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  • 1
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It has been shown that there is no significant carrier effect when low levels of [3H]octopamine (100 pg) are extracted by ethyl acetate from aqueous solutions containing a 103 or 106 times excess of unlabelled octopamine. It is also shown that there is no carrier effect when low levels of octopamine as the tetrakis-TMS derivative are injected with 100 times the amount of the [2H3] analogue on an SE 30 column.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 10 (1977), S. 216-219 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 1H n.m.r. spectra of 3-mono-oxygenated and 3,7-dioxygenated N-acetyl-17-aza-D-homoandrost-5-enes show unequal populations of the amide rotational isomers in chloroform-d1 solution. The populations are dependent upon the orientation of the C-7 oxygen substituent but are independent of concentration. In pyridine-d5 solution the two rotameric states for each compound are almost equally populated.
    Additional Material: 3 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 9 (1977), S. 210-212 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An accurate measurement of the chemical shifts and the coupling constants of some disubstituted acetophenones has been made. The acetophenones studied contained nitro, bromo or amino groups substituted in either the 3,4 or 2,5 positions. For compounds with no substituent adjacent to the acetyl group, the chemical shifts and the coupling constants estimated by the simple additivity of the substituent increments were found to be in reasonable agreement with the experimental values. The two nitro, bromo derivatives substituted in positions 2 and 5 probably prefer the conformer in which the proton H-6 is adjacent to the acetyl methyl group whilst the 3,4-disubstituted bromo, nitro and bromo, amino derivatives prefer the conformer in which the H-6 proton is adjacent to the carbonyl group.
    Additional Material: 1 Ill.
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  • 4
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The trifluoroacetate anion undergoes reaction with succinic, maleic and phthalic anhydrides to yield 1 : 1 adducts. The molecular anions of maleic and phthalic anhydride also undergo reaction with perfluoroacetic anhydride to produce [CF3CO2]-· Maleic anhydride parent ions produce [M + CF3CO·]- ions when allowed to react with perfluoroacetic anhydride.
    Additional Material: 2 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 11 (1976), S. 103-116 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The concepts of charge localization and of radical localization are considered both with regard to their validity and to their usefulness in explaining and predicting the unimolecular fragmentation pathways for positively charged ions formed from organic compounds. It is concluded that there is experimental support for these concepts.
    Additional Material: 3 Tab.
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  • 6
    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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  • 7
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Comparison of metastable peaks in the mass spectra of the monoterpenes alloöcimene and a-pyronene shows that they fragment through common ions. It is concluded that the acyclic triene (alloöcimene) undergoes electrocyclic ring closure to the cyclic diene (a-pyronene) and fragmentation then proceeds from an ionised form of a cyclic diene. The fragmentation proceeds to a series of ions [CnH2n-5]+, the decomposing forms of which are inferred to be protonated benzene (n = 6) and dihydrotropylium ions (n = 7, 8, 9). These ions react via loss of H2, the dihydrotropylium → tropylium conversion being characterised by a relatively large kinetic energy release in both un-substituted (n = 7) and methyl-substituted (n = 8, 9) cases.
    Additional Material: 4 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 11 (1976), S. 266-270 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract-Useful field desorption mass spectra can be obtained from involatile sulphonic acids and sulphonates, even when large dyestuff molecules are involved. Unusual cluster ions are commonly found, which can be singly or doubly charged. Most ions can be assigned, however, and the great potential of field desorption mass spectrometry in the identification of these involatile species is clearly established.
    Additional Material: 2 Tab.
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  • 9
    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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  • 10
    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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