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  • 33S-labelled free radicals  (1)
  • Electron spin resonance spectroscopy  (1)
  • 1
    ISSN: 0749-1581
    Keywords: Electron spin resonance spectroscopy ; Sulphur-nitrogen-containing radicals ; Dithiadiazolyl radicals ; Dithiadiazolyl radicals ; Dithiazophospholyl radicals ; Phosphaalkynes ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Further information has been obtained on the electronic structure of 1,3,2-dithiazol-2-yl radicals. The structure has been well characterized previously except for positions 4 and 5 in the ring. We have obtained solution and powder ESR spectra of radicals substituted with 13C in both positions and of radicals substituted with nitrogen or phosphorus in the 4-position. It is probably the first time that a compound has been prepared containing the ring. Two especially interesting facts emerged from the ESR spectra of these 1,3,2-dithiazolyl radicals: the 13C-substituted radical has a considerable amount of p spin density in the plane of the ring and the phosphorussubstituted radical has a very low unpaired spin density at the phosphorus atom. It is known that 1,3,2,4-dithiadiazolyl radicals isomerize readily by photolysis to the symmetrical 2,3,1,4-dithiadiazolyl radicals; we attempted the same reaction with But and a new radical was produced that we have been unable to identify.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 26 (1988), S. 755-759 
    ISSN: 0749-1581
    Keywords: ESR ; 1,3,2-Dithiazol-2-yl radicals ; 33S-labelled free radicals ; Energy calculations of conformers ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A derivative of the 1,3,2-dithiazol-2-yl radical was labelled with 33S in order to evaluate the p spin densities on the sulphur atoms. This information is required to provide a full description of the SOMO which, in turn, aids the understanding of the structure of the radical dimers. An unexpected result is that the two sulphur atoms are non-equivalent in the solid state. Calculations suggest that this is due to out-of-plane twisting of the substituent groups. Comparison of the ESR parameters of the bis(methoxycarbonyl) derivative with other members of the 1,3,2-dithiazol-2-yl group of radicals (including the parent radical) shows that it is a good model for the whole group.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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