Enhancing the Chemo-Enzymatic One-Pot Oxidation of Cyclohexane via In Situ H2O2 Production over Supported Pd-Based Catalysts

The combination of an evolved unspecific peroxygenase (UPO), from Agrocybe aegerita (PaDa-I variant) and bimetallic Pd-based catalysts, is demonstrated to be highly effective for the one-pot oxidative valorization of cyclohexane to cyclohexanol and cyclohexanone (collectively KA oil), via the in situ formation of H2O2 from the elements. The alloying of Pd with Zn in particular is found to significantly enhance catalytic performance compared to bimetallic PdAu or monometallic Pd analogues. The improved activity of the PdZn/TiO2/PaDa-I system is attributed to the facile formation of PdZn alloys and the resulting electronic modification of Pd, which results in an inhibition of competitive chemo-catalyzed H(2)O(2 )degradation reactions and the total suppression of the overoxidation of cyclohexanol. By comparison, the large population of Pd-only clusters present in both the PdAu and monometallic Pd catalysts is considered to be responsible for the promotion of further oxidation products and the unselective conversion of H2O2 to H2O, which hampers overall process efficiency. Notably, given the susceptibility of the enzyme to deactivation at moderate H(2)O(2 )concentrations, the continual supply of low levels of the oxidant via in situ production represents a highly attractive alternative to the continuous addition of preformed H2O2 or co-enzyme-based systems.

Automated summary

The combination of an evolved unspecific peroxygenase (UPO) and bimetallic Pd-based catalysts is highly effective for the oxidative valorization of cyclohexane. Alloying Pd with Zn enhances catalytic performance, while the large population of Pd-only clusters in other catalysts promotes undesired oxidation products.