FI953244A - Triatseenioksidi-siirtymämetallikompleksit hydrosilylointikatalyytteinä - Google Patents
Triatseenioksidi-siirtymämetallikompleksit hydrosilylointikatalyytteinä Download PDFInfo
- Publication number
- FI953244A FI953244A FI953244A FI953244A FI953244A FI 953244 A FI953244 A FI 953244A FI 953244 A FI953244 A FI 953244A FI 953244 A FI953244 A FI 953244A FI 953244 A FI953244 A FI 953244A
- Authority
- FI
- Finland
- Prior art keywords
- formula
- contg
- cpds
- triazene
- transition metal
- Prior art date
Links
- 229910052723 transition metal Inorganic materials 0.000 title abstract 2
- AYNNSCRYTDRFCP-UHFFFAOYSA-N triazene Chemical compound NN=N AYNNSCRYTDRFCP-UHFFFAOYSA-N 0.000 title abstract 2
- 239000003054 catalyst Substances 0.000 title 1
- 238000006459 hydrosilylation reaction Methods 0.000 title 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- -1 COCl Chemical group 0.000 abstract 3
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 229920001296 polysiloxane Polymers 0.000 abstract 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 abstract 2
- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 abstract 1
- VYXHVRARDIDEHS-UHFFFAOYSA-N 1,5-cyclooctadiene Chemical compound C1CC=CCCC=C1 VYXHVRARDIDEHS-UHFFFAOYSA-N 0.000 abstract 1
- 239000004912 1,5-cyclooctadiene Substances 0.000 abstract 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 1
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 abstract 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 1
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical compound N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 abstract 1
- 229910002651 NO3 Inorganic materials 0.000 abstract 1
- 101100030361 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) pph-3 gene Proteins 0.000 abstract 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 abstract 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 abstract 1
- 229910005948 SO2Cl Inorganic materials 0.000 abstract 1
- 229910006069 SO3H Inorganic materials 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- JRXXLCKWQFKACW-UHFFFAOYSA-N biphenylacetylene Chemical group C1=CC=CC=C1C#CC1=CC=CC=C1 JRXXLCKWQFKACW-UHFFFAOYSA-N 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 229910002091 carbon monoxide Inorganic materials 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- BITPLIXHRASDQB-UHFFFAOYSA-N ethenyl-[ethenyl(dimethyl)silyl]oxy-dimethylsilane Chemical compound C=C[Si](C)(C)O[Si](C)(C)C=C BITPLIXHRASDQB-UHFFFAOYSA-N 0.000 abstract 1
- WUOIAOOSKMHJOV-UHFFFAOYSA-N ethyl(diphenyl)phosphane Chemical compound C=1C=CC=CC=1P(CC)C1=CC=CC=C1 WUOIAOOSKMHJOV-UHFFFAOYSA-N 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 1
- 125000000743 hydrocarbylene group Chemical group 0.000 abstract 1
- 229910052741 iridium Inorganic materials 0.000 abstract 1
- 239000003446 ligand Substances 0.000 abstract 1
- SJYNFBVQFBRSIB-UHFFFAOYSA-N norbornadiene Chemical compound C1=CC2C=CC1C2 SJYNFBVQFBRSIB-UHFFFAOYSA-N 0.000 abstract 1
- 229910052762 osmium Inorganic materials 0.000 abstract 1
- 229910052763 palladium Inorganic materials 0.000 abstract 1
- 229910052697 platinum Inorganic materials 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 229910052703 rhodium Inorganic materials 0.000 abstract 1
