The H-Pd···N-H metal-ligand dual-atom sites synergistically catalyzed alkyne semi-hydrogenation with complete Z-selectivity
Abstract
In single-atom catalysts, the coordination microenvironment surrounding transition-metal centers is widely recognized as a key factor shaping their electronic structures and geometries, thereby governing catalytic behaviors. However, the synergetic catalysis between metal center and ligating atoms remains underexplored in single-atom catalysis. Herein, we construct the Pd(II)-N4 sites on carbon nitride to achieve photocatalytic semi-hydrogenation of alkynes. Under light irradiation, the Pd-N sites could transform to H-Pd···N-H moieties. The Pd-H center enhances alkyne insertion while the adjacent N-H group facilitates intramolecular proton transfer. This metal-ligand cooperativity of H-Pd···N-H sites, together with the steric-hindrance imposed by carbon nitride scaffold, lowers the energy barrier for Z-alkene formation and ensures exclusive stereoselectivity. Simultaneously, the H-Pd···N-H sites exhibit stronger adsorption toward alkynes than alkenes, effectively suppressing over-hydrogenation to alkanes. Across all evaluated substrates, Z-alkenes are the only isomers detected, excluding E-isomer and alkane. Notably, in a 5:95 mixture of diphenylacetylene and Z-stilbene, this method selectively converts only the alkyne to the Z-isomer without over-hydrogenation, highlighting its potential for product purification. Metal–ligand synergistic catalysis remains underexplored in single-atom systems. Here, inspired by homogeneous pincer complexes, the authors construct Pd(II)–N₄ sites on carbon nitride, enabling highly selective photocatalytic semi-hydrogenation of alkynes.
Fields of Study & Subjects
Catalytic C–H Functionalization Methods
Asymmetric Hydrogenation and Catalysis
Radical Photochemical Reactions
Publication details
- Journal / source
- Nature Communications
- Publisher
- Springer Science and Business Media LLC
- Volume
- 17
- Issue
- 1
- Publication date
- 23 January 2026
- Language
- EN