Hydrogen Bonding Enhances the Electrochemical Hydrogenation of Benzaldehyde in the Aqueous Phase
Udishnu Sanyal, Simuck F. Yuk, Katherine Koh, Mal‐Soon Lee, Kelsey A. Stoerzinger, Difan Zhang, Laura C. Meyer, Juan A. Lopez‐Ruiz, Abhi Karkamkar, Jamie D. Holladay, Donald M. Camaioni, Manh‐Thuong Nguyen, Vassiliki‐Alexandra Glezakou, Roger Rousseau, Oliver Y. Gutiérrez, Johannes A. Lercher
Abstract
The hydrogenation of benzaldehyde to benzyl alcohol on carbon-supported metals in water, enabled by an external potential, is markedly promoted by polarization of the functional groups. The presence of polar co-adsorbates, such as substituted phenols, enhances the hydrogenation rate of the aldehyde by two effects, that is, polarizing the carbonyl group and increasing the probability of forming a transition state for H addition. These two effects enable a hydrogenation route, in which phenol acts as a conduit for proton addition, with a higher rate than the direct proton transfer from hydronium ions. The fast hydrogenation enabled by the presence of phenol and applied potential overcompensates for the decrease in coverage of benzaldehyde caused by competitive adsorption. A higher acid strength of the co-adsorbate increases the intensity of interactions and the rates of selective carbonyl reduction.