A Heterodimeric Cluster‐Based Pair Catalyst for Electrochemical Synthesis of Cyclohexanone Oxime
Tongxin Song, Chenyang Shen, Yi-Qi Tian, Qingxi Zhai, Shisi Tang, Yan Zhu
Abstract
Abstract Heterogeneous catalysts are complex chemical ecosystems, where various functional units execute their individual responsibilities to together complete a catalysis ensemble. Here, we report a dinuclear catalyst originated from two molecular‐purity monomers including an atomically precise Ag 4 Pd 2 (SR) 8 cluster and a polyoxotitanium Ti 4 O 2 (TBC[4]) 2 ( i PrO) 4 cluster that are eventually paired off by the bridging sulfur. The heterodimeric catalyst with a unique interface consisted of the Ti─S─metal (metal = Pd and Ag) motifs exhibits selective recognition for nitrogen sources, thereby achieving high performances for the electrochemical synthesis of cyclohexanone oxime. The nitrate is favorably deoxygenated on the metal sites to generate nitrite, followed by the flipping of nitrite at the Ti─S─metal interface and the stepwise reduction of nitrite on the Ti site to produce hydroxylamine. Sequentially, a spontaneous coupling from hydroxylamine and cyclohexanone proceeds to construct the C═N bond for cyclohexanone oxime. Using this combination of distinct functional modules into one catalyst, we develop a strategy for heterogeneous catalysts being designed to increase the substrate conversion while simultaneously increasing the target product selectivity.