GB1461531A - Process for the manufacture of unsaturated optionally haloge nated hydrocarbon polymers with reactive silyl sidegroups - Google Patents
Process for the manufacture of unsaturated optionally haloge nated hydrocarbon polymers with reactive silyl sidegroupsInfo
- Publication number
- GB1461531A GB1461531A GB1277674A GB1277674A GB1461531A GB 1461531 A GB1461531 A GB 1461531A GB 1277674 A GB1277674 A GB 1277674A GB 1277674 A GB1277674 A GB 1277674A GB 1461531 A GB1461531 A GB 1461531A
- Authority
- GB
- United Kingdom
- Prior art keywords
- silyl
- groups
- silylalkenamer
- alkenamer
- cyclopentene
- 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
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L65/00—Compositions of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08C—TREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
- C08C19/00—Chemical modification of rubber
- C08C19/28—Reaction with compounds containing carbon-to-carbon unsaturated bonds
-
- 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
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/02—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes
- C08G61/04—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms
- C08G61/06—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms prepared by ring-opening of carbocyclic compounds
- C08G61/08—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms prepared by ring-opening of carbocyclic compounds of carbocyclic compounds containing one or more carbon-to-carbon double bonds in the ring
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/04—Reinforcing macromolecular compounds with loose or coherent fibrous material
- C08J5/06—Reinforcing macromolecular compounds with loose or coherent fibrous material using pretreated fibrous materials
- C08J5/08—Reinforcing macromolecular compounds with loose or coherent fibrous material using pretreated fibrous materials glass fibres
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds
- C08L101/02—Compositions of unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups
- C08L101/10—Compositions of unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups containing hydrolysable silane groups
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Manufacturing & Machinery (AREA)
- General Chemical & Material Sciences (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
1461531 Poly(silylalkenamer) preparation CHEMISCHE WERKE HULS AG 22 March 1974 [23 March 1973] 12776/74 Heading C3P A polymer containing silylalkenamer groups is obtained by subjecting to ring-opening, with a catalyst containing a niobium, tantalum, molybdenum, tungsten and/or rhenium compound, a polymerizable material comprising a hydrolysable silyl substituted, optionally halogenated, cyclic olefin or a mixture thereof with another optionally halogenated cyclic olefin and/or with an optionally halogenated hydrocarbon polymer containing double bonds. In an alternative procedure the monomeric silylsubstituted material is replaced by the corresponding polymeric silylalkenamer, obtained in a previous batch. Where polymeric starting materials are employed, they undergo an analogous rupture at the double bonds with interchange of the resulting alkenylidene groups with the polymer being formed, to produce analogous silyl alkenamer/other alkenamer copolymeric materials. Where the polymeric silyl alkenamer alone is treated with the catalyst the resulting rearrangement of the mers leads to molecular weight regulation. Where appropriate, the electron-donor functions of the hydrolysable groups on the silyl group may be compensated by addition of a Lewis acid, typically constituted by an aluminium alkyl or halide such as is employed as cocatalyst with the transition metal compounds. In the examples, 5-methyldichlorosilylnorbornene is homopolymerized or 5-trichlorosilyl norbornene is copolymerized with cyclopentene, cyclopentene and cis,cis-cyclooctadiene-1,5 or cycloctane are copolymerized with 