4.2 Article

Chemoselective hydrogenation of α,β-unsaturated aldehydes on hydrogenated MoOx nanorods supported iridium nanoparticles

Journal

JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
Volume 425, Issue -, Pages 248-254

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.molcata.2016.10.016

Keywords

Hydrogenated molybdenum oxides; Iridium; Metal-support interactions; Chemoselective hydrogenation; alpha,beta-unsaturated aldehydes

Funding

  1. National Basic Research Program of China [2013CB934101]
  2. National Natural Science Foundation of China [21373102, 21433002, 51671089, 51402110]
  3. Guangdong Natural Science Funds for Distinguished Young Scholar [2015A030306014]
  4. Guangdong Program for Support of Top-notch Young Professionals [2014TQ01N036]
  5. Guangdong Higher Education Institute [YQ2013022]
  6. Fundamental Research Funds for the Central Universities [21615402]

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As reducible supports, metal oxides present the varied charge effect after hydrogen doping and partial reduction, accomplishing the tunable metal-support interactions and the promoted catalytic turnover in heterogeneous catalysis. Herein, the one-pot fabrication of hydrogenated MoOx (H-MoOx) nanorods supported Ir (Ir/H-MoOx) was developed, which simultaneously combined the generation of active centers (Ir) and the hydrogen doping on supports (H-MoOx). Because of the accumulated electrons around MoO6 octahedras after hydrogen doping, the electronic perturbations arising from H-MoOx supports led to the negatively charge Ir delta- species being beneficial for the selective hydrogenation of C=O moiety in alpha,beta-unsaturated aldehydes. In the hydrogenation of cinnamaldehyde to cinnamyl alcohol, Ir/H-MoOx delivered selectivity as high as 93%, performing among the best of current metal-based catalysts. Additionally, the efficacy for various substrates with multiple groups further verified our Ir/H-MoOx system to be competitive for chemoselective hydrogenation. (C) 2016 Elsevier B.V. All rights reserved.

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