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  • Electronic Resource  (3)
  • 1985-1989  (3)
  • 1
    ISSN: 0749-1581
    Keywords: 2H NMR ; Reversed micelle ; Heavy water ; Anaesthetic ; Enflurane ; Clathrate formation ; Hydrogen bond breaking ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The behaviour of water in the reversed micelles of the glycerol α-monooleate (GMO)-decane-2H2O system was investigated by deuteron nuclear magnetic resonance. The chemical shifts (δ) and the spin-lattice relaxation times (T1) of heavy water were found to be dependent on temperature. The temperature dependence of the T1 and δ values reveals that the structural change in heavy water induced by the inhalation anaesthetic enflurane is very different below and above ca. 300 K. Below ca. 300 K a cage of a water polyhedron builds up around an enflurane molecule. Above ca. 300 K there is no water polyhedron cage because of the cleavage of the hydrogen bonds in the polyhedron water, and some of the water molecules are tightly adsorbed on the enflurane molecules.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 25 (1987), S. 675-679 
    ISSN: 0749-1581
    Keywords: 1H NMR ; 7Li NMR ; 13C NMR ; 15N NMR ; lithium salts of anilines ; hybridization change ; electron ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1H, 7Li, 13C, and 15N NMR spectra were observed for lithium salts of aniline derivatives in THF solutions. The delocalization of excees charge into the phenyl ring of the salts was confirmed from the 1H and 13C chemical shift data in comparison with those of the neutral molecules. Their 15N atoms were approximately 40 ppm less shielded comparison with those of the neutral molecules, and these are discussed in terms of hybridization change and electron densities at the nitrogen atoms. The one-bond 15N-1H coupling constants of the salts are approximately 55 Hz and are smaller than those of the neutral molecules.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0749-1581
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 1H NMR signals of the cations formed from bromothiophenes were observed in HSO3F solution at -70°C. Protonation occurs at one of the α-carbons in all cases studied. Some bromothiophenium ions undergo rearrangement or fluorosulphonylation with an increase in temperature. Both protonated 2,5- and 2,3-dibromothiophenes, for example, rearrange to the same 3,5-dibromo-2H-thiophenium ion. 1H and 19F NMR spectral data of the related bromothiophenesulphonyl fluorides are also presented.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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