Abstract

Copper(III) dithiocarbamate complexes [Cu(η 2-S 2CNMe 2) 2][ClO 4] and [Cu(η 2-S 2CNEt 2) 2][FeCl 4] have been characterised crystallographically. Both contain square-planar Cu(III) centres which attain an overall distorted octahedral coordination environment via long-range intermolecular interactions. In [Cu(η 2-S 2CNEt 2) 2][FeCl 4], anions and cations do not interact and Cu(III) centres form an infinite chain held together by weak copper–sulfur interactions. In [Cu(η 2-S 2CNMe 2) 2][ClO 4], perchlorate anions interact weakly with the Cu(III) centre [CuO 2.753(3) Å] which attains overall six coordination via a CuS interaction with a second copper–dithiocarbamate–perchlorate unit.

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