Search results for " DFT"

showing 10 items of 97 documents

Molecular Electron Density Theory: A Modern View of Reactivity in Organic Chemistry

2016

A new theory for the study of the reactivity in Organic Chemistry, named Molecular Electron Density Theory (MEDT), is proposed herein. MEDT is based on the idea that while the electron density distribution at the ground state is responsible for physical and chemical molecular properties, as proposed by the Density Functional Theory (DFT), the capability for changes in electron density is responsible for molecular reactivity. Within MEDT, the reactivity in Organic Chemistry is studied through a rigorous quantum chemical analysis of the changes of the electron density as well as the energies associated with these changes along the reaction path in order to understand experimental outcomes. St…

Electron densitymolecular mechanismsChemistry OrganicPharmaceutical ScienceElectronsElectron010402 general chemistry01 natural sciencesArticleAnalytical Chemistrylcsh:QD241-441Electron density distributionlcsh:Organic chemistryComputational chemistryDrug DiscoveryDFT reactivity indicesNon-covalent interactionsOrganic chemistryReactivity (chemistry)Physical and Theoretical Chemistryelectron densityQuantum chemicalchemistry.chemical_classification010405 organic chemistryOrganic Chemistrymolecular electron density theory0104 chemical scienceschemistrynon-covalent interactionsModels ChemicalChemistry (miscellaneous)molecular electron density theory; DFT reactivity indices; electron localisation function; non-covalent interactions; electron density; molecular mechanisms; chemical reactivityMolecular MedicineDensity functional theoryGround stateelectron localisation functionchemical reactivityMolecules; Volume 21; Issue 10; Pages: 1319
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Hydrogen Arrangements on Defective Quasi-Molecular BN Fragments

2019

Considering the ever-increasing interest in metal-free materials, some potential chemical applications of quasi-molecular boron nitride (BN) derivatives were tested. Specifically, the behavior of BN fragments was analyzed when given defects, producing local electron density changes, were introduced by using topological engineering approaches. The inserted structural faults were Schottky-like divacancy (BN-d) defects, assembled in the fragment frame by the subtraction of one pair of B and N atoms or Stone-Wales (SW) defects. This study is aimed at highlighting the role of these important classes of defects in BN materials hypothesizing their future use in H-2-based processes, related to eith…

Exothermic reactionElectron densityMaterials scienceHydrogenGeneral Chemical Engineeringchemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesEndothermic processArticlechemistry.chemical_compoundAdsorptionFragmentation (mass spectrometry)MoleculeQD1-999General Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesChemistrychemistryBoron nitrideChemical physicsSettore CHIM/03 - Chimica Generale E Inorganica0210 nano-technologyh-BN catalysts hydrogen surface arrangements DFT studiesACS Omega
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Toward tailorable surfaces: a combined theoretical and experimental study of lanthanum niobate layered perovskites.

2014

A comprehensive theoretical investigation of the MLaNb2O7 (M = H, Li, Na, K, Rb, and Cs) series of ion-exchangeable layered perovskite is presented. These perovskites are in particular interesting in view of their potential applications as inorganic supports for the design of new hybrid inorganic-organic proton conductors. In particular, their structural and electronic properties have been investigated by periodic calculations in the framework of Density Functional Theory, using different exchange-correlation functionals. A general very good agreement with the available experimental (XRD, NPD, and EXAFS) data has been found. The structure of the protonated HLaNb2O7 form has also been furthe…

Extended X-ray absorption fine structureChemistryInorganic chemistryGeneral Physics and AstronomyIonic bondingSpace groupperovskites MLaNb2O7 DFT CrystalCrystal structureTetragonal crystal systemChemical physicsX-ray crystallographyDensity functional theoryPhysical and Theoretical ChemistryPerovskite (structure)The Journal of chemical physics
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MODELING OF SPIRAL HALLOYSITE NANOTUBES

2013

Halloysite DFTB+ spiral nanotubes
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Metal complex-DNA binding: Insights from molecular dynamics and DFT/MM calculations.

