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showing 10 items of 59416 documents

Towards highly accurate ab initio thermochemistry of larger systems: benzene.

2011

The high accuracy extrapolated ab initio thermochemistry (HEAT) protocol is applied to compute the total atomization energy (TAE) and the heat of formation of benzene. Large-scale coupled-cluster calculations with more than 1500 basis functions and 42 correlated electrons as well as zero-point energies based on full cubic and (semi)diagonal quartic force fields obtained with the coupled-cluster singles and doubles with perturbative treatment of the triples method and atomic natural orbital (ANO) triple- and quadruple-zeta basis sets are presented. The performance of modifications to the HEAT scheme and the scaling properties of its contributions with respect to the system size are investiga…

010304 chemical physicsChemistryAb initioGeneral Physics and AstronomyBasis function010402 general chemistry01 natural sciences7. Clean energyStandard enthalpy of formation0104 chemical sciencesChemical thermodynamicsAb initio quantum chemistry methodsQuartic function0103 physical sciencesThermochemistryPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsScalingThe Journal of chemical physics
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The ensemble switch method and related approaches to obtain interfacial free energies between coexisting phases from simulations: a brief review

2015

The accurate estimation of the excess free energy due to an interface between coexisting phases of a model system by computer simulation often is a challenging task. We review here two methods, whi...

010304 chemical physicsChemistryAccurate estimationGeneral Chemical EngineeringMonte Carlo methodModel systemGeneral ChemistryCondensed Matter Physics01 natural sciencesSurface tensionModeling and Simulation0103 physical sciencesGeneral Materials ScienceFree energiesStatistical physics010306 general physicsInformation SystemsMolecular Simulation
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Theoretical investigation of the potential energy surface of the van der Waals complex CH4-N-2

2009

International audience; The interaction potential energy surface of the van der Waals CH4-N-2 complex has been calculated for a broad range of intermolecular separations and configurations in the approximation of rigid interacting molecules at the CCSD(T) and MP2 levels of theory using the correlation consistent aug-cc-pVTZ basis set. The BSSE correction was taken into account for all the calculations. The most stable configurations of the complex were found. Binding energies were calculated in the CBS limit with accounting for the molecular deformations. The harmonic and anharmonic fundamental vibrational frequencies and rotational constants for the ground and first excited vibrational sta…

010304 chemical physicsChemistryBinding energyIntermolecular forceAnharmonicityVan der Waals surfaceGeneral Physics and Astronomy010402 general chemistry01 natural sciences0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistrysymbols.namesakeLennard-Jones potentialExcited state0103 physical sciencesPotential energy surface[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistrysymbolsPhysics::Atomic and Molecular ClustersPhysical and Theoretical Chemistryvan der Waals forceAtomic physicsPhysics::Chemical Physics
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Fourier-transform spectroscopy and deperturbation analysis of the spin-orbit coupled A(1)Σ(+) and b(3)Π states of KRb.

2016

Fourier-transform A(1)Σ(+) - b(3)Π → X(1)Σ(+) laser-induced fluorescence spectra were recorded for the natural mixture of (39,41)K(85,87)Rb isotopologues produced in a heatpipe oven. Overall 4200 rovibronic term values of the spin-orbit coupled A(1)Σ(+) and b(3)Π states were determined with an uncertainty of about 0.01 cm(-1) in the energy range [10 850, 14 200] cm(-1) covering rotational quantum numbers J' ∈ [3, 280]. Direct deperturbation analysis of the A ∼ b complex performed within the framework of the A(1)Σ(+) ∼ b(3)ΠΩ=0,1,2 coupled-channel approach reproduced experimental data with a standard deviation of 0.004 cm(-1). Initial parameters of the internuclear potentials and spin-orbit …

010304 chemical physicsChemistryGeneral Physics and AstronomyElectronic structureQuantum number01 natural sciencesFourier transform spectroscopyB vitamins0103 physical sciencesKinetic isotope effectIsotopologueEmission spectrumPhysical and Theoretical ChemistryAtomic physics010306 general physicsSpectroscopyThe Journal of chemical physics
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A QM/MM Approach Using the AMOEBA Polarizable Embedding: From Ground State Energies to Electronic Excitations

2016

International audience; A fully polarizable implementation of the hybrid Quantum Mechanics/Molecular Mechanics approach is presented, where the classical environment is described through the AMOEBA polarizable force field. A variational formalism, offering a self-consistent 1 relaxation of both the MM induced dipoles and the QM electronic density is used for ground state energies and extended to electronic excitations in the framework of Time-Dependent Density Functional Theory combined with a state specific response of the classical part. An application to the calculation of the solvatochromism of the pyridinium N-phenolate betaine dye used to define the solvent ET30 scale is presented. Th…

010304 chemical physicsChemistryPolarizable force fieldSolvatochromismQuantum Chemistry010402 general chemistryElementary chargeQM/MM01 natural sciences0104 chemical sciencesComputer Science Applications[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryQM/MMQM/MM; Polarisable embedding; Physical and Theoretical ChemistryPolarizabilityQuantum mechanics0103 physical sciencesPolarisable embeddingDensity functional theorypolarizable force field AMOEBAPhysical and Theoretical ChemistryGround stateExcitationElectronic densityJournal of Chemical Theory and Computation
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Adaptive Finite Temperature String Method in Collective Variables.

