GB1360755A - Organosilicon compounds - Google Patents
Organosilicon compoundsInfo
- Publication number
- GB1360755A GB1360755A GB2031372A GB2031372A GB1360755A GB 1360755 A GB1360755 A GB 1360755A GB 2031372 A GB2031372 A GB 2031372A GB 2031372 A GB2031372 A GB 2031372A GB 1360755 A GB1360755 A GB 1360755A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkoxy
- styrene
- denotes
- peroxy
- alkoxyalkoxy
- 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
- 150000003961 organosilicon compounds Chemical class 0.000 title 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000005083 alkoxyalkoxy group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 1
- 229910018540 Si C Inorganic materials 0.000 abstract 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 abstract 1
- 239000004141 Sodium laurylsulphate Substances 0.000 abstract 1
- 239000004205 dimethyl polysiloxane Substances 0.000 abstract 1
- 238000007720 emulsion polymerization reaction Methods 0.000 abstract 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 1
- 239000011521 glass Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 abstract 1
- -1 polydimethylsiloxane Polymers 0.000 abstract 1
- 239000003505 polymerization initiator Substances 0.000 abstract 1
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 abstract 1
- 229910052710 silicon Inorganic materials 0.000 abstract 1
- 239000010703 silicon Substances 0.000 abstract 1
- 229910010271 silicon carbide Inorganic materials 0.000 abstract 1
- 150000003377 silicon compounds Chemical class 0.000 abstract 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances 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
- 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
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
Abstract
1360755 Organoperoxy silicon compounds DOW CORNING Ltd 18 April 1973 [2 May 1972] 20313/72 Headings C3S C3T and C3G Novel compounds of the formula wherein R denotes monovalent C 1 -C 18 hydrocarbonyl, C 1 -C 4 alkoxy, C 1 -C 4 alkoxyalkoxy, C 1 -C 10 tertiary alkyl peroxy or aralkyl peroxy not exceeding 10C, Q denotes a C 2 -C 10 divalent radical linked to silicon through a Si-C bond and comprising C, H and optional ether oxygen atoms, are prepared by reacting R 3 SiQO.CO.Cl with hydrogen peroxide. An example describes the preparation of [(CH 3 O) 3 Si(CH 2 ) 3 O.CO.O] 2 . Uses.-As polymerization initiators and, after hydrolysis of alkoxy or alkoxyalkoxy groups, as glass sizes. Further examples describe the emulsion polymerization of styrene and a mixture of styrene with acrylonitrile and a silanol - terminated polydimethylsiloxane (M.W. 2,500) in the presence of water, sodium lauryl sulphate and a novel compound as identified above.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2031372A GB1360755A (en) | 1973-04-18 | 1973-04-18 | Organosilicon compounds |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2031372A GB1360755A (en) | 1973-04-18 | 1973-04-18 | Organosilicon compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1360755A true GB1360755A (en) | 1974-07-24 |
Family
ID=10143907
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2031372A Expired GB1360755A (en) | 1973-04-18 | 1973-04-18 | Organosilicon compounds |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1360755A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0239961A2 (en) * | 1986-04-01 | 1987-10-07 | Shin-Etsu Chemical Co., Ltd. | A silicone rubber composition |
-
1973
- 1973-04-18 GB GB2031372A patent/GB1360755A/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0239961A2 (en) * | 1986-04-01 | 1987-10-07 | Shin-Etsu Chemical Co., Ltd. | A silicone rubber composition |
| EP0239961A3 (en) * | 1986-04-01 | 1989-02-08 | Shin-Etsu Chemical Co., Ltd. | A silicone rubber composition |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |