KR100962056B1 - 오가노하이드로겐실리콘 화합물 - Google Patents
오가노하이드로겐실리콘 화합물 Download PDFInfo
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- KR100962056B1 KR100962056B1 KR1020047017589A KR20047017589A KR100962056B1 KR 100962056 B1 KR100962056 B1 KR 100962056B1 KR 1020047017589 A KR1020047017589 A KR 1020047017589A KR 20047017589 A KR20047017589 A KR 20047017589A KR 100962056 B1 KR100962056 B1 KR 100962056B1
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 74
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 55
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 28
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 19
- -1 alkoxyether group Chemical group 0.000 claims description 130
- 238000006243 chemical reaction Methods 0.000 claims description 52
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 46
- 239000003054 catalyst Substances 0.000 claims description 45
- 125000004432 carbon atom Chemical group C* 0.000 claims description 34
- 125000000524 functional group Chemical group 0.000 claims description 33
- 125000005843 halogen group Chemical group 0.000 claims description 22
- 125000003700 epoxy group Chemical group 0.000 claims description 21
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 20
- 125000002252 acyl group Chemical group 0.000 claims description 20
- 125000003545 alkoxy group Chemical group 0.000 claims description 20
- 125000003277 amino group Chemical group 0.000 claims description 20
- 125000001033 ether group Chemical group 0.000 claims description 20
- 239000011541 reaction mixture Substances 0.000 claims description 20
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims description 19
- 239000003112 inhibitor Substances 0.000 claims description 16
- 229910004283 SiO 4 Inorganic materials 0.000 claims description 13
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- 229910052796 boron Inorganic materials 0.000 claims description 12
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- 238000002156 mixing Methods 0.000 claims description 9
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- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
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- 239000004971 Cross linker Substances 0.000 description 2
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- 239000004944 Liquid Silicone Rubber Substances 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
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- WRYNUJYAXVDTCB-UHFFFAOYSA-M acetyloxymercury Chemical compound CC(=O)O[Hg] WRYNUJYAXVDTCB-UHFFFAOYSA-M 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- ZPOLOEWJWXZUSP-WAYWQWQTSA-N bis(prop-2-enyl) (z)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C/C(=O)OCC=C ZPOLOEWJWXZUSP-WAYWQWQTSA-N 0.000 description 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
- FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 150000005690 diesters Chemical class 0.000 description 2
- GCSJLQSCSDMKTP-UHFFFAOYSA-N ethenyl(trimethyl)silane Chemical compound C[Si](C)(C)C=C GCSJLQSCSDMKTP-UHFFFAOYSA-N 0.000 description 2
- 125000005677 ethinylene group Chemical group [*:2]C#C[*:1] 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
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- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
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- 238000004448 titration Methods 0.000 description 2
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