- 229910052707 ruthenium Inorganic materials 0.000 abstract 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 abstract 1
- RXJKFRMDXUJTEX-UHFFFAOYSA-N triethylphosphine Chemical compound CCP(CC)CC RXJKFRMDXUJTEX-UHFFFAOYSA-N 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
- C07F15/0086—Platinum compounds
- C07F15/0093—Platinum compounds without a metal-carbon linkage
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
- B01J31/1805—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
- C07F15/006—Palladium compounds
- C07F15/0066—Palladium compounds without a metal-carbon linkage
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
- C07F15/0073—Rhodium compounds
- C07F15/008—Rhodium compounds without a metal-carbon linkage
-
- 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
- C08L83/04—Polysiloxanes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/30—Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
- B01J2231/32—Addition reactions to C=C or C-C triple bonds
- B01J2231/323—Hydrometalation, e.g. bor-, alumin-, silyl-, zirconation or analoguous reactions like carbometalation, hydrocarbation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/82—Metals of the platinum group
- B01J2531/821—Ruthenium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/82—Metals of the platinum group
- B01J2531/822—Rhodium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/82—Metals of the platinum group
- B01J2531/824—Palladium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/82—Metals of the platinum group
- B01J2531/825—Osmium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/82—Metals of the platinum group
- B01J2531/827—Iridium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/82—Metals of the platinum group
- B01J2531/828—Platinum
-
- 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
- C08G77/04—Polysiloxanes
- C08G77/06—Preparatory processes
- C08G77/08—Preparatory processes characterised by the catalysts used
-
- 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
- C08G77/04—Polysiloxanes
- C08G77/12—Polysiloxanes containing silicon bound to hydrogen
-
- 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
- C08G77/04—Polysiloxanes
- C08G77/20—Polysiloxanes containing silicon bound to unsaturated aliphatic groups
-
- 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
- C08G77/04—Polysiloxanes
- C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
- C08G77/26—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen nitrogen-containing groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- Inorganic Chemistry (AREA)
- Catalysts (AREA)
- Silicon Polymers (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4423195A DE4423195A1 (de) | 1994-07-01 | 1994-07-01 | Triazenoxid-Übergangsmetall-Komplexe als Hydrosilylierungskatalysatoren |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| FI953244A0 FI953244A0 (fi) | 1995-06-30 |
| FI953244A true FI953244A (fi) | 1996-01-02 |
Family
ID=6522075
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI953244A FI953244A (fi) | 1994-07-01 | 1995-06-30 | Triatseenioksidi-siirtymämetallikompleksit hydrosilylointikatalyytteinä |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US5496961A (fi) |
| EP (1) | EP0690067B1 (fi) |
