Electrocatalytic Oxyesterification Of Hydrocarbons By Tetravalent Lead

The selective catalytic oxidative monofunctionalization of gaseous alkanes found in natural gas and commodity chemicals such as benzene and cyclohexane is an important objective in the field of carbon-hydrogen bond activation. Past research has demonstrated the possibility of stoichiometric oxyesterification of such substrates using lead(IV) trifluoroacetate (Pb-IV(TFA)(4)) as oxidant, which is driven by the high 2-electron redox potential of lead(IV). However, this redox potential then precludes reoxidation of lead(II) by a convenient oxidant such as O-2, nullifying an effective catalytic cycle. In order to utilize renewable energy resources as alternatives to high-temperature thermocatalysis, we demonstrate the room-temperature electrocatalytic oxyesterification of alkanes and benzene with Pb-IV(TFA)(4) as catalysts. At 1.67 V versus SHE, alkanes and benzene yielded the corresponding trifluoroacetate esters at room temperature; typically, good yields and high faradaic efficiencies were observed. High intrinsic turnover frequencies were obtained, for example, of >1000 min(-1) for the oxyesterification of ethane at 30 bar. An analysis of the possible mechanistic pathways based on previously investigated stochiometric reactions, cyclic voltammetry measurements, kinetic isotope effects, and model compounds led to the conclusion that catalysis involves lead-mediated proton-coupled electron transfer of alkanes at and to the anode, followed by reductive elimination through an S(N)2 reaction to yield the alkyl-TFA products. Similarly, lead-mediated electron transfer from benzene at and to the anode leads to phenyl-TFA. Cyclic voltammetry also shows the viability of in situ reoxidation of Pb(II) species. The synthesis results obtained as well as the mechanistic insight are important advances towards the realization of selective alkane and arene oxidation reactions.