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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 70 (1987), S. 2065-2072 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The radical cations and the radical anions of 1,6-dithiapyrene (1) and 3,10-dithiaperylene (2) as well as those of three further Weitz-type S-donors 3, 4, and 5 have been studied by ESR spectroscopy. The experimental findings for \documentclass{article}\pagestyle{empty}\begin{document}$ 1^{\scriptstyle {{\relbar}\kern-4pt {.} }} $\end{document} (widths and behaviour on saturation of hyperfine lines) suggest that the ground state of this radical anion is effectively degenerate. With the exception of \documentclass{article}\pagestyle{empty}\begin{document}$ 1^{\scriptstyle {{\relbar}\kern-4pt {.} }} $\end{document}, the ESR studies of all radical ions could be complemented by the use of the ENDOR and general TRIPLE resonance techniques. In addition to proton hyperfine data, 33S coupling constants have been determined for \documentclass{article}\pagestyle{empty}\begin{document}$ 1^{+ \atop \dot{}} $\end{document} (0.53mT), \documentclass{article}\pagestyle{empty}\begin{document}$ 2^{+ \atop \dot{}} $\end{document} (0.46mT), and \documentclass{article}\pagestyle{empty}\begin{document}$ 4^{+ \atop \dot{}} $\end{document} (0.34mT); they are in agreement with the predicted substantial π-spin populations at the S-atoms.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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