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  • 1970-1974  (6)
  • Analytical Chemistry and Spectroscopy  (6)
  • Organic Chemistry
  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 3 (1970), S. 1055-1066 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electron-impact mass spectra and the field ionization mass spectra of 1-chloro-2-nitrosocyclohexane and 1-chloro-2-nitrosocyclopetane are presented and discussed. The two compounds investigated exist in dimeric form in the gaseous phase.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 4 (1970), S. 503-512 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Five phenarsazine derivatives with arsenic in the trivalent state and the pentavalent state are studied by mass spectrometry. Their characteristic fragmentation modes and the fragment ions with common structures are discussed. Experimental results show that the pyrolytic decompositions of the phenarsazine derivatives are closely parallel to the unimolecular ion fragmentation.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 3 (1970), S. 287-302 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Nine phenoxarsine derivatives with arsenic in the trivalent state and the pentavalent state are synthesized and studied by mass spectrometry. Their characteristic fragmentation modes and the fragment ions with common structures are discussed. Phenoxarsinic acids are found to be unstable in the gaseous phase at the temperatures studied and tend to form their corresponding anhydrides.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 833-841 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The EI Mass spectra of the polyfunctional pentaerythritol derivatives show that the molecular ions [M]+· exhibit extensive ion fragmentation. No Information about [M]+·. can be obtained. In Contrast to this, the FI Mass spectra of these compounds show intense [M]+· and/or [M + 1]+, and a characteristic ion at m/e 31, which is assumed to be the oxonium ion \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm CH}_2 = \mathop {\rm O}\limits^ + {\rm H} $\end{document}. Because of surface adsorption and field attraction, FI mass spectrometry presents a serious problem in quantitative analysis of a mixture containing compounds with quite different degrees of polarization.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 3 (1970), S. 747-751 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The predicted pyrolyzate of phenoxarsine derivatives from their mass spectra is diphenylene oxide. The prediction is verified by the experiment.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 493-500 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermally and electron-impact-induced rearrangements of the dimethylthioncarbamates to the dimethylthiolcarbamates are discussed. Owing to the competition with the ion fragmentation reactions in the mass spectrometric time, 〈 10-6 seconds, the extent of the mass spectrometrically observed ion isomerization cannot be predicted from that of the thermal induced one. In the ion fragmentations of the non-rearranged molecular ions, it was found that the relative abundance of the ion (CH3)2NC≡O⊕ to the total ionization is larger than that of the ion (CH3)2NC≡S⊕. This is believed to be attributable to the differences in the dissociation energies of the C—S bond and the C—O bond and in the stabilities of the two ions.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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