Search results for "Chemical physics"

showing 10 items of 2553 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)
researchProduct

Elucidating the Influence of the Activation Energy on Reaction Rates by Simulations Based on a Simple Particle Model

2020

An application for visualizing the dynamic properties of an equimolar binary mixture of isotropic reactive particles is presented. By introducing a user selectable choice for the activation energy, the application is useful to demonstrate qualitatively that the reaction rate depends on the above choice and on temperature. The application is based on a 2D realistic dynamic model where atoms move because of their thermal energies and the trajectories are determined by solving numerically Newton’s laws according to a Molecular Dynamics (MD) scheme. Collisions are monitored as time progresses, and every time the collision energy is larger than the selected activation energy, a reactive event oc…

010405 organic chemistry05 social sciencesIsotropyKinetics050301 educationBinary numberGeneral ChemistryActivation energy01 natural sciences0104 chemical sciencesEducationReaction rateHigh School/Introductory Chemistry First-Year Undergraduate/General Physical Chemistry Chemoinformatics Computer-Based Learning Kinetics Kinetic-Molecular TheorySimple (abstract algebra)Chemical physicsMolecule0503 educationEnergy (signal processing)Settore CHIM/02 - Chimica Fisica
researchProduct

A study on stabilization of HHeF molecule upon complexation with Xe atoms

2004

In the present work, we computationally study energetic stabilization of HHeF by its complexation with Xe atoms. For the studied HHeF ��� Xen systems ðn ¼ 1–4; 6Þ, we found a large complexation-induced decrease of energy of HHeF with respect to its dissociation into atoms. As a working hypothesis, we assume that this stabilization effect continues for the larger systems (n > 6) as well. This suggests that dissociation of HHeF via the H–He stretching coordinate might be suppressed and its lifetime might be increased by inserting it into large Xe clusters or matrices. 2004 Elsevier B.V. All rights reserved.

010405 organic chemistryChemistryChemical physicsGeneral Physics and AstronomyMoleculePhysical and Theoretical ChemistryAtomic physics010402 general chemistry01 natural sciencesDissociation (chemistry)0104 chemical sciencesChemical Physics Letters
researchProduct

The nature of interactions of benzene with CF3I and CF3CH2I

2019

In situ grown crystals of CF3I and CF3CH2I are dominated by I⋯I and F⋯F interactions. Their co-crystals with benzene, (CF3I)2·C6H6 and CF3CH2I·C6H6, contain two completely different sets of intermolecular interactions. (CF3I)2·C6H6 shows a unique halogen-bond type: above-the-bond C–I⋯πC6H6 interactions. CF3CH2I·C6H6 shows above-the-centre C–H⋯πC6H6 interactions. These interactions are electrostatically dominated type II halogen bonds between single halogenoalkane molecules and weaker dispersion dominated interactions between the co-crystal components. The observed preferences for benzene for the two binding partners match with calculated molecular electrostatic potentials.

010405 organic chemistryChemistryIntermolecular forceMetals and AlloysGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundChemical physicsHalogenMaterials ChemistryCeramics and CompositesMoleculeDispersion (chemistry)BenzeneChemical Communications
researchProduct

Theoretical Investigation of the Low-Energy States of CpMoCl(PMe 3 ) 2 and Their Role in the Spin-Forbidden Addition of N 2 and CO

2003

International audience; A recent computational investigation of Jahn−Teller effects in unsaturated 16-electron d4d6 [CpMLn] complexes (Abu-Hasanayn, F.; Cheong, P.; Oliff, M. Angew. Chem.2002, 41, 2120) highlighted the typical presence of two spin-triplet and two singlet states of competing stability in these complexes and pointed out the necessity to account for more than one electronic state in studies thereof. Consequently, we have reinvestigated the addition of N2 to all the four low-energy states of CpMoCl(PH3)2, a reaction for which previously only one singlet and one triplet state have been considered (Keogh, D. W.; Poli, R. J. Am. Chem. Soc.1997, 119, 2516). The present study was pe…

010405 organic chemistryChemistryState (functional analysis)010402 general chemistry01 natural sciencesQuantum mechanics0104 chemical sciencesElectronic statesAddition reactionsChemical calculations[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryLow energyChemical structureMathematical methodsDensity functional theory[CHIM.COOR]Chemical Sciences/Coordination chemistrySinglet statePhysical and Theoretical ChemistryAtomic physicsTriplet statePhysics::Chemical PhysicsSpin (physics)Ground state
researchProduct

Tuning the Electronic Properties of the Dative N-B Bond with Associated O-B Interaction: Electron Localizability Indicator from X-Ray Wavefunction Re…

2016

Despite the immense growth in interest in difluoroborate dyes, the nature of the interactions of the boron atom within the N-BF2 -O kernel is not yet fully understood. Herein, a set of real-space bonding indicators is used to quantify the electronic characteristics of the dative N-B bond in difluoroborate derivatives. The atoms-in-molecules (AIM) partitioning scheme is complemented by the electron localizability indicator (ELI-D) approach, and both were applied to experimental and theoretical electron-density distributions (X-ray constrained wavefunction fitting vs. DFT calculations). Additionally, Fermi orbital analysis was introduced for small DFT models to support and extend the findings…

