Search results for "Optical"

showing 10 items of 7671 documents

Towards highly luminescent phenylene vinylene films

1996

Abstract Fluorescence and electronic absorption spectra, fluorescence decay curves and fluorescence quantum yields of a series of oligo (p-phenylene vinylenes) are investigated in solution, nanoaggregates and vapour-deposited or cast ultrathin films. The film constituting molecules are varied in chain length and modified by electron donating and withdrawing substituents and bulky alkyl spacers. PPP-MO calculations serve to rationalize the resulting spectral changes. In dilute solutions, fluorescence yields of the short oligomers with alkyl or oxyalkyl substituents approach the region of unity. The yields decrease with chain length, reaching a long-chain limit of ΦF=0.4–0.7. Introduction of …

chemistry.chemical_classificationAbsorption spectroscopyDouble bondMechanical EngineeringMetals and AlloysQuantum yieldCondensed Matter PhysicsInternal conversion (chemistry)PhotochemistryElectronic Optical and Magnetic MaterialschemistryMechanics of MaterialsPhenyleneMaterials ChemistryPolar effectMoleculeAlkylSynthetic Metals
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Acid—base properties of azo dyes in the presence of surfactants

1991

Abstract The changes in the acid—base properties of an azo dye produced by the presence of surfactants, at surfactant concentrations below and above the CMC, are quantitatively described using a simple model and spectrophotometric and potentiometric measurements. The azo dye formed by aniline and N -(1-naphthyl)-ethylenediamine, and the surfactants sodium dodecyl sulphate, Triton X-100 and N -cetylpyridinium chloride (NCPC) are used. The protonation constants of the free and surfactant-bound dye species, the binding constant of the protonated and unprotonated forms of the dye, and the average aggregation number of the dye—NCPC aggregates are evaluated.

chemistry.chemical_classificationAggregation numberBase (chemistry)Potentiometric titrationInorganic chemistryProtonationCetylpyridinium chlorideBinding constantSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryAnilinechemistryPulmonary surfactantJournal of Colloid and Interface Science
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Glass-forming non-symmetric bis-styryl-DWK-type dyes for infra-red radiation amplification systems

2019

Abstract A series of D-π-A type organic dyes with bulky triphenylmethyl moiety containing 2,6-bis-(4-substituted)styryl-4H-pyran-4-ylidene donor (D) fragments and different electron acceptors (A) were synthesized and investigated, mostly for potential applications in organic solid-state lasers as infra-red (IR) radiation amplification medium. Dye glass transition temperature is above 99 °C with thermal stability in the region from 173 °C to 326 °C which was slightly influenced by the electron acceptor fragment attached to the 4H-pyrane ring in 4-position. Introducing substituents in 4-position within one of the styryl-fragments with stronger electron withdrawing properties decreased ASE exc…

chemistry.chemical_classificationAmplified spontaneous emissionActive laser mediumDye laserMaterials sciencePhotoluminescenceOrganic Chemistry02 engineering and technologyElectron acceptor010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic MaterialsInorganic ChemistrychemistryMoietyThermal stabilityElectrical and Electronic EngineeringPhysical and Theoretical Chemistry0210 nano-technologyGlass transitionSpectroscopyOptical Materials
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Single particle jumps and correlated ionic motions in glass-ceramics

1993

Using impedance spectroscopy, the ion transport in poorly Li-conducting aluminosilicate glass ceramics and their precursor glasses has been measured for temperatures 50 K < T < 550 K and covering a frequency range of more than 14 decades from 10 mHz up to 3 THz. In addition to the familiar cooperative ionic motion dominating at high temperatures, for the first time dielectric relaxation due to elementary hopping processes is observed well below room temperature.

chemistry.chemical_classificationAnalytical chemistryMineralogyIonic bondingCondensed Matter Physics530Electronic Optical and Magnetic MaterialsDielectric spectroscopychemistryAluminosilicatevisual_artMaterials ChemistryCeramics and Compositesvisual_art.visual_art_mediumIonic conductivityParticleDielectric lossCeramicInorganic compound
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ESR of Nd3+ in BaTiO3

1990

Afin d'identifier les defauts responsables de l'effet photo-refractif dans BaTiO 3 , on etudie ces cristaux. Les echantillons contiennent generalement divers etats de charge et des associations de Fe, Cr, ainsi que des trous de O − induits par le rayonnement. On trouve un nouveau centre qui doit etre attribue a Nd 3+ . Dans la presente etude, l'echantillon utilise n'est pas dope, et on l'etudie dans la phase rhomboedrique a T∼77 K. Il apparait que Na est une impurete courante dans BaTiO 3 probablement incorporee avec le materiau de depart, BaCO 3

chemistry.chemical_classificationAngular variationchemistryMineralogyPhysical chemistryCondensed Matter PhysicsInorganic compoundElectronic Optical and Magnetic Materialsphysica status solidi (b)
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Copolymers sensitive to temperature and pH in water and in water+oil mixtures: A DSC, ITC and volumetric study

