GB981268A - Organo-trifluorosilane complexes - Google Patents

Organo-trifluorosilane complexes

Info

Publication number
GB981268A
GB981268A GB1486963A GB1486963A GB981268A GB 981268 A GB981268 A GB 981268A GB 1486963 A GB1486963 A GB 1486963A GB 1486963 A GB1486963 A GB 1486963A GB 981268 A GB981268 A GB 981268A
Authority
GB
United Kingdom
Prior art keywords
trifluorosilanes
acidification
purification
solution
examples
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
GB1486963A
Inventor
Richard Muller
Christian Dathe
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.)
Institut fuer Silikon und Fluorkarbon Chemie
Original Assignee
Institut fuer Silikon und Fluorkarbon Chemie
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 Institut fuer Silikon und Fluorkarbon Chemie filed Critical Institut fuer Silikon und Fluorkarbon Chemie
Priority to GB1486963A priority Critical patent/GB981268A/en
Publication of GB981268A publication Critical patent/GB981268A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C07F7/12Organo silicon halides
    • C07F7/121Preparation or treatment not provided for in C07F7/14, C07F7/16 or C07F7/20
    • C07F7/123Preparation or treatment not provided for in C07F7/14, C07F7/16 or C07F7/20 by reactions involving the formation of Si-halogen linkages

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)

Abstract

The invention comprises complex salts of organo-trifluorosilanes and alkali metal or ammonium fluorides. They are prepared by the action of the organotrifluorsilanes on the alkali metal or ammonium fluoride in solid form or in solution-a neutral or weakly alkaline aqueous solution being advantageous. The trifluorosilanes may be liberated from the dry complex salts, or their solutions, by the action of heat, or, preferably, by acidification. When hydrofluoric acid is used for the acidification, the solution may be neutralized with a suitable hydroxide and recycled. Only trifluorosilanes and silicon tetrafluoride are thus absorbed, and the latter is not regenerated by acidification, so that the process of absorption and regeneration provides a convenient method for the separation and purification of organotrifluorosilanes. The dry complex salts are stable, and may be used for storage of the trifluorosilanes. The fluorides used are also fluorinating agents, so that it is possible to carry out processes of fluorination and purification in one step, excess fluoride acting as buffer for any acid formed. The examples describe the preparation of complexes of methyl - and phenyl - trifluorosilane with ammonium and potassium fluorides, in solution, and their decomposition by acidification, and by heat (Example 5). Examples 2-4 describe the purification of methyl trifluorsilane by complexing with ammonium fluoride and subsequent regeneration, and Examples 9 and 10 the purification of dimethyl difluorosilane by the removal of trifluorosilane impurities. In the latter case and in Example 4 the ammonium fluoride is also used to fluorinate the initial mixtures of chlorosilanes and chlorosiloxanes. Examples 11 and 12 describe respectively the decomposition of dry disodium methyl pentafluorosilicate and the re-use of a complexing solution acidified with HF, after neutralizing it with ammonia.
GB1486963A 1963-04-16 1963-04-16 Organo-trifluorosilane complexes Expired GB981268A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1486963A GB981268A (en) 1963-04-16 1963-04-16 Organo-trifluorosilane complexes

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1486963A GB981268A (en) 1963-04-16 1963-04-16 Organo-trifluorosilane complexes

Publications (1)

Publication Number Publication Date
GB981268A true GB981268A (en) 1965-01-20

Family

ID=10048946

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1486963A Expired GB981268A (en) 1963-04-16 1963-04-16 Organo-trifluorosilane complexes

Country Status (1)

Country Link
GB (1) GB981268A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3449394A (en) * 1967-04-06 1969-06-10 Inst Silikon & Fluorkarbonchem Process for making salts of perfluorovinyl fluorosilicic acids
US3517043A (en) * 1968-07-29 1970-06-23 Inst Silikon & Fluorkarbonchem Method for the preparation of salts of organofluosilicic acids in nonaqueous solvents
US3525763A (en) * 1963-04-17 1970-08-25 Inst Silikon Und Fluorkarbonch Production of salts of organofluorosilicic acids

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3525763A (en) * 1963-04-17 1970-08-25 Inst Silikon Und Fluorkarbonch Production of salts of organofluorosilicic acids
US3449394A (en) * 1967-04-06 1969-06-10 Inst Silikon & Fluorkarbonchem Process for making salts of perfluorovinyl fluorosilicic acids
US3517043A (en) * 1968-07-29 1970-06-23 Inst Silikon & Fluorkarbonchem Method for the preparation of salts of organofluosilicic acids in nonaqueous solvents

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