FR2458553A1 - Procede de preparation de composes organosiliciques porteurs de groupements chlorosilylmethyles a partir d'halogenures organiques, de polysilanes et de composes organosiliciques porteurs de groupements trichlorosilyles - Google Patents
Procede de preparation de composes organosiliciques porteurs de groupements chlorosilylmethyles a partir d'halogenures organiques, de polysilanes et de composes organosiliciques porteurs de groupements trichlorosilyles Download PDFInfo
- Publication number
- FR2458553A1 FR2458553A1 FR7915069A FR7915069A FR2458553A1 FR 2458553 A1 FR2458553 A1 FR 2458553A1 FR 7915069 A FR7915069 A FR 7915069A FR 7915069 A FR7915069 A FR 7915069A FR 2458553 A1 FR2458553 A1 FR 2458553A1
- Authority
- FR
- France
- Prior art keywords
- sep
- group
- allyl
- nickelocene
- 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.)
- Granted
Links
- -1 allyl halide Chemical class 0.000 title claims abstract description 31
- KZPXREABEBSAQM-UHFFFAOYSA-N cyclopenta-1,3-diene;nickel(2+) Chemical compound [Ni+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KZPXREABEBSAQM-UHFFFAOYSA-N 0.000 title claims abstract description 16
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 title claims abstract description 11
- 125000001309 chloro group Chemical group Cl* 0.000 title claims description 6
- 239000003054 catalyst Substances 0.000 title abstract description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 title description 6
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 title description 3
- 229910000077 silane Inorganic materials 0.000 title description 3
- 229910052710 silicon Inorganic materials 0.000 title 2
- 239000010703 silicon Substances 0.000 title 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 17
- 238000006243 chemical reaction Methods 0.000 claims abstract description 14
- 229920000548 poly(silane) polymer Polymers 0.000 claims abstract description 12
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 7
- 238000000034 method Methods 0.000 claims description 21
- 150000001875 compounds Chemical group 0.000 claims description 9
- 150000004820 halides Chemical class 0.000 claims description 7
- 150000003961 organosilicon compounds Chemical class 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 125000004970 halomethyl group Chemical group 0.000 claims description 5
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical group CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 claims description 5
- 239000005054 phenyltrichlorosilane Substances 0.000 claims description 5
- 125000001424 substituent group Chemical group 0.000 claims description 5
- ORVMIVQULIKXCP-UHFFFAOYSA-N trichloro(phenyl)silane Chemical compound Cl[Si](Cl)(Cl)C1=CC=CC=C1 ORVMIVQULIKXCP-UHFFFAOYSA-N 0.000 claims description 5
- VXEGSRKPIUDPQT-UHFFFAOYSA-N 4-[4-(4-methoxyphenyl)piperazin-1-yl]aniline Chemical compound C1=CC(OC)=CC=C1N1CCN(C=2C=CC(N)=CC=2)CC1 VXEGSRKPIUDPQT-UHFFFAOYSA-N 0.000 claims description 4
- 230000003197 catalytic effect Effects 0.000 claims description 4
- 239000005049 silicon tetrachloride Substances 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- KQHIGRPLCKIXNJ-UHFFFAOYSA-N chloro-methyl-silylsilane Chemical compound C[SiH]([SiH3])Cl KQHIGRPLCKIXNJ-UHFFFAOYSA-N 0.000 claims description 2
- 150000007530 organic bases Chemical class 0.000 claims 1
- PPDADIYYMSXQJK-UHFFFAOYSA-N trichlorosilicon Chemical group Cl[Si](Cl)Cl PPDADIYYMSXQJK-UHFFFAOYSA-N 0.000 claims 1
- 239000005047 Allyltrichlorosilane Substances 0.000 abstract description 5
- HKFSBKQQYCMCKO-UHFFFAOYSA-N trichloro(prop-2-enyl)silane Chemical compound Cl[Si](Cl)(Cl)CC=C HKFSBKQQYCMCKO-UHFFFAOYSA-N 0.000 abstract description 5
