JP2017509730A5 - - Google Patents
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- JP2017509730A5 JP2017509730A5 JP2016543607A JP2016543607A JP2017509730A5 JP 2017509730 A5 JP2017509730 A5 JP 2017509730A5 JP 2016543607 A JP2016543607 A JP 2016543607A JP 2016543607 A JP2016543607 A JP 2016543607A JP 2017509730 A5 JP2017509730 A5 JP 2017509730A5
- Authority
- JP
- Japan
- Prior art keywords
- composition
- combinations
- item
- composition according
- organosiloxane oligomer
- 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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- 239000000203 mixture Substances 0.000 claims description 73
- -1 organosiloxane compound Chemical class 0.000 claims description 29
- 125000005375 organosiloxane group Chemical group 0.000 claims description 23
- 229910052751 metal Inorganic materials 0.000 claims description 13
- 239000002184 metal Substances 0.000 claims description 13
- 239000002841 Lewis acid Substances 0.000 claims description 10
- 150000007517 lewis acids Chemical class 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 9
- GQHTUMJGOHRCHB-UHFFFAOYSA-N 2,3,4,6,7,8,9,10-octahydropyrimido[1,2-a]azepine Chemical compound C1CCCCN2CCCN=C21 GQHTUMJGOHRCHB-UHFFFAOYSA-N 0.000 claims description 8
- 125000003118 aryl group Chemical group 0.000 claims description 8
- 125000003709 fluoroalkyl group Chemical group 0.000 claims description 8
- OEBXWWBYZJNKRK-UHFFFAOYSA-N 1-methyl-2,3,4,6,7,8-hexahydropyrimido[1,2-a]pyrimidine Chemical compound C1CCN=C2N(C)CCCN21 OEBXWWBYZJNKRK-UHFFFAOYSA-N 0.000 claims description 7
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical group [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 7
- 239000000758 substrate Substances 0.000 claims description 7
- 150000001642 boronic acid derivatives Chemical class 0.000 claims description 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 6
- 125000004407 fluoroaryl group Chemical group 0.000 claims description 6
- 125000005348 fluorocycloalkyl group Chemical group 0.000 claims description 6
- 150000002357 guanidines Chemical class 0.000 claims description 6
- 125000004404 heteroalkyl group Chemical group 0.000 claims description 6
- 125000001072 heteroaryl group Chemical group 0.000 claims description 6
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 6
- GKTNLYAAZKKMTQ-UHFFFAOYSA-N n-[bis(dimethylamino)phosphinimyl]-n-methylmethanamine Chemical compound CN(C)P(=N)(N(C)C)N(C)C GKTNLYAAZKKMTQ-UHFFFAOYSA-N 0.000 claims description 6
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims description 5
- 150000001409 amidines Chemical class 0.000 claims description 5
- 239000011248 coating agent Substances 0.000 claims description 5
- 238000000576 coating method Methods 0.000 claims description 5
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 4
- 239000003054 catalyst Substances 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 4
- ZFDWWDZLRKHULH-UHFFFAOYSA-N 1,2-dimethyl-5,6-dihydro-4h-pyrimidine Chemical compound CN1CCCN=C1C ZFDWWDZLRKHULH-UHFFFAOYSA-N 0.000 claims description 3
