Search results for "Calculation"

showing 10 items of 594 documents

Study of heavy meson production in p-Pb collisions at $\sqrt{S}$=5.02 TeV in the general-mass variable-flavour-number scheme

2017

Nuclear physics / B 925, 415 - 430 (2017). doi:10.1016/j.nuclphysb.2017.10.016

CMSnucleusFOS: Physical sciencesinitial-state interaction530High Energy Physics - PhenomenologyHigh Energy Physics - Phenomenology (hep-ph)CERN LHC CollALICEproduction [bottom]heavy [meson]ddc:530High Energy Physics::Experimentcross section [p p]Nuclear Experimentnumerical calculationscharmproduction [meson]1 [higher-order]
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The one loop gluon emission light cone wave function

2017

Light cone perturbation theory has become an essential tool to calculate cross sections for various small-$x$ dilute-dense processes such as deep inelastic scattering and forward proton-proton and proton-nucleus collisions. Here we set out to do one loop calculations in an explicit helicity basis in the four dimensional helicity scheme. As a first process we calculate light cone wave function for one gluon emission to one-loop order in Hamiltonian perturbation theory on the light front. We regulate ultraviolet divergences with transverse dimensional regularization and soft divergences with using a cut-off on longitudinal momentum. We show that when all the renormalization constants are comb…

COLLISIONSParticle physicsNuclear TheoryRENORMALIZATIONQUANTUM ELECTRODYNAMICSGeneral Physics and AstronomyFOS: Physical sciencesloop calculations114 Physical sciences01 natural scienceslight cone perturbation theoryRenormalizationNuclear Theory (nucl-th)Dimensional regularizationHigh Energy Physics - Phenomenology (hep-ph)INFINITE-MOMENTUMLight cone0103 physical sciencesSCATTERINGHelicity basis010306 general physicsNuclear ExperimentQuantum chromodynamicsPhysicsCoupling constantgluon emissionta114010308 nuclear & particles physicsCOLOR GLASS CONDENSATEDeep inelastic scatteringFRONT QCDHelicityEVOLUTIONHigh Energy Physics - PhenomenologyCHROMODYNAMICSQuantum electrodynamicsgluon saturation
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Cobalt Electrolyte/Dye Interactions in Dye-Sensitized Solar Cells: A Combined Computational and Experimental Study

2012

We report a combined experimental and computational investigation to understand the nature of the interactions between cobalt redox mediators and TiO2 surfaces sensitized by :ruthenium and organic dyes, and their impact on. the performance of the corresponding dye-sensitized solar cells (DSSCs). We : focus: on different ruthenium dyes and fully organic dyes, to understand the dramatic loss of efficiency observed for the prototype Ru(II) N719 dye in conjunction with :Cobalt: electrolytes. Both N719- and Z907-based DSSCs showed an increased lifetime in iodine-based electrolyte compared to the cobalt-based redox-shuttle; While the organic D21L6 and D25L6 cycles endowed.With long alkoxy chains,…

COLLOIDAL TIO2 FILMSinorganic chemicalsLOW QUANTUM YIELDSInorganic chemistrychemistry.chemical_element02 engineering and technologyElectrolyte010402 general chemistryPhotochemistry01 natural sciencesBiochemistryRedoxREDOX COUPLECatalysisEFFECTIVE CORE POTENTIALSDENSITY-FUNCTIONAL THEORYColloid and Surface ChemistryDENSITY-FUNCTIONAL THEORY; EFFECTIVE CORE POTENTIALS; INTRAMOLECULAR ELECTRON-TRANSFER; TRANSITION-METAL-COMPLEXES; COLLOIDAL TIO2 FILMS; LOW QUANTUM YIELDS; MOLECULAR CALCULATIONS; REDOX COUPLE; MAGNETIC-PROPERTIES; PHOTOVOLTAIC CELLSMAGNETIC-PROPERTIESPHOTOVOLTAIC CELLSLigandGeneral Chemistry021001 nanoscience & nanotechnologyMOLECULAR CALCULATIONSTRANSITION-METAL-COMPLEXES0104 chemical sciencesMarcus theoryRutheniumDye-sensitized solar cellchemistryAlkoxy groupINTRAMOLECULAR ELECTRON-TRANSFER0210 nano-technologyCobalt
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Effect of electron-withdrawing substituents on the electrophilicity of carbonyl carbons

