Search results for "DFT"

showing 10 items of 361 documents

Supramolecular Aggregates in Vacuum: Positively Mono-Charged Sodium Alkanesulfonate Clusters

2010

The formation and structural features of positively mono-charged aggregates of sodium bis(2-ethylhexyl) sulfosuccinate (AOT) and sodium methane—(MetS), butane—(ButS) and octane—(OctS) sulfonate molecules in the gas phase have been investigated by electrospray ionization mass spectrometry, energy-resolved mass spectrometry and density functional theory (DFT) calculations. The experimental results show that the center-of-mass collision energy required to dissociate 50% of these mono-charged aggregates scantly depends on the length of the alkyl chain as well as on the aggregation number. This, together with the large predominance of mono-charged species in the mass spectra, was rationalized i…

AlkanesulfonatesSpectrometry Mass Electrospray IonizationAmphiphilic moleculeVacuumChemistryElectrospray ionizationSodiumSodiumSupramolecular chemistrychemistry.chemical_elementGeneral MedicineAtomic and Molecular Physics and Opticschemistry.chemical_compoundSulfonateTandem Mass SpectrometrySupramolecular aggregates amphiphilic molecules surfactants reversed micelles ESI MS ESI MS/MS energy resolved mass spectrometry DFT calculationsQuantum TheoryOrganic chemistrySpectroscopyEuropean Journal of Mass Spectrometry
researchProduct

ENANTIOSELECTIVE REDUCTION OF PROCHIRAL KETONES PROMOTED BY AMINO AMIDE RUTHENIUM COMPLEXES: A DFT STUDY

2021

International audience; The origin of enantioselectivity in the reaction of chiral Ru amino amide complexes in the asymmetric transfer hydrogenation of acetophenone was investigated using DFT calculations. For the most stable active catalysts, the full free energy profiles for the reaction were calculated according to the concerted hydrogen transfer mechanism. We succeeded in reproducing the experimentally observed enantioselectivity for the studied Ru amino amide complexes. Our results indicate that the high enantioselectivity can be explained by a stabilizing CH-π interaction existing between the phenyl group of acetophenone and the aromatic substituent of the catalyst, which plays a sign…

Amidoamide Ruthenium CatalystEnantioselective ReductionSubstituentchemistry.chemical_elementConformers010402 general chemistryTransfer hydrogenation01 natural sciencesBiochemistryDFTCatalysisInorganic Chemistrychemistry.chemical_compoundComputational chemistryMaterials ChemistryPhenyl groupPhysical and Theoretical ChemistryEnantiomeric excess010405 organic chemistryOrganic ChemistryEnantioselective synthesis3. Good health0104 chemical sciencesRuthenium[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistryMechanismAcetophenone
researchProduct

TASCAを用いたCn, Nh, Fl化学実験のためのHg, Tl, PbのSiO2及びAu表面に対するオンライン化学吸着研究

2018

Online gas-solid adsorption studies with single atom quantities of Hg, Tl, and Pb on SiO$_{2}$ and Au surfaces were carried out using short-lived radioisotopes with half-lives in the range of 4-49 s. This is a model study to measure adsorption enthalpies of superheavy elements Cn, Nh, and Fl. The short-lived isotopes were produced and separated by the gas-filled recoil separator TASCA at GSI. The products were stopped in He gas, and flushed into gas chromatography columns made of Si detectors whose surfaces were covered by SiO$_{2}$ or Au. The short-lived Tl and Pb were successfully measured by the Si detectors with the SiO$_{2}$ surface at room temperature. On the other hand, the Hg did no…

Analytical chemistrychemistry.chemical_elementElectronic structure010402 general chemistry01 natural sciencesadsorption studiethermochromatographyHomologs of superheavy elementRELATIVISTIC PERIODIC DFTMetalGSIAdsorptionCHEMISTRY0103 physical sciencesisothermal chromatographyPhysical and Theoretical ChemistrySUPERHEAVY ELEMENTS010306 general physicsCoperniciumChemistryQUARTZ SURFACE0104 chemical sciencesgas phase chromatography of single atomHEAVIEST ELEMENTSFleroviumELECTRONIC-STRUCTUREvisual_artYield (chemistry)METALvisual_art.visual_art_mediumGas chromatographyRelativistic quantum chemistryphysical preseparationSYSTEMRadiochimica acta
researchProduct

Symmetry and models of single-walled TiO2 nanotubes with rectangular morphology

2011

Abstract The formalism of line symmetry groups for one-periodic (1D) nanostructures with rotohelical symmetry has been applied for symmetry analysis of single-walled titania nanotubes (SW TiO2 NTs) formed by rolling up the stoichiometric two-periodic (2D) slabs of anatase structure. Either six- or twelve-layer (101) slabs have been cut from TiO2 crystal in a stable anatase phase. After structural optimization, the latter keeps the centered rectangular symmetry of initial slab slightly compressed along a direction coincided with large sides of elemental rectangles. We have considered two sets of SW TiO2 NTs with optimized six- and twelve-layer structures, which possess chiralities (−n, n) an…

