High-Density Palladium Single-Atom Catalysts for Photoinduced Tandem Decarbonylation/Carbonylative Reductive Coupling

In carbonylation reactions, a carbonyl source is typically required, often supplied by carbon monoxide (CO) gas or CO surrogates that release CO via decarbonylation. Herein, we report a novel carbonylative reductive coupling reaction utilizing pivaldehyde as a facile and cost-effective carbonyl source with water serving as an environmentally benign reductant. A polymeric carbon nitride semiconductor functionalized with high-density single-atom palladium was designed as a multifunctional catalytic system, simultaneously driving a cascade decarbonylation-CO migration-carbonylative coupling process while enabling photocatalytic water oxidation to supply electrons for the reductive coupling. Life cycle assessment analysis further supports the economic viability of our carbonylative reductive coupling strategy. The spatial proximity of Pd atoms is crucial in promoting efficient CO migration, and computational studies offer atomic-level insights into this high-density configuration in the reaction. The heterogeneous single-atom photocatalyst exhibits exceptional stability, maintaining its catalytic activity over 10 consecutive cycles with minimal loss in performance. The practical utility of this method was demonstrated through the efficient synthesis of pharmaceutical compounds, including a decagram-scale synthesis of AdipoRon in a high-speed circulation flow system. This work seamlessly integrates decarbonylation, photocatalytic water splitting, and reductive coupling reactions, underscoring the tremendous potential of single-atom photocatalysts in advancing sustainable cascade organic transformations.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-12-12
DOI
https://doi.org/10.1021/jacs.5c12630
Citations
2
Primary Topic
Advanced Photocatalysis Techniques
Type
article
Field-Weighted Citation Impact
0.73
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article

High-Density Palladium Single-Atom Catalysts for Photoinduced Tandem Decarbonylation/Carbonylative Reductive Coupling

Haolin Du, Qi Yu, Junli Ao, Jie Wu et al.
2 citations
Journal of the American Chemical Society
Advanced Photocatalysis Techniques
0.73
article

High-Density Palladium Single-Atom Catalysts for Photoinduced Tandem Decarbonylation/Carbonylative Reductive Coupling

Haolin Du, Qi Yu, Junli Ao, Jie Wu, Jun‐An Ma, Jiale Wu, Yucong Miao, Jun Li, Yang Shi, Kun Fu
article en
2 citations

Abstract

In carbonylation reactions, a carbonyl source is typically required, often supplied by carbon monoxide (CO) gas or CO surrogates that release CO via decarbonylation. Herein, we report a novel carbonylative reductive coupling reaction utilizing pivaldehyde as a facile and cost-effective carbonyl source with water serving as an environmentally benign reductant. A polymeric carbon nitride semiconductor functionalized with high-density single-atom palladium was designed as a multifunctional catalytic system, simultaneously driving a cascade decarbonylation-CO migration-carbonylative coupling process while enabling photocatalytic water oxidation to supply electrons for the reductive coupling. Life cycle assessment analysis further supports the economic viability of our carbonylative reductive coupling strategy. The spatial proximity of Pd atoms is crucial in promoting efficient CO migration, and computational studies offer atomic-level insights into this high-density configuration in the reaction. The heterogeneous single-atom photocatalyst exhibits exceptional stability, maintaining its catalytic activity over 10 consecutive cycles with minimal loss in performance. The practical utility of this method was demonstrated through the efficient synthesis of pharmaceutical compounds, including a decagram-scale synthesis of AdipoRon in a high-speed circulation flow system. This work seamlessly integrates decarbonylation, photocatalytic water splitting, and reductive coupling reactions, underscoring the tremendous potential of single-atom photocatalysts in advancing sustainable cascade organic transformations.

Journal of the American Chemical SocietyVol. 147(51)
Guiyang Medical University (CN), Tianjin University (CN), National University of Singapore (SG), Shaanxi University of Technology (CN), Southern University of Science and Technology (CN), Institute of Catalysis and Petrochemistry (RU), Carnegie Department of Plant Biology (US), State Key Laboratory of Synthetic Chemistry (CN), State Key Laboratory of Chemical Engineering (CN), Beijing University of Chemical Technology (CN), Tsinghua University (CN)
Openalex Percentile: Top 27%
Advanced Photocatalysis Techniques
0.73
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