文摘
The anionic hydroxyethyl-substituted gold dithiolene complex [NEt4][Au(EtOH-thiazdt)2] is synthesized and further oxidized to the neutral radical species [Au(EtOH-thiazdt)2]鈥?/sup> through electrocrystallization. Single-crystal X-ray diffraction studies highlight the existence of the two cis and trans isomers for the monoanionic complex, with involvement of the hydroxy group in intermolecular O鈥揌路路路S hydrogen-bonding interactions. The neutral radical complex, [Au(EtOH-thiazdt)2]鈥?/sup>, is isostructural with its known ethyl analogue, namely, [Au(Et-thiazdt)2]鈥?/sup>. It exhibits a semiconducting behavior (蟽RT = 0.05鈥?.07 S cm鈥?) at room temperature and ambient pressure with an activation energy of 0.14 eV. Comparison of the crystal structures and transport and magnetic properties with those of the prototypical [Au(Et-thiazdt)2]鈥?/sup> single-component conductor shows that the replacement of ethyl by a slightly bulkier hydroxyethyl substituent affects only weakly the overlap interactions, complemented here by added O鈥揌路路路S hydrogen-bonding interactions.