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  • Electronic Resource  (3)
  • 1975-1979  (3)
  • Analytical Chemistry and Spectroscopy  (3)
  • DNA adducts
  • Industrial Chemistry
  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 8 (1976), S. 327-328 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C n.m.r. chemical shifts of the sp-hybridized carbons in dialkylcarbodiimides have values of δc ≃ 140. These shifts are compared with those of similarly hybridized carbons occuring in other classes of compounds.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The natural-abundance 13C NMR spectra of cis,cis-1,5-cyclooctadiene monoepoxide and cis,syn,cis-1,5-cyclooctadiene diepoxide have been investigated over the temperature range of - 10 to - 180°C. Whereas the spectra of the former showed no dynamic NMR effect, two different conformations in the ratio of 3:1 were observed at low temperatures for the latter. The free-energy barrier (ΔG≠) for conversion of the major conformation to the minor conformation is calculated to be 5.9°0.2 kcal mol-1 from a line-shape analysis of spectra obtained at intermediate temperatures. It is shown that cis,syn,cis-1,5-cyclooctadiene diepoxide exists in solution in chair (major) and in twist-boat (minor) conformations of slightly different energies. Interconversion paths between these conformations are discussed. The monoepoxide is suggested to have a twist-boat conformation that is rapidly pseudorotating via a boat conformation even at - 180°C.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 12 (1979), S. 362-364 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 251 MHz 1H and the natural-abundance 63.1 MHz 13C NMR spectra of N,N'-dimethylimidazolidine have been measured from -50 to -170°C. Below about -140°C. nitrogen inversion in the compound becomes slow on the NMR time scale and both the 1H and the 13C spectra indicate that it exists in solution as a mixture of cis and trans conformations having nearly the same energies. The free-energy barrier (ΔG≠) for nitrogen inversion in N,N'-dimethylimidazolidine is 6.4 kcal mol-1, a value which is 1.5 kcal mol-1 lower than that for N-methylpyrrolidine.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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