Search results for "molecule"

showing 10 items of 5162 documents

Deviations from Kleinman symmetry of the second-order polarizability tensor in molecules with low-lying perpendicular electronic bands

1993

Abstract 4-Nitroaniline (pNA) and 3,5-dinitro-aniline (3,5-DNA) were studied by electric field induced second harmonic generation (EFISH) and electrooptical absorption measurements (EOAM) in dioxane solution at T = 298 K. The measurements were carried out for two polarization conditions, the electric field vector of the linearly polarized incident light being parallel or perpendicular to the static electric field. The second-order polarizability tensor of pNA is confirmed to be Kleinman symmetric, while a strong deviation from index permutation symmetry is observed for 3,5-DNA. The latter is quantitatively interpreted by contributions of a low-lying electronic band with transition dipole pe…

Condensed matter physicsChemistrybusiness.industryLinear polarizationGeneral Physics and AstronomySecond-harmonic generationPolarization (waves)RayDipoleOpticsElectric fieldPerpendicularMoleculePhysical and Theoretical ChemistrybusinessChemical Physics
researchProduct

Quantum Monte Carlo study of insulating state in NaV2O5

2003

Abstract Quantum Monte Carlo (QMC) methods are being increasingly used as complements to Hartree–Fock (HF) methods for computing the electronic structure of molecules and materials. We investigate the nature of the insulating state driven by electronic correlations in the ladder compound NaV 2 O 5 ; considered as a quarter-filled system. We use an extended Hubbard model (EHM) to study the role of on-site and inter-site Coulomb interaction. It is found that the insulating state in the charge-disordered phase of this compound take origin from the transfer of spectral density and dynamical fluctuations. Our calculation allows us also, to understand the origin of the insulating states above T C…

Condensed matter physicsHubbard modelChemistryMechanical EngineeringQuantum Monte CarloMonte Carlo methodMetals and AlloysSpectral densityGeneral MedicineState (functional analysis)Electronic structureMechanics of MaterialsPhase (matter)Materials ChemistryCoulombMoleculeCondensed Matter::Strongly Correlated ElectronsMetal–insulator transitionElectronic band structureJournal of Alloys and Compounds
researchProduct

Modelling of two step high spin⇌low spin transitions using the cluster variation method

1998

Abstract A thermodynamic description of high spin (HS)⇌low spin (LS) transition curves beyond the Bragg–Williams approximation is given using the Kikuchi cluster variation method (CVM). Transition curves of unusual behaviour (i.e. two step transition) are reproduced by short range interaction energies which are present in addition to long range elastic interaction between the spin changing molecules. The correlations in the distribution of the spin changing centers can be expressed analytically. They give rise to a reduced mixing entropy which was found experimentally in compounds with two step transitions.

Condensed matter physicsSpin statesSpin crossoverIsing systemChemistryTwo stepMoleculeGeneral Materials ScienceIsing modelGeneral ChemistryCondensed Matter PhysicsEntropy (order and disorder)Journal of Physics and Chemistry of Solids
researchProduct

Charging process in electron conducting polymers: dimerization model

2001

Abstract Theory of the charging and discharging process in electron-conducting polymer films at an electrode surface has been presented. It is based on the concept of two coexisting subsystems at the polymer matrix, ‘usual’ sites P which can exchange with the electrode by the electronic charge in a quasi-reversible manner, and sites D where intermolecular bonds between neighboring polymer molecules can be formed. The charging and discharging of the latter subsystem may be realized along different reaction pathways, e.g. via the bond formation after the generation of two cation radicals within such site D in the course of the anodic scan while the bond dissociation may take place via a parti…

Conductive polymerChemical physicsChemistryGeneral Chemical EngineeringIntermolecular forceElectrochemistryAnalytical chemistryMoleculeElectronCyclic voltammetryElementary chargeRedoxDissociation (chemistry)Electrochimica Acta
researchProduct

A glassy carbon electrode modified by a triply-fused-like Co( ii ) polyporphine and its ability for sulphite oxidation and detection

2018

This article presents a Co(II) polyporphine conductive polymer easily and rapidly obtained (less than 2 h 30 min) on the surface of a glassy carbon electrode from the transformation of an initial Mg(II) porphine solution in a four-step process (including electrochemical and chemical stages). The intimate molecular structure is argued on the basis of the electrochemical response of the modified electrode, as well as its surface characterization. Owing to its apparent stability in water over potential cycling and its high density in active Co(II) centers, the electrosynthesized film shows its ability to catalyze sulphite oxidation in aqueous solutions. The mechanism of this molecular catalysi…

Conductive polymerDetection limitAqueous solutionChemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryGlassy carbon electrodeInorganic chemistry02 engineering and technologyGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistry010402 general chemistry021001 nanoscience & nanotechnologyElectrochemistry01 natural sciencesCatalysis0104 chemical sciencesCatalysis[CHIM.ANAL]Chemical Sciences/Analytical chemistryElectrodeMaterials ChemistryMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistry0210 nano-technology
researchProduct

An approach to the electrochemical activity of poly-(phenothiazines) by complementary electrochemical impedance spectroscopy and Vis–NIR spectroscopy

