| Literature DB >> 25523894 |
Chun Wong Aaron Chan1, Abdul Hanif Mahadi1, Molly Meng-Jung Li1, Elena Cristina Corbos2, Chiu Tang3, Glenn Jones4, Winson Chun Hsin Kuo5, James Cookson2, Christopher Michael Brown2, Peter Trenton Bishop2, Shik Chi Edman Tsang1.
Abstract
Lindlar catalysts comprising of palladium/calcium carbonate modified with lead acetate and quinoline are widely employed industrially for the partial hydrogenation of alkynes. However, their use is restricted, particularly for food, cosmetic and drug manufacture, due to the extremely toxic nature of lead, and the risk of its leaching from catalyst surface. In addition, the catalysts also exhibit poor selectivities in a number of cases. Here we report that a non-surface modification of palladium gives rise to the formation of an ultra-selective nanocatalyst. Boron atoms are found to take residence in palladium interstitial lattice sites with good chemical and thermal stability. This is favoured due to a strong host-guest electronic interaction when supported palladium nanoparticles are treated with a borane tetrahydrofuran solution. The adsorptive properties of palladium are modified by the subsurface boron atoms and display ultra-selectivity in a number of challenging alkyne hydrogenation reactions, which outclass the performance of Lindlar catalysts.Entities:
Year: 2014 PMID: 25523894 DOI: 10.1038/ncomms6787
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919