2017

Here we present a modified version of the on-the-fly string method for the localization of the minimum free energy path in a space of arbitrary collective variables. In the proposed approach the shape of the biasing potential is controlled by only two force constants, defining the width of the potential along the string and orthogonal to it. The force constants and the distribution of the string nodes are optimized during the simulation, improving the convergence. The optimized parameters can be used for umbrella sampling with a path CV along the converged string as the reaction coordinate. We test the new method with three fundamentally different processes: chloride attack to chloromethane…

010304 chemical physicsChemistryString (computer science)Mathematical analysis010402 general chemistry01 natural sciences0104 chemical sciencesReaction coordinateDistribution (mathematics)0103 physical sciencesPath (graph theory)Convergence (routing)Range (statistics)Physical and Theoretical ChemistryUmbrella samplingPotential of mean forceThe journal of physical chemistry. A
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Heterogeneous Interactions between Gas-Phase Pyruvic Acid and Hydroxylated Silica Surfaces: A Combined Experimental and Theoretical Study

2019

The adsorption of gas-phase pyruvic acid (CH3COCOOH) on hydroxylated silica particles has been investigated at 296 K using transmission Fourier transform infrared (FTIR) spectroscopy and theoretical simulations. Under dry conditions (<1% relative humidity, RH), both the trans-cis (Tc) and trans-trans (Tt) pyruvic acid conformers are observed on the surface as well as the (hydrogen bonded) pyruvic acid dimer. The detailed surface interactions were further understood through ab initio molecular dynamics simulations. Under higher relative humidity conditions (above 10% RH), adsorbed water competes for surface adsorption sites. Adsorbed water is also observed to change the relative populations …

010304 chemical physicsHydrogenChemistryDimerInorganic chemistrychemistry.chemical_element010402 general chemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundAdsorption13. Climate action0103 physical sciencesRelative humidityPyruvic acid[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Physical and Theoretical ChemistryFourier transform infrared spectroscopySpectroscopyConformational isomerismComputingMilieux_MISCELLANEOUS
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Pressure‐induced widths and shifts for the ν3 band of methane

1994

International audience; Widths and shifts of methane lines perturbed by nitrogen are calculated using a complex-valued implementation of Robert-Bonamy (RB) theory. The static intermolecular potential is described as a sum of electrostatic forces and Lennard-Jones (6-12) atom-atom terms, using literature values for all physical parameters. Vibrational dependence of the isotropic potential is obtained from the polarizability of methane assuming a dispersion interaction. The repulsive part of the Lennard-Jones accounts for the greatest part of widths, while dispersion interactions are largely responsible for shifts. Although the average error between calculated and observed linewidths (up to J…

010304 chemical physicsMathematical modelAbsorption spectroscopyIntermolecular forceIsotropyGeneral Physics and Astronomy7. Clean energy01 natural sciencesMethane010309 opticschemistry.chemical_compoundLennard-Jones potentialchemistryPolarizability0103 physical sciencesDispersion (optics)Physics::Atomic and Molecular ClustersPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsThe Journal of Chemical Physics
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Matrix isolation and quantum chemical studies on the H2O2–SO2complex

2004

Complexation and photochemical reactions of hydrogen peroxide and sulfur dioxide have been studied in solid Ar, Kr and Xe. Complexes between H2O2 and SO2 are characterized using Fourier transform infrared spectroscopy and ab initio calculations. In solid Ar, the H2O2–SO2 complex absorptions are found at wavenumbers of 3572.8, 3518.7, 3511.2, 3504.3, 1340.3, 1280.2 and 1149.9 cm−1. In Kr and Xe matrices, the bonded OH stretching frequencies deviate from the values in Ar, and we propose that the matrix surrounding influences the structure of the H2O2–SO2 complex. UV photolysis of the H2O2–SO2 was also studied in solid Ar, Kr and Xe. This photolysis produces mainly a complex between sulfur tri…

010304 chemical physicsPhotodissociationMatrix isolationGeneral Physics and Astronomy010402 general chemistry7. Clean energy01 natural sciences0104 chemical scienceschemistry.chemical_compoundMatrix (mathematics)chemistryComputational chemistryAb initio quantum chemistry methods0103 physical sciencesSulfur trioxidePhysical chemistryPhysical and Theoretical ChemistryFourier transform infrared spectroscopyHydrogen peroxideSulfur dioxidePhys. Chem. Chem. Phys.
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MD Simulation Investigation on the Binding Process of Smoke-Derived Germination Stimulants to Its Receptor

2019

Karrikins (KARs) are a class of smoke-derived seed germination stimulants with great significance in both agriculture and plant biology. By means of direct binding to the receptor protein KAI2, the compounds can initiate the KAR signal transduction pathway, hence triggering germination of the dormant seeds in the soil. In the research, several molecular dynamics (MD) simulation techniques were properly integrated to investigate the binding process of KAR1 to KAI2 and reveal the details of the whole binding event. The calculated binding free energy, -7.00 kcal/mol, is in good agreement with the experimental measurement, -6.83 kcal/mol. The obtained PMF profile indicates the existence of thre…

010304 chemical physicsProtein ConformationChemistryGeneral Chemical EngineeringGerminationGeneral ChemistryPlasma protein bindingMolecular Dynamics SimulationLibrary and Information SciencesLigand (biochemistry)01 natural sciences0104 chemical sciencesComputer Science Applications010404 medicinal & biomolecular chemistryMolecular dynamicsProtein structure0103 physical sciencesMoleBiophysicsThermodynamicsMoleculeSignal transductionReceptorPlant ProteinsProtein BindingJournal of Chemical Information and Modeling
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