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Heterogeneous Enantioselective Catalysis with Chiral Encoded Mesoporous Pt−Ir Films Supported on Ni Foam
Authors:Dr Sunpet Assavapanumat  Sopon Butcha  Dr Somlak Ittisanronnachai  Prof Dr Alexander Kuhn  Asst Prof Dr Chularat Wattanakit
Institution:1. School of Energy Science and Engineering, School of Molecular Science and Engineering, Frontier Research Center (FRC), Nanocatalysts and Nanomaterials for Sustainable Energy and Environment Research Network of NANOTEC, Vidyasirimedhi Institute of Science and Technology (VISTEC), 21210 Rayong, Thailand;2. School of Energy Science and Engineering, School of Molecular Science and Engineering, Frontier Research Center (FRC), Nanocatalysts and Nanomaterials for Sustainable Energy and Environment Research Network of NANOTEC, Vidyasirimedhi Institute of Science and Technology (VISTEC), 21210 Rayong, Thailand

University of Bordeaux, CNRS, UMR 5255, Bordeaux INP, Site ENSCBP, 16 avenue Pey Berland, 33607 Pessac, France

Abstract:The development of heterogeneous catalysts for asymmetric synthesis is one of the most challenging topics in chemistry, as it allows obtaining enantiomerically pure compounds. Recently, metal layers incorporating molecular chiral cavities, obtained by electroreduction of a metal source in the simultaneous presence of a non-ionic surfactant and asymmetric molecules, have been proposed for a wide range of applications, including enantioselective electroanalysis and electrosynthesis, as well as chiral separation. In contrast to this previous work, solely based on electrochemical phenomena, herein we designed and employed nanostructured chiral encoded Pt−Ir alloys, supported on high surface area nickel foams, as heterogeneous catalysts for the asymmetric hydrogenation of aromatic ketones. Fine-tuning the experimental conditions allows achieving very high enantioselectivity (>80%), combined with improved catalyst stability.
Keywords:Chiral imprinted on Ni foam  asymmetric synthesis  chiral encoded mesoporous alloy  heterogeneous catalyst  pulsed synthesis
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