5-(trichlorosilylethyl) norbornene, 5-trimethoxysilylnorbornene or 3-(diethoxymethylsilyl)propyl - cyclooctene - 1 and cyclopentene are copolymerized and 5-(trichlorosilyl ethyl) norbornene or 1-trichlorosilyl cyclododecadiene-4,8 are reacted in the presence of cis - 1,4 - polybutadiene, the catalysts being WCl 6 -AlEtCl 2 -EtOH together with regulators such as octene-1, vinyl acetate, and 1,10 - bis(methyl - dichlorosilyl) - decene - (4). The silylpolyalkenamers may be hydrolysed and cross-linked via the silanol groups formed, or cross-linked via the double bonds using the usual sulphur and peroxy curing.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19732314543 DE2314543C3 (en) | 1973-03-23 | 1973-03-23 | Process for the preparation of polymeric hydrocarbons with reactive silyl groups |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1461531A true GB1461531A (en) | 1977-01-13 |
Family
ID=5875692
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1277674A Expired GB1461531A (en) | 1973-03-23 | 1974-03-22 | Process for the manufacture of unsaturated optionally haloge nated hydrocarbon polymers with reactive silyl sidegroups |
Country Status (7)
Country | Link |
---|---|
JP (1) | JPS5325359B2 (en) |
CA (1) | CA1026040A (en) |
DE (1) | DE2314543C3 (en) |
FR (1) | FR2222386B1 (en) |
GB (1) | GB1461531A (en) |
IT (1) | IT1003839B (en) |
NL (1) | NL7403942A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0029100A1 (en) * | 1979-09-19 | 1981-05-27 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Coating composition comprising compounds that contain silyl groups and a hydrolysable ester |
EP0050248A2 (en) * | 1980-10-03 | 1982-04-28 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Vinyl-type resin composition |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3003893A1 (en) | 1980-02-02 | 1981-10-15 | Chemische Werke Hüls AG, 4370 Marl | REACTIVE SILYL GROUPS CARRYING HOMO- OR COPOLYMERS OF 1,3-DIENES, PROCESS FOR THEIR PRODUCTION AND THE USE THEREOF |
DE3167793D1 (en) * | 1980-06-19 | 1985-01-31 | Huels Chemische Werke Ag | 1,3-diene-homo and copolymers containing reactive silyl groups, process for their preparation and their use |
DE69711378T2 (en) * | 1996-11-04 | 2002-10-24 | The B.F. Goodrich Co., Richfield | PHOTOSTRUCTURABLE DIELECTRIC COMPOSITIONS |
JP2003082074A (en) * | 2001-09-13 | 2003-03-19 | Jsr Corp | Norbornene ring-opened (co)polymer and hydrogenated product thereof |
US8889806B2 (en) | 2010-01-14 | 2014-11-18 | Zeon Corporation | Ring-opening polymer of cyclopentene and method of production of same |
-
1973
- 1973-03-23 DE DE19732314543 patent/DE2314543C3/en not_active Expired
-
1974
- 1974-03-07 FR FR7407757A patent/FR2222386B1/fr not_active Expired
- 1974-03-22 CA CA195,707A patent/CA1026040A/en not_active Expired
- 1974-03-22 IT IT4953474A patent/IT1003839B/en active
- 1974-03-22 JP JP3160274A patent/JPS5325359B2/ja not_active Expired
- 1974-03-22 GB GB1277674A patent/GB1461531A/en not_active Expired
- 1974-03-22 NL NL7403942A patent/NL7403942A/xx not_active Application Discontinuation
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0029100A1 (en) * | 1979-09-19 | 1981-05-27 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Coating composition comprising compounds that contain silyl groups and a hydrolysable ester |
EP0050248A2 (en) * | 1980-10-03 | 1982-04-28 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Vinyl-type resin composition |
EP0050248A3 (en) * | 1980-10-03 | 1983-02-16 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Vinyl-type resin composition |
Also Published As
Publication number | Publication date |
---|---|
DE2314543A1 (en) | 1974-10-03 |
FR2222386A1 (en) | 1974-10-18 |
JPS502800A (en) | 1975-01-13 |
CA1026040A (en) | 1978-02-07 |
FR2222386B1 (en) | 1978-11-10 |
NL7403942A (en) | 1974-09-25 |
IT1003839B (en) | 1976-06-10 |
DE2314543C3 (en) | 1980-09-11 |
JPS5325359B2 (en) | 1978-07-26 |
DE2314543B2 (en) | 1980-01-10 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |