Journal
JOURNAL OF COORDINATION CHEMISTRY
Volume -, Issue -, Pages -Publisher
TAYLOR & FRANCIS LTD
DOI: 10.1080/00958972.2021.1974011
Keywords
Palladium nanocatalyst; linear thiol; Sonogashira reaction; styrene hydrogenation
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The ligand-free, copper-free Sonogashira coupling reaction and styrene hydrogenation catalysis by linear organic dodecanethiol stabilized palladium nanoparticles (PdTNPs) were studied. PdTNPs catalysts showed high catalytic activity for the Sonogashira reaction of iodobenzene with phenyl acetylene and the hydrogenation of styrene at room temperature, with excellent yield and recyclability.
Ligand-free, copper-free Sonogashira coupling reaction and styrene hydrogenation catalysis by linear organic dodecanethiol stabilized palladium nanoparticles (PdTNPs) were studied. At 70 degrees C and in the presence of piperidine, PdTNPs catalysts for Sonogashira reaction of iodobenzene with phenyl acetylene afforded 90% yield in 10 min under air/nitrogen atmosphere. PdTNPs catalysts also exhibit high catalytic activity for the hydrogenation of styrene at room temperature with excellent yield and recyclability.
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