ABSTRACT
Invited for this month's cover is the group of Prof. Mahito Atobe at Yokohama National University, Japan. The image shows an anion-exchange membrane (AEM) reactor enabling selective oxidation of a primary alcohol to a corresponding aldehyde by the electrochemical reaction at the triple-phase boundary. The Communication itself is available at 10.1002/cssc.202102076.
ABSTRACT
Oxidation of primary alcohol to the corresponding aldehyde remains a significant challenge, even with the state-of-the-art chemistry. Here, a novel electrochemical system was developed for the exclusive production of aldehyde from primary alcohol using an anion-exchange membrane (AEM) reactor. Oxidation proceeded on a gold catalyst under basic conditions, which largely enhanced the reaction rate. Despite the basic nature around the reaction sites, the oxidation of primary alcohols exclusively yielded the corresponding aldehyde, which was attributed to the unique three-phase interfacial reaction sites in the AEM reactor. In addition to benzyl alcohol, the oxidation of allylic and aliphatic alcohols was also demonstrated. Comparison of constant potential electrolysis with the AEM reactor or a conventional batch-type cell revealed the crucial role of the triple-phase boundary for the selectivity of the oxidation of alcohol.
ABSTRACT
The highly efficient chemoselective electrocatalytic hydrogenation of benzoic acids (BAs) to cyclohexanecarboxylic acids (CCAs) was carried out in a proton-exchange membrane reactor under mild conditions without hydrogenation of the carboxyl group. Among the investigated catalysts, the PtRu alloy catalyst was found to be the most suitable for achieving high current efficiencies for production of CCAs. An electrochemical spillover mechanism on the PtRu alloy catalyst was also proposed.