2011

Block copolymer micelles are receiving an increasing interest because of the variety of structures and the possibilities to tune them by changing external and internal parameters achieving the desired properties for a specific purpose. We have investigated the acid/base behavior, self-assembling and solubilization ability towards polar oils of star-like copolymers named Tetronics. They are composed of branched four-arms each one consisting of two blocks made of EO and PO units linked to the diethylenediamine group, which confers pH response ability. The copolymers T1107 and T90R4 were studied with a sequential and reverse architecture. The thermodynamics of the acid/base equilibrium was stu…

chemistry.chemical_classificationAqueous solutionBase (chemistry)ChemistryCopolymers DSC ITC solubilizationMicelleSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialsColloid and Surface ChemistryDifferential scanning calorimetryMolar volumeChemical engineeringPulmonary surfactantCopolymerOrganic chemistryMacromoleculeJournal of Colloid and Interface Science
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Transfer of Some Alkyl Substituted Ferrocenes from Water to Cationic Surfactant Micelles Studied by Kinetic Method

1994

Abstract Binding of ferrocene and its 1,1′-dimethyl and n -butyl derivatives to dodecyl and tetradecyltrimethylammonium nitrate micellar aggregates has been studied at 20.0°C and ionic strength 0.02 tool dm -3 by examining the micellar retarding effects on the rates of iron(III) oxidation of these substrates. Solubilization of the ferrocenes in the cationic micellar phase increases as the substrate hydrophobic character increases and, to a lesser extent, as the surfactant hydrocarbon chain length becomes longer. The critical micelle concentrations of the surfactants used and the incremental free energy of transfer of methylene groups of both the substrate and the surfactant from the aqueous…

chemistry.chemical_classificationAqueous solutionChemistryInorganic chemistryCationic polymerizationMicelleSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryPulmonary surfactantFerroceneIonic strengthMethyleneAlkylJournal of Colloid and Interface Science
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Enthalpies of Mixing of Some Primary Hydrogenated and Fluorinated Alcohols and Sodium Dodecanoate Aqueous Solutions

1993

Abstract The enthalpies of transfer from water to the surfactant solutions ΔH(W → W + S) of some hydrogenated and fiuorinated alkanols and of sodium dodecanoate NaL were determined. In the premicellar region the measurements were carried out as functions of both the additive and the surfactant concentrations in order to evaluate the interaction parameters between the additive and the surfactant molecules. It is shown that in this region, pair, triplet, and quadruplet interaction parameters between unlike solute molecules contribute to ΔH(W → W + S). Within the large uncertainty with which these parameters are determined because of the very narrow surfactant and alcohol concentration interva…

chemistry.chemical_classificationAqueous solutionDistribution constantEnthalpyConcentration effectSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialsPropanolchemistry.chemical_compoundColloid and Surface ChemistrychemistryPulmonary surfactantPhysical chemistryOrganic chemistryAlkylHexanolJournal of Colloid and Interface Science
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Kinetic and Mechanistic Aspects of a Poly(o-toluidine)-Modified Gold Electrode. 1. Simultaneous Cyclic Spectroelectrochemistry and Electrogravimetry …

2012

International audience; Electrodeposited poly(o-toluidine) (POT) on gold electrodes was investigated in a 0.5 M H2SO4 aqueous solution using cyclic electrogravimetry with in situ vis-NIR spectroscopy. This coupling of different techniques allows the electrical, color, and mass changes during the electrochemical reactions of these polymers to be correlated. Therefore, this is a powerful tool to obtain valuable information on the physical models of polymer films and their electrochemical properties. The accurate analysis of the results from these techniques showed the contribution of three different redox transitions (leucoemeraldine-polaron transition, polaron-bipolaron transition, and bipol…

chemistry.chemical_classificationAqueous solutionInorganic chemistry02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnologyElectrochemistry01 natural sciencesRedox0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAbsorbancechemistry.chemical_compoundGeneral EnergychemistryElectrogravimetryElectrode[CHIM]Chemical SciencesPhysical and Theoretical Chemistry0210 nano-technology[CHIM.OTHE]Chemical Sciences/OtherDerivative (chemistry)
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Atomistic Simulations of Functional Au_{144}(SR)_{60} Gold Nanoparticles in Aqueous Environment

2012

Charged monolayer-protected gold nanoparticles (AuNPs) have been studied in aqueous solution by performing atomistic molecular dynamics simulations at physiological temperature (310 K). Particular attention has been paid to electrostatic properties that modulate the formation of a complex comprised of the nanoparticle together with surrounding ions and water. We focus on Au-144 nanoparticles that comprise a nearly spherical Au core (diameter similar to 2 nm), a passivating Au-S interface, and functionalized alkanethiol chains. Cationic and anionic AuNPs have been modeled with amine and carboxyl terminal groups and Cl-/Na+ counterions, respectively. The radial distribution functions show tha…

chemistry.chemical_classificationAqueous solutionta114ChemistryCationic polymerizationNanoparticleNanotechnologySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMolecular dynamicsGeneral EnergySolvation shellChemical engineeringColloidal goldSide chainPhysical and Theoretical ChemistryCounterionThe Journal of Physical Chemistry C
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