Search results for "Basis set"

showing 10 items of 193 documents

Factors Governing the Chemical Stability and NMR Parameters of Uracil Tautomers and Its 5-Halogen Derivatives

2020

We report on the density functional theory (DFT) modelling of structural, energetic and NMR parameters of uracil and its derivatives (5-halogenouracil (5XU), X = F, Cl, Br and I) in vacuum and in water using the polarizable continuum model (PCM) and the solvent model density (SMD) approach. On the basis of the obtained results, we conclude that the intramolecular electrostatic interactions are the main factors governing the stability of the six tautomeric forms of uracil and 5XU. Two indices of aromaticity, the harmonic oscillator model of aromaticity (HOMA), satisfying the geometric criterion, and the nuclear independent chemical shift (NICS), were applied to evaluate the aromaticity of ur…

Models MolecularMagnetic Resonance SpectroscopyNICSsolvent stabilizationMolecular ConformationPharmaceutical SciencePolarizable continuum modelDFTArticleAnalytical Chemistrylcsh:QD241-441tautomersHalogenslcsh:Organic chemistryComputational chemistryDrug DiscoveryHOMAPhysical and Theoretical ChemistryUracilDensity Functional TheoryBasis setMolecular Structure5-halogenouracil (5XU)ChemistryChemical shiftOrganic ChemistryAromaticityaromaticityTautomerChemistry (miscellaneous)Intramolecular forceSolventsMolecular MedicineChemical stabilityDensity functional theoryMolecules
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DFT study of zigzag (n, 0) single-walled carbon nanotubes: 13C NMR chemical shifts

2016

Abstract 13 C NMR chemical shifts of selected finite-size models of pristine zigzag single walled carbon nanotubes (SWCNTs) with a diameter of ∼0.4–0.8 nm and length up to 2.2 nm were studied theoretically. Results for finite SWCNTs models containing 1, 4 and 10 adjacent bamboo-type units were compared with data obtained for infinite tubes in order to estimate the reliability of small finite models in predicting magnetic properties of real-size nanotubes and to assess their tube-length dependence. SWCNTs were fully optimized using unrestricted density functional theory (DFT-UB3LYP/6-31G*). Cyclacenes, as the shortest models of open-ended zigzag SWCNTs, with systematically varying diameter w…

Models MolecularMaterials science02 engineering and technologyCarbon nanotube010402 general chemistryDFT01 natural sciencesMolecular physicslaw.inventionlawComputational chemistryMaterials ChemistryCarbon-13 Magnetic Resonance SpectroscopyPhysical and Theoretical ChemistrySpectroscopyBasis setNanotubes Carbontheoretical modelingChemical shiftCarbon-13Carbon-13 NMR021001 nanoscience & nanotechnologyzigzag SWCNTComputer Graphics and Computer-Aided DesignNMR0104 chemical sciencesReal sizeZigzagQuantum TheorycyclacenesDensity functional theory0210 nano-technologyJournal of Molecular Graphics and Modelling
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A quantum-chemical study of the structure, vibrations and SiH bond properties of disilylamine, NH(SiH3)2.

2002

Quantum-chemical calculations at HF, MP2 and B3LYP levels with 6-31G* and 6-311G** basis sets are reported for disilylamine, NH(SiH3)2. The equilibrium structure is found to vary with both level and basis set, all but one of the structures exhibiting a small lack of planarity of the HNSi2 system. The barrier to inversion, however, is found to be very low, at most 38 cm(-1). Vibration frequencies and intensities are calculated. The frequencies are scaled, where possible, either using updated infrared data or with the aid of factors transferred from N(CH3)(SiH3)2. Unobserved frequencies due to the v(s)NSi2, deltaNSi2 and delta(perpendicular)NH modes are predicted near 610, 210 and 360 cm(-1),…

Models MolecularSiliconSpectrophotometry InfraredChemistrySilicon CompoundsBiophysicsInfrared spectroscopyHydrogen atomHyperconjugationSpectrum Analysis RamanPotential energyAtomic and Molecular Physics and OpticsBiophysical PhenomenaAnalytical Chemistrysymbols.namesakesymbolsQuantum TheoryAtomic physicsInstrumentationMulliken population analysisSpectroscopyBasis setRaman scatteringNatural bond orbitalSpectrochimica acta. Part A, Molecular and biomolecular spectroscopy
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Accurate Treatment of Large Supramolecular Complexes by Double-Hybrid Density Functionals Coupled with Nonlocal van der Waals Corrections.

