Search results for "clusters"

showing 10 items of 1274 documents

Getting discriminant functions of antibacterial activity from physicochemical and topological parameters.

2001

Linear discriminant analysis has been demonstrated to be a very useful tool in the selection and design of new drugs. Up to now we have used it through the search of a topological pattern of activity. In this work our goal is to calculate a complete set of physicochemical parameters using semiempirical (quantum chemical) calculations as well as topological indices (TIs) and try to find out any discriminant function for antibacterial activity through the combined use of both types of descriptors. The physicochemical parameters, such as heat of formation, HOMO, LUMO, dipole moment, polarizability, hyperpolarizability, PM3 generated IR vibrational frequencies, etc., were calculated using PM3 H…

Chemical PhenomenaChemistry PhysicalHyperpolarizabilityDiscriminant AnalysisGeneral ChemistryLinear discriminant analysisTopologyComputer Science ApplicationsMaxima and minimasymbols.namesakeComputational Theory and MathematicsDiscriminantAnti-Infective AgentsPolarizabilityDrug DesignPhysics::Atomic and Molecular ClusterssymbolsRegression AnalysisHamiltonian (quantum mechanics)HOMO/LUMOTopological quantum numberInformation SystemsMathematicsJournal of chemical information and computer sciences
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Setting the photoelectron clock through molecular alignment

2020

The interaction of strong laser fields with matter intrinsically provides a powerful tool for imaging transient dynamics with an extremely high spatiotemporal resolution. Here, we study strong-field ionisation of laser-aligned molecules, and show a full real-time picture of the photoelectron dynamics in the combined action of the laser field and the molecular interaction. We demonstrate that the molecule has a dramatic impact on the overall strong-field dynamics: it sets the clock for the emission of electrons with a given rescattering kinetic energy. This result represents a benchmark for the seminal statements of molecular-frame strong-field physics and has strong impact on the interpreta…

Chemical Physics (physics.chem-ph)Atomic Physics (physics.atom-ph)ScienceChemical physicsQQuantum physicsFOS: Physical sciencesSettore FIS/03 - Fisica Della MateriaArticlePhysics - Atomic PhysicsStrong field ionizationTDDFTPhysics - Chemical Physicslcsh:QAtomic and molecular physicsddc:500Physics - Atomic and Molecular Clusterslcsh:ScienceAtomic and Molecular Clusters (physics.atm-clus)Applied optics
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Electronic Structure and Bonding of Icosahedral Core–Shell Gold–Silver Nanoalloy Clusters Au144–xAgx(SR)60

2011

Atomically precise thiolate-stabilized gold nanoclusters are currently of interest for many cross-disciplinary applications in chemistry, physics and molecular biology. Very recently, synthesis and electronic properties of "nanoalloy" clusters Au_(144-x)Ag_x(SR)_60 were reported. Here, density functional theory is used for electronic structure and bonding in Au_(144-x)Ag_x(SR)_60 based on a structural model of the icosahedral Au_144(SR)_60 that features a 114-atom metal core with 60 symmetry-equivalent surface sites, and a protecting layer of 30 RSAuSR units. In the optimal configuration the 60 surface sites of the core are occupied by silver in Au_84Ag_60(SR)_60. Silver enhances the electr…

Chemical Physics (physics.chem-ph)Condensed Matter - Materials ScienceAbsorption spectroscopyIcosahedral symmetryFermi levelSuperatomElectron shellMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesElectronic structureNanoclustersCrystallographysymbols.namesakePhysics - Chemical PhysicssymbolsGeneral Materials ScienceDensity functional theoryPhysics - Atomic and Molecular ClustersPhysical and Theoretical ChemistryAtomic and Molecular Clusters (physics.atm-clus)The Journal of Physical Chemistry Letters
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Real-time time-dependent density functional theory implementation of electronic circular dichroism applied to nanoscale metal–organic clusters

2020

| openaire: EC/H2020/838996/EU//RealNanoPlasmon Electronic circular dichroism (ECD) is a powerful spectroscopy method for investigating chiral properties at the molecular level. ECD calculations with the commonly used linear-response time-dependent density functional theory (LR-TDDFT) framework can be prohibitively costly for large systems. To alleviate this problem, we present here an ECD implementation within the projector augmented-wave method in a real-time-propagation TDDFT framework in the open-source GPAW code. Our implementation supports both local atomic basis sets and real-space finite-difference representations of wave functions. We benchmark our implementation against an existin…

Chemical Physics (physics.chem-ph)Condensed Matter - Materials Sciencemagneettiset ominaisuudetCondensed Matter - Mesoscale and Nanoscale PhysicsspektroskopiatiheysfunktionaaliteoriaMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesorganometalliyhdisteetoptiset ominaisuudetPhysics - Chemical PhysicsMesoscale and Nanoscale Physics (cond-mat.mes-hall)Physics::Atomic and Molecular Clustersnanohiukkaset
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The spectra of mixed $^3$He-$^4$He droplets

2005

The diffusion Monte Carlo technique is used to calculate and analyze the excitation spectrum of $^3$He atoms bound to a cluster of $^4$He atoms, by using a previously determined optimum filling of single-fermion orbits with well defined orbital angular momentum $L$, spin $S$ and parity quantum numbers. The study concentrates on the energies and shapes of the three kinds of states for which the fermionic part of the wave function is a single Slater determinant: maximum $L$ or maximum $S$ states within a given orbit, and fully polarized clusters. The picture that emerges is that of systems with strong shell effects whose binding and excitation energies are essentially determined over configur…

