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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 3335-3341 
    ISSN: 1434-193X
    Keywords: Catenanes ; Donor-acceptor interactions ; Self-assembly ; Supramolecular chemistry ; Tetrathiafulvalenes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of three novel macrocycles 3-5based on the two electron donors bis(2,5-dimethylpyrrolo)[3,4-d]tetrathiafulvalene (1) and 1,4-hydroquinone is presented. Their abilities to include the electron acceptor paraquat (6) have been investigated by UV/Vis and 1H NMR spectroscopy and an X-ray crystallographic analysis. Also, the complex formation between the cyclic acceptor cyclobis(paraquat-p-phenylene) (7) and different tetrathiafulvalene derivatives has been studied. A strong association between 1 and 7 facilitates the self-assembly of catenanes from the macrocycles 3-5. However, the preferred position of the cyclic acceptor 7in the catenanes around either the pyrrolo-annelated TTF or around the hydroquinone donor relies on a fine balance between all the individual noncovalent forces acting in cooperation.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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