Abstract
Isomers of a macrocycle containing two tetrathiafulvalene structural units joined by propylenedithio bridges are prepared. The electrochemical oxidation potentials are determined. Possible conformations of tetramethoxycarbonyl[5.5] tetrathiafulvalenophane are analyzed using the AM1 method.
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Riga Technical University, Riga LV-1048, Latvia. Department of Chemistry, Ben Gurion University of Negev, 84105 Israel. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 910–913, July, 1999.
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Neiland, O., Khodorkovskii, V., Utinans, M. et al. Preparation of two stereoisomers of the macrocyclic electron donor tetramethoxycarbonyl[5.5]-tetrathiafulvalenophane with bridges containing two sulfur atoms. Chem Heterocycl Compd 35, 795–798 (1999). https://doi.org/10.1007/BF02252102
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DOI: https://doi.org/10.1007/BF02252102