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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 17 (1982), S. 269-273 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Water and acetic acid eliminations from 1-tetralin radical cations have been shown previously to be highly regiospecific 1,4 processes. Utilizing deuterium labeling, high resolution peak ratio measurements and metastable ion defocusing techniques, the stereochemistry of these processes has been investigated. cis-4-d1- and trans-4-d1-1-Tetralol both lose HOH and DOH in appreciable amounts; similarly, both acetoxy derivatives lose HOAc and DOAc. These results are interpreted in terms of an ionic epimerization which operates in competition with a stereospecific 1,4 elimination mechanism. A hydrogen exchange process which occurs between the 4-carbon and the oxygen atom situated on the 1-carbon of 1-tetralol has also been observed. This process accounts for observed H/D ratios in the ethene elimination reaction of various deuterium labeled 1-tetralols.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 2
    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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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 19 (1984), S. 519-520 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 4
    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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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 17 (1982), S. 416-423 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Water and acetic acid eliminations from 1- and 2-indan derivatives have been investigated. Deuterium labeling, high resolution peak matching and the metastable peak analysis capabilities of a high resolution triple analyzer (E B E) mass spectrometer were employed to examine the eliminations. These experiments showed that water was lost from 1-indanol via 1,2 and 1,3 processes. These results contrast with those obtained for 1-tetralol, which specifically eliminates water in a 1,4 process involving the benzylic hydrogens. Water elimination from 2-indanol is preceded by a slow hydroxyl-benzylic hydrogen exchange and proceeds specifically 1,2. Water losses from both 1- and 2-indanol are characterized by large kinetic energy releases. Acetic acid elimination is shown to occur specifically 1,3 from 1-acetoxyindan and 1,2 from 2-acetoxyindan.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 6
    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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