Abstract
The synthesis and single crystal X-ray structures of two new self-assembled antimony(III)-thiolate complexes are described: Sb2L3 (1) and “anti”-Sb2L2Cl2 (2), where H2L is α,α′-dimercaptoxylene. The Sb(III) ions in both complexes exhibit tripodal coordination geometries with stereochemically-active lone pairs. The extended structure of 1 in the crystalline state reveals numerous C–H···S interactions, while the packing in 2 is dominated by numerous antimony-sulfur and antimony-chlorine secondary bonding interactions. These structures demonstrate that a supramolecular design strategy can be developed to prepare self-assembled structures based on the coordination geometry of Sb(III) and the reversible formation of antimony-thiolate bonds in solution. This strategy offers promise in the specific chelation of toxic ions such as antimony, a contaminant of increasing environmental concern.
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