Hydroxyl-assisted selective epoxidation of perillyl alcohol with hydrogen peroxide by vanadium-substituted phosphotungstic acid hinged on imidazolyl activated carbon?

New Journal of Chemistry Pub Date: 2022-03-03 DOI: 10.1039/D2NJ00040G

Abstract

Through the amidation reaction with 2-methylimidazole, organic basic groups were introduced into the carboxyl sites of activated carbon to obtain imidazolyl activated carbon. H3+xPW12?xVxO40 (x = 0, 1, 2, or 3) was chemically bonded to the surface, which was used to catalyze the oxidation of perillyl alcohol by hydrogen peroxide. After reaction at 60 °C for 5 h, AC-COIMIH+[H4PW10V2]? could catalyze almost complete oxidation of the substrate, where the conversion reached 97.4%, the selectivity for the 1,2-epoxide was 80.0%, and the stereo configuration of the epoxide product was RR/SS = 5?:?3. In addition, the catalyst could be easily recovered via centrifugation and reused five times without any significant deactivation. By calculating the Fukui function of perillyl alcohol, we consider a proper explanation for the main product from the oxidation of the allyl alcohol. A cooperative epoxidation mechanism with electrostatic adsorption of a double bond, and hydrogen-bonded adsorption of hydroxyl was proposed.

Graphical abstract: Hydroxyl-assisted selective epoxidation of perillyl alcohol with hydrogen peroxide by vanadium-substituted phosphotungstic acid hinged on imidazolyl activated carbon
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