Abstract
Solar-driven transfer hydrogenation of unsaturated bonds has received considerable attention in the research area of sustainable organic synthesis; however, water, the ultimate green source of hydrogen, has rarely been investigated due to the high barrier associated with splitting of water molecules. We report a carbon-nitride-supported palladium single-atom heterogeneous catalyst with unparalleled performance in photocatalytic water-donating transfer hydrogenation compared to its nanoparticle counterparts. Isotopic-labeling experiments and operando nuclear magnetic resonance measurements confirm the direct hydrogenation mechanism using in situ-generated protons from water splitting under visible-light irradiation. Density functional theory calculations attribute the high activity to lower barriers for hydrogenation, facilitated desorption of ethylbenzene, and facile hydrogen replenishment from water on the atomic palladium sites.
| Original language | English |
|---|---|
| Article number | e202207410 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 61 |
| Issue number | 40 |
| DOIs | |
| State | Published - 4 Oct 2022 |
Keywords
- Carbon Nitride
- Operando NMR
- Photocatalysis
- Single-Atom Catalysts
- Transfer Hydrogenation