GB1289526A - - Google Patents
Info
- Publication number
- GB1289526A GB1289526A GB1289526DA GB1289526A GB 1289526 A GB1289526 A GB 1289526A GB 1289526D A GB1289526D A GB 1289526DA GB 1289526 A GB1289526 A GB 1289526A
- Authority
- GB
- United Kingdom
- Prior art keywords
- radical
- initiator
- polymer
- carbanion
- 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.)
- Expired
Links
Classifications
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Silicon Polymers (AREA)
Abstract
1289526 Carbanion-polymerization of cyclic organosiloxanes DOW CORNING Ltd 15 April 1970 [18 April 1969] 19879/69 Headings C3P and C3T An organopolysiloxane is obtained by (1) polymerizing in the presence of a carbanion-producing initiator a cyclic organosiloxane [R 2 SiO] n , wherein each R is H or a methyl, phenyl, vinyl or CF 3 -CH 2 -CH 2 - radical and n is 3, 4 or 5, not more than 50% of the substituents R being H, and (2) reacting the product with a silane R<SP>1</SP> 2 R<SP>11</SP>SiX, wherein each R<SP>1</SP> is a C 1-4 alkyl or alkenyl radical or a phenyl radical, R<SP>11</SP> is an alkyl radical of at least 5 C atoms, and X is Cl, Br or I. Suitable initiators include the alkali metals and their hydrocarbon derivatives and complexes; a solvent, e.g. tetrahydrofuran, tetrahydropyran, dioxan, diethoxyethane dimethyl acetamide, dimethyl formamide or dimethyl sulphoxide, is preferably used; the amount of initiator is preferably such as to give a molecular weight of 400-40,000. The silane is added when the desired molecular weight is reached; it will react with one or both ends of the polymer according to the initiator, butyl lithium, for instance giving a monofunctional polymer, an alkali metal giving a difunctional polymer. In the example butyl lithium is used to polymerize hexamethylcyclotrisiloxane in tetrahydrofuran at 22‹ C.; after 2 hrs. dimethyldecylchlorosilane in benzene is added. The product, precipitated by addition of methanol is When 1% by weight of this is incorporated into polyethylene or polystyrene, reduced solid surface tension is observed.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1987969 | 1969-04-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1289526A true GB1289526A (en) | 1972-09-20 |
Family
ID=10136706
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1289526D Expired GB1289526A (en) | 1969-04-18 | 1969-04-18 |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1289526A (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2398768A1 (en) * | 1977-07-27 | 1979-02-23 | Raychem Ltd | SILICONE RESINS PRODUCTION PROCESS |
US6020430A (en) * | 1998-05-20 | 2000-02-01 | Fmc Corporation | Functionalized diene and alkenylsubstituted aromatic silicone copolymers and processes for making the same |
US6031060A (en) * | 1997-05-22 | 2000-02-29 | Fmc Corporation | Functionalized silicone polymers and processes for making the same |
US6344521B1 (en) | 1998-05-20 | 2002-02-05 | Fmc Corporation | Protected functionalized diene and alkenyl substituted aromatic silicone triblock copolymers and processes for making the same |
WO2006106361A1 (en) * | 2005-04-06 | 2006-10-12 | Dow Corning Corporation | Organosiloxane compositions |
US8487037B2 (en) | 2009-03-26 | 2013-07-16 | Dow Corning Corporation | Preparation of organosiloxane polymers |
US8735493B2 (en) | 2009-03-26 | 2014-05-27 | Dow Corning Corporation | Preparation of organosiloxane polymers |
CN101151324B (en) * | 2005-04-06 | 2014-06-25 | 陶氏康宁公司 | Organosiloxane compositions |
CN116217933A (en) * | 2022-11-21 | 2023-06-06 | 浙江开化合成材料有限公司 | Polymethylphenylsiloxane oligomer, preparation method and low-oil-separation heat-conducting silicone grease |
-
1969
- 1969-04-18 GB GB1289526D patent/GB1289526A/en not_active Expired
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2398768A1 (en) * | 1977-07-27 | 1979-02-23 | Raychem Ltd | SILICONE RESINS PRODUCTION PROCESS |
US6031060A (en) * | 1997-05-22 | 2000-02-29 | Fmc Corporation | Functionalized silicone polymers and processes for making the same |
US6271330B1 (en) | 1997-05-22 | 2001-08-07 | Fmc Corporation | Functionalized silicone polymers and processes for making the same |
US6020430A (en) * | 1998-05-20 | 2000-02-01 | Fmc Corporation | Functionalized diene and alkenylsubstituted aromatic silicone copolymers and processes for making the same |
US6344521B1 (en) | 1998-05-20 | 2002-02-05 | Fmc Corporation | Protected functionalized diene and alkenyl substituted aromatic silicone triblock copolymers and processes for making the same |
US8067519B2 (en) | 2005-04-06 | 2011-11-29 | Dow Corning Corporation | Organosiloxane compositions |
US7754800B2 (en) | 2005-04-06 | 2010-07-13 | Dow Corning Europe Sa | Organosiloxane compositions |
US8022162B2 (en) | 2005-04-06 | 2011-09-20 | Dow Corning Corporation | Organosiloxane compositions |
WO2006106361A1 (en) * | 2005-04-06 | 2006-10-12 | Dow Corning Corporation | Organosiloxane compositions |
US8076411B2 (en) | 2005-04-06 | 2011-12-13 | Dow Corning Corporation | Organosiloxane compositions |
US8084535B2 (en) | 2005-04-06 | 2011-12-27 | Dow Corning Corporation | Organosiloxane compositions |
US8088857B2 (en) | 2005-04-06 | 2012-01-03 | Dow Corning Corporation | Organosiloxane compositions |
US8153724B2 (en) | 2005-04-06 | 2012-04-10 | Dow Corning Corporation | Organosiloxane compositions |
US8344087B2 (en) | 2005-04-06 | 2013-01-01 | Dow Corning Corporation | Hydrosilylation cured organosiloxanes having diluent therein |
CN101151324B (en) * | 2005-04-06 | 2014-06-25 | 陶氏康宁公司 | Organosiloxane compositions |
US8487037B2 (en) | 2009-03-26 | 2013-07-16 | Dow Corning Corporation | Preparation of organosiloxane polymers |
US8735493B2 (en) | 2009-03-26 | 2014-05-27 | Dow Corning Corporation | Preparation of organosiloxane polymers |
CN116217933A (en) * | 2022-11-21 | 2023-06-06 | 浙江开化合成材料有限公司 | Polymethylphenylsiloxane oligomer, preparation method and low-oil-separation heat-conducting silicone grease |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |