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  • 1980-1984  (3)
  • 1983  (3)
  • Chemistry  (3)
  • Datenerhebung
  • microwave cavities
  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 18 (1983), S. 542-546 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Additional evidence for the rearrangement of the 1- and 3-phenylcyclobutene radical cations, their corresponding ring-opened 1,3-butadiene ions and 1,2-dihydronaphthalene radical cations to methylindenetype ions has been obtained for the decomposing ions by mass analysed ion kinetic energy spectroscopy (MIKES). The nature of the [C9H7]+ and [C10H8]+· daughter ions arising from the electron ionization induced fragmentation of these [C10H10]+· precursors has been investigated by collisionally activated dissociation (CAD), collisional ionization and ion kinetic energy spectroscopy. The [C9H7]+ produced from the various C10H10 hydrocarbons are of identical structure or an identical mixture of interconverting structures. These ions are similar in nature to the [C9H7]+ generated from indene by low energy electron ionization. The [C10H8]+· ions also possess a common structure, which is presumably that of the maphthalene radical cation.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 18 (1983), S. 239-244 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: C5H10 radical cations generated from a variety of olefins and cycloalkanes were investigated by collisionally activated dissociation, charge stripping, and low energy ion-molecule reactions. It has been determined that all of the isomers studied can be distinguished by charge stripping, whereas collisionally activated dissociation and the ion-molecule reactions are less informative. The radical cations from cyclopentane, methylcyclobutane and substituted cyclopropanes retain their cyclic structures for at least a fraction of the population having lifetimes in the microsecond range.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 18 (1983), S. 16-21 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The extent of isomerization of [C9H10]+· ions, with lifetimes of approximately 10-11 and 10-6 s has been investigated using field ionization, collisionally activated dissociation and charge stripping techniques. The [C9H10]+· ions which were investigated included the molecular ions of α-methylstyrene, β-methylstyrene, o-methylstyrene, m-methylstyrene, p-methylstyrene, indan, cyclopropylbenzene, allylbenzene and the product of water loss from 3-phenylpropanol. The field ionization spectra of all the C9H10 hydrocarbons were different indicating that isomerization to a common ion structure had not occurred to a measurable extent for ions with lifetimes of approximately 10-11 s. Collisionally activated dissociation and charge stripping results indicated that most of the [C9H10]+· ions continued to maintain unique ion structures (or mixtures of structures) at ion lifetimes of 10-6 s. Possible exceptions are the [C9H10]+· ions from allylbenzene and cyclopropylbenzene which gave indistinguishable collisionally activated dissociation and charge stripping spectra.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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