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- FDNBQVCBHKEDOJ-FPLPWBNLSA-N (z)-4-(6-methylheptoxy)-4-oxobut-2-enoic acid Chemical compound CC(C)CCCCCOC(=O)\C=C/C(O)=O FDNBQVCBHKEDOJ-FPLPWBNLSA-N 0.000 description 1
- VYXHVRARDIDEHS-UHFFFAOYSA-N 1,5-cyclooctadiene Chemical compound C1CC=CCCC=C1 VYXHVRARDIDEHS-UHFFFAOYSA-N 0.000 description 1
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- KUIZKZHDMPERHR-UHFFFAOYSA-N 1-phenylprop-2-en-1-one Chemical compound C=CC(=O)C1=CC=CC=C1 KUIZKZHDMPERHR-UHFFFAOYSA-N 0.000 description 1
- VMAWODUEPLAHOE-UHFFFAOYSA-N 2,4,6,8-tetrakis(ethenyl)-2,4,6,8-tetramethyl-1,3,5,7,2,4,6,8-tetraoxatetrasilocane Chemical compound C=C[Si]1(C)O[Si](C)(C=C)O[Si](C)(C=C)O[Si](C)(C=C)O1 VMAWODUEPLAHOE-UHFFFAOYSA-N 0.000 description 1
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- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
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- ZCTILCZSUSTVHT-UHFFFAOYSA-N 3,5-dimethylhex-1-yn-3-yloxy(trimethyl)silane Chemical compound CC(C)CC(C)(C#C)O[Si](C)(C)C ZCTILCZSUSTVHT-UHFFFAOYSA-N 0.000 description 1
- HMVBQEAJQVQOTI-UHFFFAOYSA-N 3,5-dimethylhex-3-en-1-yne Chemical compound CC(C)C=C(C)C#C HMVBQEAJQVQOTI-UHFFFAOYSA-N 0.000 description 1
- 125000004975 3-butenyl group Chemical group C(CC=C)* 0.000 description 1
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- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
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- 125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-L fumarate(2-) Chemical class [O-]C(=O)\C=C\C([O-])=O VZCYOOQTPOCHFL-OWOJBTEDSA-L 0.000 description 1
- XLYMOEINVGRTEX-UHFFFAOYSA-N fumaric acid monoethyl ester Natural products CCOC(=O)C=CC(O)=O XLYMOEINVGRTEX-UHFFFAOYSA-N 0.000 description 1
- NKHAVTQWNUWKEO-UHFFFAOYSA-N fumaric acid monomethyl ester Natural products COC(=O)C=CC(O)=O NKHAVTQWNUWKEO-UHFFFAOYSA-N 0.000 description 1
- 150000004687 hexahydrates Chemical group 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 230000002779 inactivation Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 150000002688 maleic acid derivatives Chemical class 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- NKHAVTQWNUWKEO-IHWYPQMZSA-N methyl hydrogen fumarate Chemical compound COC(=O)\C=C/C(O)=O NKHAVTQWNUWKEO-IHWYPQMZSA-N 0.000 description 1
- 229940043265 methyl isobutyl ketone Drugs 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- 229940074369 monoethyl fumarate Drugs 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 238000001208 nuclear magnetic resonance pulse sequence Methods 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 150000003961 organosilicon compounds Chemical class 0.000 description 1
- 229910052762 osmium Inorganic materials 0.000 description 1
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 description 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 229920001843 polymethylhydrosiloxane Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- MWWATHDPGQKSAR-UHFFFAOYSA-N propyne Chemical group CC#C MWWATHDPGQKSAR-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- XUIMIQQOPSSXEZ-OUBTZVSYSA-N silicon-29 atom Chemical compound [29Si] XUIMIQQOPSSXEZ-OUBTZVSYSA-N 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- JMTMWSZLPHDWBQ-UHFFFAOYSA-N tetrakis[ethenyl(dimethyl)silyl] silicate Chemical compound C=C[Si](C)(C)O[Si](O[Si](C)(C)C=C)(O[Si](C)(C)C=C)O[Si](C)(C)C=C JMTMWSZLPHDWBQ-UHFFFAOYSA-N 0.000 description 1
