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Metal Nodes of Metal-Organic Frameworks can Activate Molecular Hydrogen
Authors:Dr. Arianna Melillo  Dr. Antonio Franconetti  Prof. Dr. Mercedes Alvaro  Prof. Dr. Belen Ferrer  Prof. Hermenegildo Garcia
Affiliation:1. Departamento de Química, Universitat Politècnica de València, Camino de Vera s/n, 46022 Valencia, Spain

Insituto Universitario de Tecnologia Química, Consejo Superior de Investigaciones Científicas-Universitat Politècnica de València, av. De los Naranjos s/n, 46022 Valencia, Spain;2. CIC BioGUNE, Bizkaia Science and Technology Park, Building 800, 48160 Derio, Bizkaia, Spain;3. Departamento de Química, Universitat Politècnica de València, Camino de Vera s/n, 46022 Valencia, Spain

Abstract:Hydrogenation of multiple bonds are among the most general and important organic reactions. Typical heterogeneous catalysts are based on transition metal nanoparticles, including noble metals. Data are presented here showing that metal nodes of MIL-101(Cr) and UiO-66 in the absence of occluded metal nanoparticles can promote hydrogenation of polarized X=Y double bonds of nitro and carbonyl groups. The catalytic activity is a function of the composition of the metal node and the organic linker. It is proposed that the reaction mechanism is based on the operation of frustrated Lewis acid/base pairs.
Keywords:catalytic hydrogenation  heterogeneous catalysis  metal-organic frameworks as catalysts  UiO-66 as hydrogenation catalyst
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