GB832487A - Organosiloxanes - Google Patents

Organosiloxanes

Info

Publication number
GB832487A
GB832487A GB8130/57A GB813057A GB832487A GB 832487 A GB832487 A GB 832487A GB 8130/57 A GB8130/57 A GB 8130/57A GB 813057 A GB813057 A GB 813057A GB 832487 A GB832487 A GB 832487A
Authority
GB
United Kingdom
Prior art keywords
prepared
preparation
trimer
formula
temperatures
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
GB8130/57A
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.)
Midland Silicones Ltd
Original Assignee
Midland Silicones Ltd
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
Priority claimed from US594108A external-priority patent/US2979519A/en
Application filed by Midland Silicones Ltd filed Critical Midland Silicones Ltd
Publication of GB832487A publication Critical patent/GB832487A/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
    • C07F7/0834Compounds having one or more O-Si linkage
    • C07F7/0838Compounds with one or more Si-O-Si sequences
    • 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
    • C07F7/21Cyclic compounds having at least one ring containing silicon, but no carbon in the ring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Silicon Polymers (AREA)

Abstract

The invention comprises perfluoroalkyl cyclotrisiloxanes of the formula <FORM:0832487/IV (a)/1> where R is a perfluoralkyl radical containing 1 to 10 carbon atoms. They are prepared by hydrolysing the chlorosilanes RCH2CH2Si(Me) Cl2 in the usual manner and heating the hydrolysate with an alkali metal hydroxide or salt of a siloxane under conditions which cause the cyclic trimer to distil from the mixture. Alternatively, when the trimer is crystalline, the conditions are such as to remove the volatile materials, and the distillate is crystallized. The cracking is generally effected at 200 DEG to 400 DEG C., at atmospheric or reduced temperature; at the higher temperatures, a nitrogen atmosphere is preferably employed. The comounds are useful as lubricants and for the preparation of high polymers and elastomers as described in Specifications 832,488 and 832,489. The examples describe the preparation of compounds of the above formula where R=CF3, C2F5 and C3F7. Perfluoroalkyldichloromethyl silanes are prepared by reacting an alkylene RCH=CH2 (R is as above) with methyldichlorosilane in the presence of a peroxide or platinum catalyst at temperatures of 150 DEG to 300 DEG C.
GB8130/57A 1956-06-27 1957-03-12 Organosiloxanes Expired GB832487A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US594108A US2979519A (en) 1956-06-27 1956-06-27 New cyclotrisiloxanes
US834711XA 1956-09-10 1956-09-10

Publications (1)

Publication Number Publication Date
GB832487A true GB832487A (en) 1960-04-13

Family

ID=26769343

Family Applications (2)

Application Number Title Priority Date Filing Date
GB8130/57A Expired GB832487A (en) 1956-06-27 1957-03-12 Organosiloxanes
GB27930/57A Expired GB834711A (en) 1956-06-27 1957-09-04 Improvements in or relating to organosiloxanes

Family Applications After (1)

Application Number Title Priority Date Filing Date
GB27930/57A Expired GB834711A (en) 1956-06-27 1957-09-04 Improvements in or relating to organosiloxanes

Country Status (3)

Country Link
DE (1) DE1044814B (en)
FR (2) FR1176236A (en)
GB (2) GB832487A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5241097A (en) * 1992-12-21 1993-08-31 Allied-Signal Inc. Process for the preparation of cyclic siloxane

Also Published As

Publication number Publication date
FR1176236A (en) 1959-04-08
DE1044814B (en) 1958-11-27
FR1182154A (en) 1959-06-23
GB834711A (en) 1960-05-11

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