2015

In this work, we present a thorough assessment of the performance of some representative double-hybrid density functionals (revPBE0-DH-NL and B2PLYP-NL) as well as their parent hybrid and GGA counterparts, in combination with the most modern version of the nonlocal (NL) van der Waals correction to describe very large weakly interacting molecular systems dominated by noncovalent interactions. Prior to the assessment, an accurate and homogeneous set of reference interaction energies was computed for the supramolecular complexes constituting the L7 and S12L data sets by using the novel, precise, and efficient DLPNO-CCSD(T) method at the complete basis set limit (CBS). The correction of the bas…

Models MolecularWork (thermodynamics)Macromolecular SubstancesAccurate treatmentSupramolecular chemistryVan der Waals surfaceDouble-hybrid density functionalsSet (abstract data type)symbols.namesakeLarge supramolecular complexesQuantum mechanicsNon-covalent interactionsComputer SimulationQuímica FísicaLimit (mathematics)Statistical physicsPhysical and Theoretical ChemistryBasis setNonlocal van der Waals correctionschemistry.chemical_classificationChemistryComputer Science ApplicationsModels ChemicalsymbolsQuantum Theoryvan der Waals forceHydrophobic and Hydrophilic InteractionsJournal of chemical theory and computation
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The prediction of molecular equilibrium structures by the standard electronic wave functions

1997

A systematic investigation has been carried out of the accuracy of molecular equilibrium structures of 19 small closed-shell molecules containing first-row atoms as predicted by the following standard electronic ab initio models: Hartree–Fock (HF) theory, Mo/ller–Plesset theory to second, third, and fourth orders (MP2, MP3, and MP4), coupled-cluster singles and doubles (CCSD) theory; CCSD theory with perturbational triples corrections [CCSD(T)], and the configuration-interaction singles and doubles (CISD) model. For all models, calculations were carried out using the correlation-consistent polarized valence double-zeta (cc-pVDZ) basis, the correlation-consistent polarized valence triple-zet…

Modern valence bond theoryValence (chemistry)ChemistryAb initio quantum chemistry methodsPhysics::Atomic and Molecular ClustersAb initioGeneral Physics and AstronomyMoleculePhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsWave functionBasis set
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Novel second-order nonlinear optical polymer materials containing indandione derivativatives as a chromophore

2006

Second order non linear optical (NLO) properties of sPMMA based host-guest systems containing eight dimethylaminobenzylidene -1, 3 - indandione (DMABI) related chromophores have been investigated by means of quantum chemical calculations and SHG experimental characterization. Ab initio calculations with basis set 6-31G were used for molecular geometry determination as well as in the calculations of molecular hyperpolarizability by FF approach. Influence of the chromophore concentration on the host-guest film NLO performance was obtained by SHG Maker fringe experiments. The highest value of d53233 =80 pm/V (frequency corrected value d033 =12 pm/V) at chromophore concentration 15 %wt have bee…

Molecular geometryAb initio quantum chemistry methodsChemistryComputational chemistrySecond-harmonic generationPhysical chemistryHyperpolarizabilityNonlinear opticsChromophoreCorona polingBasis setSPIE Proceedings
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Nuclear Quadrupole Moment of 119Sn

