Abstract
The neutral complex [ReOBr2(tmi)] [Htmi = 2-(1-ethanolthiomethyl)-1-methylimidazole] was synthesized by reaction of (n-Bu4N)[ReOBr4(OPPh3)] with an equimolar amount of Htmi in acetonitrile. The ‘3 + 2’ complex [ReO(tmi)(mi)]Cl [Hmi = 2-(hydroxymethyl)-1-methylimidazole] was isolated from a one-pot reaction of (n-Bu4N)[ReOCl4] with Htmi and Hmi in equimolar quantities in acetonitrile. The compounds were characterized by spectroscopic methods and X-ray crystallography. Both complexes have distorted octahedral geometries with the alcoholate oxygen of tmi coordinated trans to the oxo group.