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Effect of electronic structures of Au clusters stabilized by poly(N-vinyl-2-pyrrolidone) on aerobic oxidation catalysis.

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TLDR
It is proposed that electron transfer from the anionic Au cores of Au:PVP into the LUMO (pi*) of O(2) generates superoxo- or peroxo -like species, which plays a key role in the oxidation of alcohol.
Abstract
Au clusters smaller than 1.5 nm and stabilized by poly(N-vinyl-2-pyrrolidone) (PVP) showed higher activity for aerobic oxidation of alcohol than those of larger size or stabilized by poly(allylamine) (PAA). X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy of adsorbed CO, and X-ray absorption near edge structure measurements revealed that the catalytically active Au clusters are negatively charged by electron donation from PVP, and the catalytic activity is enhanced with increasing electron density on the Au core. Based on similar observations of Au cluster anions in the gas phase, we propose that electron transfer from the anionic Au cores of Au:PVP into the LUMO (pi*) of O(2) generates superoxo- or peroxo-like species, which plays a key role in the oxidation of alcohol. On the basis of these results, a simple principle is presented for the synthesis of Au oxidation catalysts stabilized by organic molecules.

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Atomically Precise Colloidal Metal Nanoclusters and Nanoparticles: Fundamentals and Opportunities

TL;DR: This review summarizes the major progress in the field, including the principles that permit atomically precise synthesis, new types of atomic structures, and unique physical and chemical properties ofatomically precise nanoparticles, as well as exciting opportunities for nanochemists to understand very fundamental science of colloidal nanoparticles.
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Atomically Precise Clusters of Noble Metals: Emerging Link between Atoms and Nanoparticles

TL;DR: Luminescence in the visible region, especially by clusters protected with proteins, with a large Stokes shift, has been used for various sensing applications, down to a few tens of molecules/ions, in air and water.
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Quantum sized, thiolate-protected gold nanoclusters

TL;DR: Recent research advances have opened an avenue to achieving the precise control of Au(n)(SR)(m) nanoclusters at the ultimate atomic level, and may stimulate a long-lasting and wider scientific and technological interest in this special type of Au nanoparticles.
Journal ArticleDOI

Gold-catalyzed carbon-heteroatom bond-forming reactions.

TL;DR: Application to Total Synthesis 1699 6.1.
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Atomically Precise Noble Metal Nanoclusters as Efficient Catalysts: A Bridge between Structure and Properties.

TL;DR: The model catalyst role of NCs in catalysis is illustrated from theoretical and experimental perspectives, particularly in electrocatalysis, photocatalysis, photoelectric conversion, and catalysis of organic reactions.
References
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Journal ArticleDOI

Novel Gold Catalysts for the Oxidation of Carbon Monoxide at a Temperature far Below 0 °C

TL;DR: In this article, a variety of gold catalysts are used to catalyze the oxidation of carbon monoxide at temperatures as low as −70 °C and are stable in a moistened gas atmosphere.
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Supported gold nanoparticles as catalysts for organic reactions

TL;DR: This critical review is intended to attract the interest of organic chemists and researchers on green and sustainable chemistry on the catalytic activity of supported gold nanoparticles in organic transformations.
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Glutathione-Protected Gold Clusters Revisited: Bridging the Gap between Gold(I)−Thiolate Complexes and Thiolate-Protected Gold Nanocrystals

TL;DR: It is proposed that a series of the isolated Au:SG clusters corresponds to kinetically trapped intermediates of the growing Au cores, and it is revealed that the subnanometer-sized Au clusters thiolated constitute a distinct class of binary system which lies between the Au(I)-thiolate complexes and thiolate-protected Au NCs.
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Charging Effects on Bonding and Catalyzed Oxidation of CO on Au8 Clusters on MgO

TL;DR: Infrared measurements of the stretch vibration of CO adsorbed on mass-selected gold octamers soft-landed on MgO(001) with coadsorbed O2 show a red shift on an F-center–rich surface with respect to the perfect surface, agreeing with quantum ab initio calculations that predict this shift should arise via electron back-donation to the CO antibonding orbital.
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Selective oxidation with dioxygen by gold nanoparticle catalysts derived from 55-atom clusters

TL;DR: The observations suggest that catalytic activity arises from the altered electronic structure intrinsic to small gold nanoparticles, and that the use of 55-atom gold clusters may prove a viable route to the synthesis of robust gold catalysts suited to practical application.
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