Search results for "Atomic orbital"

showing 10 items of 233 documents

A computational study of some electric and magnetic properties of gaseous BF3 and BCl3

2005

We present the results of an extended computational study of the electric and magnetic properties connected to Cotton-Mouton birefringences, on the trifluoro- and trichloroborides in the gas phase. The electric dipole polarizabilities, magnetizabilities, quadrupole moments, and higher-order hypersusceptibilities—expressed as quadratic and cubic frequency-dependent response functions—are computed within Hartree-Fock, density-functional, and coupled-cluster response theories employing singly and doubly augmented correlation-consistent basis sets and London orbitals in the magnetic property calculations. The results, which illustrate the capability of time-dependent density-functional theory f…

BirefringenceBirefringenceCondensed matter physicsChemistryElectron correlationsGeneral Physics and AstronomyMagnetic susceptibilityBoron compounds; Polarisability Quadrupole moments ; HF calculations ; Density functional theory ; Coupled cluster calculations ; Electron correlations ; Magnetic anisotropy ; Magnetic susceptibility ; BirefringenceUNESCO::FÍSICA::Química físicaMagnetic susceptibilityMagnetic anisotropyDipoleAtomic orbitalBoron compoundsCoupled cluster calculationsQuadrupolePolarisability Quadrupole momentsDensity functional theoryDensity functional theoryPhysical and Theoretical ChemistryAtomic physicsAnisotropy:FÍSICA::Química física [UNESCO]HF calculationsMagnetic anisotropy
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Unveiling the role of upper excited electronic states in the photochemistry and laser performance of: anti -B18H22

2020

13 pags., 7 figs., -- This article is part of the themed collection: Journal of Materials Chemistry C HOT Papers

Blue lasereducation.field_of_studyMaterials sciencePopulationGeneral ChemistryBoraneLaserPhotochemistryQuantum chemistrylaw.inventionchemistry.chemical_compoundchemistryAtomic orbitallawExcited stateMaterials ChemistrySpectroscopyeducationJournal of Materials Chemistry C 8: 12806-12818 (2020)
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Phonon calculations in cubic and tetragonal phases of SrTiO3: A comparative LCAO and plane-wave study

2011

The atomic, electronic structure and phonon frequencies have been calculated in cubic and low-temperature tetragonal SrTiO${}_{3}$ phases at the ab initio level. We demonstrate that the use of the hybrid exchange-correlation PBE0 functional gives the best agreement with experimental data. The results for the standard generalized gradient approximation (PBE) and hybrid PBE0 functionals are compared for the two types of approaches: a linear combination of atomic orbitals (CRYSTAL09 computer code) and plane waves (VASP5.2 code). The relation between cubic and tetragonal phases and the relevant antiferrodistortive phase transition is discussed in terms of group theory and is illustrated with an…

Brillouin zonePhysicsCondensed Matter::Materials ScienceTetragonal crystal systemTight bindingCondensed matter physicsPhononLinear combination of atomic orbitalsPlane waveAb initioCondensed Matter PhysicsHeat capacityElectronic Optical and Magnetic MaterialsPhysical Review B
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A first-principles DFT study of UN bulk and (001) surface: comparative LCAO and PW calculations.

2008

LCAO and PW DFT calculations of the lattice constant, bulk modulus, cohesive energy, charge distribu- tion, band structure, and DOS for UN single crystal are analyzed. It is demonstrated that a choice of the uranium atom relativistic effective core potentials considerably affects the band structure and magnetic structure at low tem- peratures. All calculations indicate mixed metallic-covalent chemical bonding in UN crystal with U5f states near the Fermi level. On the basis of the experience accumulated in UN bulk simulations, we compare the atomic and elec- tronic structure as well as the formation energy for UN(001) surface calculated on slabs of different thickness using both DFT approach…

Bulk modulusChemistryFermi levelGeneral ChemistryMolecular physicsComputational Mathematicssymbols.namesakeCrystallographyDelocalized electronAtomic orbitalLinear combination of atomic orbitalsAtomsymbolsElectronic band structureBasis setJournal of computational chemistry
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A CNDO/2 study on the additivity and the nature of the non-additivity of the substituent effects on13C NMR shifts in chlorobenzenes and chlorophenols

1980

The general correlation between the electron densities and the 13C NMR chemical shifts is found to be quite poor in the cases discussed. The non-additivities of the substituent effects on the chemical shifts and the CNDO/2 electron densities correlate only weakly. However, when the electron densities are made specific to different types of atomic orbitals, the s electrons have a pronounced effect in all the models tested. This is explained by an indirect effect on the 〈1/r3〉 term of the p electrons. Good correlations are found between the sums of the chemical shifts and the corresponding sums of the substituent charge excesses. The different behaviour of OH and Cl substituents in the additi…

