Carboxylated dithiafulvenes and tetrathiafulvalene vinylogues: Synthesis, electronic properties, and complexation with zinc ions

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Abstract

A class of carboxyl and carboxylate ester-substituted dithiafulvene (DTF) derivatives and tetrathiafulvalene vinylogues (TTFVs) has been synthesized and their electronic and electrochemical redox properties were characterized by UV-vis spectroscopic and cyclic voltammetric analyses. The carboxyl-TTFV was applied as a redox-active ligand to complex with Zn(II) ions, forming a stable Zn-TTFV coordination polymer. The structural, electrochemical, and thermal properties of the coordination polymer were investigated by infrared spectroscopy, cyclic voltammetry, powder X-ray diffraction, and differential scanning calorimetric analyses. Furthermore, the microscopic porosity and surface area of the Zn-TTFV coordination polymer were measured by nitrogen gas adsorption analysis, showing a BET surface of 148.2 m 2 g -1 and an average pore diameter of 10.2 nm.

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Wang, Y., & Zhao, Y. (2015). Carboxylated dithiafulvenes and tetrathiafulvalene vinylogues: Synthesis, electronic properties, and complexation with zinc ions. Beilstein Journal of Organic Chemistry, 11, 957–965. https://doi.org/10.3762/bjoc.11.107

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