| JP (1) | JP2820640B2 (fi) |
| KR (1) | KR0150097B1 (fi) |
| CN (1) | CN1127756A (fi) |
| AT (1) | ATE193293T1 (fi) |
| CA (1) | CA2149393A1 (fi) |
| DE (2) | DE4423195A1 (fi) |
| FI (1) | FI953244A (fi) |
Families Citing this family (63)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5693735A (en) * | 1995-07-12 | 1997-12-02 | Shin-Etsu Chemical Co., Ltd. | Trimethylsiloxy group-containing polysiloxane and a process for producing the same |
| DE19535005A1 (de) * | 1995-09-21 | 1997-03-27 | Wacker Chemie Gmbh | Wäßrige Organopolysiloxanemulsionen sowie Emulgatoren zu deren Herstellung |
| DE19644561C2 (de) * | 1996-10-26 | 2003-10-16 | Degussa | Verfahren zur Herstellung von Fluoralkyl-Gruppen tragenden Silicium-organischen Verbindungen |
| US6907176B2 (en) * | 2002-06-24 | 2005-06-14 | Dow Corning Corporation | Planar optical waveguide assembly and method of preparing same |
| DE10235267A1 (de) | 2002-08-01 | 2004-02-12 | Wacker-Chemie Gmbh | Verwendung von Rhodium-vernetzenden Siliconelastomeren für die Herstellung von Backformen |
| DE10394275T5 (de) * | 2003-07-28 | 2006-06-22 | Dow Corning Corp., Midland | Verfahren zur Ätzung einer Siliconschicht in Musterform |
| EP1820065A2 (en) | 2004-08-11 | 2007-08-22 | Dow Corning Corporation | Photopolymerizable silicone materials forming semipermeable membranes for sensor applications |
| US20060105483A1 (en) * | 2004-11-18 | 2006-05-18 | Leatherdale Catherine A | Encapsulated light emitting diodes and methods of making |
| US7314770B2 (en) | 2004-11-18 | 2008-01-01 | 3M Innovative Properties Company | Method of making light emitting device with silicon-containing encapsulant |
| US7192795B2 (en) * | 2004-11-18 | 2007-03-20 | 3M Innovative Properties Company | Method of making light emitting device with silicon-containing encapsulant |
| US8092910B2 (en) * | 2005-02-16 | 2012-01-10 | Dow Corning Toray Co., Ltd. | Reinforced silicone resin film and method of preparing same |
| ATE551398T1 (de) * | 2005-02-16 | 2012-04-15 | Dow Corning | Verstärkte silikonharzfolie und herstellungsverfahren dafür |
| CN101238181B (zh) * | 2005-08-04 | 2011-10-05 | 陶氏康宁公司 | 增强的有机硅树脂膜及其制备方法 |
| US20070092736A1 (en) * | 2005-10-21 | 2007-04-26 | 3M Innovative Properties Company | Method of making light emitting device with silicon-containing encapsulant |
| US20070092737A1 (en) * | 2005-10-21 | 2007-04-26 | 3M Innovative Properties Company | Method of making light emitting device with silicon-containing encapsulant |
| EP1949459A4 (en) * | 2005-10-24 | 2014-04-30 | 3M Innovative Properties Co | METHOD FOR MANUFACTURING A LIGHT EMITTING DEVICE COMPRISING A MOLDED ENCAPSULANT |
| US7595515B2 (en) | 2005-10-24 | 2009-09-29 | 3M Innovative Properties Company | Method of making light emitting device having a molded encapsulant |
| JP5362363B2 (ja) * | 2005-12-21 | 2013-12-11 | ダウ・コーニング・コーポレイション | シリコーン樹脂フィルム、その調製方法、及びナノ材料充填シリコーン組成物 |
| WO2008051242A2 (en) * | 2006-01-19 | 2008-05-02 | Dow Corning Corporation | Silicone resin film, method of preparing same, and nanomaterial-filled silicone compositon |
| US8084097B2 (en) * | 2006-02-20 | 2011-12-27 | Dow Corning Corporation | Silicone resin film, method of preparing same, and nanomaterial-filled silicone composition |