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract description 4
- 229910003910 SiCl4 Inorganic materials 0.000 abstract description 4
- FDNAPBUWERUEDA-UHFFFAOYSA-N silicon tetrachloride Chemical compound Cl[Si](Cl)(Cl)Cl FDNAPBUWERUEDA-UHFFFAOYSA-N 0.000 abstract description 4
- 229920001296 polysiloxane Polymers 0.000 abstract description 2
- 239000007767 bonding agent Substances 0.000 abstract 1
- PZPGRFITIJYNEJ-UHFFFAOYSA-N disilane Chemical compound [SiH3][SiH3] PZPGRFITIJYNEJ-UHFFFAOYSA-N 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 239000003153 chemical reaction reagent Substances 0.000 description 7
- 238000010992 reflux Methods 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
- 125000000746 allylic group Chemical group 0.000 description 4
- YGZSVWMBUCGDCV-UHFFFAOYSA-N chloro(methyl)silane Chemical class C[SiH2]Cl YGZSVWMBUCGDCV-UHFFFAOYSA-N 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- OSDWBNJEKMUWAV-UHFFFAOYSA-N Allyl chloride Chemical compound ClCC=C OSDWBNJEKMUWAV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 239000012429 reaction media Substances 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 229910003902 SiCl 4 Inorganic materials 0.000 description 2
- GONOPSZTUGRENK-UHFFFAOYSA-N benzyl(trichloro)silane Chemical class Cl[Si](Cl)(Cl)CC1=CC=CC=C1 GONOPSZTUGRENK-UHFFFAOYSA-N 0.000 description 2
- ZJDOJJKRTWHPOY-UHFFFAOYSA-N but-2-enyl(trichloro)silane Chemical compound CC=CC[Si](Cl)(Cl)Cl ZJDOJJKRTWHPOY-UHFFFAOYSA-N 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- YTKRILODNOEEPX-NSCUHMNNSA-N crotyl chloride Chemical compound C\C=C\CCl YTKRILODNOEEPX-NSCUHMNNSA-N 0.000 description 2
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 description 2
- JZALIDSFNICAQX-UHFFFAOYSA-N dichloro-methyl-trimethylsilylsilane Chemical compound C[Si](C)(C)[Si](C)(Cl)Cl JZALIDSFNICAQX-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- LXEXBJXDGVGRAR-UHFFFAOYSA-N trichloro(trichlorosilyl)silane Chemical compound Cl[Si](Cl)(Cl)[Si](Cl)(Cl)Cl LXEXBJXDGVGRAR-UHFFFAOYSA-N 0.000 description 2
- TXEDGTTUEVJNPE-UHFFFAOYSA-N trichloro(trimethylsilyl)silane Chemical compound C[Si](C)(C)[Si](Cl)(Cl)Cl TXEDGTTUEVJNPE-UHFFFAOYSA-N 0.000 description 2
- PVGYYKBIUKOMTG-UHFFFAOYSA-N trichloro-[chloro(dimethyl)silyl]silane Chemical compound C[Si](C)(Cl)[Si](Cl)(Cl)Cl PVGYYKBIUKOMTG-UHFFFAOYSA-N 0.000 description 2
- ZDHXKXAHOVTTAH-UHFFFAOYSA-N trichlorosilane Chemical compound Cl[SiH](Cl)Cl ZDHXKXAHOVTTAH-UHFFFAOYSA-N 0.000 description 2
- 239000005052 trichlorosilane Substances 0.000 description 2
- AVMHMVJVHYGDOO-NSCUHMNNSA-N (e)-1-bromobut-2-ene Chemical compound C\C=C\CBr AVMHMVJVHYGDOO-NSCUHMNNSA-N 0.000 description 1
- AVQQQNCBBIEMEU-UHFFFAOYSA-N 1,1,3,3-tetramethylurea Chemical compound CN(C)C(=O)N(C)C AVQQQNCBBIEMEU-UHFFFAOYSA-N 0.000 description 1
- RBSYGFLXVMWYGD-UHFFFAOYSA-N 2-chloro-3-methylbut-1-ene Chemical compound CC(C)C(Cl)=C RBSYGFLXVMWYGD-UHFFFAOYSA-N 0.000 description 1
- OHXAOPZTJOUYKM-UHFFFAOYSA-N 3-Chloro-2-methylpropene Chemical compound CC(=C)CCl OHXAOPZTJOUYKM-UHFFFAOYSA-N 0.000 description 1
- BEZYMHYZKNSRQV-UHFFFAOYSA-N CCC=CCl.Cl Chemical compound CCC=CCl.Cl BEZYMHYZKNSRQV-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- BHELZAPQIKSEDF-UHFFFAOYSA-N allyl bromide Chemical compound BrCC=C BHELZAPQIKSEDF-UHFFFAOYSA-N 0.000 description 1
- 150000001491 aromatic compounds Chemical group 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- NNCKZOPOZPBPOZ-UHFFFAOYSA-N benzyl-dichloro-phenylsilane Chemical class C=1C=CC=CC=1[Si](Cl)(Cl)CC1=CC=CC=C1 NNCKZOPOZPBPOZ-UHFFFAOYSA-N 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- COUMSRIIJWJSSY-UHFFFAOYSA-N chloro(chlorosilyl)silane Chemical compound Cl[SiH2][SiH2]Cl COUMSRIIJWJSSY-UHFFFAOYSA-N 0.000 description 1