AnataseNanostructureMaterials scienceline groupsBand gaptio2 nanotubesPhysicsQC1-999Ab initiohybrid hf-dft pbe0 calculationsGeneral Physics and AstronomyNanotechnologyanatase structureMolecular physicsCondensed Matter::Materials ScienceReflection symmetryLinear combination of atomic orbitalsSlabrotohelical symmetryStoichiometryOpen Physics
researchProduct

Theoretical Determination of the pK a Values of Betalamic Acid Related to the Free Radical Scavenger Capacity: Comparison Between Empirical and Quant…

2015

Health benefits of dietary phytochemicals have been suggested in recent years. Among 1000s of different compounds, Betalains, which occur in vegetables of the Cariophyllalae order (cactus pear fruits and red beet), have been considered because of reducing power and potential to affect redox-modulated cellular processes. The antioxidant power of Betalains is strictly due to the dissociation rate of the acid moieties present in all the molecules of this family of phytochemicals. Experimentally, only the pK a values of betanin were determined. Recently, it was evidenced it was evidenced as the acid dissociation, at different environmental pHs, affects on its electron-donating capacity, and fur…

AntioxidantPyridinesmedicine.medical_treatmentBetalainsHealth Informatics010402 general chemistry01 natural sciencesGeneral Biochemistry Genetics and Molecular BiologyAcid dissociation constantAntioxidantschemistry.chemical_compoundComputational chemistryBetalamic Acid antioxidants pKa predictions empirical methods DFTmedicineOrganic chemistryA valueMoleculeBetaninQuantum chemical010405 organic chemistryFree Radical ScavengersFree radical scavengerSettore CHIM/08 - Chimica Farmaceutica0104 chemical sciencesComputer Science ApplicationschemistryModels ChemicalBetalamic acid
researchProduct

Insight into the Mechanism of Action of Marine Cytotoxic Thiazinoquinones

2017

The electrochemical response of four natural cytotoxic thiazinoquinones isolated from the Aplidium species was studied using conventional solution-phase and solid-state techniques, based on the voltammetry of immobilized particles methodology. The interaction with O-2 and electrochemically generated reactive oxygen species (ROS) was electrochemically monitored. At the same time, a molecular modeling study including density functional theory (DFT) calculations was performed in order to analyze the conformational and electronic properties of the natural thiazinoquinones, as well as those of their reduced intermediates. The obtained electrochemical and computational results were analyzed and c…

Aquatic OrganismsMolecular modelStereochemistryBioactive natural products; Cytotoxic activity; DFT calculations; Electrochemistry; Reactive radical species; Thiazinoquinones; Animals; Electrochemistry; Quinones; Reactive Oxygen Species; Aquatic Organisms; Urochordata; Drug Discovery3003 Pharmaceutical ScienceThiazinoquinoneDFT calculationPharmaceutical Science02 engineering and technologyDFT calculationsElectrochemistry01 natural sciencesArticleAplidiumbioactive natural products; thiazinoquinones; electrochemistry; DFT calculations; reactive radical species; cytotoxic activityComputational chemistryDrug DiscoverymedicineAnimalsCytotoxic T cellUrochordataBioactive natural productlcsh:QH301-705.5Pharmacology Toxicology and Pharmaceutics (miscellaneous)Voltammetrycytotoxic activitychemistry.chemical_classificationReactive oxygen speciesbiology010405 organic chemistryDrug Discovery3003 Pharmaceutical ScienceQuinonesReactive radical specie021001 nanoscience & nanotechnologybiology.organism_classification0104 chemical scienceslcsh:Biology (General)electrochemistryMechanism of actionchemistryreactive radical speciesbioactive natural productsthiazinoquinonesDensity functional theorymedicine.symptomReactive Oxygen Species0210 nano-technologyMarine Drugs
researchProduct

Ab initio angle- and energy-resolved photoelectron spectroscopy with time-dependent density-functional theory

2012

We present a time-dependent density-functional method able to describe the photoelectron spectrum of atoms and molecules when excited by laser pulses. This computationally feasible scheme is based on a geometrical partitioning that efficiently gives access to photoelectron spectroscopy in time-dependent density-functional calculations. By using a geometrical approach, we provide a simple description of momentum-resolved photoemission including multiphoton effects. The approach is validated by comparison with results in the literature and exact calculations. Furthermore, we present numerical photoelectron angular distributions for randomly oriented nitrogen molecules in a short near-infrared…

