Search results for " quantum chemistry"

showing 10 items of 549 documents

High-pressure structural and vibrational properties of monazite-type BiPO4, LaPO4, CePO4, and PrPO4

2018

[EN] Monazite-type BiPO4, LaPO4, CePO4, and PrPO4 have been studied under high pressure by ab initio simulations and Raman spectroscopy measurements in the pressure range of stability of the monazite structure. A good agreement between experimental and theoretical Raman-active mode frequencies and pressure coefficients has been found which has allowed us to discuss the nature of the Raman-active modes. Besides, calculations have provided us with information on how the crystal structure is modified by pressure. This information has allowed us to determine the equation of state and the isothermal compressibility tensor of the four studied compounds. In addition, the information obtained on th…

Equation of stateMaterials scienceAb initioThermodynamics02 engineering and technology010402 general chemistry01 natural sciencessymbols.namesakeAb initio quantum chemistry methodsorthophospahtemonaziteGeneral Materials ScienceMonaziteTensorAnisotropyOrthophosphateRamanequation of stateEquation of state021001 nanoscience & nanotechnologyCondensed Matter PhysicsAb initio calculations; Raman; equation of state; high pressure; monazite; orthophospahte0104 chemical sciencesHigh pressurehigh pressureMonaziteFISICA APLICADACompressibilitysymbolsAb initio calculations0210 nano-technologyRaman spectroscopy
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Towards an accurate molecular orbital theory for excited states : Ethene, butadiene, and hexatriene

1993

A newly proposed quantum chemical approach for ab initio calculations of electronic spectra of molecular systems is applied to the molecules ethene, trans‐1,3‐butadiene, and trans‐trans‐1,3,5‐hexatriene. The method has the aim of being accurate to better than 0.5 eV for excitation energies and is expected to provide structural and physical data for the excited states with good reliability. The approach is based on the complete active space (CAS) SCF method, which gives a proper description of the major features in the electronic structure of the excited state, independent of its complexity, accounts for all near degeneracy effects, and includes full orbital relaxation. Remaining dynamic ele…

ErrorsGeneral Physics and AstronomyPolyenesElectronic structuresymbols.namesakeRydberg StatesAb initio quantum chemistry methodsComputational chemistrySinglet statePhysical and Theoretical ChemistryTriplet state:FÍSICA::Química física [UNESCO]AccuracyExcitationCalculation MethodsButadieneTripletsChemistryMolecular orbital theoryScf CalculationsExcited StatesCalculation Methods ; Quantum Chemistry ; Ab Initio Calculations ; Electron Spectra ; Butadiene ; Accuracy ; Scf Calculations ; Triplets ; Rydberg States ; Excitation ; Errors ; Polyenes ; Excited StatesQuantum ChemistryUNESCO::FÍSICA::Química físicaElectron SpectraExcited stateRydberg formulasymbolsRydberg stateAtomic physicsAb Initio Calculations
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Bond length compressibility in hard ReB2 investigated by x-ray absorption under high pressure

2010

International audience; This work describes x-ray absorption measurements under high pressure in ReB2 , complemented by ab initio calculations. The EXAFS analysis yields the average Re–B bond compressibility, which turns out to be χReB = 5.6(9) × 10− 4 GPa−1 . Combining this information with previous x-ray diffraction experiments we have characterized the network of covalent bonds responsible for the rigidity of the structure. The main conclusion is that the compression is anisotropic and nonhomogeneous, reflecting bonding differences between Re–B and B–B bonds and also between nonequivalent Re–B bonds. The layer defined by boron atoms tends to become flatter under high pressure. As a conse…

Extended X-ray absorption fine structureChemistry02 engineering and technology021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesMolecular physicsBond lengthCrystallographyChemical bondCovalent bondAb initio quantum chemistry methods[PHYS.COND.CM-GEN]Physics [physics]/Condensed Matter [cond-mat]/Other [cond-mat.other]0103 physical sciencesX-ray crystallographyCompressibilityGeneral Materials Science010306 general physics0210 nano-technologyStructural rigidity
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Extension of the MIRS computer package for the modeling of molecular spectra : from effective to full ab initio ro-vibrational hamiltonians in irredu…

