JP2009526105A5 - - Google Patents
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- JP2009526105A5 JP2009526105A5 JP2008553688A JP2008553688A JP2009526105A5 JP 2009526105 A5 JP2009526105 A5 JP 2009526105A5 JP 2008553688 A JP2008553688 A JP 2008553688A JP 2008553688 A JP2008553688 A JP 2008553688A JP 2009526105 A5 JP2009526105 A5 JP 2009526105A5
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- JP
- Japan
- Prior art keywords
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- formula
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- compound
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- 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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- 150000001875 compounds Chemical class 0.000 claims 17
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims 6
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 5
- 150000004696 coordination complex Chemical class 0.000 claims 5
- 239000001257 hydrogen Substances 0.000 claims 5
- 229910052739 hydrogen Inorganic materials 0.000 claims 5
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 4
- 230000003647 oxidation Effects 0.000 claims 4
- 238000007254 oxidation reaction Methods 0.000 claims 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims 3
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 claims 3
- 229910002651 NO3 Inorganic materials 0.000 claims 3
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 3
- 125000003545 alkoxy group Chemical group 0.000 claims 3
- 125000002877 alkyl aryl group Chemical group 0.000 claims 3
- 150000001413 amino acids Chemical class 0.000 claims 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 3
- 150000007942 carboxylates Chemical class 0.000 claims 3
- 150000004820 halides Chemical class 0.000 claims 3
- 150000002466 imines Chemical class 0.000 claims 3
- 239000003446 ligand Substances 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- 229910052759 nickel Inorganic materials 0.000 claims 3
- 150000002894 organic compounds Chemical class 0.000 claims 3
- 229910052763 palladium Inorganic materials 0.000 claims 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 3
- 229910052697 platinum Inorganic materials 0.000 claims 3
- 229920000642 polymer Polymers 0.000 claims 3
- 229920005862 polyol Polymers 0.000 claims 3
- 150000003077 polyols Chemical class 0.000 claims 3
- 229910052703 rhodium Inorganic materials 0.000 claims 3
- 239000010948 rhodium Substances 0.000 claims 3
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 2
- 125000002252 acyl group Chemical group 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 238000006243 chemical reaction Methods 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
- 239000002638 heterogeneous catalyst Substances 0.000 claims 2
- 150000002484 inorganic compounds Chemical class 0.000 claims 2
- 229910010272 inorganic material Inorganic materials 0.000 claims 2
- 239000007788 liquid Substances 0.000 claims 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims 2
- 229910052751 metal Inorganic materials 0.000 claims 2
- 239000002184 metal Substances 0.000 claims 2
- 102000004169 proteins and genes Human genes 0.000 claims 2
- 108090000623 proteins and genes Proteins 0.000 claims 2
- 239000002516 radical scavenger Substances 0.000 claims 2
- 239000011541 reaction mixture Substances 0.000 claims 2
- 239000002699 waste material Substances 0.000 claims 2
- 239000002351 wastewater Substances 0.000 claims 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 102000004190 Enzymes Human genes 0.000 claims 1
- 108090000790 Enzymes Proteins 0.000 claims 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims 1
- 229910052768 actinide Inorganic materials 0.000 claims 1