- CKMVRBFKYLMXHU-UHFFFAOYSA-N tetrakis[hex-1-enyl(dimethyl)silyl] silicate Chemical compound CCCCC=C[Si](C)(C)O[Si](O[Si](C)(C)C=CCCCC)(O[Si](C)(C)C=CCCCC)O[Si](C)(C)C=CCCCC CKMVRBFKYLMXHU-UHFFFAOYSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 125000005628 tolylene group Chemical group 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- JNRUXZIXAXHXTN-UHFFFAOYSA-N trimethyl(2-methylbut-3-yn-2-yloxy)silane Chemical compound C#CC(C)(C)O[Si](C)(C)C JNRUXZIXAXHXTN-UHFFFAOYSA-N 0.000 description 1
- ZGBHPZUKKNSAOS-UHFFFAOYSA-N tris(ethenyl)borane Chemical compound C=CB(C=C)C=C ZGBHPZUKKNSAOS-UHFFFAOYSA-N 0.000 description 1
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
- 125000006839 xylylene group Chemical group 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
-
- 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
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
-
- 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
- C07F7/21—Cyclic compounds having at least one ring containing silicon, but no carbon in the ring
-
- 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
-
- 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
- C08G77/48—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 in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms
- C08G77/50—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 in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms by carbon linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Silicon Polymers (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US37742502P | 2002-05-01 | 2002-05-01 | |
| US60/377,425 | 2002-05-01 | ||
| PCT/US2003/013203 WO2003093349A1 (en) | 2002-05-01 | 2003-04-29 | Organohydrogensilicon compounds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20040106442A KR20040106442A (ko) | 2004-12-17 |
| KR100962056B1 true KR100962056B1 (ko) | 2010-06-08 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020047017589A Expired - Lifetime KR100962056B1 (ko) | 2002-05-01 | 2003-04-29 | 오가노하이드로겐실리콘 화합물 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US7429636B2 (enExample) |
| EP (1) | EP1499661B1 (enExample) |
| JP (1) | JP4755824B2 (enExample) |
| KR (1) | KR100962056B1 (enExample) |
| CN (1) | CN100334134C (enExample) |
| AT (1) | ATE363504T1 (enExample) |
| AU (1) | AU2003234276A1 (enExample) |
| DE (1) | DE60314126T2 (enExample) |
| MY (1) | MY129816A (enExample) |
| WO (1) | WO2003093349A1 (enExample) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| KR100949448B1 (ko) * | 2002-05-01 | 2010-03-29 | 다우 코닝 코포레이션 | 바스 수명이 연장된 조성물 |
| KR101028347B1 (ko) | 2002-12-20 | 2011-04-11 | 다우 코닝 코포레이션 | 유기 수소화 규소 화합물로부터의 분지된 중합체 |
| EP1572779B1 (en) | 2002-12-20 | 2008-05-21 | Dow Corning Corporation | Branched polymers from organohydrogensilicon compounds |
| US7687591B2 (en) * | 2003-03-17 | 2010-03-30 | Dow Corning Corporation | Solventless silicone pressure sensitive adhesives with improved high temperature cohesive strength |
| GB0316162D0 (en) | 2003-07-10 | 2003-08-13 | Dow Corning | Silicone release coating compositions |
| JP2006073950A (ja) * | 2004-09-06 | 2006-03-16 | Kansai Electric Power Co Inc:The | 高耐熱半導体装置 |
| US20060134440A1 (en) * | 2004-10-27 | 2006-06-22 | Crivello James V | Silicone encapsulants for light emitting diodes |
| KR101216576B1 (ko) * | 2004-11-19 | 2012-12-31 | 다우 코닝 코포레이션 | 오가노하이드로겐폴리실록산 수지 및 실리콘 조성물 |
| KR101351815B1 (ko) * | 2005-07-28 | 2014-01-15 | 다우 코닝 코포레이션 | 향상된 박리력 프로파일을 갖는 박리 피막 조성물 |