2012

The MIRS software for the modeling of ro-vibrational spectra of polyatomic molecules was considerably extended and improved. The original version (Nikitin, et al. JQSRT, 2003, pp. 239--249) was especially designed for separate or simultaneous treatments of complex band systems of polyatomic molecules. It was set up in the frame of effective polyad models by using algorithms based on advanced group theory algebra to take full account of symmetry properties. It has been successfully used for predictions and data fitting (positions and intensities) of numerous spectra of symmetric and spherical top molecules within the vibration extrapolation scheme. The new version offers more advanced possib…

ExtrapolationAb initioFOS: Physical sciences02 engineering and technologyPoint group01 natural scienceshigh-resolution infrared spectroscopyTheoretical physicsAb initio quantum chemistry methodsPhysics - Chemical PhysicsQuantum mechanics0103 physical sciencesMolecular symmetrypolyadsSpectroscopycomputational spectroscopyChemical Physics (physics.chem-ph)Physics[PHYS.PHYS.PHYS-AO-PH]Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph]Radiation010304 chemical physicsab initio calculationseffective hamiltoniansRotational–vibrational spectroscopy021001 nanoscience & nanotechnologyAtomic and Molecular Physics and Opticsmolecular symmetryPhysics - Atmospheric and Oceanic Physicsvibration-rotation spectroscopy[ PHYS.PHYS.PHYS-AO-PH ] Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph]Atmospheric and Oceanic Physics (physics.ao-ph)Curve fittingirreducible tensors0210 nano-technologyGroup theory
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Magnetic and electronic properties of double perovskites and estimation of their Curie temperatures byab initiocalculations

2008

First principles electronic structure calculations have been carried out on ordered double perovskites Sr_2B'B"O_6 (for B' = Cr or Fe and B" 4d and 5d transition metal elements) with increasing number of valence electrons at the B-sites, and on Ba_2MnReO_6 as well as Ba_2FeMoO_6. The Curie temperatures are estimated ab initio from the electronic structures obtained with the local spin-density functional approximation, full-potential generalized gradient approximation and/or the LDA+U method (U - Hubbard parameter). Frozen spin-spirals are used to model the excited states needed to evaluate the spherical approximation for the Curie temperatures. In cases, where the induced moments on the oxy…

FOS: Physical sciences02 engineering and technologyElectronic structure01 natural sciencesCondensed Matter::Materials ScienceCurie's lawAb initio quantum chemistry methods0103 physical sciences010306 general physicsPhysicsCondensed Matter - Materials ScienceCurie–Weiss lawCondensed matter physicsMaterials Science (cond-mat.mtrl-sci)021001 nanoscience & nanotechnologyCondensed Matter Physics3. Good healthElectronic Optical and Magnetic MaterialsCondensed Matter - Other Condensed MatterCurie temperatureCondensed Matter::Strongly Correlated ElectronsCurie constantLocal-density approximation0210 nano-technologyValence electronOther Condensed Matter (cond-mat.other)Physical Review B
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Molecular equilibrium structures from experimental rotational constants and calculated vibration–rotation interaction constants

2002

A detailed study is carried out of the accuracy of molecular equilibrium geometries obtained from least-squares fits involving experimental rotational constants B(0) and sums of ab initio vibration-rotation interaction constants alpha(r)(B). The vibration-rotation interaction constants have been calculated for 18 single-configuration dominated molecules containing hydrogen and first-row atoms at various standard levels of ab initio theory. Comparisons with the experimental data and tests for the internal consistency of the calculations show that the equilibrium structures generated using Hartree-Fock vibration-rotation interaction constants have an accuracy similar to that obtained by a dir…

FREQUENCIESChemistryGAUSSIAN-BASIS SETSAb initioGeneral Physics and AstronomyDiatomic moleculeSTATEBORONBond lengthVibrationHOFMETHANEMolecular geometryCCSD(T) 2ND DERIVATIVESAb initio quantum chemistry methodsACIDWAVE-FUNCTIONSPhysics::Atomic and Molecular ClustersMoleculeQUARTIC FORCE-FIELDPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsRotation (mathematics)The Journal of Chemical Physics
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Concise Chemistry Modulation of the SMM Behavior within a Family of Mononuclear Dy(III) Complexes.