- SGUVLZREKBPKCE-UHFFFAOYSA-N 1,5-diazabicyclo[4.3.0]-non-5-ene Chemical compound C1CCN=C2CCCN21 SGUVLZREKBPKCE-UHFFFAOYSA-N 0.000 claims description 3
- YQHJFPFNGVDEDT-UHFFFAOYSA-N 2-tert-butyl-1,1,3,3-tetramethylguanidine Chemical compound CN(C)C(N(C)C)=NC(C)(C)C YQHJFPFNGVDEDT-UHFFFAOYSA-N 0.000 claims description 3
- FVKFHMNJTHKMRX-UHFFFAOYSA-N 3,4,6,7,8,9-hexahydro-2H-pyrimido[1,2-a]pyrimidine Chemical compound C1CCN2CCCNC2=N1 FVKFHMNJTHKMRX-UHFFFAOYSA-N 0.000 claims description 3
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims description 3
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 claims description 3
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 claims description 3
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 claims description 3
- 125000005647 linker group Chemical group 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- POPHMOPNVVKGRW-UHFFFAOYSA-N 1,2,3,4,4a,5,6,7-octahydronaphthalene Chemical compound C1CCC2CCCCC2=C1 POPHMOPNVVKGRW-UHFFFAOYSA-N 0.000 claims description 2
- 125000003342 alkenyl group Chemical group 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 2
- 125000000962 organic group Chemical group 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- 229910052797 bismuth Inorganic materials 0.000 description 3
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 125000000732 arylene group Chemical group 0.000 description 2
- 125000002993 cycloalkylene group Chemical group 0.000 description 2
- SHZIWNPUGXLXDT-UHFFFAOYSA-N ethyl hexanoate Chemical compound CCCCCC(=O)OCC SHZIWNPUGXLXDT-UHFFFAOYSA-N 0.000 description 2
- 125000005549 heteroarylene group Chemical group 0.000 description 2
- 125000006588 heterocycloalkylene group Chemical group 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- GXTAADIYVXOPAM-UHFFFAOYSA-N 1-phosphabicyclo[3.3.3]undecane Chemical compound C1CCP2CCCC1CCC2 GXTAADIYVXOPAM-UHFFFAOYSA-N 0.000 description 1
- AURKDQJEOYBJSQ-UHFFFAOYSA-N 2-hydroxypropanoyl 2-hydroxypropanoate Chemical compound CC(O)C(=O)OC(=O)C(C)O AURKDQJEOYBJSQ-UHFFFAOYSA-N 0.000 description 1
- VSCBATMPTLKTOV-UHFFFAOYSA-N 2-tert-butylimino-n,n-diethyl-1,3-dimethyl-1,3,2$l^{5}-diazaphosphinan-2-amine Chemical compound CCN(CC)P1(=NC(C)(C)C)N(C)CCCN1C VSCBATMPTLKTOV-UHFFFAOYSA-N 0.000 description 1
- YPIFGDQKSSMYHQ-UHFFFAOYSA-M 7,7-dimethyloctanoate Chemical compound CC(C)(C)CCCCCC([O-])=O YPIFGDQKSSMYHQ-UHFFFAOYSA-M 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 1
- PTFCDOFLOPIGGS-UHFFFAOYSA-N Zinc dication Chemical class [Zn+2] PTFCDOFLOPIGGS-UHFFFAOYSA-N 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 125000004474 heteroalkylene group Chemical group 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- NSRBCQCXZAYQHF-UHFFFAOYSA-N n-[[tert-butylimino-bis[[tris(dimethylamino)-$l^{5}-phosphanylidene]amino]-$l^{5}-phosphanyl]imino-bis(dimethylamino)-$l^{5}-phosphanyl]-n-methylmethanamine Chemical compound CN(C)P(N(C)C)(N(C)C)=NP(=NC(C)(C)C)(N=P(N(C)C)(N(C)C)N(C)C)N=P(N(C)C)(N(C)C)N(C)C NSRBCQCXZAYQHF-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 description 1
