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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 941-950 
    ISSN: 0009-2940
    Keywords: Donor-acceptor compounds ; Fluorescence ; Electrochemistry ; Viologens ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis and Properties of of σ-Bridged Anthracene-Viologens[1]The synthesis of the donor-acceptor compounds 2, 7, and 12 where the anthracene donor and the viologen acceptor are linked by a saturated bridge (polymethylene or the bicyclo[2.2.2]octanyl moiety) is described. While the preparation of 2a-c is straightforward, new procedures for the synthesis of the bicyclo compounds 7 and 12 had to be developed. Unexpectedly, the viologens 13d, e could be obtained by direct nucleophilic substitution of the corresponding tertiary and neopentyl-type alkyl tosylates with 4,4′-bipyridine. By comparison of the emission spectra of the compounds 2a and 12a, b the strong fluorescence quenching indicates an electron transfer from the donor to the acceptor.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 2000 (2000), S. 425-437 
    ISSN: 1434-193X
    Keywords: Cyclic voltammetry ; Fluorescence spectroscopy ; Mixed oligomers ; Structure-property relationships ; Organic light-emitting diodes ; Oligothiophenes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---Novel mixed oligoheterocycles 1-5, containing thiophene/thiazole, thiophene/1,3,4-thiadiazole, thiophene/oxazole, or thiophene/1,3,4-oxadiazole moieties, were synthesized. The introduction of electronegative heteroatoms such as oxygen and nitrogen into the conjugated π-system leads to a more pronounced acceptor character than that found in the analogous oligothiophenes. Characterization of the redox properties reveals that the reduction of the mixed oligomers is facilitated while oxidation is shifted to higher potentials. For this series, clear structure-property relationships could be found by comparing optical properties, in particular absorptions, emissions and fluorescence quantum yields in solution. The X-ray structural determination of mixed thiophene/1,3,4-oxadiazole heptamer 5 indicates that the replacement of thiophene units by 1,3,4-oxadiazoles has a strong influence on the molecular arrangement and intermolecular interactions in the solid state.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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