Abstract

The syntheses, crystal structures, and electrochemical of the transition metal coordination complexes, Cu(acac)2(EDO-TTF-3-py)2 (2) and Zn(acac)2(EDO-TTF-3-py)2 (3) are reported, where acac = acetylacetonate; EDO-TTF-3-py (L1) = 4,5-ethylenedioxy-3′-(3′-pyridyl)-tetrathiafulvalene). In the complexes 2 and 3, the ligand L1 is coordinated to the metal atom through pyridine nitrogen. The similarly oxidation potentials were observed for the ligand L1 and 2 and 3, indicating the negligible interaction between the ligand and the metal in solution.

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