- 150000001255 actinides Chemical class 0.000 claims 1
- 230000010933 acylation Effects 0.000 claims 1
- 238000005917 acylation reaction Methods 0.000 claims 1
- 238000007259 addition reaction Methods 0.000 claims 1
- 230000029936 alkylation Effects 0.000 claims 1
- 238000005804 alkylation reaction Methods 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 150000001450 anions Chemical class 0.000 claims 1
- 238000006254 arylation reaction Methods 0.000 claims 1
- 238000006664 bond formation reaction Methods 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 claims 1
- 230000006315 carbonylation Effects 0.000 claims 1
- 238000005810 carbonylation reaction Methods 0.000 claims 1
- 230000021523 carboxylation Effects 0.000 claims 1
- 238000006473 carboxylation reaction Methods 0.000 claims 1
- 230000003197 catalytic effect Effects 0.000 claims 1
- 150000001768 cations Chemical class 0.000 claims 1
- 230000032050 esterification Effects 0.000 claims 1
- 238000005886 esterification reaction Methods 0.000 claims 1
- 239000007789 gas Substances 0.000 claims 1
- 238000007037 hydroformylation reaction Methods 0.000 claims 1
- 238000005342 ion exchange Methods 0.000 claims 1
- 150000002500 ions Chemical class 0.000 claims 1
- 229910052742 iron Inorganic materials 0.000 claims 1
- 238000006317 isomerization reaction Methods 0.000 claims 1
- 229910052747 lanthanoid Inorganic materials 0.000 claims 1
- 150000002602 lanthanoids Chemical class 0.000 claims 1
- 229910021645 metal ion Inorganic materials 0.000 claims 1
- 102000039446 nucleic acids Human genes 0.000 claims 1
- 108020004707 nucleic acids Proteins 0.000 claims 1
- 150000007523 nucleic acids Chemical class 0.000 claims 1
- 125000002524 organometallic group Chemical group 0.000 claims 1
- 229920000768 polyamine Polymers 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 claims 1
- 102000004196 processed proteins & peptides Human genes 0.000 claims 1
- 108090000765 processed proteins & peptides Proteins 0.000 claims 1
- 238000000746 purification Methods 0.000 claims 1
- 238000006462 rearrangement reaction Methods 0.000 claims 1
- 229910052702 rhenium Inorganic materials 0.000 claims 1
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 claims 1
- 229910052707 ruthenium Inorganic materials 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 229920006395 saturated elastomer Polymers 0.000 claims 1
- 229910052710 silicon Inorganic materials 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- 125000000101 thioether group Chemical group 0.000 claims 1
- 238000005809 transesterification reaction Methods 0.000 claims 1
- 229910052723 transition metal Inorganic materials 0.000 claims 1
- 150000003624 transition metals Chemical class 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0602811.2 | 2006-02-10 | ||
| GBGB0602811.2A GB0602811D0 (en) | 2006-02-10 | 2006-02-10 | Substituted Organopolysiloxanes And Use Thereof |
| PCT/EP2007/001137 WO2007090676A1 (en) | 2006-02-10 | 2007-02-09 | Subtituted organopolysiloxanes and use thereof |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2009526105A JP2009526105A (ja) | 2009-07-16 |
| JP2009526105A5 true JP2009526105A5 (enExample) | 2010-05-06 |
| JP5449782B2 JP5449782B2 (ja) | 2014-03-19 |
Family
ID=36119938
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008553688A Expired - Fee Related JP5449782B2 (ja) | 2006-02-10 | 2007-02-09 | 置換オルガノポリシロキサン及びその使用 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8343474B2 (enExample) |
| EP (1) | EP1987082B1 (enExample) |
| JP (1) | JP5449782B2 (enExample) |
| CN (1) | CN101405325B (enExample) |
| AT (1) | ATE556105T1 (enExample) |
| ES (1) | ES2386906T3 (enExample) |
| GB (1) | GB0602811D0 (enExample) |