CNDO/2chemistry.chemical_compoundAtomic orbitalComputational chemistryChemistryChlorobenzeneChemical shiftAdditive functionSubstituentGeneral Materials ScienceGeneral ChemistryElectronCarbon-13 NMROrganic Magnetic Resonance
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Donor–anion interactions at the charge localization and charge ordering transitions of (TMTTF)2AsF6 probed by NEXAFS

2015

High-resolution near-edge X-ray absorption fine structure (NEXAFS) measurements at the As M-edge, F K-edge and S L-edge of the Fabre salt (TMTTF)2AsF6 were performed from room temperature (RT) to 90 K, allowing to reach the charge localization regime below Tρ ≈ 230 K and to cross the charge ordering (CO) transition at TCO ≈ 102 K. The F K-edge and S L-edge spectra exhibit several transitions which have been indexed on the basis of first-principles DFT calculations. Upon cooling from RT significant energy shifts up to +0.8 eV and -0.4 eV were observed in transitions exhibited by the F 1s and S 2p spectra respectively, while the As 3p doublet does not show a significant shift. Opposite energy…

Charge orderingAtomic orbitalComputational chemistryChemistryPoint reflectionGeneral Physics and AstronomyCharge (physics)Symmetry breakingPhysical and Theoretical ChemistryMolecular physicsXANESSpectral lineIonPhysical Chemistry Chemical Physics
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Generalized Many-Body Expanded Full Configuration Interaction Theory

2019

Facilitated by a rigorous partitioning of a molecular system's orbital basis into two fundamental subspaces - a reference and an expansion space, both with orbitals of unspecified occupancy - we generalize our recently introduced many-body expanded full configuration interaction (MBE-FCI) method to allow for electron-rich model and molecular systems dominated by both weak and strong correlation to be addressed. By employing minimal or even empty reference spaces, we show through calculations on the one-dimensional Hubbard model with up to 46 lattice sites, the chromium dimer, and the benzene molecule how near-exact results may be obtained in a entirely unbiased manner for chemical and physi…

Chemical Physics (physics.chem-ph)010304 chemical physicsBasis (linear algebra)Computer scienceFOS: Physical sciences010402 general chemistrySpace (mathematics)01 natural sciencesFull configuration interactionMany body0104 chemical sciencesTheoretical physicsAtomic orbitalPhysics - Chemical Physics0103 physical sciencesGeneral Materials ScienceAstrophysics::Earth and Planetary AstrophysicsPhysical and Theoretical Chemistry
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Anomalous High-Pressure Jahn-Teller Behavior inCuWO4

2012

High-pressure optical-absorption measurements performed in CuWO4 up to 20 GPa provide experimental evidence of the persistence of the Jahn-Teller (JT) distortion in the whole pressure range both in the low-pressure triclinic and in the highpressure monoclinic phase. The electron-lattice coupling associated with the eg(Exe) and t2g(Txe) orbitals of Cu2+ in CuWO4 are obtained from correlations between the JT distortion of the CuO6 octahedron and the associated structure of Cu2+ d-electronic levels. This distortion and its associated JT energy (EJT) decrease upon compression in both phases. However, both the distortion and associated EJT increase sharply at the phase transition pressure (PT = …

Chemical Physics (physics.chem-ph)Condensed Matter - Materials ScienceMaterials scienceStrongly Correlated Electrons (cond-mat.str-el)Condensed matter physicsJahn–Teller effectMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesGeneral Physics and AstronomyTriclinic crystal systemCondensed Matter - Strongly Correlated ElectronsAtomic orbitalOctahedronPhysics - Chemical PhysicsDistortionPhase (matter)MultiferroicsMonoclinic crystal systemPhysical 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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Virtual Orbital Many-Body Expansions: A Possible Route towards the Full Configuration Interaction Limit

2017

In the present letter, it is demonstrated how full configuration interaction (FCI) results in extended basis sets may be obtained to within sub-kJ/mol accuracy by decomposing the energy in terms of many-body expansions in the virtual orbitals of the molecular system at hand. This extension of the FCI application range lends itself to two unique features of the current approach, namely that the total energy calculation can be performed entirely within considerably reduced orbital subspaces and may be so by means of embarrassingly parallel programming. Facilitated by a rigorous and methodical screening protocol and further aided by expansion points different from the Hartree-Fock solution, al…

Chemical Physics (physics.chem-ph)Physics010304 chemical physicsBasis (linear algebra)Embarrassingly parallelFOS: Physical sciences010402 general chemistry01 natural sciencesFull configuration interactionLinear subspace0104 chemical sciencesRange (mathematics)Atomic orbitalComputational chemistryPhysics - Chemical Physics0103 physical sciencesGeneral Materials ScienceLimit (mathematics)Statistical physicsPhysical and Theoretical ChemistryEnergy (signal processing)
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