| WO2008088570A1 (en) * | 2006-04-18 | 2008-07-24 | Itn Energy Systems, Inc. | Reinforcing structures for thin-film photovoltaic device substrates, and associated methods |
| KR20090005184A (ko) * | 2006-04-18 | 2009-01-12 | 다우 코닝 코포레이션 | 구리 인듐 디셀레나이드-기재 광전지 장치 및 그의 제조 방법 |
| WO2007123898A1 (en) * | 2006-04-18 | 2007-11-01 | Dow Corning Corporation | Copper indium diselenide-based photovoltaic device and method of preparing the same |
| KR20080112381A (ko) * | 2006-04-18 | 2008-12-24 | 다우 코닝 코포레이션 | 카드뮴 텔루라이드 기재 광전지 장치 및 그 제조 방법 |
| US7655486B2 (en) * | 2006-05-17 | 2010-02-02 | 3M Innovative Properties Company | Method of making light emitting device with multilayer silicon-containing encapsulant |
| US20070269586A1 (en) * | 2006-05-17 | 2007-11-22 | 3M Innovative Properties Company | Method of making light emitting device with silicon-containing composition |
| CN101501571B (zh) * | 2006-08-14 | 2013-08-21 | 道康宁公司 | 使用显影溶剂制备图案化膜的方法 |
| US8092735B2 (en) * | 2006-08-17 | 2012-01-10 | 3M Innovative Properties Company | Method of making a light emitting device having a molded encapsulant |
| WO2008036769A2 (en) * | 2006-09-19 | 2008-03-27 | Itn Energy Systems, Inc. | Semi-transparent dual layer back contact for bifacial and tandem junction thin-film photovolataic devices |
| CN101522838B (zh) * | 2006-10-05 | 2012-07-04 | 陶氏康宁公司 | 有机硅树脂膜及其制备方法 |
| US8277945B2 (en) * | 2006-12-20 | 2012-10-02 | Dow Corning Corporation | Glass substrates coated or laminated with multiple layers of cured silicone resin compositions |
| CN101563300B (zh) * | 2006-12-20 | 2012-09-05 | 陶氏康宁公司 | 用固化的有机硅树脂组合物涂布或层压的玻璃基底 |
| EP2125936A1 (en) * | 2007-02-06 | 2009-12-02 | Dow Corning Corporation | Silicone resin, silicone composition, coated substrate, and reinforced silicone resin film |
| US9944031B2 (en) * | 2007-02-13 | 2018-04-17 | 3M Innovative Properties Company | Molded optical articles and methods of making same |
| EP2111651A4 (en) | 2007-02-13 | 2011-08-17 | 3M Innovative Properties Co | LED DEVICES HAVING ASSOCIATED LENSES AND METHODS OF MANUFACTURE |
| KR20090120468A (ko) * | 2007-02-22 | 2009-11-24 | 다우 코닝 코포레이션 | 우수한 내화성을 갖는 복합체 물품 |
| US8283025B2 (en) * | 2007-02-22 | 2012-10-09 | Dow Corning Corporation | Reinforced silicone resin films |
| CN101652245A (zh) * | 2007-02-22 | 2010-02-17 | 陶氏康宁公司 | 具有优良耐火性的复合制品 |
| JP2010519381A (ja) * | 2007-02-22 | 2010-06-03 | ダウ コーニング コーポレーション | 強化シリコーン樹脂フィルムおよびその調製方法 |
| US8323797B2 (en) * | 2007-02-22 | 2012-12-04 | Dow Corning Corporation | Composite article having excellent fire and impact resistance and method of making the same |
| WO2008103229A1 (en) * | 2007-02-22 | 2008-08-28 | Dow Corning Corporation | Reinforced silicone resin film and method of preparing same |
| CN101636270B (zh) * | 2007-02-22 | 2012-07-04 | 道康宁公司 | 增强硅树脂膜 |
| EP2142589A2 (en) * | 2007-05-01 | 2010-01-13 | Dow Corning Corporation | Reinforced silicone resin film |
| WO2008134241A1 (en) * | 2007-05-01 | 2008-11-06 | Dow Corining Corporation | Nanomaterial-filled silicone composition and reinforced silicone resin film |
| CN101848960A (zh) * | 2007-10-12 | 2010-09-29 | 陶氏康宁公司 | 强化的硅酮树脂膜和纳米纤维填充的硅酮组合物 |
| WO2009051905A2 (en) * | 2007-10-12 | 2009-04-23 | Dow Corning Corporation | Aluminum oxide dispersion and method of preparing same |
