Bifunctional N-Doped Co@C Catalysts for Base-Free Transfer Hydrogenations of Nitriles: Controllable Selectivity to Primary Amines vs Imines

The transfer hydrogenation of nitriles is an important and alternative strategy to produce primary amines or imines, both of which play a crucial role in the synthesis of fine chemicals and pharmaceuticals. Nevertheless, developing highly active bifunctional catalyst system with controllable selectivity for these reactions still remains a huge challenge. In this study, we presented a bifunctional N-doped Co@C catalyst system (Co@NC) for the selective transfer hydrogenation of nitriles into either primary amines or imines. The Co@NC was prepared by the direct pyrolysis of an N-containing Co-MOF under an inert atmosphere, where the N-containing ligands could be transformed into highly graphitic N-doped carbon, endowing the catalysts with high-density special basic sites, while the Co' ions were reduced to uniform Co nanoparticles which were dispersed on or embedded in N-doped graphitic structures. Under base-free conditions with isopropyl alcohol as both proton donor and solvent, the optimized Co@NC-900 (obtained at 900 degrees C) catalyst could convert nitriles into primary amines or imines at will with surprising selectivities (mostly higher than 90%), depending on the solvent volume added to the reaction systems. Furthermore, a possible reaction mechanism was proposed. The N-derived basic sites on Co@NC could play a role similar to that of the base additives, which not only inhibit the formation of polyamine or prevent the products stacked on the surface of catalysts but also effectively promote the transfer hydrogenation of nitriles. The generated corresponding primary imines could controllably attack the primary imine intermediates to form imines by adjusting the concentration of Co@ NC. It is clear that this strategy offers a high-performance catalyst system for base-free transfer hydrogenations of nitriles to selectively produce primary amines vs imines.