Search results for "gold clusters"

showing 9 items of 9 documents

Towards Atomically Precise Supported Catalysts from Monolayer‐Protected Clusters: The Critical Role of the Support

2020

Abstract Controlling the size and uniformity of metal clusters with atomic precision is essential for fine‐tuning their catalytic properties, however for clusters deposited on supports, such control is challenging. Here, by combining X‐ray absorption spectroscopy and density functional theory calculations, it is shown that supports play a crucial role in the evolution of monolayer‐protected clusters into catalysts. Based on the acidic nature of the support, cluster‐support interactions lead either to fragmentation of the cluster into isolated Au–ligand species or ligand‐free metallic Au0 clusters. On Lewis acidic supports that bind metals strongly, the latter transformation occurs while pre…

010402 general chemistry01 natural sciencesgold clustersNanomaterials | Hot PaperCatalysiskultaCatalysisNanomaterialsmonolayer-protected clustersMetalklusteritnoncovalent interactionskatalyytitMonolayerCluster (physics)Non-covalent interactionschemistry.chemical_classificationX-ray absorption spectroscopyFull Paper010405 organic chemistryOrganic ChemistryX-ray absorption spectroscopyGeneral ChemistryFull Papersgold0104 chemical sciencesX-Ray Absorption SpectroscopychemistryChemical physicsvisual_artdensity functional calculationsvisual_art.visual_art_mediumDensity functional theorynanohiukkasetcluster-support interactionChemistry (Weinheim an Der Bergstrasse, Germany)
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Stabilized Naked Sub-nanometric Cu Clusters within a Polymeric Film Catalyze C-N, C-C, C-O, C-S, and C-P Bond-Forming Reactions

2015

[EN] Sub-nanometric Cu clusters formed by endogenous reduction of Cu salts and Cu nanoparticles are active and selective catalysts for C−N, C−C, C−O, C−S, and C−P bond-forming reactions. Sub-nanometric Cu clusters have also been generated within a polymeric film and stored with full stability for months. In this way, they are ready to be used on demand and maintain high activity (TONs up to 104 ) and selectivity for the above reactions. A potential mechanism for the formation of the sub-nanometric clusters and their electronic nature is presented.

ARYL HALIDESTECNOLOGIA DE ALIMENTOSDIAMINE LIGANDSULLMANNHeterogeneous catalysisBiochemistryCatalysisCoupling reactionCatalysisMECHANISMSColloid and Surface ChemistryQUIMICA ORGANICAOn demandPolymer chemistryOxidationHigh activityOrganic chemistryPotential mechanismTEMPERATURECu nanoparticlesChemistryGeneral ChemistryHETEROGENEOUS CATALYSISCROSS-COUPLING REACTIONSGOLD CLUSTERSSelectivityCOPPER CLUSTERS
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Electrocrystallization of Monolayer-Protected Gold Clusters : Opening the Door to Quality, Quantity, and New Structures

2017

Thiolate-protected metal clusters are materials of ever-growing importance in fundamental and applied research. Knowledge of their single-crystal X-ray structures has been instrumental to enable advanced molecular understanding of their intriguing properties. So far, however, a general, reliable, chemically clean approach to prepare single crystals suitable for accurate crystallographic analysis was missing. Here we show that single crystals of thiolate-protected clusters can be grown in large quantity and very high quality by electrocrystallization. This method relies on the fact that charged clusters display a higher solubility in polar solvents than their neutral counterparts. Nucleation…

ChemistryChemistry (all)Nucleation02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyCatalysis; Chemistry (all); Biochemistry; Colloid and Surface Chemistry01 natural sciencesBiochemistrygold clustersCatalysis0104 chemical sciencesCrystallographyColloid and Surface ChemistryQuality (physics)Chemical physicsElectrodeMonolayerCluster (physics)PolarSolubility0210 nano-technologyta116Metal clusters
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Induced Chirality in Confined Space on Halogen Gold Complexes

2015

The solubilization of HAuCl4 in toluene within optically active reverse micelles and lamellar structures formed by (1R,2S)-Dodecyl(2-hydroxy-1-methyl-2-phenylethyl)- dimethylammonium bromide (DMEB) has allowed us to evidence the complex phenomenology accompanying the confinement of Au salt within these nanostructures. Together with a chloride/bromide exchange process occurring in the first coordination sphere of an Au ion, UV−vis and electronic circular dichroism (ECD) spectra reveal the appearance of an induced dichroic signal attributable to Au complexes entrapped in the hydrophilic domain of the DMEB chiral nanostructures. Interestingly, change of the effective oxidation state and coordi…

Circular dichroismSupramolecular chiralityCoordination spherechirality confined space DMEBPhotochemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundGeneral EnergychemistryBromideRAY-ABSORPTION SPECTROSCOPY; BODY DISTRIBUTION-FUNCTIONS; NEAR-EDGE STRUCTURE; STABILIZED MICROEMULSIONS; SUPRAMOLECULAR CHIRALITY; CINCHONIDINE ADSORPTION; ELECTRONIC-STRUCTURES; CHIROPTICAL ACTIVITY; UNDECAGOLD CLUSTERS; CONDENSED MATTERPhysical and Theoretical ChemistryAbsorption (chemistry)SpectroscopyChirality (chemistry)Settore CHIM/02 - Chimica FisicaCoordination geometryThe Journal of Physical Chemistry C
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Exploring the atomic structure of 1.8 nm monolayer-protected gold clusters with aberration-corrected STEM

