Cu2O hydrides promote the selective semihydrogenation of alkynes on Pd-Cu2O/TiO2 under mild conditions

The selective semihydrogenation of alkynes is of importance in many industrial applications, but great challenges still remain in the full utilization of noble metals for the catalysis of hydrogen spillover on mixed supports. As Pd-0 is chemically loaded on Cu2O/TiO2, this work reports that Pd-0 is imparted with a high electron density to dissociate H-2 efficiently and the active Cu2O hydride is responsible for the high catalytic activity in spillover semihydrogenations. As compared with inert Pd-Cu2O/SiO2 interfaces, the studies demonstrate that the high chemoselectivity and stereoselectivity originate from the well-defined p-n junctions of Cu2O/TiO2, therein alkynes are adsorbed in their trans configurations and the product is desorbed from them. As catalyzed by 1.3Pd-3.6Cu(2)O/TiO2 in 1 atm H-2 at 30 degrees C, the semihydrogenations can be completed in 90 min with 97.6% chemoselectivity for phenylacetylene, and in 45 min with 92.4% stereoselectivity for methyl non-2-ynoate. These studies provide new ideas to design and synthesize noble metal-based catalysts through manipulating the interface properties of the mixed supports.

Automated summary

By chemically loading Pd-0 on Cu2O/TiO2, high electron density is imparted to Pd-0 for efficient H2 dissociation, while the active Cu2O hydride is responsible for the high catalytic activity in spillover semihydrogenations. Studies show that the well-defined p-n junctions of Cu2O/TiO2 contribute to high chemoselectivity and stereoselectivity, allowing for the adsorption of alkynes in their trans configurations and desorption of the product. The research provides new ideas for designing and synthesizing noble metal-based catalysts by manipulating the interface properties of mixed supports.