Search results for "Quantum chemical"

showing 10 items of 56 documents

Preparation and molecular structures of N′-(2-heteroarylmethylidene)-3-(3-pyridyl)acrylohydrazides

2018

Abstract The crystal and molecular structures of N′-(2-furylmethylidene)-3-(3-pyridyl)acrylohydrazide and N′-(2-thienylmethylidene)-3-(3-pyridyl)acrylohydrazide are reported, and the influence of the type of the heteroatom on the aromaticity of the aromatic rings is discussed. Both molecules are nearly planar. The geometry of the acrylohydrazide arrangement is comparable to that of homologous compounds. Density functional theory (DFT) calculations were performed in order to analyze the changes in the geometry of the studied compounds in the crystalline state and for the isolated molecule. The most significant changes were observed in the values of the N–N and C–N bond lengths. The harmonic …

0301 basic medicinecrystal structure010405 organic chemistryChemistryacroylhydrazidesaromaticityGeneral ChemistryX-ray structure determination01 natural sciences0104 chemical sciences03 medical and health sciences030104 developmental biologyPolymer chemistryquantum chemical calculationsdensity functional theoryheteroaryl substituentsZeitschrift für Naturforschung B
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The Coordination of Uranyl in Water: A Combined Quantum Chemical and Molecular Simulation Study

2005

The coordination environment of uranyl in water has been studied using a combined quantum mechanical and molecular dynamics approach. Multiconfigurational wave function calculations have been performed to generate pair potentials between uranyl and water. The quantum chemically determined energies have been used to fit parameters in a polarizable force field with an added charge transfer term. Molecular dynamics simulations have been performed for the uranyl ion and up to 400 water molecules. The results show a uranyl ion with five water molecules coordinated in the equatorial plane. The U-O(H(2)O) distance is 2.40 A, which is close to the experimental estimates. A second coordination shell…

Ab initioMolecular simulationBiochemistryCatalysisIonMolecular dynamicschemistry.chemical_compoundColloid and Surface ChemistryAb initio quantum chemistry methodsComputational chemistryComputer SimulationPhysics::Chemical PhysicsQuantum chemicalHydrogen bondSolvationWaterGeneral ChemistryGeneral MedicineUranylSolvation shellchemistryModels ChemicalChemical physicsddc:540Quantum TheoryUranium
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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
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Quantum chemical calculations of formyl radicals

1975

The ground state (2 A′) of the fluoroformyl radical, FCO, has been investigated by the unrestricted Hartree-Fock method. Pulay's force method for open-shell systems has been applied to calculate the complete quadratic force field and the diagonal cubic force constants. The force relaxation method has been used to determine the equilibrium geometry of FCO: . Adjusting the diagonal force constants to the observed vibrational frequencies of 19F12C16O and taking the values for the off-diagonal force constants from the UHF calculations, the force field of FCO is found to be: . This force field is compared with experiment and with the force fields of HCO, H2CO, and F2CO. The ground state of the F…

Coupling constantQuantum chemicalChemistryRadicalDiagonalBiophysicsCondensed Matter PhysicsForce field (chemistry)IonQuadratic equationPhysical and Theoretical ChemistryAtomic physicsGround stateMolecular BiologyMolecular Physics
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Synthesis and stereochemical studies of 1- and 2-phenyl-substituted 1,3-oxazino[4,3-a]isoquinoline derivatives

2003

Abstract Starting from the 1′- or 2′-phenyl-substituted 1-(2′-hydroxyethyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline diastereomers 3 and 6 , 4-unsubstituted and 4-(p-nitrophenyl)- and 4-oxo-substituted 1-phenyl- and 2-phenyl-9,10-dimethoxy-2H,4H-1,6,7,11b-tetrahydro-1,3-oxazino[4,3-a]isoquinolines ( 7–12 ) were prepared. The relative configurations and the predominant conformations of the products were determined by NMR spectroscopy, by quantum chemical calculations and, for (2R∗,4S∗,11bR∗)-9,10-dimethoxy-4-(p-nitrophenyl)-2-phenyl-2H,4H-1,6,7,11b-tetrahydro-1,3-oxazino[4,3-a]isoquinoline ( 11 ), by X-ray diffraction.

