Homogeneous and Semi-Heterogeneous Magnetically Retrievable Bis-N-Heterocyclic Carbene Rhodium(I) Based Catalysts for Selective Hydroaminomethylation Reactions

The preparation of various bis‐N‐heterocyclic carbene (bis‐NHC) complexes of rhodium and their application in the hydroaminomethylation of vinyl arenes was investigated. Various reaction parameters such as solvent, temperature, and pressure were tested, and the optimized protocol was applied to a wi...

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Veröffentlicht in:European journal of organic chemistry 2015-03, Vol.2015 (9), p.1961-1969
Hauptverfasser: Dutta, Bishnu, Schwarz, Rony, Omar, Suheir, Natour, Suzana, Abu-Reziq, Raed
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Sprache:eng
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Zusammenfassung:The preparation of various bis‐N‐heterocyclic carbene (bis‐NHC) complexes of rhodium and their application in the hydroaminomethylation of vinyl arenes was investigated. Various reaction parameters such as solvent, temperature, and pressure were tested, and the optimized protocol was applied to a wide variety of vinyl arenes and amines to afford the corresponding amines in good yields with high selectivity towards the branched product. The bis‐NHC‐based catalyst demonstrated superior reactivity and selectivity compared to catalysts containing bidentate phosphine or monodentate NHC ligands. A triethoxysilyl‐functionalized bis‐NHC ligand was immobilized on magnetic nanoparticles and then utilized to bind a rhodium catalyst. The resulting catalytic system was successfully employed in hydroaminomethylation reactions. The catalyst exhibited excellent reactivity, high selectivity, and was simply recovered from the reaction medium by applying an external magnetic field. Various bis‐N‐heterocyclic carbene (bis‐NHC) ligands are prepared and complexed with rhodium(I). Some of these complexes show excellent reactivity and high selectivity in homogeneous hydroaminomethylation reactions. A bis‐NHC ligand derivative is supported on magnetite nanoparticles and after complexation with RhI is was applied successfully in semi‐heterogeneous hydroaminomethylations.
ISSN:1434-193X
1099-0690
DOI:10.1002/ejoc.201403526