2018

By means of the facile chemistry, structural assembly, and transformation of four mononuclear Dy(III) complexes, Dy(bpad)3·CH3OH·H2O (1), Dy(bpad)2(H2O)2·NO3 (2), [Dy(bpad)2(tmhd)] (3), and [Dy(bpad)2(btfa)] (4) (Hbpad = N3-benzoylpyridine-2-carboxamidrazone, tmhd = 2,2,6,6-tetramethylheptane-3,5-dione, btfa = 3-benzoyl-1,1,1-trifluoroacetone), with distinct architectures and local symmetries were established. The disparity of the coordination geometries around the Dy(III) ion among these complexes impacts the strength of the crystal field and the local tensor of anisotropy ( D) of each Dy site and their relative orientations, therefore giving rise to diverse SIM behaviors with distinguishi…

Field (physics)010405 organic chemistryChemistryRelaxation (NMR)010402 general chemistry01 natural sciences0104 chemical sciencesIonInorganic ChemistryCrystalCrystallographyMagnetic anisotropyAb initio quantum chemistry methodsModulation (music)Physical and Theoretical ChemistryAnisotropyInorganic chemistry
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Gas-phase detection of HSOH: synthesis by flash vacuum pyrolysis of di-tert-butyl sulfoxide and rotational-torsional spectrum.

2003

Gas-phase oxadisulfane (HSOH), the missing link between the well-known molecules hydrogen peroxide (HOOH) and disulfane (HSSH), was synthesized by flash vacuum pyrolysis of di-tert-butyl sulfoxide. Using mass spectrometry, the pyrolysis conditions have been optimized towards formation of HSOH. Microwave spectroscopic investigation of the pyrolysis products allowed-assisted by high-level quantum-chemical calculations--the first measurement of the rotational-torsional spectrum of HSOH. In total, we have measured approximately 600 lines of the rotational-torsional spectrum in the frequency range from 64 GHz to 1.9 THz and assigned some 470 of these to the rotational-torsional spectrum of HSOH …

Flash vacuum pyrolysisChemistryAb initio quantum chemistry methodsTotal angular momentum quantum numberOrganic ChemistryAnalytical chemistryMoleculeGeneral ChemistryRotational spectroscopyMass spectrometryCatalysisCis–trans isomerismIsotopomersChemistry (Weinheim an der Bergstrasse, Germany)
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Flexibility of TTF. a theoretical study

1999

Abstract The folding of tetrathiafulvalene along the S···S axes has been investigated using highly-accurate quantum-chemical calculations. A very flat, two-fold potential is found for neutral TTF where minima correspond to boat conformations (θ ≈ 15–20 °). The flatness of the folding potential indicates that TTF is conformationally more flexible than usually thought.

Flexibility (anatomy)ChemistryMechanical EngineeringFlatness (systems theory)Metals and AlloysCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsFolding (chemistry)Maxima and minimachemistry.chemical_compoundmedicine.anatomical_structureMechanics of MaterialsChemical physicsAb initio quantum chemistry methodsComputational chemistryMaterials ChemistrymedicineMoleculeTetrathiafulvaleneSynthetic Metals
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The mechanism of formamide hydrolysis in water from ab initio calculations and simulations.

2005

The neutral hydrolysis of formamide in water is a suitable reference to quantify the efficiency of proteolytic enzymes. However, experimental data for this reaction has only very recently been obtained and the kinetic constant determined experimentally is significantly higher than that predicted by previous theoretical estimations. In this work, we have investigated in detail the possible mechanisms of this reaction. Several solvent models have been considered that represent a considerable improvement on those used in previous studies. Density functional and ab initio calculations have been carried out on a system which explicitly includes the first solvation shell of the formamide molecule…

FormamideModels MolecularReaction mechanismFormamidesMolecular StructureReaction stepHydrolysisOrganic ChemistryProteolytic enzymesHydrogen BondingGeneral ChemistryReaction intermediateCrystallography X-RayCatalysischemistry.chemical_compoundSolvation shellchemistrySolvent modelsAb initio quantum chemistry methodsComputational chemistryThermodynamicsComputer SimulationChemistry (Weinheim an der Bergstrasse, Germany)
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