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  • Analytical Chemistry and Spectroscopy  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 4 (1970), S. 365-372 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mass spectra of nitraminopyridines can be obtained by careful introduction of the sample direct to the ion source. Electron-impact fragmentation of the molecular ion is largely by expulsion of nitrogen dioxide. Introduction of samples through a heated glass inlet results in extensive pyrolysis with formation of nitric oxide, nitrous oxide and ions corresponding to an aminopyridine. In addition, the 2-nitraminopyridines give strong ions for the corresponding pyridones and ions at high mass resulting from an undefined bimolecular reaction.Similarly in the direct inlet spectrum of N-methyl-2-nitriminopyridine loss of nitrogen dioxide is the only significant reaction of the parent ion but the heated inlet causes extensive pyrolysis. This is largely restricted to expulsion of nitrous oxide with formation of N-methylpyridone.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 5 (1971), S. 317-324 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The low resolution mass spectra of a number of homologous 5-alkylthio-1,3,4-thiadiazolyl-2-amines have been determined. With the methylthio compound the only significant loss from the molecular ion is the sulphydryl radical. As the homologous series is ascended this reaction becomes less important and is insignificant with the butylthio isomers. The ethylthio compound suffers extensive loss of ethylene and when the alkyl group contains three or more carbon atoms the main reaction is always loss of the olefin coresponding to the alkyl group.All of the n-alkylthio compounds showed in addition loss of methylthio radical from the molecular ion. A mechanism is proposed and comparisons made with alkyl phenyl thioethers and alkylthio substituted heterocycles.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
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