Search results for "Density Functional Theory."

showing 10 items of 935 documents

Cavitation of electron bubbles in liquid parahydrogen

2011

Within a finite-temperature density functional approach, we have investigated the structure of electron bubbles in liquid parahydrogen below the saturated vapour pressure, determining the critical pressure at which electron bubbles explode as a function of temperature. The electron-parahydrogen interaction has been modelled by a Hartree-type local potential fitted to the experimental value of the conduction band-edge for a delocalized electron in pH(2). We have found that the pressure for bubble explosion is, in absolute value, about a factor of two smaller than that of the homogeneous cavitation pressure in the liquid. Comparison with the results obtained within the capillary model shows t…

Capillary actionChemistryVapor pressureBubbleBiophysicselectron bubblesElectronCondensed Matter PhysicsSpin isomers of hydrogenThermal conductionMolecular physicsPhysics::Fluid Dynamicscapillary approximationNuclear magnetic resonanceCavitationliquid parahydrogenPhysics::Atomic and Molecular ClustersDensity functional theoryPhysical and Theoretical ChemistryMolecular Biologydensity functional theoryMolecular Physics
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Isotropic-nematic interface in suspensions of hard rods: Mean-field properties and capillary waves

2006

We present a study of the isotropic-nematic interface in a system of hard spherocylinders. First we compare results from Monte Carlo simulations and Onsager density functional theory for the interfacial profiles of the orientational order parameter and the density. Those interfacial properties that are not affected by capillary waves are in good agreement, despite the fact that Onsager theory overestimates the coexistence densities. Then we show results of a Monte Carlo study of the capillary waves of the interface. In agreement with recent theoretical investigations (Eur.Phys.J. E {\bf 18} 407 (2005)) we find a strongly anistropic capillary wave spectrum. For the wave-numbers accessed in o…

Capillary waveCondensed matter physicsField (physics)Monte Carlo methodIsotropy: Physics [G04] [Physical chemical mathematical & earth Sciences]FOS: Physical sciencesCondensed Matter - Soft Condensed MatterCondensed Matter::Soft Condensed MatterMean field theory: Physique [G04] [Physique chimie mathématiques & sciences de la terre]Liquid crystalNatuur- en SterrenkundeSoft Condensed Matter (cond-mat.soft)Density functional theoryAnisotropyMathematics
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8-Hydroxyquinoline-2-Carboxylic Acid as Possible Molybdophore: A Multi-Technique Approach to Define Its Chemical Speciation, Coordination and Sequest…

2020

8-hydroxyquinoline-2-carboxylic acid (8-HQA) has been found in high concentrations (0.5&ndash

Carboxylic acidInorganic chemistryPotentiometric titrationlcsh:QR1-502metal complexesMolybdate010402 general chemistry01 natural sciencesBiochemistryFerric Compoundschemical speciation; metal complexes; metallophores; molybdate; natural chelants; sequestration; stability constantslcsh:MicrobiologyArticlemetal complexechemistry.chemical_compoundSettore CHIM/01 - Chimica AnaliticaMolecular BiologyVoltammetryDensity Functional TheorySettore CHIM/02 - Chimica Fisicachemistry.chemical_classificationMolybdenumAqueous solutionmetallophore010405 organic chemistryLigandWatersequestrationchemical speciationhumanities0104 chemical sciencesSolutionsmolybdatestability constantsnatural chelantschemistryHydroxyquinolinesnatural chelantTitrationCyclic voltammetrymetallophoresBiomolecules
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New fitting scheme to obtain effective potential from Car-Parrinello molecular dynamics simulations: Application to silica

2008

A fitting scheme is proposed to obtain effective potentials from Car-Parrinello molecular dynamics (CPMD) simulations. It is used to parameterize a new pair potential for silica. MD simulations with this new potential are done to determine structural and dynamic properties and to compare these properties to those obtained from CPMD and a MD simulation using the so-called BKS potential. The new potential reproduces accurately the liquid structure generated by the CPMD trajectories, the experimental activation energies for the self-diffusion constants and the experimental density of amorphous silica. Also lattice parameters and elastic constants of alpha-quartz are well-reproduced, showing th…

