Syntheses and exploration of the catalytic activities of organotin(IV) compounds.

Abstract

Six organotin(IV) compounds (1-6) have been synthesized by reaction of the polydentate pro-ligands H3L and H2L, respectively, with the corresponding diorganotin chlorides. All of the compounds were characterized by FT-IR spectroscopy, 1H, 13C{1H}, and 119Sn (1H) NMR spectroscopy, HRMS spectrometry, and single-crystal X-ray diffraction. The solid-state structures show that all of the compounds are monomeric (except compound 3) and contain a penta-coordinated tin atom. Compound 3 is a dimer with two hexa-coordinated tin atoms. Compounds 1-3 contain a non-coordinated hydroxymethyl group. All of the compounds have been screened for their catalytic efficacy in the synthesis of 1,2 disubstituted benzimidazoles using o-phenylenediamine and aldehyde derivatives. It has been observed that both the Lewis acidic Sn(IV) centre and the hydroxymethyl group (hydrogen bond donor) catalyse the reactions with a product yield of up to 92%.