2005

Indexación: Scopus The substituent effects on the carbonyl carbon atom for a series of twelve substituted phenyl acetates have been rationalized using a global electrophilicity index. This index is linearly correlated with the experimental reaction rate coefficients. We found that, in contrast to the proposed interpretation based on experimental 13C NMR chemical shifts and ground state destabilization calculations, the electrophilicity of carbonyl compounds increases due to the effect promoted by electron-withdrawing groups in these systems. https://www.sciencedirect.com/science/article/pii/S0040402004018046?via%3Dihub

Carbon atomChemistryChemical shiftOrganic ChemistrySubstituentcarbonyl derivativecarbonylCarbon-13 NMRcarbon nuclear magnetic resonancePhotochemistryDFT calculationsBiochemistryMedicinal chemistryParrReaction rateElectron-withdrawing effectschemistry.chemical_compoundElectronegativityDrug DiscoveryElectrophilePolar effectChemical Reactivityphenylacetic acid derivativeElectrophilicityGround state
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Assessment for the mean value total dressing method: Comparison with coupled cluster including triples methods for BF, NO+, CN+, C2, BeO, NH3, CH2, H…

1997

Limited previous experience with the mean value total dressing (MVTD) method had shown that MVTD energies for closed shell systems are generally better than CCSD(T) ones compared to FCI. The method, previously published as total dressing 2′(td-2′), is based on the single reference intermediate Hamiltonian theory. It is not a CC method but deals in a great part with the same physical effects that CC methods that incorporate amplitudes of triples such as CCSDT or its CCSDT-1n approaches. A number of test calculations comparing to diverse CC methods, as well as FCI and experiment when available, have been performed. The tests concern equilibrium energies in NH3 and CH2, equilibrium energies an…

Carbon compoundsGeneral Physics and AstronomyBoron compounds ; Nitrogen compounds ; Water ; Ammonia ; Ozone ; Organic compounds ; Carbon compounds ; Beryllium compounds ; Hydrogen compounds ; Silicon compounds ; Lithium ; Lithium compounds ; Carbon ; Neon compounds ; Coupled cluster calculations ; Dissociation ; Dissociation energies ; Positive ionsLithiumDissociation (chemistry)Nitrogen compoundsIonDissociation energiesOzoneCoupled cluster calculationsAmmoniaBeryllium compoundsOrganic compoundsMoleculeSilicon compoundsPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]Open shellChemistryNeon compoundsMean valueWaterLithium compoundsHydrogen compoundsDiatomic moleculeCarbonUNESCO::FÍSICA::Química físicaCoupled clusterAmplitudeBoron compoundsPositive ionsAtomic physicsDissociation
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New fitting scheme to obtain effective potential from Car-Parrinello molecular dynamics simulations: Application to silica

2008

A fitting scheme is proposed to obtain effective potentials from Car-Parrinello molecular dynamics (CPMD) simulations. It is used to parameterize a new pair potential for silica. MD simulations with this new potential are done to determine structural and dynamic properties and to compare these properties to those obtained from CPMD and a MD simulation using the so-called BKS potential. The new potential reproduces accurately the liquid structure generated by the CPMD trajectories, the experimental activation energies for the self-diffusion constants and the experimental density of amorphous silica. Also lattice parameters and elastic constants of alpha-quartz are well-reproduced, showing th…

Car–Parrinello molecular dynamicsMaterials sciencemolecular dynamics calculations (Car-Parrinello) and other numerical simulationsTransferabilityGeneral Physics and AstronomyFOS: Physical sciences02 engineering and technologyglasses01 natural sciencesMolecular physicsMolecular dynamicsLattice (order)0103 physical sciences[PHYS.COND.CM-DS-NN]Physics [physics]/Condensed Matter [cond-mat]/Disordered Systems and Neural Networks [cond-mat.dis-nn]010306 general physicsdensity functional theoryCondensed Matter - Materials Sciencegradient and other correctionsMaterials Science (cond-mat.mtrl-sci)Disordered Systems and Neural Networks (cond-mat.dis-nn)computer simulation of liquid structureCondensed Matter - Disordered Systems and Neural Networks021001 nanoscience & nanotechnologylocal density approximation[PHYS.COND.CM-MS]Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]Amorphous silica0210 nano-technologyPair potential
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Anion-driven encapsulation of cationic guests inside pyridine[4]arene dimers

2019

Pyridine[4]arenes have previously been considered as anion binding hosts due to the electron-poor nature of the pyridine ring. Herein, we demonstrate the encapsulation of Me4N+ cations inside a dimeric hydrogen-bonded pyridine[4]arene capsule, which contradicts with earlier assumptions. The complexation of a cationic guest inside the pyridine[4]arene dimer has been detected and studied by multiple gas-phase techniques, ESI-QTOF-MS, IRMPD, and DT-IMMS experiments, as well as DFT calculations. The comparison of classical resorcinarenes with pyridinearenes by MS and NMR experiments reveals clear differences in their host–guest chemistry and implies that cation encapsulation in pyridine[4]arene…

