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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 19 (1984), S. 193-195 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The field ionization mass spectra of monosubstituted cyclopentenes and cyclohexenes with C1-C7 n-alkyl and C4-C5 isoalkyl substituents in positions 1 and 3 have been investigated and compared with the previously reported electron impact mass spectra of these compounds. The cleavage of the C—C bond β to the double bond in the non-isomerized molecular ion was found to be a typical degradation reaction of the higher homologues in the strong electric field. So, by means of the field ionization mass spectra, the 〉C1 alkyl substituent can be readily located in the parent molecule. The electron impact mass spectra exhibit a less specific fragment ion distribution for positional isomers due to the extensive molecular ion isomerization prior to decomposition, but provide useful information on the ring size. For structure determination it is appropriate to use both ionization techniques.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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