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  • 1
    Electronic Resource
    Electronic Resource
    Biomethylation of tin (II) complexes in the presence of pure strains of Saccharomyces cerevisiae (1987)
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 1 (1987), S. 275-279 
    Details
    ISSN: 0268-2605
    Keywords: Biomethylation ; Methyl tin compounds ; Environmental methylation ; Saccharomyces cerevisiae ; Yeasts ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The methylation of several tin compounds by strains of Saccharomyces cerevisiae strains (yeast) is described. The production of the methyl tin species was established by gas chromatography and mass spectrometry. Monomethyl tin (IV) products dominated but some dimethyl tin products were observed. This appears to be the first report of a tin methylation by a pure strain of a methylating species rather than a complex mixture obtained from an environmental source.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aoc.590010310
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Speciation for analysis of organotin compounds by GC AA and GC MS after ethylation by sodium tetraethylborate (1991)
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 5 (1991), S. 173-181 
    Details
    ISSN: 0268-2605
    Keywords: Ethylation ; analysis ; organotins ; sodium tetraethylborate ; tributyltin ; tricyclohexyltin ; triphenyltin ; gas chromatography ; mass spectroscopy ; atomic absorption ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A range of organotin compounds has been ethylated using the reagent sodium tetraethylborate in a simple one-step procedure. Analysis of the volatile, fully alkylated derivatives has been achieved by GC AA with confirmation of the identity of the resulting ethylated derivatives by GC MS. Conditions for the GC AA and GC MS analysis of the organometallic ethyl derivatives are given.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aoc.590050306
    Library Location Call Number Volume/Issue/Year Availability
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    Paper (German National Licenses)
    Fulltext
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