Abstract

The synthesis of a Mo(VI) Schiff base complex, cis-[MoO 2{(4,6-bis( tert-butyl)-2-{(benzyl)iminomethyl}phenolate) 2}], cis-[MoO 2(L) 2] where L = 4,6-bis( tert-butyl)-2-{(benzyl)iminomethyl}phenol, derived from benzylamine and 3,5-di- tert-butylsalycilaldehyde is reported. Full characterization of this complex was accomplished with elemental analyses, spectroscopic studies (NMR, IR and electronic) and X-ray structure analysis. This complex was tested as a catalyst for the homogeneous oxidation of olefins. The Mo(VI) complex is catalytically active for the epoxidation of aliphatic substrates at 80 °C, yielding the epoxide as the sole product in yields up to 100% and turnover numbers up to 5000. Under the optimized conditions styrene was oxidized in an 81% conversion to produce styrene oxide, benzaldehyde, and acetophenone.

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