Summary
[CuCl(Vn3S3)]·2THF (8) and [CuCl(Me2S)3] (9) can directly be obtained by reacting copper (I) chloride either with 5,10,15-trithia-cyclo-triveratrylene (Vn3S3) in a 1∶1 molar ratio in tetrahydrofuran (THF) as a solvent or in an excess of dimethylsulphide (Me2S). In both complexes the copper ion has a tetrahedral coordination which is, however, strongly distorted in the case of (8) because of the fixed geometry of the Vn3S3 ligand (mean values: Cl−Cu−S 124.1° and 110.2°, S−Cu−S 91.7° and 108.7°). In spite of similar Cu−S distances [232.2(2) and 231.2(3)pm] the donor ability of Vn3S3 is not as good as that of three Me2S ligands due to the less optimal bond angles formed in (8); consequently, in (8) the Cu−Cl distance is significantly shorter than in (9) [220.4(2) versus 226.3(3) pm].
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Olbrich, F., Maelger, H. & Klar, G. Cyclic ligands with fixed coordination geometry, Part 8(1). Structure of [CuCl(Vn3S3)]·2THF and of [CuCl(Me2S)3] for comparison (Vn3S3 = 5,10,15-trithia-cyclo-triveratrylene). Transition Met. Chem. 17, 525–529 (1992). https://doi.org/10.1007/BF02910749
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DOI: https://doi.org/10.1007/BF02910749