DiffractionQuantum chemicalchemistry.chemical_classificationStereochemistryChemistryOrganic ChemistryDiastereomerOxazinesNuclear magnetic resonance spectroscopyBiochemistrychemistry.chemical_compoundComputational chemistryDrug DiscoveryIsoquinolineTetrahedron
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The nature of inter- and intramolecular interactions in F2OXe…HX (X= F, Cl, Br, I) complexes

2015

Electronic structure of the XeOF2 molecule and its two complexes with HX (X= F, Cl, Br, I) molecules have been studied in the gas phase using quantum chemical topology methods: topological analysis of electron localization function (ELF), electron density, ρ(r), reduced gradient of electron density |RDG(r)| in real space, and symmetry adapted perturbation theory (SAPT) in the Hilbert space. The wave function has been approximated by the MP2 and DFT methods, using APF-D, B3LYP, M062X, and B2PLYP functionals, with the dispersion correction as proposed by Grimme (GD3). For the Xe-F and Xe=O bonds in the isolated XeOF2 molecule, the bonding ELF-localization basins have not been observed. Accord…

Electron densityQuantum chemical topologyXenonksenonElectronic structure010402 general chemistrynoble gas complexes01 natural sciencesCatalysisNoble gas complexesInorganic ChemistryComputational chemistry0103 physical sciencesMoleculePhysical and Theoretical ChemistryTopology (chemistry)Original Paper010304 chemical physicsSAPTHydrogen bondChemistryOrganic ChemistryElectron localization function0104 chemical sciencesComputer Science ApplicationsCrystallographyELFComputational Theory and MathematicsCovalent bondIntramolecular forcequantum chemical topology
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Experimental and theoretical insights in the alkene-arene intramolecular π-stacking interaction

2016

Chiral acrylic esters derived from biomass were developed as models to have a better insight in the aryl-vinyl π-stacking interactions. Quantum chemical calculations, NMR studies and experimental evidences demonstrated the presence of equilibriums of at least four different conformations: π-stacked and face-to-edge, each of them in an s-cis/s-trans conformation. The results show that the stabilization produced by the π-π interaction makes the π-stacked conformation predominant in solution and this stabilization is slightly affected by the electron density of the aromatic counterpart. Fil: Corne, Valeria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológi…

Electron densityStereochemistryasymmetric synthesisStackingBiomass010402 general chemistry01 natural sciencesFull Research PaperBIOMASS//purl.org/becyt/ford/1 [https]lcsh:QD241-441lcsh:Organic chemistryASYMMETRIC SYNTHESISComputational chemistryCONFORMATIONAL EQUILIBRIUMΠ-STACKING INTERACTION//purl.org/becyt/ford/1.4 [https]conformational equilibriumACRYLIC ESTERSlcsh:Sciencechemistry.chemical_classificationQuantum chemicalbiomass010405 organic chemistryAlkeneacrylic estersOtras Ciencias QuímicasOrganic ChemistryEnantioselective synthesisCiencias Químicasπ-stacking interaction0104 chemical sciencesChemistrychemistryIntramolecular forcelcsh:QCIENCIAS NATURALES Y EXACTAS
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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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Ion-Track Template Synthesis and Characterization of ZnSeO3 Nanocrystals

2022

A.I.P. thanks the Institute of Solid-State Physics, University of Latvia. ISSP UL as the Center of Excellence is supported through the Framework Program for European universities. The work was carried out within the framework of the grant AP05134367 of the Ministry Funding: The work was carried out within the framework of the grant AP05134367 of the Ministry of education and Science Science of of the Republic Republic of Kazakhstan.

Inorganic ChemistrySiO<sub>2</sub>/Si track template; chemical and electrochemical deposition; ZnSeO<sub>3</sub> nanocrystals; XRD study; quantum chemical calculationchemical and electrochemical depositionGeneral Chemical Engineering:NATURAL SCIENCES::Physics [Research Subject Categories]General Materials ScienceSiO2/Si track templateZnSeO3 nanocrystalsCondensed Matter Physicsquantum chemical calculationXRD studyCrystals
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Breathing-Dependent Redox Activity in a Tetrathiafulvalene-Based Metal–Organic Framework

2018

"Breathing" metal-organic frameworks (MOFs) that involve changes in their structural and physical properties upon an external stimulus are an interesting class of crystalline materials due to their range of potential applications including chemical sensors. The addition of redox activity opens up a new pathway for multifunctional "breathing" frameworks. Herein, we report the continuous breathing behavior of a tetrathiafulvalene (TTF)-based MOF, namely MUV-2, showing a reversible swelling (up to ca. 40% of the volume cell) upon solvent adsorption. Importantly, the planarity of the TTF linkers is influenced by the breathing behavior of the MOF, directly impacting on its electrochemical proper…

MECHANISMNIChemistry MultidisciplinarySOLIDSQuímica organometàl·lica010402 general chemistryElectrochemistry01 natural sciencesBiochemistryArticleCatalysisMOFSRedox Activitychemistry.chemical_compoundsymbols.namesakeColloid and Surface ChemistryAdsorptionReacció d'oxidació-reduccióCATIONCONDUCTIVITYQuantum chemicalScience & Technology010405 organic chemistryUNITSGeneral Chemistry0104 chemical sciencesSolventChemistryChemical engineeringchemistryHYBRID FRAMEWORKSPhysical SciencessymbolsMetal-organic frameworkRaman spectroscopy03 Chemical SciencesTetrathiafulvaleneJournal of the American Chemical Society
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