Car–Parrinello molecular dynamicsMaterials sciencemolecular dynamics calculations (Car-Parrinello) and other numerical simulationsTransferabilityGeneral Physics and AstronomyFOS: Physical sciences02 engineering and technologyglasses01 natural sciencesMolecular physicsMolecular dynamicsLattice (order)0103 physical sciences[PHYS.COND.CM-DS-NN]Physics [physics]/Condensed Matter [cond-mat]/Disordered Systems and Neural Networks [cond-mat.dis-nn]010306 general physicsdensity functional theoryCondensed Matter - Materials Sciencegradient and other correctionsMaterials Science (cond-mat.mtrl-sci)Disordered Systems and Neural Networks (cond-mat.dis-nn)computer simulation of liquid structureCondensed Matter - Disordered Systems and Neural Networks021001 nanoscience & nanotechnologylocal density approximation[PHYS.COND.CM-MS]Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]Amorphous silica0210 nano-technologyPair potential
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Simulations of a Graphene Nanoflake as a Nanovector To Improve ZnPc Phototherapy Toxicity: From Vacuum to Cell Membrane

2017

International audience; We propose a new approach to improving photodynamic therapy (PDT) by transporting zinc phthalocyanine (ZnPc) in biological systems via a graphene nanoflake, to increase its targeting. Indeed, by means of time-dependent density functional theory simulations, we show that the ZnPc molecule in interaction with a graphene nanoflake preserves its optical properties not only in a vacuum but also in water. Moreover, molecular dynamic simulations demonstrate that the graphene nanoflake/ZnPc association, as a carrier, permits one to stabilize the ZnPc/graphene nanoflake system on the cellular membrane, which was not possible when using ZnPc alone. We finally conclude that the…

Cellular membraneIndolesMaterials scienceVacuum[SPI.NANO] Engineering Sciences [physics]/Micro and nanotechnologies/MicroelectronicsNanotechnology02 engineering and technology[SPI.MAT] Engineering Sciences [physics]/Materials010402 general chemistry01 natural sciences[SPI.MAT]Engineering Sciences [physics]/Materialslaw.inventionCell membraneMolecular dynamicslawCell Line TumorOrganometallic CompoundsmedicineHumansMoleculeGeneral Materials Science[SPI.NANO]Engineering Sciences [physics]/Micro and nanotechnologies/Microelectronics[SPI.ACOU]Engineering Sciences [physics]/Acoustics [physics.class-ph]Zinc phthalocyanine[SPI.ACOU] Engineering Sciences [physics]/Acoustics [physics.class-ph]Photosensitizing AgentsGrapheneCell Membrane021001 nanoscience & nanotechnologyNanostructures0104 chemical sciencesmedicine.anatomical_structurePhotochemotherapyGraphiteDensity functional theory0210 nano-technology
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The effect of the fused-ring substituent on anthracene chalcones: crystal structural and DFT studies of 1-(anthracen-9-yl)-3-(naphthalen-2-yl)prop-2-…

2018

Two new anthracene chalcones, namely 1-(anthracen-9-yl)-3-(naphthalen-2-yl)prop-2-en-1-one and 1-(anthracen-9-yl)-3-(pyren-1-yl)prop-2-en-1-one, have been successfully synthesized and the effect of the different fused ring substituent system attached to the anthracene chalcone derivative investigated. These compounds show a very narrow band gap due to the large p-conjugated systems, making them promising candidates as optoelectronic materials. Hirshfeld surface analysis has been carried out to show the contribution of inter­molecular contacts and weak inter­actions to supra­molecular stabilization.