| EP2265674A1 (en) * | 2008-03-04 | 2010-12-29 | Dow Corning Corporation | Silicone composition, silicone adhesive, coated and laminated substrates |
| US8450442B2 (en) * | 2008-03-04 | 2013-05-28 | Dow Corning Corporation | Borosiloxane composition, borosiloxane adhesive, coated and laminated substrates |
| WO2009146254A1 (en) * | 2008-05-27 | 2009-12-03 | Dow Corning Corporation | Adhesive tape and laminated glass |
| TW201004795A (en) * | 2008-07-31 | 2010-02-01 | Dow Corning | Laminated glass |
| KR101625545B1 (ko) | 2008-10-31 | 2016-05-30 | 다우 코닝 코포레이션 | 광전지 모듈 및 이의 형성 방법 |
| DE102009027215A1 (de) * | 2009-06-25 | 2010-12-30 | Wacker Chemie Ag | Verfahren zur Hydrosilylierung |
| US9012547B2 (en) | 2010-11-09 | 2015-04-21 | Dow Corning Corporation | Hydrosilylation cured silicone resins plasticized by organophosphorous compounds |
| JP2013544949A (ja) | 2010-12-08 | 2013-12-19 | ダウ コーニング コーポレーション | 封止材を形成するのに好適な二酸化チタンナノ粒子を含むシロキサン組成物 |
| EP2649113A1 (en) | 2010-12-08 | 2013-10-16 | Dow Corning Corporation | Siloxane compositions including metal-oxide nanoparticles suitable for forming encapsulants |
| KR20130140815A (ko) | 2010-12-08 | 2013-12-24 | 다우 코닝 코포레이션 | 봉지재의 형성에 적합한 실록산 조성물 |
| US9731245B2 (en) | 2012-09-26 | 2017-08-15 | Dow Corning Corporation | Method of separating a gas using at least one membrane in contact with an organosilicon fluid |
| CN105209474B (zh) * | 2013-03-14 | 2017-07-14 | 国立研究开发法人产业技术综合研究所 | 具有二硅氧烷作为配体的金属络合物和负载型金属络合物、它们的制备方法和通过使用负载型金属络合物制备的负载型金属催化剂 |
| CN106804110B (zh) | 2014-09-17 | 2020-11-27 | 美国陶氏有机硅公司 | 使用可光固化的有机硅组合物的3d印刷方法 |
| CN104788363B (zh) * | 2015-03-22 | 2017-10-03 | 东莞理工学院 | 一种三氮烯‑钴(iii)单核配合物及其制备方法 |
| CN106977923B (zh) * | 2017-03-31 | 2020-10-23 | 广东工业大学 | 一种三氮烯混合物及其制备方法 |
| CN109453812B (zh) * | 2017-09-06 | 2021-09-07 | 中国科学院大连化学物理研究所 | 有机含氮聚合物载体负载Rh基催化剂及其制备和应用 |
| KR102171374B1 (ko) * | 2018-07-27 | 2020-10-29 | 주식회사 비에스피 | 마이크로 소자 리워크 방법 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3814730A (en) * | 1970-08-06 | 1974-06-04 | Gen Electric | Platinum complexes of unsaturated siloxanes and platinum containing organopolysiloxanes |
| DE4242469A1 (de) * | 1992-12-16 | 1994-06-23 | Wacker Chemie Gmbh | Katalysatoren für Hydrosilylierungsreaktionen |
| DE4324685A1 (de) * | 1993-07-22 | 1995-01-26 | Wacker Chemie Gmbh | Organosiloxangebundene Übergangsmetallkomplexe |
-
1994
- 1994-07-01 DE DE4423195A patent/DE4423195A1/de not_active Withdrawn
-
1995
- 1995-05-10 US US08/437,830 patent/US5496961A/en not_active Expired - Fee Related
- 1995-05-15 CA CA002149393A patent/CA2149393A1/en not_active Abandoned
- 1995-06-22 AT AT95109673T patent/ATE193293T1/de active
- 1995-06-22 DE DE59508374T patent/DE59508374D1/de not_active Expired - Fee Related
- 1995-06-22 EP EP95109673A patent/EP0690067B1/de not_active Expired - Lifetime
- 1995-06-30 CN CN95108153A patent/CN1127756A/zh active Pending
- 1995-06-30 FI FI953244A patent/FI953244A/fi unknown
- 1995-06-30 JP JP7166589A patent/JP2820640B2/ja not_active Expired - Lifetime
- 1995-06-30 KR KR1019950018824A patent/KR0150097B1/ko not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| KR0150097B1 (ko) | 1998-10-15 |
| CN1127756A (zh) | 1996-07-31 |
| KR960004358A (ko) | 1996-02-23 |
| CA2149393A1 (en) | 1996-01-02 |
| DE59508374D1 (de) | 2000-06-29 |