Cation bindingmassaspektrometriaanionitDimerpyridinearenes010402 general chemistryDFT calculations01 natural sciencesFull Research Paperdft calculationsIonlcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryPolymer chemistryPyridinesupramolekulaarinen kemiaresorcinarenesInfrared multiphoton dissociationcation bindingAnion bindinglcsh:Science010405 organic chemistryChemistrytiheysfunktionaaliteoriaOrganic ChemistryCationic polymerizationkationit5470104 chemical sciences3. Good healthChemistryion mobility mass spectrometrymacrocycleslcsh:QBeilstein Journal of Organic Chemistry
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High efficiency of Pt2+ - CeO2 novel thin film catalyst as anode for proton exchange membrane fuel cells

2016

Abstract The elevated price of Pt limits the large-scale implementation of commercial proton exchange membrane fuel cells, which effectively convert chemical energy into electricity. In order to increase the cost-efficiency in proton-exchange membrane fuel cells, we have designed a family of novel anode catalysts consisting of thin films of ceria with low Pt loadings sputtered on a nanostructured carbon support. Remarkably, only such small amounts of Pt are necessary for achieving power density values comparable to the reference commercial catalysts, which results in excellent specific activities of our samples. By combining photoelectron spectroscopy and catalytic performance analysis, we …

Cerium oxideMaterials scienceSURFACEInorganic chemistrychemistry.chemical_elementProton exchange membrane fuel cell02 engineering and technology010402 general chemistry7. Clean energy01 natural sciencesCatalysisCatalysisWAVE BASIS-SETX-ray photoelectron spectroscopyNANOPARTICLESSPECTRAHYDROGENATIONThin filmThin filmGeneral Environmental SciencePLATINUMProcess Chemistry and TechnologyTOTAL-ENERGY CALCULATIONSCERIUM OXIDE-FILMSNANOSTRUCTUREFuel cellCerium oxide021001 nanoscience & nanotechnology0104 chemical sciencesAnodeELECTRONIC-STRUCTUREMembranechemistry0210 nano-technologyPlatinum
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Theoretical study of the electronic spectrum of magnesium-porphyrin

1999

Multiconfigurational self-consistent field (SCF) and second order perturbation methods have been used to study the electronic spectrum of magnesium-porphyrin (MgP). An extended ANO-type basis set including polarization functions on all heavy atoms has been used. Four allowed singlet states of E1u symmetry have been computed and in addition a number of forbidden transitions and a few triplet states. The results lead to a consistent interpretation of the electronic spectrum, where the Q band contains one transition, the B band two, and the N band one. The computed transition energies are consistently between 0.1 and 0.5 too low compared to the measured band maxima. The source of the discrepan…

ChemistryGeneral Physics and AstronomyPerturbation theoryTriplet stateSpectraB bandMolecular biophysicsPolarization (waves)Spectral lineOrbital calculationsUNESCO::FÍSICA::Química físicaQ bandSCF calculations ; Perturbation theory ; Orbital calculations ; Triplet state ; Organic compounds ; Spectra ; Molecular biophysicsOrganic compoundsSCF calculationsSinglet statePhysical and Theoretical ChemistryAtomic physicsTriplet state:FÍSICA::Química física [UNESCO]MaximaBasis setThe Journal of Chemical Physics
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Semiempirical calculations on the interaction between dimethyltin(IV) and DNA model system

1999

Abstract The interaction between a dinucleotide triphosphate duplex (DD), mimicking the DNA molecule, and the dimethyltin(IV) cation is studied by the semiempirical PM3 method. The results show that the interaction can occur involving the tin atom and the electron-donor centres of DD, requiring in some cases the presence of water molecules. In particular, the binding of the dimethyltin(IV) moiety with two adjacent phosphate oxygen atoms is allowed by the presence of water molecules coordinating to the tin atom. In this case the tin environment shows a geometry in agreement with 119 Sn Mossbauer and X-ray data.

ChemistryMolecular models of DNAchemistry.chemical_elementequipment and suppliesCondensed Matter PhysicsBiochemistryOrganotin moietychemistry.chemical_compoundCrystallographyOxygen atomSettore CHIM/03 - Chimica Generale E InorganicaComputational chemistryMössbauer spectroscopyDNA modelMoleculeMoietyPM3 calculationPhysical and Theoretical ChemistryTinDNAJournal of Molecular Structure: THEOCHEM
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