2017

Abstract Monolayer-protected (MP) Au clusters present attractive quantum systems with a range of potential applications e.g. in catalysis. Knowledge of the atomic structure is needed to obtain a full understanding of their intriguing physical and chemical properties. Here we employed aberration-corrected scanning transmission electron microscopy (ac-STEM), combined with multislice simulations, to make a round-robin investigation of the atomic structure of chemically synthesised clusters with nominal composition Au 144 (SCH 2 CH 2 Ph) 60 provided by two different research groups. The MP Au clusters were “weighed” by the atom counting method, based on their integrated intensities in the high …

Icosahedral symmetrymonolayer-Protected Gold Clusters02 engineering and technology010402 general chemistry01 natural sciencesMolecular physicsatomic structureatom counting methodMonolayerScanning transmission electron microscopyAu144(SR)60ta116InstrumentationQuantumaberration-Corrected STEMRange (particle radiation)ta114Chemistry021001 nanoscience & nanotechnologyDark field microscopyAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic MaterialsAmorphous solidExponentAtomic physics0210 nano-technologyUltramicroscopy
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Role of Donor and Acceptor Substituents on the Nonlinear Optical Properties of Gold Nanoclusters

2018

In recent years, a large number of monolayer-protected clusters (MPCs) have been studied by means of single crystal structure characterization. A central aspect of research on MPCs is the correlation of their interesting optical properties with structural features and the formulation of a theoretical framework that allows interpretation of their unique properties. For this, superatom and jellium models have been proven successful. Little attention, however, has been paid to the influence of the protecting ligands. Here, we investigate the effect of changes in [Au25(SR)18-x(SR′)x]−, where SR′ represents a para-substituted thiophenolate derivative (SPh-4-X). We computed the first hyperpolariz…

Materials scienceJelliumnanoclustersSubstituent02 engineering and technology010402 general chemistrygold clusters01 natural sciencesmonolayer-protected clustersNanoclusterschemistry.chemical_compoundPhysical and Theoretical Chemistryta116ta114ThiophenolSuperatomgoldOrders of magnitude (numbers)021001 nanoscience & nanotechnologyAcceptor0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyGeneral Energychemistry0210 nano-technologySingle crystalThe Journal of Physical Chemistry C
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A magnetic look into the protecting layer of Au25 clusters

2016

The field of molecular metal clusters protected by organothiolates is experiencing a very rapid growth. So far, however, a clear understanding of the fine interactions between the cluster core and the capping monolayer has remained elusive, despite the importance of the latter in interfacing the former to the surrounding medium. Here, we describe a very sensitive methodology that enables comprehensive assessment of these interactions. Pulse electron nuclear double resonance (ENDOR) was employed to study the interaction of the unpaired electron with the protons of the alkanethiolate ligands in four structurally related paramagnetic Au25(SR)0 18 clusters (R ¼ ethyl, propyl, butyl, 2-methylpro…

molecular metal clusterselectronic distributionkemiaIcosahedral symmetryAnalytical chemistry02 engineering and technologychemistry010402 general chemistrygold clusters01 natural sciencesSpectral lineAu25ParamagnetismMolecular dynamicsNMR spectroscopyMonolayerthiolate-cappedCluster (physics)ta116Electron nuclear double resonanceChemistryChemistry (all)paramagnetic gols nanoclustersGeneral ChemistryENDOR spectroscopy021001 nanoscience & nanotechnology0104 chemical sciencesUnpaired electronChemical physics0210 nano-technology
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The Role of Donor and Acceptor Substituents on the Nonlinear Optical Properties of Gold Nanoclusters

2018

In recent years, a large number of monolayer-protected clusters (MPCs) have been studied by means of single crystal structure characterization. A central aspect of research on MPCs is the correlation of their interesting optical properties with structural features and the formulation of a theoretical framework that allows interpretation of their unique properties. For this, superatom and jellium models have been proven successful. Little attention, however, has been paid to the influence of the protecting ligands. Here, we investigate the effect of changes in [Au25(SR)18-x(SR′)x]−, where SR′ represents a para-substituted thiophenolate derivative (SPh-4-X). We computed the first hyperpolariz…

nanoclustersgold clusterskultamonolayer-protected clusters
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Symmetry breaking in ligand-protected gold clusters probed by nonlinear optics

2016

The first hyperpolarizabilities of [Au25(SR)18](-1/0) and Au38(SR)24 clusters were determined by Hyper-Rayleigh Scattering. A strong dependence on the molecular symmetry was observed, and we explore two strategies to destroy the center of inversion in [Au25(SR)18](-1/0), protection by chiral ligands and alloying of the cluster with silver. This may open new avenues to applications of Au : SR clusters in second-order nonlinear optics.

ta114Condensed matter physicsligandsChemistryScatteringLigandnonlinear opticsNonlinear optics02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologygold clusters01 natural sciencesMolecular physics0104 chemical sciencesmolecular symmetryMolecular symmetryCluster (physics)General Materials ScienceSymmetry breaking0210 nano-technologyta116Nanoscale
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