2010

Abstract The electroactivity of two poly-(phenothiazine), the poly-(Azure A) and the poly-(Methylene Blue), has been compared in this work. The spectroelectrochemical results prove clearly the existence of two electroactive moieties integrated in the polymeric lattice, the phenothiazine ring (detected by changes of absorbance at 590 and 685 nm) and the newly formed covalent links which fixes the monomers in the backbone of the polymer (detected by changes of absorbance at 460 and 875 nm). Differences in the electrochemical response of both polymers are due to differences in this covalent link. However in both polymers, the charge balance during electrochemical reactions takes place by the e…

Conductive polymerGeneral Chemical EngineeringAnalytical chemistryInfrared spectroscopyIonic bondingAzure APhotochemistryDielectric spectroscopyAbsorbancechemistry.chemical_compoundchemistryPhenothiazineElectrochemistryMoleculeElectrochimica Acta
researchProduct

Mixed Grotthuss and Vehicle Transport Mechanism in Proton Conducting Polymers from Ab initio Molecular Dynamics Simulations

2011

We elucidate the microscopic mechanism of long-range proton conduction in poly[vinyl phosphonic acid] (PVPA), a highly promising proton conducting polymer. Using a steered ab initio molecular dynamics approach, we characterize the charge transport functionality of acid groups interacting with nonbulk water molecules intercalated in the polymer. Our results show that in PVPA, unlike in Nafion, water has a local vehicle/carrier function for excess protons. This function must however be combined with the Grotthuss-type conduction mechanism that is supplied by the acid groups in order to yield long-range charge transport. As an additional aspect, we find that contrary to common intuition, syste…

Conductive polymerchemistry.chemical_classificationMaterials scienceProtonGeneral Chemical EngineeringGeneral ChemistryPolymerThermal conductionAmorphous solidchemistry.chemical_compoundchemistryComputational chemistryChemical physicsYield (chemistry)NafionMaterials ChemistryMoleculeChemistry of Materials
researchProduct

Bis(2-ethylhexyl)phosphoric acid/bis(2-ethylhexyl)amine mixtures as solvent media for lithium-ions: A dynamical study

2016

Abstract The self-diffusion coefficient, the spin-lattice relaxation times and ionic conductivity of lithium ions in liquid mixtures composed of bis(2-ethylhexyl)amine (BEEA) and bis(2-ethylhexyl)phosphoric acid (HDEHP) have been thoroughly investigated as a function of composition and temperature by NMR spectroscopy and conductometry. While the temperature and composition dependence of diffusion coefficients of lithium ions follow the same trend observed for those of the surfactant molecules, the spin-lattice relaxation times of lithium ions and 1 H are remarkably different. The observed behavior has been interpreted in terms of lithium ions diffusion occurring through its association with…

ConductometrySurfactantsInorganic chemistrychemistry.chemical_element02 engineering and technology010402 general chemistrySelf-diffusion coefficients01 natural sciencesSpin-lattice relaxation timechemistry.chemical_compoundColloid and Surface ChemistryPulmonary surfactantLithium ionSpin-lattice relaxation timeSelf-diffusion coefficientsSurfactantsLithium ionMoleculeIonic conductivityPhysics::Chemical PhysicsPhosphoric acidSettore CHIM/02 - Chimica FisicaChemistryNuclear magnetic resonance spectroscopy021001 nanoscience & nanotechnology0104 chemical sciencesSolventLithium0210 nano-technology
researchProduct

Double- and Multi-Calixarentes

2006

Calixarenes are easily (and often selectively) functionalized and therefore they can be combined in various ways to larger molecules containing more than one calixarene substructure. In the following chapter we will try to give an overview on such multicalixarenes held together by "conventional" covalent links. Self-assembled structures are treated separately in Chapter 8. The earliest examples for double calixarenes of importance are the carcerands and hemicarcerands of D. Cram in which two resorcarene derived cavitands are combined. Due to their unique properties to include (more or less permanently) smaller molecules, they are treated separately in Chapter 10. Further combinations of cav…

Cone conformationCovalent bondChemistrySILVER CATIONCalixareneSubstructureMoleculeResorcinareneCombinatorial chemistry
researchProduct

Imaging and force transduction in correlative scanning force and confocal fluorescence microscopy

2018

Correlative scanning force and confocal fluorescence microscopy has been used to study individual molecules, nanoparticles and nanoparticle oligomers. By applying a compressive force via the AFM cantilever, spectral blue and red shifts in the range of several meV/GPa have been observed for single dye molecules and semiconductor quantum dots. Moreover, individual Au nanoparticle dimers linked by a chlorophyll binding protein have been imaged in both modes and plasmonic fluorescence enhancement of the chlorophyll emission of up to a factor of 15 has been found.

ConfocalPhysicsQC1-999technology industry and agricultureNanoparticle02 engineering and technologymacromolecular substances010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesFluorescence0104 chemical sciencesTransduction (biophysics)Chlorophyll bindingBiophysicsFluorescence microscopeMolecule0210 nano-technologyPlasmonEPJ Web of Conferences
researchProduct