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Updated: Dec 8, 2025

Development of Heterogeneous Enantioselective Catalysts using Chiral Metal-Organic Frameworks MOFs
Published on: January 17, 2020
Heterogeneous Single-Site Catalysts for C-H Activation Reactions: Pd(II)-Loaded S,O-Functionalized Metal
Niels Van Velthoven1, Yanhui Wang2, Hannah Van Hees1
1Centre For Membrane Separations, Adsorption, Catalysis and Spectroscopy for Sustainable Solutions (cMACS), KU Leuven, Celestijnenlaan 200F, P.O. Box 2461, 3001 Leuven, Belgium.
Abstract:
Heterogeneous single-site catalysts contain spatially isolated, well-defined active sites. This allows not only their easy recovery by solid-liquid separation but also the detailed active site design similar to homogeneous catalysts. Here, heterogeneous Pd(II) single-site catalysts were assembled, based on mesoporous metal oxide-bisphosphonate materials as supports. This new family of hybrid organic-inorganic materials with tunable porosity was further functionalized with thioether ligands containing S,O-binding sites that enhance the activity of Pd(II) for C-H activation reactions. The structures of the resulting Pd(II) single-site catalysts were carefully analyzed via solid-state NMR spectroscopy, via texture analysis by N2 physisorption, infrared spectroscopy, and transmission electron microscopy. Furthermore, the immediate environment of the isolated Pd(II) active sites was studied with X-ray absorption spectroscopy. A clear relationship between the thioether ligand surface density and catalyst activity could be established. Significantly higher yields were obtained using highly porous metal oxide-bisphosphonate materials as supports compared to materials with lower porosities, such as conventional metal oxides, indicating that the high surface area facilitates the presence of isolated, well-accessible S,O-supported Pd(II) active sites. A wide scope of model substrates, including industrially relevant arenes, can be converted with high yields by the optimal heterogeneous Pd catalyst.
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