Search results for "potential energy"

showing 10 items of 274 documents

Relativistic coupled cluster calculations of the electronic structure of KrH+, XeH+ and RnH+

2012

Potential energy curves of NgH+ cations (Ng = Kr, Xe, Rn) were obtained by using four-component relativistic CCSD(T) coupled cluster calculations. Dissociation energies, equilibrium bond lengths, electronic properties, such as dipole moments and electric field gradients at the nuclei, and the related spectroscopic parameters of the electronic ground state have been determined. The results obtained for KrH+ and XeH+ are in good agreement with available experimental data, while those for RnH+ have been determined for the first time at this level of theory.

Bond lengthDipoleCoupled clusterChemistryElectric fieldRelativistic effects Coupled cluster Protonated noble gasesElectronic structurePhysical and Theoretical ChemistryAtomic physicsGround statePotential energyDissociation (chemistry)Theoretical Chemistry Accounts
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GERMANIUM DICARBIDE: EVIDENCE FOR A T−SHAPED GROUND STATE STRUCTURE

2017

The equilibrium structure of germanium dicarbide GeC2 has been an open question since the late 1950s. Although most high-level quantum calculations predict an L-shaped geometry, a T-shaped or even a linear geometry cannot be ruled out because of the very flat potential energy surface. By recording the rotational spectrum of this dicarbide using sensitive microwave and millimeter techniques, we unambiguously establish that GeC2 adopts a vibrationally averaged T-shaped structure in its ground state. From analysis of 14 isotopologues, a precise r0 structure has been derived, yielding a Ge–C bond length of 1.952(1) A and an apex angle of 38.7(2)°.

Bond lengthMaterials sciencechemistryPotential energy surfacechemistry.chemical_elementMillimeterIsotopologueGermaniumLinear molecular geometryGround stateMolecular physicsMicrowaveNuclear chemistryProceedings of the 72nd International Symposium on Molecular Spectroscopy
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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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Resonating valence bond quantum Monte Carlo: Application to the ozone molecule

2015

We study the potential energy surface of the ozone molecule by means of Quantum Monte Carlo simulations based on the resonating valence bond concept. The trial wave function consists of an antisymmetrized geminal power arranged in a single-determinant that is multiplied by a Jastrow correlation factor. Whereas the determinantal part incorporates static correlation effects, the augmented real-space correlation factor accounts for the dynamics electron correlation. The accuracy of this approach is demonstrated by computing the potential energy surface for the ozone molecule in three vibrational states: symmetric, asymmetric and scissoring. We find that the employed wave function provides a de…

Chemical Physics (physics.chem-ph)PhysicsQuantum PhysicsStrongly Correlated Electrons (cond-mat.str-el)Electronic correlationGeminalQuantum Monte CarloFOS: Physical sciencesComputational Physics (physics.comp-ph)Condensed Matter PhysicsBond-dissociation energyMolecular physicsAtomic and Molecular Physics and OpticsCondensed Matter - Strongly Correlated ElectronsPhysics - Chemical PhysicsScissoringPotential energy surfaceValence bond theoryPhysics::Chemical PhysicsPhysical and Theoretical ChemistryQuantum Physics (quant-ph)Wave functionPhysics - Computational PhysicsInternational Journal of Quantum Chemistry
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Observable Electric Potential and Electrostatic Potential in Electrochemical Systems

1999

The role of the electric potential in the description of transport processes in electrochemical systems is critically analyzed. Since the electrostatic potential drop between two parts of a system ...

Chemical physicsChemistryComputational chemistryElectric potential energyMaterials ChemistryObservableElectric potentialPhysical and Theoretical ChemistryElectrochemistryVoltage dropSurfaces Coatings and FilmsElectrochemical potentialThe Journal of Physical Chemistry B
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Improving the QM/MM Description of Chemical Processes:  A Dual Level Strategy To Explore the Potential Energy Surface in Very Large Systems.

2005

Potential energy surfaces are fundamental tools for the analysis of reaction mechanisms. The accuracy of these surfaces for reactions in very large systems is often limited by the size of the system even if hybrid quantum mechanics/molecular mechanics (QM/MM) strategies are employed. The large number of degrees of freedom of the system requires hundreds or even thousands of optimization steps to reach convergence. Reactions in condensed media (such as enzymes or solutions) are thus usually restricted to be analyzed using low level quantum mechanical methods, thus introducing a source of error in the description of the QM region. In this paper, an alternative method is proposed, coupled to t…

Chemical processComputer scienceDegrees of freedom (physics and chemistry)computer.software_genreTopologyPotential energyComputer Science ApplicationsQM/MMConvergence (routing)Potential energy surfaceData miningPhysical and Theoretical ChemistrycomputerQuantumEnergy (signal processing)Journal of chemical theory and computation
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Assessment of the Potential Energy Hypersurfaces in Thymine within Multiconfigurational Theory: CASSCF vs. CASPT2