| WO (1) | WO2007090676A1 (enExample) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0720579D0 (en) * | 2007-10-20 | 2007-11-28 | Phosphonics Ltd | Functionalised materials and uses thereof |
| GB201006368D0 (en) * | 2010-04-15 | 2010-06-02 | Phosphonics Ltd | Functionalised materials and uses thereof |
| FR2968301B1 (fr) * | 2010-09-23 | 2020-05-01 | Gelest Technologies, Inc. | Derives d'alcoxysilane des acides amines a groupement n-acyle, des dipeptides a groupement n-acyle et des tripeptides a groupement n-acyle, ainsi que les particules et formulations huile dans l'eau stables les utilisant |
| EP2446965A1 (en) * | 2010-11-02 | 2012-05-02 | Evonik Degussa GmbH | Process for preparation of supported catalysts and use of the catalyst for the esterification of free fatty acids in vegetable oil |
| GB201100531D0 (en) * | 2011-01-13 | 2011-03-02 | Phosphonics | Functionalised materials, processes for the production and uses thereof |
| DE102011085492A1 (de) | 2011-10-31 | 2013-05-02 | Evonik Goldschmidt Gmbh | Neue aminogruppenhaltige Siloxane, Verfahren zu deren Herstellung und Anwendung |
| GB2508350A (en) * | 2012-11-28 | 2014-06-04 | Phosphonics Ltd | A process for the selective removal of a catalyst from a liquid phase |
| CN103877952B (zh) * | 2014-03-20 | 2017-01-18 | 江苏大学 | 类软糖状聚硅氧烷吸附材料及其表面改性海绵的制备与应用 |
| GB201505977D0 (en) | 2015-04-08 | 2015-05-20 | Johnson Matthey Davy Technologies Ltd | Catalyst system and process |
| GB201505981D0 (en) | 2015-04-08 | 2015-05-20 | Johnson Matthey Davy Technologies Ltd | Process |
| GB201515414D0 (en) | 2015-08-29 | 2015-10-14 | Advance Performance Materials Ltd | Polyorganic groups modified silica, processes to make and use therof |
| GB201515411D0 (en) * | 2015-08-29 | 2015-10-14 | Advance Performance Materials Ltd | Substituted materials, process for the production and uses thereof |
| CN106397472B (zh) * | 2016-08-06 | 2020-08-11 | 湖北硒诺唯新功能化硅胶材料有限公司 | 功能化材料及其生产工艺与使用 |
| GB201615762D0 (en) | 2016-09-16 | 2016-11-02 | Johnson Matthey Davy Technologies Ltd | Process |
| CN106866975B (zh) * | 2017-02-24 | 2020-10-23 | 苏州硒诺唯新新材料科技有限公司 | 有机聚合官能团改性二氧化硅及其生产工艺和用途 |
| CN107129575B (zh) * | 2017-04-07 | 2020-10-16 | 苏州硒诺唯新新材料科技有限公司 | 功能化材料及其生产工艺与用途 |
| CN107930601B (zh) * | 2017-11-02 | 2020-12-08 | 苏州硒诺唯新新材料科技有限公司 | 新型多聚有机改性硅胶材料的新组分及其使用 |
| CN119056412B (zh) * | 2024-11-05 | 2025-04-25 | 苏州硒诺唯新新材料科技有限公司 | 一种交叉网格结构功能化硅胶材料及其制备方法和应用 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1527598A (en) * | 1974-11-12 | 1978-10-04 | Dow Corning Ltd | Catalysts and carriers therefor |
| JP3522860B2 (ja) * | 1994-10-31 | 2004-04-26 | 信越化学工業株式会社 | ハイドロシリレーション法 |
| DE19536363A1 (de) * | 1995-09-29 | 1997-04-03 | Degussa | Sulfonat- und mercaptogruppenhaltige Organopolysiloxane, Verfahren zu ihrer Herstellung und Verwendung |
| JPH10101801A (ja) * | 1996-10-02 | 1998-04-21 | Showa Denko Kk | 水酸基含有ポリオルガノシルセスキオキサンおよびその製造方法 |
| US7301042B2 (en) * | 2002-04-23 | 2007-11-27 | Cruse Richard W | Blocked mercaptosilane hydrolyzates as coupling agents for mineral-filled elastomer compositions |
| US9982095B2 (en) | 2004-08-04 | 2018-05-29 | Phosphonics Ltd | Substituted organopolysiloxanes and use thereof |
-
2006
- 2006-02-10 GB GBGB0602811.2A patent/GB0602811D0/en not_active Ceased
-
2007
- 2007-02-09 US US12/278,939 patent/US8343474B2/en not_active Expired - Fee Related
- 2007-02-09 AT AT07703381T patent/ATE556105T1/de active
- 2007-02-09 ES ES07703381T patent/ES2386906T3/es active Active
- 2007-02-09 CN CN2007800100169A patent/CN101405325B/zh not_active Expired - Fee Related
- 2007-02-09 JP JP2008553688A patent/JP5449782B2/ja not_active Expired - Fee Related
- 2007-02-09 EP EP07703381A patent/EP1987082B1/en not_active Not-in-force
- 2007-02-09 WO PCT/EP2007/001137 patent/WO2007090676A1/en not_active Ceased
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