- 125000005429 oxyalkyl group Chemical group 0.000 description 1
- 125000005702 oxyalkylene group Chemical group 0.000 description 1
- PVNUIRUAPVSSOK-UHFFFAOYSA-N tert-butylimino(tripyrrolidin-1-yl)-$l^{5}-phosphane Chemical compound C1CCCN1P(N1CCCC1)(=NC(C)(C)C)N1CCCC1 PVNUIRUAPVSSOK-UHFFFAOYSA-N 0.000 description 1
- 239000012974 tin catalyst Substances 0.000 description 1
- AJSTXXYNEIHPMD-UHFFFAOYSA-N triethyl borate Chemical compound CCOB(OCC)OCC AJSTXXYNEIHPMD-UHFFFAOYSA-N 0.000 description 1
- WRECIMRULFAWHA-UHFFFAOYSA-N trimethyl borate Chemical compound COB(OC)OC WRECIMRULFAWHA-UHFFFAOYSA-N 0.000 description 1
- MDCWDBMBZLORER-UHFFFAOYSA-N triphenyl borate Chemical compound C=1C=CC=CC=1OB(OC=1C=CC=CC=1)OC1=CC=CC=C1 MDCWDBMBZLORER-UHFFFAOYSA-N 0.000 description 1
- NHDIQVFFNDKAQU-UHFFFAOYSA-N tripropan-2-yl borate Chemical compound CC(C)OB(OC(C)C)OC(C)C NHDIQVFFNDKAQU-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361922160P | 2013-12-31 | 2013-12-31 | |
| US61/922,160 | 2013-12-31 | ||
| US201462073106P | 2014-10-31 | 2014-10-31 | |
| US62/073,106 | 2014-10-31 | ||
| PCT/US2014/071786 WO2015102979A1 (en) | 2013-12-31 | 2014-12-22 | Curable organosiloxane oligomer compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2017509730A JP2017509730A (ja) | 2017-04-06 |
| JP2017509730A5 true JP2017509730A5 (cg-RX-API-DMAC7.html) | 2018-02-08 |
Family
ID=53493911
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016543607A Withdrawn JP2017509730A (ja) | 2013-12-31 | 2014-12-22 | 硬化性オルガノシロキサンオリゴマー組成物 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US10370499B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP3090008A4 (cg-RX-API-DMAC7.html) |
| JP (1) | JP2017509730A (cg-RX-API-DMAC7.html) |
| KR (1) | KR20160105844A (cg-RX-API-DMAC7.html) |
| CN (1) | CN105873984A (cg-RX-API-DMAC7.html) |
| SG (1) | SG11201605193YA (cg-RX-API-DMAC7.html) |
| WO (1) | WO2015102979A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6583821B2 (ja) * | 2015-12-01 | 2019-10-02 | 国立大学法人山口大学 | 硬化性樹脂組成物 |
| US9897914B2 (en) * | 2015-12-28 | 2018-02-20 | Shin-Etsu Chemical Co., Ltd. | Resist composition and patterning process |
| KR102024252B1 (ko) * | 2016-09-09 | 2019-09-23 | 주식회사 엘지화학 | 폴더블(foldable) 디스플레이용 점착제 조성물 |
| CN109467707B (zh) * | 2017-09-07 | 2022-02-01 | 青岛科技大学 | 线性聚磷腈化合物及其制备方法和用途 |
| FR3079238B1 (fr) * | 2018-03-21 | 2020-05-15 | Bostik Sa | Composition catalytique pour composition adhesive a base de polymere silyle reticulable |
| CN110734550A (zh) * | 2018-07-20 | 2020-01-31 | 东莞市博君来胶粘材料科技有限公司 | 一种甲基苯基硅油的制备方法 |
| BR112021015373B1 (pt) | 2019-02-13 | 2024-03-05 | Dow Global Technologies Llc | Formulação de poliolefina curável por umidade, método para fazer uma formulação de poliolefina curável por umidade, produto de poliolefina curada por umidade, artigo fabricado, condutor revestido e método para conduzir eletricidade |
| US11840587B2 (en) | 2019-02-13 | 2023-12-12 | Dow Global Technologies Llc | Moisture-curable polyolefin formulation |
| EP3938456B1 (en) * | 2019-03-07 | 2024-11-06 | Dow Global Technologies Llc | Formaldehyde free adhesive composition |
