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  • Analytical Chemistry and Spectroscopy  (3)
  • 13C NMR  (1)
  • Wiley-Blackwell  (3)
  • 1985-1989  (2)
  • 1980-1984  (1)
  • 1987  (2)
  • 1983
  • 1982  (1)
  • 1
    ISSN: 0749-1581
    Schlagwort(e): 13C NMR ; Heteronuclear ; NOE ; Conformation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The 20.15 MHz 13C NMR spectra of five 3,6,9-trioxanthracenes and four 3,6-dioxa-9-thianthracenes have been assigned using a variety of one-dimensional techniques. These include spin-echo multiplicity sorting (SEFT), long-range heteronuclear coupling constant determination via gated decoupling and selective heteronuclear 13C{1H} NOE difference spectroscopy. The axial position of substituents on C-10 has been demonstrated.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 25 (1987), S. 539-543 
    ISSN: 0749-1581
    Schlagwort(e): Indirect heteronuclear NOEs ; 1H-19F-1H and 1H-19F-13C systems ; Three-spin effects ; Anomalous intensity effects ; Conformational analysis ; Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Indirect nuclear Overhauser enhancements through 19F have been determined for the three-spin systems 1H-19F-1H and 1H-19F-13C by steady-state presaturation of the appropriate proton, and applied to the conformational analysis of 5-bromo-2-fluoro-4-nitroacetanilide. The 1H NOE difference spectra at 400 MHz showed antiphase doublets for protons undergoing simultaneous dipolar relaxation with, and scalar coupling to, 19F. Similarly, in the 13C selective NOE difference spectrum at 100 MHz, the two lines of the fluorine-bearing carbon showed negative enhancement factors of different magnitude on presaturation of the appropriate proton. The use of these anomalous intensity effects in conformational analysis is illustrated.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 12 (1982), S. 68-72 
    ISSN: 0377-0486
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Amorphous V2O5 can be obtained by cooling from the melt. This amorphous oxide is very sensitive to water vapour and can even be dissolved in water to give a vanadium pentoxide gel. The hydration process has been followed by infrared and Raman spectroscopy between 20 and 4000 cm-1. Short-range order in the amorphous oxide appears to be almost the same as in orthorhombic V2O5. The amorphous phase could even be described as made of small crystallites about 100 Å in diameter. The structure of amorphous V2O5 does not seem to be modified by water adsorption, at least during the first stages of the hydration process. However, a drastic modification occurs when enough water is added to give a gel. A general shift to lower frequencies is observed, indicating a weakening of the V—O bonds, presumably associated with the formation of new V—OH2 bonds. Two different water species have been identified, one of which seems to be almost free of hydrogen bonding. Short-range order in the gels seems to be quite well defined and the spectra could be interpreted either in terms of crystallites, as in amorphous V2O5, or in terms of molecular (or macromolecular) species containing V2O5, (H2O), groups.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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