Search results for "Basis set"

showing 10 items of 193 documents

1,3-Di(hetero)aryl-7-substituted Pyrenes—An Undiscovered Area of Important Pyrene Derivatives

2019

Despite the pyrene derivatives have been covered extensively by scientists during the last years, many interesting properties and applications of pyrene derivatives have been presented, nowadays there are still areas of pyrenes’ chemistry that need to be fulfilled. Most of the described in literature pyrenes are 1,3,6,8-tetrasubstituted followed by 4,5,9,10-tetrasubstituted, 2,7-, and 1,6-, and 1,8-disubstituted pyrene derivatives. In the case of 1,3-di(hetero)aryl-7-substituted, there are only a few examples of derivatives containing at position 7 - tert-butyl group. In this work, the necessity of synthesis of 1,3-di(hetero)aryl-7-substituted pyrenes is presented based on the results of th…

chemistry.chemical_compoundChemistryGroup (periodic table)ArylNitroMoleculePyreneDensity functional theoryAmine gas treatingCombinatorial chemistryBasis setThe 23rd International Electronic Conference on Synthetic Organic Chemistry
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Synthesis and Conformational Analysis of Saturated3,1,2-Benzoxazaphosphinine 2-Oxides

2005

N-Unsubstituted, N-methyl and N-benzyl cis- and trans-2(hydroxymethyl)cyclohexylamines were subjected to ring closure with phenylphosphonic dichloride, phenyl dichlorophosphate and bis(2-chloroethyl)phosphoramidic dichloride in order to synthesize P-epimeric diastereomers of the corresponding unsubsituted and N-substituted 2-phenyl-, 2phenoxy- and 2-[bis(2-chloroethyl)amino]octahydro-2H3,1,2-benzoxazaphosphinine 2-oxides. The stereochemistry and conformations of the prepared compounds were analyzed mainly by variable-temperature 1 H, 13 C and 31 P NMR spectroscopy. Geometry optimizations were performed for some trans-fused molecules by utilizing the B3LYP DFT method and a locally dense basi…

chemistry.chemical_compoundChemistryStereochemistryOrganic ChemistryDiastereomerMoleculeCyclohexylaminesHydroxymethylNuclear magnetic resonance spectroscopyPhysical and Theoretical ChemistryRing (chemistry)Phenyl dichlorophosphateBasis setEuropean Journal of Organic Chemistry
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ChemInform Abstract: A Theoretical Determination of the Dissociation Energy of the Nitric Oxide Dimer.

2010

Multi-reference CI methods have been applied to determine the dissociation energy and structure of thecis-N2O2 molecule. The convergence of the theoretical result has been checked with respect to a systematic expansion of the one-electron basis set and the multi-reference CI wave function. The best calculated value, 13.8 kJ/mol, is in agreement with the experimental value, 12.2 kJ/mol. It has been obtained with an extended ANO-type basis set [6s5p3d2f], including the effect of the basis set superposition error (BSSE) in the geometry optimization, and additional effects, such as the electron correlation of core electrons and relativistic corrections, using the average coupled pair functional…

chemistry.chemical_compoundElectronic correlationCore electronStereochemistryChemistryDimerMoleculeThermodynamicsGeneral MedicineEnergy minimizationWave functionBond-dissociation energyBasis setChemInform
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Rotational spectra of isotopic species of silyl fluoride. Part II: theoretical and empirical equilibrium structure

2010

Abstract The equilibrium structure of silyl fluoride, SiH 3 F, has been reinvestigated using both theoretical and experimental data. With respect to the former, quantum-chemical calculations at the coupled-cluster level have been employed together with extrapolation to the basis set limit, consideration of higher excitations in the cluster operator, and inclusion of core correlation as well as relativistic corrections ( r (Si–F) = 1.5911 A, r (Si–H) = 1.4695 A, and ∠FSiH = 108.30°). A semi-experimental equilibrium structure has been determined based on the available rotational constants for the various isotopic species of silyl fluoride ( 28 SiH 3 F, 28 SiD 3 F, 29 SiH 3 F, 29 SiD 3 F, 30 S…

chemistry.chemical_compoundMaterials sciencechemistrySilylationOperator (physics)ExtrapolationPhysical chemistryPhysical and Theoretical ChemistryFluorideSpectroscopyAtomic and Molecular Physics and OpticsSpectral lineBasis set
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Interpretation of the electronic absorption spectrum of free base porphin by using multiconfigurational second-order perturbation theory

1998

Abstract Multiconfigurational second-order perturbation (CASPT2) calculations have been performed on the low-lying optically allowed valence excited states of the free base porphin molecule in order to assign the four lowest bands of the spectrum. The low-lying triplet states have also been characterized. A basis set of the atomic natural orbital type of split-valence plus polarization quality for first-row atoms has been employed. Polarization functions are important for an accurate description of the transitions. These CASPT2 results provide a consistent picture of the experimental spectrum. Each band of the spectrum up to 4.5 eV is composed of a pair of states, which become degenerate in…

chemistry.chemical_compoundValence (chemistry)Absorption spectroscopychemistryAb initio quantum chemistry methodsExcited stateDegenerate energy levelsGeneral Physics and AstronomyPhysical and Theoretical ChemistryAtomic physicsBasis setSpectral linePorphinChemical Physics Letters
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Comparison of the molecular structure and spectra of benzene and borazine