| EP0690067B1 (de) | 2000-05-24 |
| FI953244A0 (fi) | 1995-06-30 |
| ATE193293T1 (de) | 2000-06-15 |
| US5496961A (en) | 1996-03-05 |
| JPH0848778A (ja) | 1996-02-20 |
| DE4423195A1 (de) | 1996-01-04 |
| JP2820640B2 (ja) | 1998-11-05 |
| EP0690067A1 (de) | 1996-01-03 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| FI953244A (fi) | Triatseenioksidi-siirtymämetallikompleksit hydrosilylointikatalyytteinä | |
| CA2111643A1 (en) | Catalysts for Hydrosilylation Reactions | |
| Ouderkirk et al. | Observation of coordinatively unsaturated intermediates following the pulsed UV photolysis of iron pentacarbonyl (Fe (CO) 5) | |
| Vol'Pin et al. | Reactions of carbon dioxide with transition metal compounds | |
| Sakamoto et al. | Synthesis of the first carbon dioxide coordinated palladium (0) complex, Pd (. eta. 2-CO2)(PMePh2) 2 | |
| SG34298A1 (en) | Offsite regeneration process for a catalyst containing at least one precious metal | |
| GB9601603D0 (en) | Terpyridine-platinum (II) complexes | |
| ATE131187T1 (de) | Organosiloxangebundene übergangsmetallkomplexe. | |
| Kinting et al. | Metal controlled enantioselectivity in the catalytic asymmetric hydrosilylation | |
| CA2289503A1 (en) | A catalyst comprising pd and au deposited on a copper containing carrier for production of vinyl acetate | |
| Reger et al. | Alkyl group isomerization studies with unusually stable alkylmetal complexes of palladium and platinum. Secondary-primary alkyl isomerization equilibria in the absence of steric influences from ancillary ligands | |
| Moseley et al. | Bis-and tris-(dibenzylideneacetone) platinum and the stabilization of zerovalent complexes by an unsaturated ketone | |
| Schrod et al. | Investigation of the synthesis of acetic anhydride by homogeneous catalysis: II. Spectroscopic studies of the mechanism | |
| Sustmann et al. | Dimerization of methyl acrylate by homogeneous transition-metal catalysis. Part I. Activation of hydrido (carbonyl) chloro-[bis (triisopropylphosphane)] ruthenium by CF3SO3Ag | |
| Li et al. | EXAFS and fourier transform IR characterization of platinum carbonyl clusters [Pt3 (CO) 6] n2–(n= 3, 4) encapsulated in nay zeolites and their effective catalysis in the CO+ NO reaction | |
| Bailey | The cleavage of a cluster carbonyl C O bond by trifluoromethanesulphonic anhydride | |
| Lyashenko et al. | Effect of the method of photoactivating immobilized catalytic properties in the reaction of isobutylene oxidation | |
| Drage et al. | Synthesis, structure, and dynamic properties of a fulvalene-bound Fischer-type carbene complex. A novel thermal elimination of propene | |
| Wong et al. | Synthesis and X-ray crystal structure of (cis-PdCl2) 2 [Ph2PNH)(NH) CC6H4C (NH)(NHPPh2)]· 6DMF | |
| JPH07114966B2 (ja) | 水性ガス転化反応及びオキソ合成反応用触媒の調整方法 | |
| JPS6144850A (ja) | アミノ酸又は／及びペプチドの製造法 | |
| West et al. | JOURNAL OF ORGANOMETALLIC CHEMWI’RY, VOL. 393 (1990) | |
| Dent et al. | Interaction of acyl chlorides and triethylsilane catalysed by cis-di-chlorobis (triphenylphosphine) platinum (II) and related complexes | |
| Plackett | Activation of carbon monoxide by ruthenium carbonyl complexes in solution | |
| Pompeo | Studies of the coordination and ring-opening transformations of thietane ligands in triosmium carbonyl cluster complexes. |