Nigra, Michael M. Ha, Jeong-Myeong Katz, Alexander 2024-01-20T11:04:48Z 2024-01-20T11:04:48Z 2021-08-31 2013-11 2044-4753 https://pubs.kist.re.kr/handle/201004/127523 The homogeneous versus heterogeneous nature of the active site of gold catalysis of the 4-nitrophenol reduction to 4-aminophenol is investigated using poisoning experiments that employ various organic ligands and 4 nm gold nanoparticles as catalysts. DDT (dodecanethiol)-bound gold nanoparticles are unable to catalyze this reaction, whereas nanoparticles capped with calixarene ligands consisting of calix[6] arene phosphine C6P and calix[4] arene thiol MBC are active. Poisoning of residual terrace sites upon addition of 2-naphthalenethiol (2-NT) in these latter two catalysts results in a gold nanoparticle that consists solely of ostensibly similar pinhole defect sites. However, the reaction rate for the catalyst consisting of C6P + 2-NT is 6.5-fold higher relative to the rate for catalyst consisting of MBC + 2-NT. This observation along with lack of activity for the DDT-bound catalyst suggests that pinhole defect sites and the gold nanoparticle surface cannot be the active site for catalysis. Instead, the active site is suggested to be a leached gold species that is present in exceedingly small concentrations (cannot be detected by disappearance of gold nanoparticles from solution during catalysis). Such a supposition is supported by observations of induction time and the interplay between observed induction time and kinetics. It is observed that the composition of the organic ligands in the system controls the kinetics and the induction time. Additionally, there is an absence of an induction time in a solution containing used catalyst, to which reactants are added. In the initial catalysis, it is observed that as the thiol ligand concentration on the surface increases, the induction time increases and the reaction rate decreases. The leached species were unable to be detected via changes in the surfaceplasmon resonance absorption of the gold nanoparticles in solution before and after catalysis, as well as electron microscopy studies of used nanoparticle catalysts. This suggests that the leached species concentration is low, and their catalytic activity in turn must be quite high. English ROYAL SOC CHEMISTRY METAL SIZE PLATINUM ACCESSIBILITY PARTICLES OXIDATION SILVER OXIDE CORE Identification of site requirements for reduction of 4-nitrophenol using gold nanoparticle catalysts Article 10.1039/c3cy00298e 1 CATALYSIS SCIENCE & TECHNOLOGY, v.3, no.11, pp.2976 - 2983 CATALYSIS SCIENCE & TECHNOLOGY 3 11 2976 2983 scie scopus 000325727500016 2-s2.0-84885631176 Chemistry, Physical Chemistry Article METAL SIZE PLATINUM ACCESSIBILITY PARTICLES OXIDATION SILVER OXIDE CORE gold nanoparticle catalyst hydrogenation calixarene