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  • Digitale Medien  (2)
  • Analytical Chemistry and Spectroscopy  (2)
Materialart
  • Digitale Medien  (2)
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  • Analytical Chemistry and Spectroscopy  (2)
  • Chemistry  (2)
  • 1
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 12 (1979), S. 263-270 
    ISSN: 0030-4921
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 13C and 15N spectroscopies at natural abundance have been applied to the study of nitrogen lone-pair delocalization in N—N containing compounds: nitrosamines, nitramines, hydrazines, hydrazones and triazenes. Structure-chemical shift correlations have been derived for nitrosamines; the 13C upfield effect of a γ substituent has been used for assigning the configuration of both diastereoisomers in N,N-unsymmetrically substituted nitrosamines. Equations have been computed which permit the prediction of the electronic delocalization, expressed in terms of free enthalpy of activation ΔG≠298, as a function of δ15N and of the length of the N—N bond. 15N spectroscopy has also been applied to the study of the protonated species of nitrosamines and of acceptor-donor complexes of nitrosamines with Lewis acids. The behaviour of such N—N containing compounds is compared to that of amides.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 13 (1980), S. 126-131 
    ISSN: 0030-4921
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 13C and 15N spectra of unsymmetrically N-substituted formamides and alkyl-, substituted alkyl-, and arylcarboxamides, which can be considered as model peptide compounds, were determined and discussed in terms of nitrogen lone pair delocalization. Differential solvent shifts and through-space steric effects are considered as a tentative explanation of the difference in screening between geometrical diastereoisomers. Z-E assignment and the thermodynamic stability of diastereoisomers can also be predicted in some circumstances from a consideration of the 15N chemical shifts. Data concerning small peptides are discussed in the light of the results obtained using the model compounds.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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