Search results for " Quantum chemistry"

showing 10 items of 549 documents

Island Homoaromaticity in the W-Shaped 2,4-Diphospha-3-arsapentadienide Anion and Related Compounds - Theoretical and Experimental Investigations

2012

A series of anions with general formula (R2C=P)2Pn– (Pn = N, P, As, Sb; R = H, Me, CF3, SiH3, SiMe3, SiF3) was investigated theoretically at the DFT (RI-BP86/TZVP) and RI-MP2/TZVP levels of approximation. Significantly sharpened central PPnP bond angles were predicted for the species with π-acceptor R substituents. The corresponding bond angle values decrease in the order Pn = N >> P > As > Sb. This finding is in agreement with the previously published structural data for [(Me3Si)2C=P]2P–. An island homoaromaticity was proposed as a suitable explanation for the observed effect. In more detail, it consists of shifting negative charge to the electron-withdrawing terminal groups with formation…

AnionsHomoaromaticity010405 organic chemistryChemistryCharge (physics)010402 general chemistry01 natural sciencesHomoaromaticity0104 chemical sciencesIonInorganic ChemistryCrystallographyDensity functional calculationsMolecular geometryComputational chemistryAb initio quantum chemistry methodsMolecular orbitalsMoleculeMoietyMolecular orbitalAb initio calculations
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Development of La3+ Doped CeOthick film humidity sensors

2014

Published version of an article in the journal: Abstract and Applied Analysis. Also available from the publisher at: http://dx.doi.org/10.1155/2014/297632 Open Access The humidity sensitive characteristics of the sensor fabricated from 10 mol% Ladoped CeOnanopowders with particle size 17.26 nm synthesized via hydrothermal method were investigated at different frequencies. It was found that the sensor shows high humidity sensitivity, rapid response-recovery characteristics, and narrow hysteresis loop at 100 Hz in the relative humidity range from 11% to 95%. The impedance of the sensor decreases by about five orders of magnitude as relative humidity increases. The maximum humidity hysteresis …

Applied MathematicsVDP::Mathematics and natural science: 400::Chemistry: 440::Theoretical chemistry quantum chemistry: 444Analysis; Applied MathematicsVDP::Mathematics and natural science: 400::Mathematics: 410::Analysis: 411Analysis
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A new force field including charge directionality for TMAO in aqueous solution

2016

We propose a new force field for trimethylamine N-oxide (TMAO), which is designed to reproduce the long-lived and highly directional hydrogen bond between the TMAO oxygen (OTMAO) atom and surrounding water molecules. Based on the data obtained by ab initio molecular dynamics simulations, we introduce three dummy sites around OTMAO to mimic the OTMAO lone pairs and we migrate the negative charge on the OTMAO to the dummy sites. The force field model developed here improves both structural and dynamical properties of aqueous TMAO solutions. Moreover, it reproduces the experimentally observed dependence of viscosity upon increasing TMAO concentration quantitatively. The simple procedure of the…

Aqueous solution010304 chemical physicsChemistryHydrogen bondGeneral Physics and Astronomy010402 general chemistry01 natural sciencesForce field (chemistry)0104 chemical sciencesMolecular dynamicsChemical physicsComputational chemistryAb initio quantum chemistry methods0103 physical sciencesMoleculeDirectionalityPhysical and Theoretical ChemistryLone pairThe Journal of Chemical Physics
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Calculation of the relative basicities of methylamines in solution

1990

Abstract The relative basicities in solution of the methylamines have been calculated using the model of Miertus, Scrocco and Tomasi to describe the solvent effect. The surface of the cavity is defined with the GEPOL method. The ab initio calculations have been performed using a 4-31G basis set. The relative order is reproduced using a combination of the gas-phase proton affinities obtained with quantum-mechanical methods by Eades, Weil, Dixon and Douglass and the solvation values obtained by us. The results seem to point out that the irregular order is not due to solvent but to basis-set effects.

Aqueous solutionProtonChemistrySolvationGeneral Physics and AstronomyThermodynamicsAffinitiesComputational chemistryAb initio quantum chemistry methodsPhysics::Chemical PhysicsPhysical and Theoretical ChemistrySolvent effectsMethylaminesBasis set
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Application of SQMFF Vibrational Calculations to Transition States:  DFT and ab Initio Study of the Kinetics of Methyl Azide and Ethyl Azide Thermoly…

1998

DFT including nonlocal corrections and ab initio calculations at MP2 and MP4 levels of theory have been performed in order to provide information concerning the mechanism of the rate limiting step of the thermal decomposition of methyl azide and ethyl azide. The chemically interesting points of the ground-state potential energy surface have been fully optimized, and a detailed normal-mode analysis for the reagents and the transition states is presented. The well-established scaled quantum mechanical force field method has been used to obtain reliable vibrational frequencies for these molecular structures. The force fields of transition states have been modified by using the scale factors co…

Arrhenius equationAb initioThermodynamicsTransition statesymbols.namesakeTransition state theorychemistry.chemical_compoundchemistryAb initio quantum chemistry methodsComputational chemistryPotential energy surfacesymbolsPhysics::Chemical PhysicsPhysical and Theoretical ChemistryGround stateMethyl azideThe Journal of Physical Chemistry A
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Modeling of Point Defects in Corundum Crystals

1994

Several different approaches including Hartree-Fock ab initio cluster calculations, semiempirical INDO calculations, and atom-atom potentials were used for modeling of the spatial and electronic structure as well as migration mechanisms of both intrinsic defects (self-trapped and defect-trapped holes, O and Al vacancies) and impurities (transition-metal ions like Co, Fe, Mg, Mn, Ti). The atomic structure of all hole centers is found to be similar to V[sub K] centers in alkali halides (two-site model); their formation is energetically favorable. The energy required for 60[degree] hole reorientations inside the basic oxygen triangles is found to be similar to both the energy for hops between …

