JP2018504452A5 - - Google Patents
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- JP2018504452A5 JP2018504452A5 JP2017551996A JP2017551996A JP2018504452A5 JP 2018504452 A5 JP2018504452 A5 JP 2018504452A5 JP 2017551996 A JP2017551996 A JP 2017551996A JP 2017551996 A JP2017551996 A JP 2017551996A JP 2018504452 A5 JP2018504452 A5 JP 2018504452A5
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- JP
- Japan
- Prior art keywords
- substituted
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- reaction product
- group
- formula
- 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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- 239000007795 chemical reaction product Substances 0.000 claims 15
- 150000001875 compounds Chemical class 0.000 claims 8
- 238000000034 method Methods 0.000 claims 8
- -1 6-phenylpyridyl Chemical group 0.000 claims 6
- 230000004913 activation Effects 0.000 claims 6
- 125000002947 alkylene group Chemical group 0.000 claims 6
- 229910052751 metal Inorganic materials 0.000 claims 6
- 239000002184 metal Substances 0.000 claims 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 6
- 125000004076 pyridyl group Chemical group 0.000 claims 6
- 239000012190 activator Substances 0.000 claims 5
- 125000000962 organic group Chemical group 0.000 claims 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 4
- 239000002243 precursor Substances 0.000 claims 4
- 125000001931 aliphatic group Chemical group 0.000 claims 3
- 125000000217 alkyl group Chemical group 0.000 claims 3
- 125000000732 arylene group Chemical group 0.000 claims 3
- 239000003638 chemical reducing agent Substances 0.000 claims 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims 3
- 229910021580 Cobalt(II) chloride Inorganic materials 0.000 claims 2
- 229910021575 Iron(II) bromide Inorganic materials 0.000 claims 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical group [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims 2
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims 2
- CWSCMEBPTGNWML-UHFFFAOYSA-M [Co]Cl Chemical compound [Co]Cl CWSCMEBPTGNWML-UHFFFAOYSA-M 0.000 claims 2
- 230000003796 beauty Effects 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- 229910017052 cobalt Inorganic materials 0.000 claims 2
- 239000010941 cobalt Substances 0.000 claims 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims 2
- GVPFVAHMJGGAJG-UHFFFAOYSA-L cobalt dichloride Chemical compound [Cl-].[Cl-].[Co+2] GVPFVAHMJGGAJG-UHFFFAOYSA-L 0.000 claims 2
- 239000000945 filler Substances 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 229910052742 iron Inorganic materials 0.000 claims 2
- GYCHYNMREWYSKH-UHFFFAOYSA-L iron(ii) bromide Chemical group [Fe+2].[Br-].[Br-] GYCHYNMREWYSKH-UHFFFAOYSA-L 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 239000003446 ligand Substances 0.000 claims 2
- 229910052707 ruthenium Inorganic materials 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims 1
- 239000004970 Chain extender Substances 0.000 claims 1
- 239000004606 Fillers/Extenders Substances 0.000 claims 1
- 229910021577 Iron(II) chloride Inorganic materials 0.000 claims 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 239000012962 antiaging additive Substances 0.000 claims 1
- 230000003115 biocidal effect Effects 0.000 claims 1
- 239000003139 biocide Substances 0.000 claims 1
- 238000005260 corrosion Methods 0.000 claims 1
- 230000007797 corrosion Effects 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
- 239000003063 flame retardant Substances 0.000 claims 1
- 230000004907 flux Effects 0.000 claims 1
- 238000006459 hydrosilylation reaction Methods 0.000 claims 1
- 239000003112 inhibitor Substances 0.000 claims 1
- NMCUIPGRVMDVDB-UHFFFAOYSA-L iron dichloride Chemical compound Cl[Fe]Cl NMCUIPGRVMDVDB-UHFFFAOYSA-L 0.000 claims 1
- 239000003607 modifier Substances 0.000 claims 1
- 229910052759 nickel Inorganic materials 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 239000000049 pigment Substances 0.000 claims 1