010405 organic chemistryChemistryX-raychemistry.chemical_elementElectron010402 general chemistry01 natural sciencesQuantum chemistryAtomic and Molecular Physics and Optics0104 chemical sciencesChemical bondChemical physicsKernel (statistics)Physical and Theoretical ChemistryAtomic physicsWave functionBoronFermi Gamma-ray Space TelescopeChemphyschem : a European journal of chemical physics and physical chemistry
researchProduct

A Generalized Semiempirical Approach to the Modeling of the Optical Band Gap of Ternary Al-(Ga, Nb, Ta, W) Oxides Containing Different Alumina Polymo…

2021

A generalization of the modeling equation of optical band gap values for ternary oxides, as a function of cationic ratio composition, is carried out based on the semiempirical correlation between the differences in the electronegativity of oxygen and the average cationic electronegativity proposed some years ago. In this work, a novel approach is suggested to account for the differences in the band gap values of the different polymorphs of binary oxides as well as for ternary oxides existing in different crystalline structures. A preliminary test on the validity of the proposed modeling equations has been carried out by using the numerous experimental data pertaining to alumina and gallia p…

010405 organic chemistryGeneralizationChemistryBand gapCationic polymerizationThermodynamicsFunction (mathematics)Aluminum oxideComposition (combinatorics)010402 general chemistry01 natural sciencesArticleMixed oxides0104 chemical sciencesInorganic ChemistryCondensed Matter::Materials ScienceSettore ING-IND/23 - Chimica Fisica ApplicataBand GapPhysics::Atomic and Molecular ClustersPhysics::Chemical PhysicsPhysical and Theoretical ChemistryTernary operation
researchProduct

Water-Soluble Squaramide Dihydrates: N-Methylation Modulates the Occurrence of One- and Two-Dimensional Water Clusters through Hydrogen Bonding and D…

2018

Water confined in molecular size domains is distinct to bulk water. The altered interactions between adjacent water molecules, and between water molecules and molecular wall components of the confinement system, determine aspects of important phenomena in material science, biology, and nanotechnology. The structural determination of confined water, however, has proven to be challenging. Here, we describe the crystal structures of three related squaramides 1–3 whose molecular structures are modulated by the gradual incorporation of N-methyl groups to the squaramide moiety. The three squaramides differ in their hydrogen bonding capabilities due to the different degree of N-methylation of each…

010405 organic chemistryHydrogen bondChemistrySquaramideGeneral ChemistryCrystal structureN methylation010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical sciencesDipoleWater solubleChemical physicsMoleculeMoietyGeneral Materials ScienceCrystal Growth & Design
researchProduct

Room-Temperature Phosphorescence and Efficient Singlet Oxygen Production by Cyclometalated Pt(II) Complexes with Aromatic Alkynyl Ligands

2020

The synthesis of five novel cyclometalated platinum(II) compounds containing five different alkynyl-chromophores was achieved by the reaction of the previously synthesized Pt–Cl cyclometalated compound (1) with the corresponding RC≡CH by a Sonogashira reaction. It was observed that the spectral and photophysical characteristics of the cyclometalated platinum(II) complexes (Pt–Ar) are essentially associated with the platinum-cyclometalated unit. Room-temperature emission of the Pt–Ar complexes was attributed to phosphorescence in agreement with DFT calculations. Broad nanosecond (ns)-transient absorption spectra were observed with decays approximately identical to those obtained from the emi…

010405 organic chemistrySinglet oxygenPhosphorescenceluminesenssichemistry.chemical_elementkompleksiyhdisteetorganometalliyhdisteetOxigen010402 general chemistryLigands01 natural sciencesCombinatorial chemistry0104 chemical sciencesInorganic ChemistryOxygenchemistry.chemical_compoundhappiLligandschemistryFosforescènciaPhysical and Theoretical ChemistryPhysics::Chemical PhysicsPhosphorescencePlatinum
researchProduct

Controlling the Host-Guest Interaction Mode through a Redox Stimulus

2017

International audience; A proof-of-concept related to the redox-control of the binding/releasing process in a host-guest system is achieved by designing a neutral and robust Pt-based redox-active metallacage involving two extended-tetrathiafulvalene (exTTF) ligands. When neutral, the cage is able to bind a planar polyaromatic guest (coronene). Remarkably, the chemical or electrochemical oxidation of the host-guest complex leads to the reversible expulsion of the guest outside the cavity, which is assigned to a drastic change of the host-guest interaction mode, illustrating the key role of counteranions along the exchange process. The reversible process is supported by various experimental d…

010405 organic chemistryStereochemistrySupramolecular chemistryGeneral MedicineGeneral ChemistryReversible processself-assembly010402 general chemistryElectrochemistry01 natural sciencesRedoxsupramolecular cageCatalysisCoronene0104 chemical scienceschemistry.chemical_compoundchemistryChemical physicsDensity functional theory[CHIM.COOR]Chemical Sciences/Coordination chemistrySelf-assemblyTetrathiafulvaleneexTTF
researchProduct