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Supramolecular bimetallic vanadium(V) complex driven by hydrogen bonding and O∙∙∙O chalcogen bonding interaction: Oxidation of cyclohexane and its application toward C H bond activation

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Abstract Vanadium(V) complex was synthesized in good yield and characterized by FT-IR, UV–Visible and NMR spectroscopy. The structure of the complex was confirmed by single X-ray crystallography. X-ray structural analysis… Click to show full abstract

Abstract Vanadium(V) complex was synthesized in good yield and characterized by FT-IR, UV–Visible and NMR spectroscopy. The structure of the complex was confirmed by single X-ray crystallography. X-ray structural analysis the complex featuring O∙∙∙O chalcogen bonding interaction and other short interaction. The O∙∙∙O intermolecular interactions distance is 2.794 A. Clearly, the O∙∙∙O intermolecular distance in the O-linked complex is less than the sum of van der Waals atomic radii of oxygen 3.00 A (rvdW (O) = 1.50 A). Oxidations of cyclohexane to cyclohexanol were also carried out, using the synthetic complex as a catalyst. The catalytic studies were carried out successfully using m-chloroperbenzoic acid as oxidant at 100 °C, under solvents free conditions. The catalytic protocols are very simple and the catalyst can be recovered without any lost in products formation in the next consecutive cycle.

Keywords: bonding interaction; vanadium complex; chalcogen bonding; interaction

Journal Title: Inorganica Chimica Acta
Year Published: 2020

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