GB761505A - Improvements in or relating to novel silanes and organosiloxane polymers and processes for preparing same - Google Patents

Improvements in or relating to novel silanes and organosiloxane polymers and processes for preparing same

Info

Publication number
GB761505A
GB761505A GB24533/54A GB2453354A GB761505A GB 761505 A GB761505 A GB 761505A GB 24533/54 A GB24533/54 A GB 24533/54A GB 2453354 A GB2453354 A GB 2453354A GB 761505 A GB761505 A GB 761505A
Authority
GB
United Kingdom
Prior art keywords
silanes
trichloro
solvent
silane
hexachlorobicyclo
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
Application number
GB24533/54A
Inventor
Morton Kleiman
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Velsicol Chemical LLC
Original Assignee
Velsicol Chemical LLC
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Velsicol Chemical LLC filed Critical Velsicol Chemical LLC
Priority to GB24533/54A priority Critical patent/GB761505A/en
Publication of GB761505A publication Critical patent/GB761505A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04Polysiloxanes
    • C08G77/22Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
    • C08G77/24Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen halogen-containing groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/18Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • C07F7/1804Compounds having Si-O-C linkages

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

The invention comprises silanes of the formula <FORM:0761505/IV(a)/1> where R is chlorine or an alkoxy radical of 1 to 5 carbon atoms, and polysiloxanes derived therefrom. The silanes are prepared by reacting hexachlorocyclopentadiene with vinyl trichloro- or vinyl trialkoxy silane. The reaction may be effected between about 75 DEG and 250 DEG C. in the presence of an inert solvent or in the absence of a solvent. The trialkoxy silanes may also be prepared by reacting the trichloro silane with absolute ethanol. The examples describe the preparation of [1,2,3,4,7,7-hexachlorobicyclo-(2.2.1) - 2 - heptenyl - 5] - triethoxy - and trichloro-silanes. By hydrolysing only two R groups in the monomer, linear polysiloxanes of the formula <FORM:0761505/IV(a)/2> are obtained, R being as above defined and X being the 1,2,3,4,7,7-hexachlorobicyclo-(2.2.1)-2-heptenyl-5 radical. Complete hydrolysis yields cross-linked polymers having an X/Si ratio of 1. The silanes may also be cohydrolysed with other silanes, e.g. dimethyl silane diol. Hydrolysis is effected by water in the presence or absence of a solvent, with or without heating. The polymers are useful as ingredients in fireproofing agents, water-repellent compositions, impregnants for laminations, hydraulic fluids and low temperature lubricants.
GB24533/54A 1954-08-23 1954-08-23 Improvements in or relating to novel silanes and organosiloxane polymers and processes for preparing same Expired GB761505A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB24533/54A GB761505A (en) 1954-08-23 1954-08-23 Improvements in or relating to novel silanes and organosiloxane polymers and processes for preparing same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB24533/54A GB761505A (en) 1954-08-23 1954-08-23 Improvements in or relating to novel silanes and organosiloxane polymers and processes for preparing same

Publications (1)

Publication Number Publication Date
GB761505A true GB761505A (en) 1956-11-14

Family

ID=10213143

Family Applications (1)

Application Number Title Priority Date Filing Date
GB24533/54A Expired GB761505A (en) 1954-08-23 1954-08-23 Improvements in or relating to novel silanes and organosiloxane polymers and processes for preparing same

Country Status (1)

Country Link
GB (1) GB761505A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0168645A2 (en) * 1984-06-27 1986-01-22 Th. Goldschmidt AG Perfluoralkylnorbornyl silanes or -siloxanes, process for preparing them and their use

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0168645A2 (en) * 1984-06-27 1986-01-22 Th. Goldschmidt AG Perfluoralkylnorbornyl silanes or -siloxanes, process for preparing them and their use
EP0168645A3 (en) * 1984-06-27 1986-02-05 Th. Goldschmidt Ag Fluoroalkyl silanes and fluoroalkyl siloxanes, process for preparing them and their use

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