| WO2007046399A1 (ja) | 2005-10-18 | 2007-04-26 | Asahi Kasei Kabushiki Kaisha | 熱硬化性樹脂組成物及び光半導体封止材 |
| WO2007120197A2 (en) * | 2005-11-04 | 2007-10-25 | Dow Corning Corporation | Encapsulation of photovoltaic cells |
| JP5424866B2 (ja) * | 2006-03-21 | 2014-02-26 | ダウ・コーニング・コーポレイション | シリコーンポリエーテルエラストマーゲル |
| CN101432340B (zh) * | 2006-03-21 | 2012-03-28 | 陶氏康宁公司 | 硅氧烷聚醚弹性体凝胶 |
| KR101387209B1 (ko) | 2006-03-21 | 2014-04-21 | 다우 코닝 코포레이션 | 실리콘-유기 엘라스토머 겔 |
| US8110630B2 (en) | 2006-03-21 | 2012-02-07 | Dow Corning Corporation | Silicone elastomer gels |
| US7642332B2 (en) * | 2006-08-14 | 2010-01-05 | The University Of Akron | Amphiphilic networks, process for producing same, and products made therefrom |
| EP2097471B1 (en) | 2006-12-21 | 2014-09-10 | Dow Corning Corporation | Dual curing polymers and methods for their preparation and use |
| US8618233B2 (en) | 2006-12-21 | 2013-12-31 | Dow Corning Corporation | Dual curing polymers and methods for their preparation and use |
| EP2114366A2 (en) * | 2006-12-29 | 2009-11-11 | Dow Corning Corporation | Personal care compositions containing silicone elastomer gels |
| EP2138525B1 (en) * | 2007-04-17 | 2012-12-26 | Asahi Kasei Chemicals Corporation | Epoxy silicone and method for production thereof, and curable resin composition using the same and use thereof |
| JP5248032B2 (ja) | 2007-04-23 | 2013-07-31 | 株式会社Adeka | ケイ素含有化合物、硬化性組成物及び硬化物 |
| JP5248033B2 (ja) * | 2007-04-23 | 2013-07-31 | 株式会社Adeka | ケイ素含有化合物、硬化性組成物及び硬化物 |
| JP5248034B2 (ja) * | 2007-04-23 | 2013-07-31 | 株式会社Adeka | ケイ素含有化合物、硬化性組成物及び硬化物 |
| CN101743282B (zh) * | 2007-05-30 | 2013-03-27 | 陶氏康宁公司 | 由天然油衍生的硅氧烷共聚物和弹性体 |
| ATE539122T1 (de) | 2007-09-25 | 2012-01-15 | Dow Corning | Emulsionen aus silikonelastomer und organische silikonelastomergele |
| KR20100061699A (ko) | 2007-09-26 | 2010-06-08 | 다우 코닝 코포레이션 | 유기폴리실록산 수지로부터의 실리콘 유기 엘라스토머 겔 |
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| JP5139882B2 (ja) * | 2008-05-08 | 2013-02-06 | 旭化成ケミカルズ株式会社 | 感光性樹脂組成物及びこれを用いた樹脂層付き基材の製造方法 |
| DE102008053788A1 (de) * | 2008-10-22 | 2010-04-29 | Beiersdorf Ag | Kosmetische Formulierung mit Siloxanelastomeren zur Verbesserung der mikrobiologischen Stabilität |
| DE102008054434A1 (de) * | 2008-12-09 | 2010-06-10 | Wacker Chemie Ag | Siloxancopolymere und Verfahren zu deren Herstellung |
| US8633478B2 (en) | 2009-06-19 | 2014-01-21 | Dow Corning Corporation | Use of ionomeric silicone thermoplastic elastomers in electronic devices |
| JP5671854B2 (ja) * | 2009-07-17 | 2015-02-18 | 信越化学工業株式会社 | 付加硬化型シリコーン組成物 |
| TWI495666B (zh) * | 2009-07-17 | 2015-08-11 | Shinetsu Chemical Co | 有機氫聚矽氧烷,製造方法,及加成固化聚矽氧組成物 |
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| TWI502004B (zh) * | 2009-11-09 | 2015-10-01 | Dow Corning | 群集官能性聚有機矽氧烷之製法及其使用方法 |
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Also Published As
| Publication number | Publication date |
|---|---|
| WO2003093349A1 (en) | 2003-11-13 |
| CN1656152A (zh) | 2005-08-17 |
| CN100334134C (zh) | 2007-08-29 |
| EP1499661B1 (en) | 2007-05-30 |
| JP2005523980A (ja) | 2005-08-11 |
| DE60314126D1 (de) | 2007-07-12 |
| ATE363504T1 (de) | 2007-06-15 |
| MY129816A (en) | 2007-05-31 |
| AU2003234276A1 (en) | 2003-11-17 |
| JP4755824B2 (ja) | 2011-08-24 |
| KR20040106442A (ko) | 2004-12-17 |
| EP1499661A1 (en) | 2005-01-26 |
| DE60314126T2 (de) | 2008-01-31 |
| US7429636B2 (en) | 2008-09-30 |
| US20050256286A1 (en) | 2005-11-17 |
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