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Vanadium catalysts were successfully used to oxidize benzene in two-phase reaction system under Udenfriend-like conditions. The selectivity of the reaction changed completely as a function of the type of reducing agents. Relatively high turnover numbers were obtained as the reductant/V molar ratio increased. High selectivity to phenol production was achieved by using ascorbate as reducing agent, while the use of a different reductant (dithiocompounds) changed completely the selectivity toward more oxidized products, i.e., hydroquinone. Thioreducing agents favored the oxidation of the aromatic ring of benzene, while ascorbate selectively favored the introduction of only one oxygen. The exploitation of the reducing capacity of the system was remarkable. The reaction yield depended on the amount of ascorbate present or, more precisely, upon the ascorbate/V molar ratio. Vanadyl concentrations tended to slowly decrease as the benzene oxidation reaction rate increased, generating VVions.
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Reference:
Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI