Origins of solvent-induced enhancement in catalytic reactivity and product selectivity are discussed with computational methods to study them.

The utilization of low frequency ultrasound (US) offers a straightforward and powerful tool for the production of nanostructured materials, in particular for structurally stable, highly crystalline, and shape-controlled catalytic materials. Herein, we report an unconventional strategy for the synthesis of CuO nanoleaves within 5 min of US irradiation. The as-obtained CuO nanoleaves were found to be selective in the base-free aqueous oxidation of glycerol to dicarboxylic acids (78% yield of tartronic and oxalic acids), in the presence of hydrogen peroxide (H₂O₂) and under mild reaction conditions. Density Functional Theory (DFT) investigations revealed a synergy between the CuO catalyst and H₂O₂ in maintaining the structural integrity of the catalyst during the reaction, creating alternative efficient pathways for the selective formation of dicarboxylic acids. Isotope labeling experiments using H₂ ¹⁸O₂ further confirmed that oxygen from hydrogen peroxide, not from CuO, was preferentially incorporated into the dicarboxylic acid, significantly preserving the monoclinic structure of the CuO catalyst.