- 239000004014 plasticizer Substances 0.000 claims 1
- 238000000518 rheometry Methods 0.000 claims 1
- 229910000077 silane Inorganic materials 0.000 claims 1
- 125000006850 spacer group Chemical group 0.000 claims 1
- 239000003381 stabilizer Substances 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- IVKIMFIYYJJVSH-UHFFFAOYSA-N C(c1ccccn1)=N/c(cccc1)c1P(c1ccccc1)c1ccccc1 Chemical compound C(c1ccccn1)=N/c(cccc1)c1P(c1ccccc1)c1ccccc1 IVKIMFIYYJJVSH-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462094316P | 2014-12-19 | 2014-12-19 | |
| US62/094,316 | 2014-12-19 | ||
| PCT/US2015/060593 WO2016099727A2 (en) | 2014-12-19 | 2015-11-13 | Ligand components, associated reaction products, activated reaction products, hydrosilylation catalysts and hydrosilylation curable compositions including the ligand components, and associated methods for preparing same |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018504452A JP2018504452A (ja) | 2018-02-15 |
| JP2018504452A5 true JP2018504452A5 (enExample) | 2018-11-29 |
| JP6824189B2 JP6824189B2 (ja) | 2021-02-03 |
Family
ID=56127813
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017551996A Active JP6824189B2 (ja) | 2014-12-19 | 2015-11-13 | 配位子成分、関連する反応生成物、活性化反応生成物、ヒドロシリル化触媒、及び配位子成分を含むヒドロシリル化硬化性組成物、及びそれを調製するための関連する方法 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US10046318B2 (enExample) |
| EP (1) | EP3233800A4 (enExample) |
| JP (1) | JP6824189B2 (enExample) |
| CN (1) | CN107207546B (enExample) |
| WO (1) | WO2016099727A2 (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6808281B2 (ja) * | 2015-12-16 | 2021-01-06 | 東ソー株式会社 | 置換シクロペンタジエニルコバルト錯体及びその製造方法、コバルト含有薄膜及びその作製方法 |
| JP7201625B2 (ja) * | 2017-06-26 | 2023-01-10 | ダウ シリコーンズ コーポレーション | 脂肪族不飽和アルコキシシラン及び水素末端オルガノシロキサンオリゴマーをヒドロシリル化して、コバルト触媒を使用してポリオルガノシロキサンを官能化するのに有用なアルコキシシリル末端ポリマーを調製する方法 |
| EP3655157A1 (en) | 2017-07-17 | 2020-05-27 | Dow Silicones Corporation | Catalyst and related methods involving hydrosilylation and dehydrogenative silylation |
| JP7777817B2 (ja) * | 2020-10-08 | 2025-12-01 | 公立大学法人大阪 | ヒドロシリル化反応触媒助剤 |
| CN112986065B (zh) * | 2021-02-08 | 2021-08-31 | 杭州同创医学检验实验室有限公司 | 一种用于血细胞分析仪的全血质控品及其制备方法 |
| FR3126418B1 (fr) * | 2021-08-31 | 2023-08-04 | Elkem Silicones France Sas | Procédé d’hydrosilylation catalysé par un complexe de cobalt |
| EP4198167A1 (de) * | 2021-12-14 | 2023-06-21 | Gühring KG | Körper aus metall, einem metallkeramischen verbund oder keramik mit einem auf einer verschleissbeanspruchten funktionsfläche mehrschichtig ausgebildeten verschleissschutzschichtsystem, und verfahren zur herstellung dieses körpers |
| CN114602557B (zh) * | 2022-03-23 | 2024-03-29 | 国科广化精细化工孵化器(南雄)有限公司 | 一种咪唑啉改性钴金属催化剂及其制备方法与应用 |
Family Cites Families (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2676182A (en) | 1950-09-13 | 1954-04-20 | Dow Corning | Copolymeric siloxanes and methods of preparing them |
| US3159601A (en) | 1962-07-02 | 1964-12-01 | Gen Electric | Platinum-olefin complex catalyzed addition of hydrogen- and alkenyl-substituted siloxanes |
| US3296291A (en) | 1962-07-02 | 1967-01-03 | Gen Electric | Reaction of silanes with unsaturated olefinic compounds |
| US3330972A (en) | 1964-10-09 | 1967-07-11 | Gen Dynamics Corp | Sine wave threshold and phase comparator |
| NL131800C (enExample) | 1965-05-17 | |||
| US3516946A (en) | 1967-09-29 | 1970-06-23 | Gen Electric | Platinum catalyst composition for hydrosilation reactions |
| US3814730A (en) | 1970-08-06 | 1974-06-04 | Gen Electric | Platinum complexes of unsaturated siloxanes and platinum containing organopolysiloxanes |
| US3989668A (en) | 1975-07-14 | 1976-11-02 | Dow Corning Corporation | Method of making a silicone elastomer and the elastomer prepared thereby |
| US4370358A (en) | 1980-09-22 | 1983-01-25 | General Electric Company | Ultraviolet curable silicone adhesives |
| US4591622A (en) | 1984-10-29 | 1986-05-27 | Dow Corning Corporation | Silicone pressure-sensitive adhesive process and product thereof |
