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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 1171-1181 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Negative ion mass spectra obtained under chemical ionization conditions (NCI) employing methane, isobutane or methylene chloride as the enhancement gas are presented for a series of chlorinated polycyclic insecticides. All of the compounds examined except 1-hydroxychlordene yielded molecular anions of substantial relative abundance (6 to 39%). The most significant features of the spectra are the prominent peaks at masses greater than that of the molecule ion formed via ionmolecule association reactions. Peaks representing association of the parent molecule with ionic species such as H-, O-, OH-, Cl-, H2OCl-, HCl2-, ClO- and Cl3- were observed in some cases. The base peak in all spectra was associated with the isotopic group of the [M + Cl]- on if contributions from other negative, even electron ions of low mass values present in high concentrations (Cl-, H2OCl- Cl2- and HCl2-) are neglected. Fragmentation processes were limited to elimination reactions involving loss of combinations of the even electron neutral species H, Cl and HCl. In addition, fragmentation resulting from a nucleophilic radical displacement of Cl by O- from the parent molecule was observed in all cases except 1-hydroxychlordene when the source was modestly wet (methane as reactant gas). NCI mass spectra of polycyclic chlorinated pesticides are reproducible, intense, interpretable in terms of classical carbanion chemistry and thus may have important analytical utility, particularly when used in conjunction with positive electron-impact and chemical ionization mass spectral methods and selective use of different enhancement gases.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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