2008

Second-order scalar-relativistic Douglas-Kroll-Hess density functional calculations of the electric field gradient, including an analytic correction of the picture change error, were performed for 34 tin compounds of which molecular structures and Sn-119 Mossbauer spectroscopy parameters are experimentally known. The components of the diagonalized electric field gradient tensor, V-xx,V-yy, V-zz, were used to determine the quantity V, which is proportional to the nuclear quadrupole splitting parameter Delta E. The slope of the linear correlation plot of the experimentally determined Delta E parameter versus the corresponding calculated V data allowed us to obtain an absolute value of the nuc…

Mössbauer spectroscopyrelativistic effectAnalytical chemistrychemistry.chemical_elementAbsolute valueQuadrupole splittingelectric field gradientchemistryCore electronSettore CHIM/03 - Chimica Generale E InorganicaElectric fieldtinQuadrupolePhysical and Theoretical ChemistryAtomic physicsTinElectric field gradientBasis setnuclear quadrupole splitting
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Method and basis set dependence of the NICS indexes of aromaticity for benzene

2018

The role of theory level in prediction of benzene magnetic indexes of aromaticity is analysed and compared with calculated nuclear magnetic shieldings of 3 He used as NMR probe. Three closely related nucleus-independent chemical shift (NICS) based indexes were calculated for benzene at SCF-HF, MP2, and DFT levels of theory and the impact of basis set on these quantities was studied. The changes of benzene NICS(0), NICS(1), and NICS(1)zz parameters calculated using SCF-HF, MP2 and several density functionals were within 1 to 3 ppm. Similar deviations between magnetic indexes of aromaticity were observed for values calculated with selected basis sets. Only very small effect of polar solvent o…

NICS010304 chemical physicsHelium atomIsotropyAromaticityaromaticityGeneral Chemistry010402 general chemistryRing (chemistry)DFT01 natural sciencesMolecular physicsNMR0104 chemical sciencesbenzenechemistry.chemical_compoundchemistry0103 physical sciencesAtomPhysics::Atomic and Molecular ClustersPolarGeneral Materials SciencePhysics::Chemical PhysicsBenzeneBasis setMagnetic Resonance in Chemistry
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Electron Correlation or Basis Set Quality: How to Obtain Converged and Accurate NMR Shieldings for the Third-Row Elements?

2022

The quality of theoretical NMR shieldings calculated at the quantum-chemical level depends on various theoretical aspects, of which the basis set type and size are among the most important factors. Nevertheless, not much information is available on the basis set effect on theoretical shieldings of the NMR-active nuclei of the third row. Here, we report on the importance of proper basis set selection to obtain accurate and reliable NMR shielding parameters for nuclei from the third row of the periodic table. All calculations were performed on a set of eleven compounds containing the elements Na, Mg, Al, Si, P, S, or Cl. NMR shielding tensors were calculated using the SCF-HF, DFT-B3LYP, and C…

NMR shieldingsbasis set dependencethird-row elementsMolecules
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Structure Validation of Natural Products by Quantum-Mechanical GIAO Calculations of 13C NMR Chemical Shifts GIAO=gauge including atomic orbitals.

2002

Geometry optimization and GIAO (gauge including atomic orbitals) 1 3 C NMR chemical shift calculations at Hartree-Fock level, using the 6-31G(d) basis set, are proposed as a tool to be applied in the structural characterization of new organic compounds, thus providing useful support in the interpretation of experimental NMR data. Parameters related to linear correlation plots of computed versus experimental 1 3 C NMR chemical shifts for fourteen low-polar natural products, containing 10-20 carbon atoms, were employed to assess the reliability of the proposed structures. A comparison with the hybrid B3LYP method was carried out to evaluate electron correlation contributions to the calculatio…

NMR spectra databaseElectronic correlationAb initio quantum chemistry methodsComputational chemistryChemistryChemical shiftOrganic ChemistryStructure validationGeneral ChemistryNuclear magnetic resonance spectroscopyCarbon-13 NMRCatalysisBasis setChemistry - A European Journal
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