Magnetically Recoverable Nanoparticles: Highly Efficient Catalysts for Asymmetric Transfer Hydrogenation of Aromatic Ketones in Aqueous Medium
Two magnetic chiral iridium and rhodium catalysts were prepared via directly postgrafting 1,2‐diphenylethylenediamine‐derived organic silica or 1,2‐cyclohexanediamine‐derived organic silica onto the silica‐coated iron oxide nanoparticles followed by complexation with iridium(III) or rhodium(III) com...
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Veröffentlicht in: | Advanced synthesis & catalysis 2011-05, Vol.353 (8), p.1317-1324 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Two magnetic chiral iridium and rhodium catalysts were prepared via directly postgrafting 1,2‐diphenylethylenediamine‐derived organic silica or 1,2‐cyclohexanediamine‐derived organic silica onto the silica‐coated iron oxide nanoparticles followed by complexation with iridium(III) or rhodium(III) complexes. During the asymmetric transfer hydrogenation of aromatic ketones in aqueous medium, the magnetic chiral catalysts exhibited high catalytic activities (up to 99% conversion) and enantioselectivities (up to 92% ee). Both catalysts could be recovered easily by magnetic separation and be reused ten times without significantly affecting their catalytic activities and enantioselectivities. |
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ISSN: | 1615-4150 1615-4169 1615-4169 |
DOI: | 10.1002/adsc.201100017 |