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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 3 (1989), S. 67-68 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Aluminium-clad fused silica capillary columns can be used with magnetic sector mass spectrometers. The column end needs to be pulled back a millimetre or so from the ion source to avoid electrical arcing. The chromatographic integrity is maintained. This brings the benefits of robust construction and high temperature gas chromatography/mass spectrometry to sector mass spectrometers.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1982), S. i 
    ISSN: 0306-042X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Mass Spectrometry Reviews 10 (1991), S. 225-279 
    ISSN: 0277-7037
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 17 (1973), S. 2213-2222 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The rate of polymerization of a methacrylate monomer was influenced by the molar ratio of benzoyl peroxide to an aromatic tertiary amine accelerator when the product of the concentrations of these was kept constant. The maximum rate, measured as the minimum gel time, occurred in monomer solutions containing about 1.5 moles of peroxide per mole of amine.
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 12 (1977), S. 453-460 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The concept that the slow, unimolecular reactions of the homologous series of radical cations are largely determined by the relative energetics of the possible product combinations is discussed. The concept is shown to provide a reasonably consistent rationalization of the known metastable dissociations of and correctly predicts the reactions undergone by . The concept may be useful in discussing the unimolecular chemistry of isomers.
    Additional Material: 4 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 12 (1977), S. 475-476 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A method for estimating the heats of formation of gaseous, open chain cations via a suitable isodesmic substitution is reported.
    Additional Material: 2 Tab.
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 13 (1978), S. 721-728 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The unimolecular decompositions of two isomers of [C3H8N]+, \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm CH}_{\rm 3} {\rm CH}_{\rm 2} {\rm CH} = \mathop {\rm N}\limits^ + {\rm H}_2 $\end{document} and \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm CH}_{\rm 3} {\rm CH}_{\rm 2} \mathop {\rm N}\limits^ + {\rm H = CH}_{\rm 2} $\end{document}, are discussed in terms of the potential energy profile over which reaction may be considered to occur. The energy needed to promote slow (metastable) dissociations of either ion is found to be less than that required to cause isomerization to the other structure. This finding is supported by the observation of different decomposition pathways, different metastable peak shapes for C2H4 loss, the results of 2H labelling studies, and energy measurements on the two ions. The corresponding potential energy profile for decomposition of the oxygen analogues, \documentclass{article}\pagestyle{empty}\begin{document}${\rm CH}_{\rm 3} {\rm CH}_{\rm 2} {\rm CH =\!= }\mathop {\rm O}\limits^ + {\rm H} $\end{document} and \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm CH}_{\rm 3} {\rm CH}_{\rm 2} \mathop {\rm O}\limits^ + {\rm = CH}_{\rm 2} $\end{document}, is compared and contrasted with that proposed for the [C3H8N]+ isomers. This analysis indicates that for the oxygen analogues, the energy needed to decompose either ion is very similar to that required to cause isomerization to the other structure. Consequently, dissociation of either ion is finely balanced with rearrangement to the other and similar reactions are observed. Detailed mechanisms are proposed for loss of H2O and C2H4 from each ion and it is shown that these mechanisms are consistent with 2H and 13C labelling studies, the kinetic energy release associated with each decomposition channel, the relative competition between H2O and C2H4 loss and energy measurements.
    Additional Material: 2 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 11 (1976), S. 223-230 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It is shown that the ‘metastable’ mass spectra of a series of monosubstituted benzenes are consistent with reaction over the lowest available energy surfaces. The non-occurrence of some qualitatively possible decomposition pathways may therefore be used to place lower limits on the heats of formation of gaseous cations. Conversely, where characterized reactions are preempted by new reactions upon introduction of additional substituents, upper limits may be placed upon the heats of formation of the ionic products of the new reactions. The concepts are employed to deduce that C3H6 elimination from n-butylbenzence subsequent to ionization leads to ionized toluene rather than ionized methyleneclohexadience.
    Additional Material: 3 Tab.
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 15 (1980), S. 51-52 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 16 (1981), S. 180-182 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several small immonium ions of general formula \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm R}^{\rm 1} {\rm R}^{\rm 2} {\rm C = }\mathop {\rm N}\limits^{\rm + } {\rm R}^{\rm 3} {\rm CH}_{\rm 3} $\end{document} (R1, R2, R3 = H or alkyl) eliminate .CH3; this reaction occurs in the mass spectrometer in both fast (source) and slow (metastable) dissociations. Such behaviour violates the even-electron rule, which states that closed-shell cations usually decompose to give closed-shell daughter ions and neutral molecules. The heats of formation of the observed product ions (for example, [(CH3)2C=NH]+.) can be bracketed using arguments based on energy data. Deuterium labelling results reveal that the methyl group originally bound to nitrogen is not necessarily lost in the course of dissociation. Thus, for instance, \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm{(CH}}_{\rm{3}})_2 = \mathop {\rm{N}}\limits^{\rm{ + }} {\rm{HCD}}_{\rm{3}} $\end{document} eliminates both CH3. and CD3., via different mechanisms, but very little CH2D. or CHD2. loss occurs.
    Additional Material: 1 Tab.
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