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.
Acknowledgments
This work was supported by the National Natural Science Foundation of China (21104037, 20971075), Ningbo Science and Technology Innovation Team (2011B82002), Foundation of the Education Committee of Zhejiang Province (Y201120345), and SRF for ROCS, SEM.