Special Feature

User Panel

My Panel

My Panel

Bookmark Science Articles

Recent News
Bookmark / Share This Science Site

Catalytic alcoholysis of tetramethylsilane via Pt-mediated C-H bond activation.

Catalytic alcoholysis of tetramethylsilane via Pt-mediated C-H bond activation. Research Abstract Details 

Research Abstract Table of Contents

Jump to the:

  • Abstract Text of This Paper
  • Journal Published
  • MeSH Keywords of This Abstract
  • Chemicals and Substances Used in this Paper
  • Grants and Granting Agency of this Research
  • Database Accession Numbers Used in this Paper
  • Related Papers
  • Related Research Tags
  • Rate this Research Paper
  • Catalytic alcoholysis of tetramethylsilane via Pt-mediated C-H bond activation. Abstract Text:

    alan f heydukAlan F Heyduk,jay a labingerJay A Labinger,john e bercawJohn E Bercaw,

    Tetramethylsilane reacts with 2,2,2-trifluoroethanol (TFE) in the presence of a cationic platinum(II) catalyst [(NN)PtMe(TFE)]+ (NN = 1,2-bis(3,5-dimethylphenylimino)butane). Catalytic Si-C bond heterolysis results in the formation of the trimethylsilyl ether, Me3SiOCH2CF3, accompanied by liberation of one equivalent of methane. Preliminary experiments suggest that a rate-determining C-H bond activation precedes rapid attack by solvent at silicon to yield the silyl ether product and regenerate the active platinum methyl cation.

    Catalytic alcoholysis of tetramethylsilane via Pt-mediated C-H bond activation. Publishing Authors By Initials

    af heydukAF Heyduk,ja labingerJA Labinger,je bercawJE Bercaw,

    For similar organic chemicals: organosilicon compounds: trimethylsilyl compounds research abstracts see: organic chemicals: organosilicon compounds: trimethylsilyl compounds research

    PUBMED ID PMID:

    MEDLINE DATE:

    Catalytic alcoholysis of tetramethylsilane via Pt-mediated C-H bond activation. Journal Published:

    PUBLICATION TYPE: Research Support, U.S. Gov't,

    Journal: Journal of the American Chemical Society

    VOLUME: 125

    Page Numbers: 6366-7

    Journal Abbreviation: J. Am. Chem. Soc.

    ISSN: 0002-7863

    DAY: 28

    MONTH: May

    YEAR: 2003

    Catalytic alcoholysis of tetramethylsilane via Pt-mediated C-H bond activation. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 7503056

    Catalytic alcoholysis of tetramethylsilane via Pt-mediated C-H bond activation. Keywords Mesh Terms:

    KEYWORDS: Trimethylsilyl Compounds

    MESH TERMS: chemistry

    Chemical & Substance for Abstract: Catalytic alcoholysis of tetramethylsilane via Pt-mediated C-H bond activation. Information

    Substance Name: tetramethylsilane

    Registry Number: 75-76-3

    Grant and Affiliation Information for Catalytic alcoholysis of tetramethylsilane via Pt-mediated C-H bond activation.

    AFFILIATION: Arnold and Mabel Beckman Laboratories of Chemical Synthesis, California Institute of Technology, Pasadena, California 91125.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NCI

    GRANT: CA 94589

    ACRONYM: CA

    MEDLINETA: J Am Chem Soc

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

    Catalytic alcoholysis of tetramethylsilane via Pt-mediated C-H bond activation Related Publications

     

    Molecular Station USER Menu

    Welcome to Molecular Station!

    You have to register before you can post on our forums or use our advanced features. Register Now! Its Free and Fast!

    Already registered? Login now below.

    User Name:

    Password:

    Already registered and Forgot your password? Click below to recover it.

    Recover Lost Password

    Join now - it's fast and free!

    Molecular Station is THE largest network of researchers, scientists and science lovers anywhere!

    Research Terms of Usage and Disclaimer
    Home
    Features

    Protocols

    DNA Forum

    Science Forum

    DNA Forum
    Biology Forum

    Science News


    [CaRP] XML error: Invalid document end at line 2

    For more click here:Science News