Chalconecrystal structureSubstituentchalconeCrystal structure010402 general chemistry010403 inorganic & nuclear chemistryRing (chemistry)01 natural sciencesMedicinal chemistryDFTResearch Communicationschemistry.chemical_compoundMoietyGeneral Materials ScienceAnthraceneCrystallographyHirshfeld surfaceUV-VisGeneral ChemistryCondensed Matter Physics0104 chemical scienceschemistryQD901-999Density functional theoryEnoneActa crystallographica. Section E, Crystallographic communications
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Applications of the Conceptual Density Functional Theory Indices to Organic Chemistry Reactivity.

2016

Indexación: Web of Science Theoretical reactivity indices based on the conceptual Density Functional Theory (DFT) have become a powerful tool for the semiquantitative study of organic reactivity. A large number of reactivity indices have been proposed in the literature. Herein, global quantities like the electronic chemical potential μ, the electrophilicity ω and the nucleophilicity N indices, and local condensed indices like the electrophilic and nucleophilic Parr functions, as the most relevant indices for the study of organic reactivity, are discussed. http://www.mdpi.com/1420-3049/21/6/748

Chemical PhenomenaNucleophilicityChemistry OrganicPharmaceutical ScienceElectronsnucleophilicityReview010402 general chemistry01 natural sciencesreactivity indicesAnalytical ChemistryMolecular electron density theorylcsh:QD241-441Reactivity indicesNucleophilelcsh:Organic chemistryconceptual DFTParr functionsComputational chemistryDrug DiscoveryOrganic chemistryReactivity (chemistry)Physical and Theoretical ChemistryElectrophilicity010405 organic chemistryChemistryOrganic Chemistrymolecular electron density theory0104 chemical sciencesChemistry (miscellaneous)Conceptual DFTElectrophileMolecular MedicineQuantum TheoryDensity functional theoryelectrophilicityMolecules (Basel, Switzerland)
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On the role of interfacial hydrogen bonds in "on-water" catalysis.

2014

Numerous experiments have demonstrated that many classes of organic reactions exhibit increased reaction rates when performed in heterogeneous water emulsions. Despite enormous practical importance of the observed "on-water" catalytic effect and several mechanistic studies, its microscopic origins remains unclear. In this work, the second generation Car-Parrinello molecular dynamics method is extended to self-consistent charge density-functional based tight-binding in order to study "on-water" catalysis of the Diels-Alder reaction between dimethyl azodicarboxylate and quadricyclane. We find that the stabilization of the transition state by dangling hydrogen bonds exposed at the aqueous inte…

Chemical Physics (physics.chem-ph)Aqueous solutionHydrogen bondGeneral Physics and AstronomyFOS: Physical sciencesCondensed Matter - Soft Condensed MatterPhotochemistryCatalysisReaction rateMolecular dynamicschemistry.chemical_compoundchemistryOrganic reactionBiological Physics (physics.bio-ph)Physics - Chemical PhysicsSoft Condensed Matter (cond-mat.soft)Density functional theoryPhysics - Biological PhysicsPhysical and Theoretical ChemistryQuadricyclaneThe Journal of chemical physics
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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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Inverse simulated annealing for the determination of amorphous structures

2013

We present a new and efficient optimization method to determine the structure of disordered systems in agreement with available experimental data. Our approach permits the application of accurate electronic structure calculations within the structure optimization. The new technique is demonstrated within density functional theory by the calculation of a model of amorphous carbon.

Chemical Physics (physics.chem-ph)Condensed Matter - Materials ScienceMaterials scienceStatistical Mechanics (cond-mat.stat-mech)Structure (category theory)Experimental dataInverseMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesElectronic structureDisordered Systems and Neural Networks (cond-mat.dis-nn)Computational Physics (physics.comp-ph)Condensed Matter - Disordered Systems and Neural NetworksCondensed Matter PhysicsMolecular physicsElectronic Optical and Magnetic MaterialsAmorphous solidAmorphous carbonPhysics - Chemical PhysicsSimulated annealingDensity functional theoryPhysics - Computational PhysicsCondensed Matter - Statistical Mechanics
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