| US11254838B2 (en) | 2019-03-29 | 2022-02-22 | Ppg Industries Ohio, Inc. | Single component hydrophobic coating |
| EP3980428B1 (en) | 2019-06-04 | 2023-04-26 | Dow Silicones Corporation | Thermally initiated acid catalyzed reaction between silyl hydride and alpha-beta unsaturated esters |
| JP7560488B2 (ja) | 2019-06-04 | 2024-10-02 | ダウ シリコーンズ コーポレーション | シリルヒドリドとシロキサンとの熱開始酸触媒反応 |
| KR20220016906A (ko) | 2019-06-04 | 2022-02-10 | 다우 실리콘즈 코포레이션 | 실릴 수소화물과 실릴 에테르 및/또는 실라놀 사이의 열적으로 개시되는 산 촉매 반응 |
| JP7560489B2 (ja) * | 2019-06-04 | 2024-10-02 | ダウ シリコーンズ コーポレーション | Ｓｉ－Ｈとアルファ－ベータ不飽和エステルとの反応のための熱トリガとしての架橋型フラストレイテッドルイスペア |
| WO2020247334A1 (en) * | 2019-06-04 | 2020-12-10 | Dow Silicones Corporation | Bridged frustrated lewis pairs as thermal trigger for reactions between si-h and si-or |
| US12421421B2 (en) | 2019-08-02 | 2025-09-23 | 3M Innovative Properties Company | Composition including a polyorganosiloxane and an amino-functional silane and method of using the same |
| KR20230029858A (ko) * | 2020-06-24 | 2023-03-03 | 다우 글로벌 테크놀로지스 엘엘씨 | 플루오르화 아릴보란 루이스 산에 의해 촉매되는 실릴 하이드라이드 반응을 위한 조성물 및 방법 |
| EP4174043A4 (en) * | 2020-06-29 | 2024-07-10 | Sobute New Materials Co., Ltd. | Organic silicon nanoprecursor medium transmission inhibitor, preparation method therefor and use thereof |
| CN117120572A (zh) | 2021-04-27 | 2023-11-24 | 美国陶氏有机硅公司 | 硅氢加成反应固化的有机硅压敏粘合剂、组合物及其制备方法以及在柔性显示设备中的用途 |
| JP7343721B2 (ja) | 2021-04-27 | 2023-09-12 | ダウ シリコーンズ コーポレーション | ラジカル硬化シリコーン感圧接着剤及び組成物、並びにその調製方法及びフレキシブルディスプレイデバイスにおける使用方法 |
| US12454125B2 (en) | 2021-11-01 | 2025-10-28 | Dow Silicones Corporation | Method for preparation of a laminate article including a silicone pressure sensitive adhesive adhered to silicone rubber |
| CN118325465A (zh) * | 2024-04-17 | 2024-07-12 | 海南核电有限公司 | 一种多尺度交联的氟硅基陶瓷修补剂及其制备方法 |
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| KR101346410B1 (ko) | 2008-11-25 | 2014-01-02 | 블루스타 실리콘즈 프랑스 에스에이에스 | 구아니딘 구조를 갖는 화합물 및 오르가노폴리실록산 중축합 촉매로서의 이의 용도 |
| CN102575011B (zh) * | 2009-06-19 | 2014-03-12 | 蓝星有机硅法国公司 | 通过在非金属催化剂存在下脱氢缩合可交联的有机硅组合物 |
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| JP5925201B2 (ja) | 2010-06-30 | 2016-05-25 | スリーエム イノベイティブ プロパティズ カンパニー | 二重反応性シラン官能基を含むオンデマンド型硬化性組成物 |
| US9006357B2 (en) | 2011-12-29 | 2015-04-14 | 3M Innovative Properties Company | Curable polysiloxane composition |
| JP6336398B2 (ja) * | 2011-12-29 | 2018-06-06 | スリーエム イノベイティブ プロパティズ カンパニー | オンデマンド型硬化性ポリシロキサンコーティング組成物 |
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2014
- 2014-12-22 JP JP2016543607A patent/JP2017509730A/ja not_active Withdrawn
- 2014-12-22 KR KR1020167020854A patent/KR20160105844A/ko not_active Withdrawn
- 2014-12-22 US US15/108,827 patent/US10370499B2/en active Active
- 2014-12-22 SG SG11201605193YA patent/SG11201605193YA/en unknown
- 2014-12-22 WO PCT/US2014/071786 patent/WO2015102979A1/en not_active Ceased
- 2014-12-22 EP EP14876642.1A patent/EP3090008A4/en not_active Withdrawn
- 2014-12-22 CN CN201480071633.XA patent/CN105873984A/zh active Pending