Selective Hydrogenation of Heteroarenes Using Supported Ruthenium Phosphide Nanoparticle Catalysts
Hooman Ghazi Zahedi1,2, Jannis Hertel1, Bhaskar Paul1
1Max Planck Institute for Chemical Energy Conversion, Stiftstrasse 34-36, 45470 Mülheim an der Ruhr, Germany.
Abstract:
The selective hydrogenation of heteroarenes, including quinolines, indoles, benzofurans, and benzothiophenes, to the corresponding aromatic compounds is enabled by ruthenium phosphide nanoparticles on imidazolium-based supported ionic liquid phases, RuxP100-x@SILP, as catalysts. The organometallic approach to the synthesis and immobilization of ruthenium phosphide nanoparticles (NPs) allows preparation under mild wet-chemistry conditions and systematic variation of the Ru/P ratio. The novel materials are characterized using various techniques, including electron microscopy and X-ray spectroscopies, and are found to be highly active, selective, and robust for application under batch and continuous flow conditions. The synthetic potential of Ru50P50@SILP as the most promising catalyst is demonstrated for a wide variety of substrates, enabling the synthesis of valuable drug molecules (e.g., cuspareine and salsolidine) and providing access to useful synthons including isotope labeling for fine chemicals and pharmaceuticals.
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