- KMVZWUQHMJAWSY-UHFFFAOYSA-N chloro-dimethyl-prop-2-enylsilane Chemical compound C[Si](C)(Cl)CC=C KMVZWUQHMJAWSY-UHFFFAOYSA-N 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 150000001879 copper Chemical class 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- KTPJDYNQZVAFBU-UHFFFAOYSA-N dichloro-[chloro(dimethyl)silyl]-methylsilane Chemical compound C[Si](C)(Cl)[Si](C)(Cl)Cl KTPJDYNQZVAFBU-UHFFFAOYSA-N 0.000 description 1
- YCEQUKAYVABWTE-UHFFFAOYSA-N dichloro-methyl-prop-2-enylsilane Chemical compound C[Si](Cl)(Cl)CC=C YCEQUKAYVABWTE-UHFFFAOYSA-N 0.000 description 1
- IGFFTOVGRACDBL-UHFFFAOYSA-N dichloro-phenyl-prop-2-enylsilane Chemical compound C=CC[Si](Cl)(Cl)C1=CC=CC=C1 IGFFTOVGRACDBL-UHFFFAOYSA-N 0.000 description 1
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- NEXSMEBSBIABKL-UHFFFAOYSA-N hexamethyldisilane Chemical compound C[Si](C)(C)[Si](C)(C)C NEXSMEBSBIABKL-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000006459 hydrosilylation reaction Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- IQCYANORSDPPDT-UHFFFAOYSA-N methyl(silyl)silane Chemical class C[SiH2][SiH3] IQCYANORSDPPDT-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
- 150000003057 platinum Chemical class 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/12—Organo silicon halides
- C07F7/121—Preparation or treatment not provided for in C07F7/14, C07F7/16 or C07F7/20
- C07F7/122—Preparation or treatment not provided for in C07F7/14, C07F7/16 or C07F7/20 by reactions involving the formation of Si-C linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7915069A FR2458553A1 (fr) | 1979-06-06 | 1979-06-06 | Procede de preparation de composes organosiliciques porteurs de groupements chlorosilylmethyles a partir d'halogenures organiques, de polysilanes et de composes organosiliciques porteurs de groupements trichlorosilyles |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7915069A FR2458553A1 (fr) | 1979-06-06 | 1979-06-06 | Procede de preparation de composes organosiliciques porteurs de groupements chlorosilylmethyles a partir d'halogenures organiques, de polysilanes et de composes organosiliciques porteurs de groupements trichlorosilyles |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| FR2458553A1 true FR2458553A1 (fr) | 1981-01-02 |
| FR2458553B1 FR2458553B1 (https=) | 1982-10-01 |
Family
ID=9226509
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FR7915069A Granted FR2458553A1 (fr) | 1979-06-06 | 1979-06-06 | Procede de preparation de composes organosiliciques porteurs de groupements chlorosilylmethyles a partir d'halogenures organiques, de polysilanes et de composes organosiliciques porteurs de groupements trichlorosilyles |
Country Status (1)
| Country | Link |
|---|---|
| FR (1) | FR2458553A1 (https=) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2677358A1 (fr) * | 1991-06-05 | 1992-12-11 | Rhone Poulenc Chimie | Composes organosilyles et leur procede de synthese. |
| US5532288A (en) * | 1992-07-10 | 1996-07-02 | Aerospatiale Societe Nationale Industrille | Process for the preparation of a polysilane crosslinked by ionizing radiation and process for the production of a composite material having a polysilane matrix |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2163579A1 (https=) * | 1971-12-15 | 1973-07-27 | Dow Corning | |
| FR2342981A1 (fr) * | 1976-03-05 | 1977-09-30 | Rhone Poulenc Ind | Procede de preparation d'hydrogenosilanes |
| US4059607A (en) * | 1976-12-20 | 1977-11-22 | Union Carbide Corporation | Preparation of hydrocarbon chlorosilanes from polysilanes |
-
1979
