau GmbH | Härtbare silikonkautschukmassen |
| MX2020012307A (es) * | 2018-05-18 | 2021-01-29 | Henkel Ag & Co Kgaa | Composiciones curables que comprenden promotores de adhesion. |
-
2018
- 2018-11-30 EP EP18209567.9A patent/EP3660116B1/en active Active
- 2018-11-30 ES ES18209567T patent/ES2955777T3/es active Active
- 2018-11-30 PL PL18209567.9T patent/PL3660116T3/pl unknown
-
2019
- 2019-11-22 KR KR1020217015923A patent/KR20210096610A/ko not_active Ceased
- 2019-11-22 CA CA3120914A patent/CA3120914A1/en active Pending
- 2019-11-22 JP JP2021531060A patent/JP2022509300A/ja active Pending
- 2019-11-22 WO PCT/EP2019/082324 patent/WO2020109187A1/en not_active Ceased
- 2019-11-22 MX MX2021006105A patent/MX2021006105A/es unknown
-
2021
- 2021-05-25 US US17/329,449 patent/US12037461B2/en active Active
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