Abstract

Organic–inorganic hybrids, based on the Lindqvist-type polyoxometalate (POM) and dioxomolybdenum(VI) complexes, have been synthesized by hydrolysis of [MoO2(acac)2] (acac = acetylacetonate) in the presence of aroylhydrazone ligands in weak donor solvents. This provides an efficient route to materials that contain open coordination sites or sites occupied by labile ligands. Removal upon grinding or heating of the labile acetonitrile and acetone molecules on the dioxomolybdenum centres and the reaction in the solid-state represent a way for designing structures with the Lindqvist Mo6O192− anion coordinated to the metal centres of two complex cations. The compounds were characterised by the single crystal and powder X-ray diffraction methods, elemental analysis, IR spectroscopy, TG and DSC analyses.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call