Search results for "Quantum"

showing 10 items of 9714 documents

Comparative computational analysis of different active site conformations and substrates in a chalcone isomerase catalyzed reaction.

2006

Chalcone isomerase catalyzes the transformation of chalcones to flavanones. We present a computational study of the rate-limiting chemical step, an intramolecular Michael addition of a 2'-oxyanion to the alpha,beta-double bound. By using quantum mechanical/molecular mechanical hybrid methods we traced the free-energy profiles associated with the reaction of two different substrates (chalcone and 6'-deoxychalcone) in two different conformations of the active site that are described in the different crystallographic structures available. We have obtained significant differences (about 4 kcal/mol) in the free-energy barriers calculated for the two active sites. According to our results, the ac…

Chalcone isomeraseAnionsModels MolecularChalconeStereochemistryProtein ConformationMolecular ConformationCatalysisCatalysischemistry.chemical_compoundAtomMaterials ChemistryComputer SimulationPhysical and Theoretical ChemistryIntramolecular LyasesBinding SitesbiologyActive siteSubstrate (chemistry)Hydrogen-Ion ConcentrationCarbonSurfaces Coatings and FilmsKineticschemistryModels ChemicalIntramolecular forcebiology.proteinMichael reactionQuantum TheoryThermodynamicsSoftwareThe journal of physical chemistry. B
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On groups having a p-constant character

2020

Let G G be a finite group, and p p a prime number; a character of G G is called p p -constant if it takes a constant value on all the elements of G G whose order is divisible by p p . This is a generalization of the very important concept of characters of p p -defect zero. In this paper, we characterize the finite p p -solvable groups having a faithful irreducible character that is p p -constant and not of p p -defect zero, and we will show that a non- p p -solvable group with this property is an almost-simple group.

Character (mathematics)Applied MathematicsGeneral MathematicsQuantum mechanicsCharacter theoryMathematicsofComputing_GENERALCharacter Theory; Finite GroupsConstant (mathematics)GeneralLiterature_REFERENCE(e.g.dictionariesencyclopediasglossaries)Mathematics
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Electromagnetic transitions of heavy baryons in theSU(2Nf)⊗O(3)symmetry

2001

We apply heavy quark symmetry to the radiative decays of heavy baryons. Even with this symmetry in place there are too many couplings to make a meaningful set of predictions. We show that if, in addition, light-diquark symmetries are applied, the number of electromagnetic couplings among S wave and P wave states as well as those between P wave to S wave transitions can be reduced significantly. Using this constituent quark model picture a number of predictions are made that will be testable in the near future.

Charmed baryonsPhysicsBaryonQuarkNuclear and High Energy PhysicsParticle physicsQuantum electrodynamicsHigh Energy Physics::PhenomenologyS-waveHomogeneous spaceRadiative transferConstituent quarkSymmetry (physics)Physical Review D
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Fourier transform spectroscopy and direct potential fit of a shelflike state: application to E(4)1Σ(+) KCs.

2011

The paper presents high-resolution experimental study and a direct potential construction of a shelflike state E(4)(1)Σ(+) of the KCs molecule converging to K(4(2)S) + Cs(5(2)D) atomic limit; such data are of interest for selecting optical paths for producing and monitoring cold polar diatomics. The collisionally enhanced laser induced fluorescence (LIF) spectra corresponding to both spin-allowed E(4)(1)Σ(+) → X(1)(1)Σ(+) and spin-forbidden E(4)(1)Σ(+) → a(1)(3)Σ(+) transitions of KCs were recorded in visible region by Fourier transform spectrometer with resolution of 0.03 cm(-1). Overall about 1650 rovibronic term values of the E(4)(1)Σ(+) state of (39)K(133)Cs and (41)K(133)Cs isotopologu…

Chebyshev polynomialsChemistryAnalytical chemistryGeneral Physics and AstronomyIsotopologuePhysical and Theoretical ChemistryAtomic physicsQuantum numberLaser-induced fluorescencePotential energyDiatomic moleculeSpectral lineFourier transform spectroscopyThe Journal of chemical physics
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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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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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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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Lower Bounds on the Exchange-Correlation Energy in Reduced Dimensions

2009

Bounds on the exchange-correlation energy of many-electron systems are derived and tested. By using universal scaling properties of the electron-electron interaction, we obtain the exponent of the bounds in three, two, one, and quasi-one dimensions. From the properties of the electron gas in the dilute regime, the tightest estimate to date is given for the numerical prefactor of the bound, which is crucial in practical applications. Numerical tests on various low-dimensional systems are in line with the bounds obtained, and give evidence of an interesting dimensional crossover between two and one dimensions.

Chemical Physics (physics.chem-ph)Condensed Matter - Materials ScienceStrongly Correlated Electrons (cond-mat.str-el)Condensed Matter - Mesoscale and Nanoscale PhysicsCrossoverMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesGeneral Physics and AstronomyCondensed Matter - Strongly Correlated ElectronsQuantum dotPhysics - Chemical PhysicsQuantum mechanicsMesoscale and Nanoscale Physics (cond-mat.mes-hall)Line (geometry)POÇOS QUÂNTICOSExponentDensity functional theoryStatistical physicsFermi gasScalingEnergy (signal processing)MathematicsPhysical Review Letters
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Coupled-cluster theory for atoms and molecules in strong magnetic fields

2015

An implementation of coupled-cluster (CC) theory to treat atoms and molecules in finite magnetic fields is presented. The main challenges for the implementation stem from the magnetic-field dependence in the Hamiltonian, or, more precisely, the appearance of the angular momentum operator, due to which the wave function becomes complex and which introduces a gauge-origin dependence. For this reason, an implementation of a complex CC code is required together with the use of gauge-including atomic orbitals to ensure gauge-origin independence. Results of coupled-cluster singles-doubles-perturbative-triples (CCSD(T)) calculations are presented for atoms and molecules with a focus on the depende…

Chemical Physics (physics.chem-ph)Physics010304 chemical physicsAtoms in moleculesBinding energyFOS: Physical sciencesGeneral Physics and Astronomy01 natural sciencesMagnetic fieldsymbols.namesakeCoupled clusterAtomic orbitalPhysics - Chemical Physics0103 physical sciencessymbolsPhysical and Theoretical ChemistryAtomic physicsAngular momentum operator010306 general physicsHamiltonian (quantum mechanics)The Journal of Chemical Physics
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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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