Atomic Physics (physics.atom-ph)Photoemission spectroscopyAb initioFOS: Physical sciences02 engineering and technology01 natural sciences7. Clean energySpectral lineSettore FIS/03 - Fisica Della MateriaPhysics - Atomic PhysicsX-ray photoelectron spectroscopyTDDFTABOVE-THRESHOLD IONIZATION; LASER FIELDS; WAVE-FUNCTIONS; PHOTOEMISSION; CLUSTERS; SYSTEMS; PULSESMesoscale and Nanoscale Physics (cond-mat.mes-hall)0103 physical sciencesPhysics::Atomic and Molecular ClustersPhysics - Atomic and Molecular ClustersPhysics::Atomic Physics010306 general physicsPhysicsCondensed Matter - Mesoscale and Nanoscale PhysicsAtoms in moleculesTime-dependent density functional theory021001 nanoscience & nanotechnologyAtomic and Molecular Physics and Optics3. Good healthStrong field ionizationExcited stateDensity functional theoryAtomic physicsAtomic and Molecular Clusters (physics.atm-clus)0210 nano-technology
researchProduct

Dissociative adsorption of water on Au/MgO/Ag(001) from first principles calculations

2015

Abstract The molecular and dissociative adsorption of water on a Ag-supported 1 ML, 2 ML and 3 ML-a six atomic layer-thick MgO films with a single Au adatom is investigated using density functional theory calculations. The obtained results are compared to a bulk MgO(001) surface with an Au atom. On thin films the negatively charged Au strengthens the binding of the polar water molecule due to the attractive Au–H interaction. The adsorption energy trends of OH and H with respect to the film thickness depend on an adsorption site. In the case OH or H binds atop Au on MgO/Ag(001), the adsorption becomes more exothermic with the increasing film thickness, while the reverse trend is seen when th…

Au adatomsExothermic reactionta114Chemistrydissociation of waterSurfaces and InterfacesDFT calculationsCondensed Matter PhysicsRedoxSurfaces Coatings and FilmsAdsorptionComputational chemistryAtomMaterials ChemistryCoulombadsorption of waterMoleculePhysical chemistryDensity functional theoryThin filmta116Ag-supported MgO thin filmsSurface Science
researchProduct

Disorder in the crystals of trans-4-fluoroazoxybenzene. Synthesis, spectral properties, crystal structures and DFT calculations

2005

Abstract Two crystals of trans-4-fluoroazoxybenzene were obtained using two different methods. Oxidation of 4-fluoroazobenzene provided crystals of trans-4-fluoroazoxybenzene (I) consisting of two isomers; 51% α (ONN) and 49% β (NNO) isomer. From trans-amino-azoxybenzenes in Schiemann reaction it were obtained crystals of trans-4-fluoro-NNO-azoxybenzenes (II, β isomer) containing 4.7% of the α-isomer according to the HPLC analysis. The crystal structures of I and II were determined by the X-ray diffraction method. In the crystal I two nitrogen atoms of azoxy bridge and fluorine atom are disordered. In the crystal II, there are two independent molecules of trans-4-fluoroazoxybenzene; the mol…

AzoxyTrans-4-fluoroazoxybenzeneHydrogen bondChemistryAromaticityCrystal structureOrganic ChemistryAromaticityCrystal structureDFT calculationsAnalytical ChemistryInorganic ChemistryCrystalCrystallographychemistry.chemical_compoundMolecular geometryComputational chemistrySchiemann reactionMolecular symmetryDisorderMoleculeSpectroscopyJournal of Molecular Structure
researchProduct

Crystal and molecular structure studies of (Z)-N-methyl-C-4-substituted phenyl nitrones by XRD, DFT, FTIR and NMR methods

2017

Abstract (Z)-N-methyl-C-4-substituted phenyl nitrones –O+N(Me)=C(H)R (Z-2a R = 4-ClC6H4, Z-2b R = 4-NO2C6H4, Z-2c R = 4-CH3OC6H4) were synthesized and characterized by elemental analyses, FTIR, 1H, 13C and DEPT-135 NMR spectroscopy and also by single crystal X-ray diffraction (in the case of Z-2a and Z-2b). The geometries of the nitrone molecules Z-2a, Z-2b and Z-2c and their E-isomers; (E)-N-methyl-C-4-chlorophenyl nitrone E-2a, (E)-N-methyl-C-4-nitrophenyl nitrone E-2b and (E)-N-methyl-C-4-methoxyphenyl nitrone E-2c were optimized using density functional theory (DFT) at the B3LYP/6-311++G(d,p) level of theory. The theoretical vibrational frequencies obtained by DFT calculations are in go…

B3LYP010402 general chemistry01 natural sciencesDFTAnalytical ChemistryNitroneInorganic ChemistryComputational chemistry(Z)-N-methyl-C-4-substituted phenyl nitronessingle crystal X-rayMoleculeHOMO/LUMOta116Spectroscopychemistry.chemical_classification010405 organic chemistryChemistryChemical shiftOrganic ChemistryNuclear magnetic resonance spectroscopyNMR0104 chemical sciencesNMR spectra databaseCrystallographyDensity functional theorySingle crystalJournal of Molecular Structure
researchProduct