| US4585836A (en) | 1984-10-29 | 1986-04-29 | Dow Corning Corporation | Silicone pressure-sensitive adhesive process and product with improved lap-shear stability-II |
| US4584355A (en) | 1984-10-29 | 1986-04-22 | Dow Corning Corporation | Silicone pressure-sensitive adhesive process and product with improved lap-shear stability-I |
| JPS61195129A (ja) | 1985-02-22 | 1986-08-29 | Toray Silicone Co Ltd | 有機けい素重合体の製造方法 |
| US4784879A (en) | 1987-07-20 | 1988-11-15 | Dow Corning Corporation | Method for preparing a microencapsulated compound of a platinum group metal |
| US4766176A (en) | 1987-07-20 | 1988-08-23 | Dow Corning Corporation | Storage stable heat curable organosiloxane compositions containing microencapsulated platinum-containing catalysts |
| JP2630993B2 (ja) | 1988-06-23 | 1997-07-16 | 東レ・ダウコーニング・シリコーン株式会社 | ヒドロシリル化反応用白金系触媒含有粒状物およびその製造方法 |
| JPH0214244A (ja) | 1988-06-30 | 1990-01-18 | Toray Dow Corning Silicone Co Ltd | 加熱硬化性オルガノポリシロキサン組成物 |
| US5036117A (en) | 1989-11-03 | 1991-07-30 | Dow Corning Corporation | Heat-curable silicone compositions having improved bath life |
| GB9103191D0 (en) | 1991-02-14 | 1991-04-03 | Dow Corning | Platinum complexes and use thereof |
| JP2511348B2 (ja) | 1991-10-17 | 1996-06-26 | 東レ・ダウコーニング・シリコーン株式会社 | オルガノポリシロキサンおよびその製造方法 |
| WO2003093369A1 (en) | 2002-05-01 | 2003-11-13 | Dow Corning Corporation | Compositions having improved bath life |
| WO2003093349A1 (en) | 2002-05-01 | 2003-11-13 | Dow Corning Corporation | Organohydrogensilicon compounds |
| US20050070718A1 (en) | 2003-09-30 | 2005-03-31 | Abbott Gmbh & Co. Kg | Heteroaryl-substituted 1,3-dihydroindol-2-one derivatives and medicaments containing them |
| WO2007013931A2 (en) * | 2005-07-21 | 2007-02-01 | Chevron Phillips Chemical Company Lp | Diimine metal complexes, synthesis, and use in oligomerization and polymerization |
| US7271121B2 (en) * | 2005-07-21 | 2007-09-18 | Chevron Phillips Chemical Company Lp | Diimine metal complexes, methods of synthesis, and methods of using in oligomerization and polymerization |
| JP5294303B2 (ja) * | 2008-03-31 | 2013-09-18 | 国立大学法人神戸大学 | 新規なｎ，ｎ，ｐ−三座シッフ塩基配位子化合物および該化合物を用いた不斉合成 |
| US8236915B2 (en) | 2009-07-10 | 2012-08-07 | Momentive Performance Materials Inc. | Hydrosilylation catalysts |
| TWI490224B (zh) | 2010-11-10 | 2015-07-01 | Dow Corning | 表面處理組合物、製造該表面處理組合物之方法及經表面處理之物件 |
| CN110105399B (zh) * | 2011-08-18 | 2022-08-05 | 德米特里·顾塞维 | 氢化和脱氢催化剂、以及制备和使用它们的方法 |
| CN103814037A (zh) * | 2011-09-20 | 2014-05-21 | 道康宁公司 | 含锰硅氢加成催化剂及含有该催化剂的组合物 |
| JP6101695B2 (ja) * | 2011-09-20 | 2017-03-22 | ダウ コーニング コーポレーションＤｏｗ Ｃｏｒｎｉｎｇ Ｃｏｒｐｏｒａｔｉｏｎ | ニッケル含有ヒドロシリル化触媒及びその触媒を含有する組成物 |
| CN104024267A (zh) * | 2011-09-20 | 2014-09-03 | 道康宁公司 | 含铁硅氢加成催化剂及含有该催化剂的组合物 |
| WO2013043787A2 (en) * | 2011-09-20 | 2013-03-28 | Dow Corning Corporation | Ruthenium containing hydrosilylation catalysts and compositions containing the catalysts |
| WO2013043766A1 (en) | 2011-09-20 | 2013-03-28 | Dow Corning Corporation | Molybdenum containing hydrosilylation reaction catalysts and compositions containing the catalysts |
| WO2013043783A2 (en) * | 2011-09-20 | 2013-03-28 | Dow Corning Corporation | Cobalt containing hydrosilylation catalysts and compositions containing the catalysts |
| WO2014201082A1 (en) * | 2013-06-12 | 2014-12-18 | Arizona Board Of Regents On Behalf Of Arizona State University | First-row transition metal hydrogenation and hydrosilylation catalysts |
| CN104513146B (zh) | 2013-10-08 | 2016-08-17 | 中国科学院大连化学物理研究所 | 一种由β-酮酸不对称合成手性β-乙炔基酮的方法 |
-
2015
- 2015-11-13 EP EP15870559.0A patent/EP3233800A4/en not_active Withdrawn
- 2015-11-13 CN CN201580069247.1A patent/CN107207546B/zh not_active Expired - Fee Related
- 2015-11-13 US US15/537,630 patent/US10046318B2/en active Active
- 2015-11-13 JP JP2017551996A patent/JP6824189B2/ja active Active
- 2015-11-13 WO PCT/US2015/060593 patent/WO2016099727A2/en not_active Ceased
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