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  • Analytical Chemistry and Spectroscopy  (2)
  • 1
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 19 (1982), S. 49-53 
    ISSN: 0030-4921
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Lanthanide induced shifts using Yb(fod)3 and Pr(fod)3 were used for the signal assignments of the 13C spectra of the 1,4-benzodiazepines diazepam, desmethyldiazepam, prazepam and flurazepam, and for characterizing their solution conformation with respect to the substituents at N-1 and C-5. The phenyl substituent at C-5 is found to be nearly coplanar with the π-bond between C-5 and N-4, and the substituents at N-1 seem to be orientated towards the carbonyl group with dihedral angles of either 60° or 120° between the bonds N-1 and C-2 and C-12 and C-13. The metal ions seem to bind to O-2 with metal-oxygen distances between 0.19 and 0.26 nm and bond angles between 117° and 167°. Contact shifts induced by Pr(fod)3 are slightly larger than obtained for Yb(fod)3, whereas the latter reagent causes a stronger broadening.
    Zusätzliches Material: 2 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 21 (1983), S. 319-321 
    ISSN: 0030-4921
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Carbon-13 NMR spectra of 1,4-benzodiazepines, substituted differently at C-7, are reported. With increasing electron demand of the substituent the signal of C-2 is shifted upfield, an effect which is interpreted in terms of a π-polarization of the carbonyl π-electrons. This mechanism also seems to be of importance for the π-electrons of the 5-phenyl substituent and of the (N-4)=(C-5) bond. Owing to the formation of hydrogen-bonded self-associates, compounds with a free amide group show concentration-dependent shifts of some resonances. This is most obvious for C-2, the proposed proton accepting site for hydrogen-bonded cyclic dimers.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
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