1970

Ab initio SCF MO and CI calculations for two different gaussian basis sets are carried out for the isoelectronic molecules benzene C6H6 and borazine B3N3H3 in order to investigate the effect of increasing the flexibility in the representation of their respective π systems. In the process it is found from comparison of orbital charge density contour diagrams and inner shell orbital energies of borazine with analogous data for other systems that the BN bonds of this compound are considerably less polar (B+N−) than that of ammonia borane BNH6 (B−N+). CI calculations employing the larger basis set produce generally better agreement with the experimental transition energies of benzene than do th…

chemistry.chemical_compoundchemistryBorazineAb initioCharge densityMoleculeChiropracticsPhysical and Theoretical ChemistryAtomic physicsBenzeneExcitationBasis setSpectral lineTheoretica Chimica Acta
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Ferromagnetic exchange in a twisted, oxime-bridged [mniii2] dimer

2012

Journal article The dimeric complex [MnIII2(Naphth-sao)2(Naphth-saoH)2(MeOH)2][middle dot]4MeOH (1[middle dot]4MeOH), acts as a simple model complex with which to examine the magneto-structural relationship in polymetallic, oxime-bridged MnIII complexes. Dc magnetic susceptibility studies reveal that ferromagnetic exchange is mediated through the heavily twisted Mn-O-N-Mn moiety (J = +1.24 cm-1) with magnetisation measurements at low temperatures and high fields suggesting significant anisotropy. Simulations of high field, high frequency EPR data reveal a single ion anisotropy, D(MnIII) = -3.94 cm-1. Theoretical studies on simplified model complexes of 1 reveal that calculated values of the…

complexes/dk/atira/pure/subjectarea/asjc/1600/1604familyni(ii)ligandsDimerMagnetic susceptibilityIonlaw.inventionInorganic Chemistryatoms lichemistry.chemical_compoundCrystallographyMagnetizationaxis extra linesSingle-Molecule Magnetselectron-paramagnetic-resonancechemistryFerromagnetismlawkrgaussian-basis setsMoietyAnisotropyElectron paramagnetic resonance
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Synthesis, crystal structure, DFT calculations, Hirshfeld surface, vibrational and optical properties of a novel hybrid non-centrosymmetric material …

2019

This present work undertakes the study of a novel organic–inorganic hybrid material, which has been obtained successfully by an acid-base reaction at room temperature and structurally studied by the single crystal X-ray diffraction method. (C10H15N2)2H2P2O7 crystallizes in the triclinic system with the non-centrosymmetric space group P1 with the following lattice parameters: a = 5.9159(2) Å, b = 13.8451(6) Å, c = 14.5973(5) Å, ? = 74.507(2)°, ? = 89.980(2)°, ? = 89.231(2)° with V = 1152.06(8) Å3 and Z = 2. The X-ray structural analysis supported by a detailed Hirshfeld 2D fingerprint plots has been performed to elucidate the different inter-contacts in the crystal structure mainly associate…

crystal structure010405 organic chemistryChemistryOrganic ChemistryMulliken chargesCrystal structureTriclinic crystal systemMEP010402 general chemistry01 natural sciencesDFT0104 chemical sciencesAnalytical Chemistrynon-centrosymmetric hybrid materialInorganic ChemistryCrystallographyMolecular vibrationNon–centrosymmetric hybrid materialDensity functional theoryHOMO-LUMOGround stateMulliken population analysisSingle crystalSpectroscopyBasis set
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Crystal structure, Hirshfeld surface analysis and DFT studies of (E)-1-(4-bromophenyl)-3-(3-fluorophenyl)prop-2-en-1-one

2018

The title halogenated organic chalcone was prepared by a Claisen–Schmidt condensation reaction. A Hirshfeld surface analysis was carried out to reveal the percentage contributions of the inter­molecular inter­actions. A theoretical study was performed using the density functional theory (DFT) at B3LYP with the 6–311 G++(d,p) basis set level to compare with the experimental results of the X-ray analysis and UV–vis absorption analysis in term of the geometrical parameters, HOMO-LUMO energy gap and charge distributions.

crystal structureCrystal structure010402 general chemistry010403 inorganic & nuclear chemistryDFT01 natural sciencesResearch Communicationslcsh:ChemistryCrystalHOMO–LUMOmolecular electrostatic potentialNucleophileGeneral Materials ScienceHOMO/LUMOBasis setmol­ecular electrostatic potentialUV–visHydrogen bondChemistryHirshfeld surfaceGeneral ChemistryCondensed Matter Physics0104 chemical sciencesCrystallographylcsh:QD1-999Electrophilehalogen chalconeDensity functional theoryActa Crystallographica Section E Crystallographic Communications
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Calculation of the conformational dependence of valence and Rydberg states in n-tetrasilane

1999

Abstract Previous CIS/6-31G ∗∗ and CASSCF/6-31G ∗ calculations of valence excited states of n -tetrasilane accounted qualitatively for the observed conformational dependence of condensed-phase UV absorption spectra. In an attempt to understand this result, we have performed CIS calculations with a larger basis set (MC-311G(2d) on Si, 6-311G on H, and 2s, 2p, and 2d diffuse orbitals at molecular center of mass). The first two excited states are of valence character at all dihedral angles if the molecule is isolated. When it is embedded in a rare gas cluster, the lowest four states are of valence character, and the results are nearly identical with those obtained without diffuse orbitals in t…

education.field_of_studyValence (chemistry)PopulationGeneral Physics and Astronomychemistry.chemical_compoundModern valence bond theorysymbols.namesakechemistryExcited stateRydberg formulasymbolsPhysical and Theoretical ChemistryAtomic physicseducationGeneralized valence bondDisileneBasis setChemical Physics
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