- 1979-06-06 FR FR7915069A patent/FR2458553A1/fr active Granted
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2163579A1 (https=) * | 1971-12-15 | 1973-07-27 | Dow Corning | |
| FR2342981A1 (fr) * | 1976-03-05 | 1977-09-30 | Rhone Poulenc Ind | Procede de preparation d'hydrogenosilanes |
| US4059607A (en) * | 1976-12-20 | 1977-11-22 | Union Carbide Corporation | Preparation of hydrocarbon chlorosilanes from polysilanes |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2677358A1 (fr) * | 1991-06-05 | 1992-12-11 | Rhone Poulenc Chimie | Composes organosilyles et leur procede de synthese. |
| US5532288A (en) * | 1992-07-10 | 1996-07-02 | Aerospatiale Societe Nationale Industrille | Process for the preparation of a polysilane crosslinked by ionizing radiation and process for the production of a composite material having a polysilane matrix |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2458553B1 (https=) | 1982-10-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP4351058B2 (ja) | アルケン−白金−シリル錯体 | |
| EP1235836B1 (fr) | Catalyseurs pour reactions d'hydrosilylation | |
| CA1312874C (en) | Rhodium colloid, method of making, and use | |
| FR2576023A1 (fr) | Procedes de preparation de bis(aminopropyl) disiloxanes et compositions ainsi obtenues | |
| EP1309647B1 (fr) | Procede de preparation d'huiles silicones par hydrosilylation de synthons contenant au moins un cycle hydrocarbone dans lequel est inclus un atome d'oxygene en presence d'un complexe metallique catalytique | |
| EP0166638B1 (fr) | Procédé de préparation d'organosilanes et d'organopolysilanes à partir d'organodisilanes | |
| FR2458553A1 (fr) | Procede de preparation de composes organosiliciques porteurs de groupements chlorosilylmethyles a partir d'halogenures organiques, de polysilanes et de composes organosiliciques porteurs de groupements trichlorosilyles | |
| US3546266A (en) | Process for the preparation of an organic silicon compound by reacting in the presence of a rhodium catalyst | |
| CA2259255A1 (fr) | Utilisation de complexes du platine notamment a titre de catalyseurs d'hydrosilylation homogenes et thermoactivables | |
| EP2876111B1 (en) | Composition containing nitrogen-containing organoxysilane compound and method for making the same | |
| JP4216354B2 (ja) | ヒドロシリル化方法 | |
| US5416230A (en) | 2-(aryl)propylhydridopolysiloxane type silicone fluids and methods for preparing the same | |
| CN118475587A (zh) | 通过氢化硅烷化制备3-卤代丙基三卤代硅烷的方法 | |
| EP0373059B1 (fr) | Compositions de précurseurs de céramiques à base de polysilazanes et céramiques obtenues par pyrolyse desdites compositions | |
| EP0191260B1 (fr) | Complexes de silicium pentacoordinés, leur procédé de préparation et leur application à la préparation d'organosilanes | |
| EP0971933B1 (fr) | Procede d'obtention d'organosilanes mettant en oeuvre une reaction de redistribution | |
| FR2650599A1 (fr) | Procede electrochimique de preparation de composes organosilicies | |
| FR2583420A1 (fr) | Procede de preparation des silazanes olefiniques. | |
| FR2777006A1 (fr) | Procede de preparation d'hydrogenosilanes par hydrogenolyse catalytique de polysilanes | |
| FR2693204A1 (fr) | Procédé de préparation en milieu solvant de polysilylhydrazines. | |
| WO2022229519A1 (fr) | Procédé d'hydrosilylation catalysé par un complexe de gallium | |
| JPH06279460A (ja) | 含フッ素有機ケイ素化合物およびその製造方法 | |
| KR950009313B1 (ko) | 실릴화 방법 | |
| FR2612190A1 (fr) | Procede de preparation de cetenes acetals silyles | |
| EP1448675A2 (fr) | Procede de preparation d'huiles silicones portant un groupement contenant au moins un cycle hydrocarbone dans lequel est inclus un atome d'oxygene |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| ST | Notification of lapse |