Synergistic C─N Coupling for Efficient Cyclohexanone Oxime Synthesis from Ambient Air by Supported Molecular Catalysts

Abstract Electrocatalytic synthesis of cyclohexanone oxime from rich nitrogen resources is a promising alternative to traditional industrial processes. However, the difficulties in unraveling atomic‐scale catalytic mechanisms and managing selective C─N coupling still pose great challenges to realizing considerable yield and selectivity, and therefore rational catalyst design to boost collaborative C─N coupling for oxime synthesis is particularly attractive. In the present work, molecular catalysts are demonstrated to be unique for oxime synthesis under mild conditions, i. e. , iron bis (pyridyl) amine‐bipyridine (FeBPAbipyH) modified MWCNTs@CP (multi‐walled carbon nanotubes coated carbon fiber paper) cathodes produced cyclohexanone oxime from NO 2 − and cyclohexanone, attaining mass‐specific efficiency of 87. 00 mg h −1 cm −2 mg cat −1, Faradaic efficiency (FE) of 77. 3%, and exclusive carbon selectivity, which is the best efficiency known to date in H‐cell. Mechanistic studies showed that the FeBPAbipyH molecular skeleton exhibited intimate interaction with both cyclohexanone and NO 2 −, and catalyzed selective NO 2 − ‐to‐NH 2 OH reduction for C─N bond in situ. The in‐depth understanding of substrate‐catalyst interactions and synergic C─N coupling from molecular points of view offers valuable insights to boost collaborative synthesis of organic nitrogen compounds. Further integrating plasma‐driven N 2 oxidation and electrocatalysis enabled cyclohexanone oxime formation at 61. 73 mg h −1 cm −2 mg cat −1 on the FeBPAbipyH/MWCNTs@CP electrode, and the whole synthetic and separation process is projected to be profitable with a promising cost of 2709 ton −1, which is much lower than the breakeven point (∼10 000 ton −1), representing a sustainable pathway to nitrogenous chemical synthesis from abundant resources under ambient conditions.