Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Articles: DFG German National Licenses  (2)
  • Electronic Resource  (2)
  • Analytical Chemistry and Spectroscopy  (2)
Source
  • Articles: DFG German National Licenses  (2)
Material
  • Electronic Resource  (2)
Years
Keywords
  • Analytical Chemistry and Spectroscopy  (2)
  • Chemistry  (2)
  • 1
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 13 (1980), S. 126-131 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...