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  • Organic Chemistry  (92)
  • Analytical Chemistry and Spectroscopy  (13)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 8 (1994), S. 1-9 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The noise in a sector or quadrupele mass spectrometer is determined by the source, i.e. the number of ions present in the signal, whereas in Fourier-transform ion cyclotron resonance it is detector limited. In addition, the Fourier transform spreads white noise equally over the whole spectrum. Thus the accuracy for broad-band spectra is generally rather low. However, the precision, i.e. the reproducibility of successive spectra, is astonishingly high. This fact has been used with much success, for example in collisionally activated dissociation in Hadamard spectra. It is shown that photofragmentation spectra are also very reproducible and thus allow - at least in principle - a ‘kinetic deconvolution’ of a series of such spectra. In such a case, nonlinear regression has to be applied to the data. Since in most kinetics problems several exponential functions are involved, and since it is well known that these exponential functions are notoriously difficult to approximate with a Marquardt-Levenberg algorithm, the validity of the results may be questionable. Three examples (protonated benzene, cycloheptatriene, deuterated toluene) are chosen to demonstrate some of the difficulties and pitfalls of the procedure.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 59 (1976), S. 119-124 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The chemical ionization spectra of linear alkyl halides with up to nine carbon atoms have been studied using water as protonating agent. An alkyl ion with the same number of carbon atoms as the halide is produced. With more than six carbon atoms in the chain, fragmentation becomes important. The results show that excited hydronium ions participate as intermediates and the fragments of the resulting alkyl ions have branched structures.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 59 (1976), S. 987-998 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 70 eV mass spectra of a number of 13C- and D-labelled analogs of 1-heptene have been measured, as well as the metastable transitions in the non-labelled compound. Isotopic distributions in the major fragment ions have been calculated from the high and low resolution data. The results show that considerable skeletal rearrangement must take place before formation of most of the fragment ions. Loss of methyl and ethyl radicals occurs mainly from the two ends of the molecule. Ethylene fragments come primarily from the unsaturated end of the molecule, but show evidence of significant prior skeletal rearrangement. The predicted McLafferty rearrangement accounts for only 2/3 of the C4H8+ ions formed, less for the C3H6+ ions. At least 80% of C4H9+ ions appear to be formed by allylic cleavage, as expected, but this mechanism can only account for a maximum of 20% of the formation of the complementary ion C3H5+. Both, this latter ion and C3H6+, are probably generated by loss of hydrogen from C3H7+.Figures obtained for label retention in 1-[13C]- and 1-D-labelled analogs were nearly identical for most fragment ions, probably indicating that the hydrogen atoms in position 1 remain on C(1) even following skeletal rearrangement. A similar result was found for the 7-[13C]- and 7-D-labelled compounds. The main exceptions in the case of the products labelled in position 1 (C4H7+, C3H3+) seem to be due to initial loss of an hydrogen atom from this position followed by further fragmentation.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The deuterium isotope partition coefficient α has been determined as a function of total pressure, temperature and degree of deuteriation for methylcyclohexane/hydrogen over Ni/Al2O3. Good agreement with theory has been obtained for the dependence on temperature but not for that on total pressure or on the degree of deuteriation.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 59 (1976), S. 1935-1937 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinematic viscosity of mixtures of perdeuteriated and protiated heptane has been measured between 15° and 35° and is given in polynomial form as a function of concentration and temperature. Using the McAllister equation to describe viscosity [4], it can be shown that the interactions between molecules containing the same or different isotopic species differ slightly.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 59 (1976), S. 107-119 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The chemical ionization spectra of linear alkenes have been measured using H2O, CH4 or CD3OD as ionizing gas. In the case of 1-heptene the dependence of spectra on pressure, temperature and repeller field strength has been measured and is discussed.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 58 (1975), S. 2267-2271 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The molar volumes of mixtures of perdeuteriated and protiated heptane have been measured between -10° and 40° and expressed as a second order polynomial of the weight fraction. The difference in molar volumes of about 0.4 ml/mol decreases with temperature. The possibility of using the density measurement to determine the degree of deuteriation of mixtures of partially deuteriated heptanes was examined. The percent deuteriation calculated by this method deviates systematically from the true values.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 22 (1987), S. 145-153 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The cis- and trans-annulated isomers of 8-(N-pyrrolidyl)bicyclo[4.3.0]nona-3,7-diene show different propensities for the retro Diels-Alder fragmentation following electron impact ionization. Molecular ions of the cis-annulated isomer decompose predominantly via the retro Diels-Alder reaction to give [C9H13N] +· fragments of the appearance energy (AE)=8.45±0.05eV and critical energy Ec=133±8kJ mol-1. The trans-annulated isomer gives abundant [M-H]+ (AE=9.34±0.08eV) and [M-C6H6]+· fragments, in addition to [C9H13N]+· ions of AE=8.98±0.05eV and Ec=181±8kJ mol-1. The ionization energies (IE) were determined as IEcis=7.07±0.05 eV and IEtrans=7.10±0.06eV. The stereochemical information is much less pronounced in unimolecular decompositions of long-lived (metastable) molecular ions which show very similar fragmentation patterns for both geometrical isomers. Nevertheless, the isomers exhibit different kinetic energy release values in the retro Diels-Alder fragmentation; T0.5=3.8±0.3 and 4.8±0.2 kJ mol-1 for the cis and trans isomer respectively. Topological molecular orbital calculations indicate that the retro Diels-Alder reaction prefers a two-step path, with a subsequent cleavage of the C(5)—C(6) and C(1)—C(2) bonds. The open-ring distonic intermediate represents the absolute minimum on the reaction energy hypersurface. The cleavage of the C(1)—C(2) bond is the rate-determining step in the decomposition of the cis isomer, with the critical energy calculated as 137 kJ mol-1. The cleavage of the C(5)—C(6) bond becomes the rate-determining step in the trans-annulated isomer because of stereoelectronic control. The difference in the energy barriers to this cleavage in the isomers (ΔE=95k Jmol-1) provides a quantitative estimate of the magnitude of the stereoelectronic effect in cation radicals.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 27 (1992), S. 428-434 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The photofragmentation of an equimolar mixture of cycloheptatriene and [1, Me-13C2]toluene was studied with photons of wavelength 488 nm in order to obtain a direct comparison between the two isomers. The idea was to check the extent to which these photons could be used as a probe to study the fragmentation processes. Whenever feasible, the data were treated by a kinetic scheme and rate constants were obtained by a non-linear regression. It could be shown that the decay of both isomers follows a time behaviour described by two exponential decays. Evidence is presented that the faster decay leads to the benzyl ion. The photofragmentation of the [C7H7]+ ions follows a complex behaviour that can be superimposed by selective ion-molecule reactions.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The ion-molecule reactions of allyl bromide with the molecular ion of allyl bromide and with its major fragment, the allyl ion, yield the C6H7+ and C6H9+ ions. The structure of these product ions was explored by means of photofragmentation with laser light in the 10 μm region and by proton transfer reaction to selected reagents. These product ions were also formed by other reactions and their reactivities compared. In both cases the presence of at least two populations is demonstrated. For C6H9+ these two populations are initially present, whereas for C6H7+ an isomer is formed by the infrared light before the loss of H2. When this ion is produced by photofragmentation of C6H7+, at least one third, stable isomer is formed. Two isomers of C6H5+ are formed in the photofragmentation of C6H7+, but only one form photofragments further by loss of C2H2. The use of non-linear least-squares fitting does not allow definite conclusions to be drawn concerning the kinetics of the consecutive photofragmentations.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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