2016

The present study provides new insights into the topography of the potential energy hypersurfaces (PEHs) of the thymine nucleobase in order to rationalize its main ultrafast photochemical decay paths by employing two methodologies based on the complete active space self-consistent field (CASSCF) and the complete active space second-order perturbation theory (CASPT2) methods: (i) CASSCF optimized structures and energies corrected with the CASPT2 method at the CASSCF geometries and (ii) CASPT2 optimized geometries and energies. A direct comparison between these strategies is drawn, yielding qualitatively similar results within a static framework. A number of analyses are performed to assess t…

Chemistry Multidisciplinary2-DIMENSIONAL ELECTRONIC SPECTROSCOPYPharmaceutical Sciencephotostability0305 Organic Chemistry01 natural sciencesLOWEST TRIPLET-STATEAnalytical ChemistryInterpretation (model theory)Molecular dynamicschemistry.chemical_compoundComputational chemistryDrug DiscoveryComplete active spacePerturbation theoryRETINAL CHROMOPHORE MODELComputingMilieux_MISCELLANEOUSAB-INITIOphotochemistry010304 chemical physicsBasis (linear algebra)ChemistryCOUPLED-CLUSTER METHODSPhotochemical ProcessesPotential energy[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryChemistryChemistry (miscellaneous)2ND-ORDER PERTURBATION-THEORYPhysical SciencesANO BASIS-SETSCASSCF/CASPT2Molecular MedicineThermodynamicsLife Sciences & BiomedicineBiochemistry & Molecular BiologyField (physics)INITIO MOLECULAR-DYNAMICSMolecular Dynamics Simulation010402 general chemistryMolecular physicsArticlelcsh:QD241-441lcsh:Organic chemistryCASSCF/CASPT2; photochemistry; DNA; thymine; photostability0103 physical sciencesthyminePhysical and Theoretical ChemistryULTRAFAST INTERNAL-CONVERSIONScience & TechnologyOrganic ChemistryDNAEXCITED-STATE DYNAMICS0104 chemical sciencesThymineModels ChemicalMolecules; Volume 21; Issue 12; Pages: 1666
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Energy landscapes of ligand-receptor couples probed by dynamic force spectroscopy.

2013

Playing a dominant role in many biochemical processes are the dynamic properties of molecular linkages; examples include cell adhesion, enzyme-catalyzed reactions, and molecular recognition by antibodies. Dynamic force spectroscopy, namely separating molecular bonds under external force ramps has rapidly become a powerful tool to study the rugged energy landscape of noncovalent ligand-receptor bonds. The picture shows a surface and tip-bound pair being pulled apart and the derived potential energy diagram.

ChemistryAnalytical chemistryEnergy landscapeProteinsLigand (biochemistry)LigandsMicroscopy Atomic ForcePotential energyAtomic and Molecular Physics and OpticsDynamic force spectroscopyKineticsMolecular recognitionChemical physicsCovalent bondPhysical and Theoretical ChemistryEnergy (signal processing)Protein BindingChemphyschem : a European journal of chemical physics and physical chemistry
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On the approximation of the similarity-transformed Hamiltonian in single-reference and multireference coupled cluster theory

2012

Abstract We consider the recursive single commutator (RSC) approximation of the Baker–Campbell–Hausdorff expansion introduced by Yanai and Chan [T. Yanai, G.K.-L. Chan, J. Chem. Phys. 124 (2006) 194106] and apply it in order to approximate the similarity transformation of the Hamiltonian in both traditional and unitary coupled cluster theory. The equilibrium bond distance, harmonic vibrational frequency, and anharmonic constant of H2, HF, N2, CuH, and Cu2 were computed using the coupled cluster approach with single and double excitations (CCSD) and CCSD with the RSC approximation of the similarity-transformed Hamiltonian (CCSD-RSC). Our results demonstrate that the RSC approximation introdu…

ChemistryAnharmonicityGeneral Physics and AstronomyPotential energyMatrix similarityBond lengthsymbols.namesakeCoupled clusterQuantum mechanicsMolecular vibrationPotential energy surfacesymbolsPhysics::Chemical PhysicsPhysical and Theoretical ChemistryHamiltonian (quantum mechanics)Chemical Physics
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High resolution spectroscopy and potential determination of the (3)1Pi state of NaCs.

2006

The (3)(1)Pi state of the NaCs molecule was studied by high resolution Fourier-transform spectroscopy. The (3)(1)Pi--X (1)Sigma(+) laser induced fluorescence was excited by an Ar(+) ion laser or by a single-mode frequency-doubled cw Nd:YAG laser. The presence of argon buffer gas yielded rich rotational relaxation spectra allowing to enlarge the data set for the (3)(1)Pi state term values, as well as to observe Lambda splittings in a wide range of vibrational (v(')) and rotational (J(')) quantum numbers. The data field includes about 820 energy levels of (3)(1)Pi NaCs in the range from v(')=0 to 37 and from J(')=3 to 190, which corresponds to ca. 95% of the potential well depth. Direct fit o…

ChemistryBuffer gasGeneral Physics and AstronomyIon laserQuantum numberLaserPotential energylaw.inventionlawExcited statePhysical and Theoretical ChemistryAtomic physicsLaser-induced fluorescenceSpectroscopyThe Journal of chemical physics
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