4.8 Article

Mechanistic interpretation of selective catalytic hydrogenation and isomerization of alkenes and dienes by ligand deactivated Pd nanoparticles

期刊

NANOSCALE
卷 7, 期 42, 页码 17786-17790

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c5nr05090a

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  1. National Institute of General Medical Science [SC3GM089562]
  2. W. M. Keck Foundation

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Unsupported thiolate-capped palladium nanoparticle catalysts are found to be highly substrate-selective for alkene hydrogenation and isomerization. Steric and poisoning effects from thiolate ligands on the nanoparticle surface control reactivity and selectivity by influencing alkene adsorption and directing either di-sigma or mono-sigma bond formation. The presence of overlapping p orbitals and a protons in alkenes greatly influences the catalytic properties of deactivated palladium nanoparticles leading to easily predictable hydrogenation or isomerization products.

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