Chemical Physics (physics.chem-ph)Excitation spectrumdiffusion[PHYS.PHYS.PHYS-ATM-PH]Physics [physics]/Physics [physics]/Atomic and Molecular Clusters [physics.atm-clus]wave functionsFOS: Physical sciencesMonte Carlo methodsbinding energyMonte Carlo technique ; Excitation spectrum ;Monte Carlo techniqueliquid theoryliquid helium 3-4 mixturesPhysics - Chemical Physics[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Physics - Atomic and Molecular ClustersAtomic and Molecular Clusters (physics.atm-clus)67.60.-g 66.10.Cb 61.20.Jadrops
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NMR chemical shift computations at second-order Møller-Plesset perturbation theory using gauge-including atomic orbitals and Cholesky-decomposed two-…

2021

We report on a formulation and implementation of a scheme to compute NMR shieldings at second-order Moller-Plesset (MP2) perturbation theory using gauge-including atomic orbitals (GIAOs) to ensure gauge-origin independence and Cholesky decomposition (CD) to handle unperturbed as well as perturbed two-electron integrals. We investigate the accuracy of the CD for the derivatives of the two-electron integrals with respect to an external magnetic field as well as for the computed NMR shieldings, before we illustrate the applicability of our CD based GIAO-MP2 scheme in calculations involving up to about one hundred atoms and more than one thousand basis functions.

Chemical Physics (physics.chem-ph)PhysicsChemical shiftMøller–Plesset perturbation theoryFOS: Physical sciencesGeneral Physics and AstronomyBasis functionElectronMagnetic fieldAtomic orbitalQuantum mechanicsPhysics::Atomic and Molecular ClustersPhysical and Theoretical ChemistryPerturbation theoryCholesky decompositionThe Journal of chemical physics
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The MOF-driven synthesis of supported palladium clusters with catalytic activity for carbene-mediated chemistry

2016

The development of catalysts able to assist industrially important chemical processes is a topic of high importance. In view of the catalytic capabilities of small metal clusters, research efforts are being focused on the synthesis of novel catalysts bearing such active sites. Here we report a heterogeneous catalyst consisting of Pd4 clusters with mixed-valence 0/+1 oxidation states, stabilized and homogeneously organized within the walls of a metal-organic framework (MOF). The resulting solid catalyst outperforms state-of-the-art metal catalysts in carbene-mediated reactions of diazoacetates, with high yields (>90%) and turnover numbers (up to 100,000). In addition, the MOF-supported Pd4 c…

Chemical processMechanical Engineeringchemistry.chemical_element02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsHeterogeneous catalysis01 natural sciencesCombinatorial chemistry0104 chemical sciencesCatalysischemistry.chemical_compoundchemistryMechanics of MaterialsOrganic chemistryGeneral Materials ScienceMetal catalyst0210 nano-technologyCarbenePalladiumMetal clustersNature Materials
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Atomically Precise Alkynyl-Protected Metal Nanoclusters as a Model Catalyst: Observation of Promoting Effect of Surface Ligands on Catalysis by Metal…

2016

Metal nanoclusters whose surface ligands are removable while keeping their metal framework structures intact are an ideal system for investigating the influence of surface ligands on catalysis of metal nanoparticles. We report in this work an intermetallic nanocluster containing 62 metal atoms, Au34Ag28(PhC≡C)34, and its use as a model catalyst to explore the importance of surface ligands in promoting catalysis. As revealed by single-crystal diffraction, the 62 metal atoms in the cluster are arranged as a four-concentric-shell Ag@Au17@Ag27@Au17 structure. All phenylalkynyl (PA) ligands are linearly coordinated to the surface Au atoms with staple "PhC≡C-Au-C≡CPh" motif. Compared with reporte…

Chemical substanceIntermetallic02 engineering and technology010402 general chemistry01 natural sciencesBiochemistrycatalystsCatalysisCatalysisNanoclustersMetalHydrolysisColloid and Surface ChemistryPolymer chemistryCluster (physics)Organic chemistryta116intermetallic nanoclustersta114ChemistryphenylalkynylGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencessurface ligandsvisual_artvisual_art.visual_art_medium0210 nano-technologyScience technology and societyJournal of the American Chemical Society
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The kinetic MC modelling of reversible pattern formation in initial stages of thin metallic film growth on crystalline substrates

2003

Abstract The results of kinetic MC simulations of the reversible pattern formation during the adsorption of mobile metal atoms on crystalline substrates are discussed. Pattern formation, simulated for submonolayer metal coverage, is characterized in terms of the joint correlation functions for a spatial distribution of adsorbed atoms. A wide range of situations, from the almost irreversible to strongly reversible regimes, is simulated. We demonstrate that the patterns obtained are defined by a key dimensionless parameter: the ratio of the mutual attraction energy between atoms to the substrate temperature. Our ab initio calculations for the nearest Ag–Ag adsorbate atom interaction on an MgO…

Chemistry(all)ChemistryD. Kinetic propertiesSubstrate (chemistry)Crystal growthGeneral ChemistryA. Surfaces and interfacesKinetic energyCondensed Matter PhysicsCrystallographyCondensed Matter::Materials ScienceAdsorptionB. Crystal growthAb initio quantum chemistry methodsChemical physicsAtomPhysics::Atomic and Molecular ClustersMaterials ChemistryMoleculeThin filmSolid State Communications
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FT-IR spectroscopy studies of the breast cancer cell composition changes induced by Au-BSA nanoclusters

2016

Chemistry010401 analytical chemistryBioengineering02 engineering and technologyGeneral Medicine021001 nanoscience & nanotechnology01 natural sciencesApplied Microbiology and Biotechnology0104 chemical sciencesNanoclustersFt ir spectroscopyComposition (visual arts)Breast cancer cells0210 nano-technologyBiotechnologyNuclear chemistryJournal of Biotechnology
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