Arrhenius equationMaterials scienceAb initioIonic bondingElectronic structureActivation energyMolecular physicsIonsymbols.namesakeAb initio quantum chemistry methodsVacancy defectPhysics::Atomic and Molecular ClustersMaterials ChemistryCeramics and CompositessymbolsPhysical chemistryJournal of the American Ceramic Society
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A theoreticalab initiostudy on the H2NO + O3reaction

2003

The deviation of the NH2 pseudo-first-order decay Arrhenius plots of the NH2 + O3 reaction at high ozone pressures measured by experimentalists, has been attributed to the regeneration of NH2 radicals due to the subsequent reactions of the products of this reaction with ozone. Although these products have not yet been characterized experimentally, the radical H2NO has been postulated, because it can regenerate NH2 radicals through the reactions: H2NO + O3 NH2 + O2 and H2NO + O3 HNO + OH + O2. With the purpose of providing a reasonable explanation from a theoretical point of view to the kinetic observed behaviour of the NH2 + O3 system, we have carried ab initio electronic structure calculat…

Arrhenius equationReaction mechanismChemistryRadicalAb initioGeneral ChemistryElectronic structureKinetic energyComputational Mathematicssymbols.namesakeAb initio quantum chemistry methodsComputational chemistryAtmospheric chemistrysymbolsJournal of Computational Chemistry
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Study of the reflection spectrum of the accreting neutron star GX 3+1 using XMM-Newton and INTEGRAL

2015

Broad emission features of abundant chemical elements, such as Iron, are commonly seen in the X-ray spectra of accreting compact objects and their studies can provide useful information about the geometry of the accretion processes. In this work, we focus our attention on GX 3+1, a bright, persistent accreting low mass X-ray binary, classified as an atoll source. Its spectrum is well described by an accretion disc plus a stable comptonizing, optically thick corona which dominates the X-ray emission in the 0.3-20 keV energy band. In addition, four broad emission lines are found and we associate them with reflection of hard photons from the inner regions of the accretion disc where doppler an…

Astrophysics::High Energy Astrophysical PhenomenaFOS: Physical sciencesAstrophysicsAstrophysics::Cosmology and Extragalactic AstrophysicsSpectral lineSettore FIS/05 - Astronomia E AstrofisicaIonizationAstrophysics::Solar and Stellar AstrophysicsEmission spectrumAccretion accretion discAstrophysics::Galaxy AstrophysicsSolar and Stellar Astrophysics (astro-ph.SR)PhysicsHigh Energy Astrophysical Phenomena (astro-ph.HE)Accretion (meteorology)AstronomyAstronomy and AstrophysicsX-rays: binarieStars: neutronNeutron starAstrophysics - Solar and Stellar AstrophysicsSpace and Planetary ScienceReflection (physics)X-rays: individual (GX 3+1)Low MassRelativistic quantum chemistryAstrophysics - High Energy Astrophysical Phenomena
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First-principles nonequilibrium Green's-function approach to transient photoabsorption: Application to atoms

2015

We put forward a first-principle NonEquilibrium Green's Function (NEGF) approach to calculate the transient photoabsorption spectrum of optically thin samples. The method can deal with pump fields of arbitrary strength, frequency and duration as well as for overlapping and nonoverlapping pump and probe pulses. The electron-electron repulsion is accounted for by the correlation self-energy, and the resulting numerical scheme deals with matrices that scale quadratically with the system size. Two recent experiments, the first on helium and the second on krypton, are addressed. For the first experiment we explain the bending of the Autler-Townes absorption peaks with increasing the pump-probe d…

Atomic Physics (physics.atom-ph)FOS: Physical sciencesNon-equilibrium thermodynamicschemistry.chemical_elementPhysics - Atomic PhysicsSettore FIS/03 - Fisica della MateriaIonsymbols.namesakeAtomic and Molecular Physics; OpticsAb initio quantum chemistry methodsAtomic and Molecular PhysicsMesoscale and Nanoscale Physics (cond-mat.mes-hall)nonequilibrium Green's-functionAbsorption (electromagnetic radiation)HeliumPhysicsta114Condensed Matter - Mesoscale and Nanoscale PhysicsKryptonOpticsFunction (mathematics)Atomic and Molecular Physics and OpticsphotoabsorptionchemistryGreen's functionsymbolsAtomic physicsPhysical Review A
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Systematic trends in (0 0 1) surface ab initio calculations of ABO 3 perovskites

2018

This work was supported by the Latvian Council of Science Grant No. 374/2012 and the Latvian National Research Program IMIS2. Many stimulating discussions with D. Vanderbilt, K.M. Rabe, M. Rohlfing, E. Heifets, J. Maier, G. Borstel and E.A. Kotomin are greatly acknowledged.

B3LYPBand gapABO3 perovskitesPopulation02 engineering and technology01 natural scienceslcsh:ChemistryCrystalAb initio quantum chemistry methodsComputational chemistry0103 physical sciences:NATURAL SCIENCES:Physics [Research Subject Categories]Surface layer010306 general physicseducationPerovskite (structure)(0 0 1) surfaceseducation.field_of_studyCondensed matter physicsChemistryRelaxation (NMR)General Chemistry021001 nanoscience & nanotechnologyB3PWlcsh:QD1-999Chemical bondAb initio calculations0210 nano-technologyJournal of Saudi Chemical Society
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