Stabilisation of trivalent platinum by structurally accommodating thiamacrocycles

Abstract
The complex cation [Pt(1)2]2+[(1)= 1,4,7-trithiacyclononane] shows a quasi square based pyramidal structure with one non-bonding sulphur donor atom; electrochemical oxidation at +0.5 V. vs. Fc0/Fc+(Fc = ferrocene) at 20 °C in MeCN affords a paramagnetic platinum(III) species.

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