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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 897-902 
    ISSN: 0009-2940
    Keywords: Biphenylophane ; Kharasch coupling reaction ; Macrocycles ; TCNQ ; TTF ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Molecules of the TTF and TCNQ Type with Macrocyclic SkeletonsThe electron-rich and electron-poor macrocycles 1 - 3 have been synthesized. Their [1.1](3,3′)biphenylophane framework is formed by Kharasch reaction. Whereas in the well-known donors and acceptors I-III the functionalities are conjugated, in their macrocyclic “analogues” 1-3 the conjugation is prevented by the meta-connection of the phenylene rings. The redox properties  - studied by cyclovoltammetry  -  are discussed. The X-ray analysis of 3 shows considerable deviations from a planar structure.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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