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  • Conformational analysis  (1)
  • Self-diffusion  (1)
  • Synchronous nutation experiments  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 27 (1989), S. 1148-1154 
    ISSN: 0749-1581
    Keywords: Self-diffusion ; Pulsed gradient ; Complexation phenomena ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1H and 133Cs NMR self-diffusion measurements were performed by means of the pulsed gradient spin-echo method (PGSE) to evaluate the complex formation constants of Cs and 18-crown-6 and those of Cs and some ethylene glycols in D2O. The calculated complex formation constants were checked as far as possible by using similar calculations based on relaxation data. Chemical shift measurements do not allow the evaluation of complex formation constants in these systems. A cross-check was introduced to verify the calculations based on the diffusion data. Similar investigations were performed on Na, K, Cs complexes and N-phenylaza-15-crown-5 in methanol. In this case, analysis of the diffusion data and as the relaxation rate and chemical shift data led to complex formation constants for 1:1 complexes, which is in contrast to a previous report suggesting the formation of 2:1 complexes.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 30 (1992), S. S3 
    ISSN: 0749-1581
    Keywords: Transient NOE experiments ; Synchronous nutation experiments ; NAD stack interactions ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cross-relaxation interactions between the nicotinamide moiety and the adenine moiety of NAD in D2O solution were unambiguously revealed by steady-state NOE experiments, transient NOE experiments and synchronous nutation experiments. The experimental results, which allow a concise description in terms of auto-relaxation and cross-relaxation, are interpreted as the result of a stacking interaction. Studies of 13C relaxation and investigations on ternary mixtures with 6-methylpurine give evidence for an inter- rather than intra-molecular stack interaction, at least in the NMR concentration range.
    Additional Material: 5 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 29 (1991), S. 580-586 
    ISSN: 0749-1581
    Keywords: [Lys8]-vasopressin homologues ; NMR assignments in peptides ; Conformational analysis ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The assignment of proton NMR signals and the conformational analysis of N-(Gly)-[Lys8]-vasopressin and N-(Gly—Gly—Gly)—[Lys8]-vasopressin in dimethyl sulfoxide solution by means of one- and two-dimensional NMR techniques are presented. Dihedral angles obtained from 3J (HN—C—α-H) vicinal couplings, intramolecular distances estimated from nuclear Overhauser enhancements (NOEs) and two-dimensional experiments in the rotating frame (ROESY), as well as temperature dependences of the amide protons, suggest a more or less rigid ring conformation with an inverse γ-turn for both cyclic peptides.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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