The selective oxidation of light hydrocarbons and their valorization with only dioxygen (O2) are important transformations toward development of efficient chemical processes. Monooxygenase enzymes can catalyze selective aerobic reactions under… Click to show full abstract
The selective oxidation of light hydrocarbons and their valorization with only dioxygen (O2) are important transformations toward development of efficient chemical processes. Monooxygenase enzymes can catalyze selective aerobic reactions under reducing and protic conditions. The translation of such enzymatic pathways to the practical electrocatalytic oxidation of light, gaseous hydrocarbons, using O2 as sole oxidant is now reported. An iron–tungsten oxide inorganic molecular catalyst with a capsular structure {Fe30W72} stabilized inside by sulfate/bisulfate anions provides a protic environment where three iron atoms are located at each of the pores of the capsule leading to a unique and potent active site for the oxidation reactions. Under mild electrochemical conditions, 1.8 V, in water at room temperature, using O2 from air, we demonstrate the low-pressure (1–2 bar) hydroxylation of alkanes, notably ethane to acetic acid, and the ozone like cleavage of the carbon–carbon double bonds of alkenes. Typical ...
               
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