2012

Molecular dynamics (MD) simulations, followed by density functional theory/molecular mechanics (DFT/MM) calculations, provided a detailed structure of the binding site between the cationic metallointercalator (dipyrido [3,2-a:2',3'-c]phenazine)(glycinato)copper(II), [Cu(gly)(dppz)](+), and the two dodeca-deoxynucleotide duplexes [dodeca(dG-dC)]2 and [dodeca(dA-dT)]2. Three simultaneous DNA binding types were detected in the fully optimized DFT/MM structures: 1) metal coordination through exocyclic oxygen atoms of nitrogen bases; 2) intercalation of the dppz chromophore between stacked Watson-Crick AT-AT and GC-GC bases; and 3) hydrogen bonding between the glycinato ligand and amine groups o…

Hydrogen bondChemistryEntropyEnthalpyDNAChromophoreMolecular Dynamics SimulationBiochemistryComputational chemistry Copper DFT DNA MD QM/MMStandard enthalpy of formationGibbs free energyInorganic ChemistryQM/MMCrystallographysymbols.namesakeMolecular dynamicsModels ChemicalComputational chemistrySettore CHIM/03 - Chimica Generale E InorganicasymbolsDensity functional theoryCopperJournal of inorganic biochemistry
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Molecular and crystal structure of Ac-(Z)-ΔAbu-NMe2 and Ac-DL-Abu-NMe2 as compared to those of related molecules

2004

Abstract The molecular and crystal structures of two homologous amino acid derivatives: N-acetyl-α,β-dehydro-butyrine N´,N´-dimethylamide (1) and N-acetyl-DL-butyrine N´,N´-dimethylamide (2), have been determined by X-ray crystallography. Similar solid-state association of both compounds is observed; despite different molecular conformation, they form centrosymmetric dimers linked by the intermolecular N–H…O hydrogen bonds. The conformation of two crystallographically independent molecules of 1 [with torsion angles ϕ, ψ, χ 1 ≈ (–47°, 130°, 3°), respectively] is also characteristic of other related diamides – ΔAla, ΔPhe and ΔLeu – previously studied in the solid state. To analyse whether thi…

Hydrogen bondStereochemistryChemistryIntermolecular forceAb initioN′Crystal structureSingle crystal structure analysisCondensed Matter PhysicsN′-dimethylamidesX-ray diffractionInorganic ChemistryCrystallographyButyridine derivativeAb initio quantum chemistry methodsX-ray crystallographyMoleculePeptide designGeneral Materials ScienceAb initio DFT calculationsConformational isomerismZeitschrift Fur Kristallographie
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DFT studies on catalytic properties of isolated and carbon nanotube supported Pd9 cluster–I: adsorption, fragmentation and diffusion of hydrogen

2009

The processes of adsorption, fragmentation and diffusion of hydrogen on a small palladium cluster have been investigated by means of DFT and DFT/MM approaches. These studies have been performed by considering a D(3h) symmetry Pd(9) in the isolated state as well as when supported on a portion of single-walled armchair(6,6) carbon nanotube. The hydrogen fragmentation process easily occurs on the bare Pd(9) cluster, involving energy barriers of 25-35 kJ mol(-1) and the drop in spin multiplicity on passing from the reactant to the product. The atomic hydrogen diffuses through the cluster atoms with energy barriers, which do not exceed 20 kJ mol(-1), with some positions clearly identifiable as t…

HydrogenChemistryDrop (liquid)General Physics and Astronomychemistry.chemical_elementCarbon nanotubeCatalysislaw.inventionAdsorptionTransition metalFragmentation (mass spectrometry)lawPhysical chemistryPhysical and Theoretical Chemistryadsorption fragmentation diffusion hydrogen DFTPalladiumPhysical Chemistry Chemical Physics
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Computation of adsorbate IR spectrum by means of ab initio molecular dynamics

2014

IR spectrum DFT
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Sr Doping and Oxygen Vacancy Formation in La1−xSrxScO3−δ Solid Solutions: Computational Modelling

2022

The study was performed with the financial support from the Latvian Council of Science under the grant agreement LZP-2020/2-0009. Calculations were performed at the HLRS, University of Stuttgart, within the project 12939 DEFTD. The Institute of Solid State Physics, University of Latvia (Latvia), as the Centre of Excellence has received funding from the European Union’s Horizon 2020 Frame-work Programme H2020-WIDESPREAD-01-2016-2017-Teaming Phase2 under grant agreement No. 739508, project CAMART2.

Inorganic ChemistryF-centreGeneral Chemical Engineering:NATURAL SCIENCES::Physics [Research Subject Categories]General Materials Scienceoxygen stoichiometryoxygen vacancyCondensed Matter PhysicsDFTlanthanum scandate; oxygen vacancy; oxygen stoichiometry; F-centre; DFTlanthanum scandateCrystals
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L-Arabinose adsorption on a Ru cluster

2011

L-Arabinose ruthenium DFT
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