Nonelectrochemical synthesis, crystal structure, and physical properties of the radical salt [ET]2[CuCl4] (ET = bis(ethylenedithio)tetrathiafulvalene)

Inorg Chem. 2013 Dec 16;52(24):14376-81. doi: 10.1021/ic402478h. Epub 2013 Nov 20.

Abstract

The radical salt [ET]2[CuCl4] was obtained by chemical oxidation of bis(ethylenedithio)tetrathiafulvalene (ET) with the tetranuclear copper(II) halide cluster [Cu4OCl10](4-). Although a complex mixture of anions forms in solution during the redox reaction, only this product is obtained as large (>3 mm) single crystals. X-ray diffraction analysis determined that the ET molecules stack in the solid state forming dimerized 1D chains along the a axis, interleaved by [CuCl4](2-) anions. The ET dimers show very short S···S contacts (<3.41 Å). The physical properties are dominated by these intradimer ET interactions. The magnetic behavior shows antiferromagnetic coupling with a singlet-triplet gap >620 K (430 cm(-1)). The Cu(2+) (S = 1/2) centers are magnetically isolated and yield a narrow EPR line in the X-band at g = 2.01. The ET moieties are EPR silent.