This article presents the catalysis investigation of
octanethiolate-capped
palladium nanoparticles (C8 PdNP) and phenylethanethiolate-capped
palladium nanoparticles (PhC2 PdNP) for chemoselective catalytic hydrogenation
reactions of styrene derivatives in the presence of other reducible
functionalities. The results show that the C8 PdNP is highly active
under mild reaction conditions (room temperature and atmospheric pressure)
and selective for hydrogenating monosubstituted alkene groups without
reducing other reactive functional groups such as nitro, halo, carbonyls,
and so forth. In comparison, the noncovalent interactions between
surface phenyl ligands and aromatic substrates are found to hinder
the hydrogenation activity of PhC2 PdNP.