Radical intermediates in chloroform reactions over triphenylphosphine-protected Au nanoparticles

Marco Conte, Karen Wilson, Victor Chechik

Research output: Contribution to journalArticlepeer-review


Reactions of chloroform over triphenylphosphine-protected Au nanoparticles have been studied using electron paramagnetic resonance (EPR) spectroscopy and a spin trapping technique. Two competing reactions, abstraction of hydrogen and halogen atoms, were identified. The hydrogen abstraction reaction showed an inverse kinetic isotope effect. Treatment of nanoparticles with oxidizing or reducing reagents made it possible to tune the selectivity of radical formation from halogen to hydrogen (deuterium) abstraction. Treatment with PbO2 promoted the deuterium abstraction reaction followed by the loss of nanoparticle activity, whereas treatment with NaBH4 regenerated the nanoparticle activity towards Cl atom abstraction. X-ray photoelectron spectroscopy showed an increased Au:P ratio upon treatment with oxidizing reagents. This is likely due to the oxidation of some phosphine ligands to phosphine oxides which then desorb from the nanoparticle surface.
Original languageEnglish
Pages (from-to)1361-1367
Number of pages7
JournalOrganic and Biomolecular Chemistry
Issue number7
Early online date3 Feb 2009
Publication statusPublished - 2009


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