Abstract
The catalytic potentials of dioxomolybdenum(VI) and dioxouranium(VI) homobimetallic bis-ONO tridentate (2-hydroxy-1-benzylidene)malonyl-, succinyl-, and terephthalo-dihydrazone complexes were studied in homogeneous oxidation processes of various aliphatic and cyclic alkenes using aqueous H2O2 or TBHP (tert-butyl hydroperoxide) as a terminal oxidant. The catalytic potentiality is quantitative and highly selective to afford the corresponding oxide product with MoVIO2 complexes which is 5 times more than that with UVIO2 complexes using aqueous H2O2 or TBHP. Effect of various solvents and temperatures was investigated in the oxidation of 1,2-cyclooctene catalyzed by MoVIO2 complexes using aqueous H2O2 results that the most favored solvent is acetonitrile at an optimal temperature is 70 °C. The mechanistic pathway was tentatively described and discussed.
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Adam, M.S.S. Catalytic potentials of homodioxo-bimetallic dihydrazone complexes of uranium and molybdenum in a homogeneous oxidation of alkenes. Monatsh Chem 146, 1823–1836 (2015). https://doi.org/10.1007/s00706-015-1477-9
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DOI: https://doi.org/10.1007/s00706-015-1477-9