Search results for "polymers"

showing 10 items of 3567 documents

Slow Dynamics of the Magnetization in One-Dimensional Coordination Polymers: Single-Chain Magnets

2009

18 pages; International audience; Slow relaxation of the magnetization (i.e., "magnet-like" behavior) in materials composed of magnetically isolated chains was observed for the first time in 2001. This type of behavior was predicted in the 1960s by Glauber in a chain of ferromagnetically coupled Ising spins (the so-called Glauber dynamics). In 2002, this new class of nanomagnets was named single-chain magnets (SCMs) by analogy to single-molecule magnets that are isolated molecules displaying related superparamagnetic properties. A long-range order occurs only at T = 0 K in any pure one-dimensional (1D) system, and thus such systems remain in their paramagnetic state at any finite temperatur…

One-dimensional coordination PolymersCondensed matter physics010405 organic chemistryMagnetismChemistryRelaxation (NMR)MagnetismSingle-Chain Magnets010402 general chemistry01 natural sciencesNanomagnet0104 chemical sciencesInorganic ChemistryParamagnetismMagnetizationMagnet[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryGlauberSuperparamagnetism
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Efficient photo-thermal activation of gold nanoparticle-doped polymer plasmonic switches

2012

International audience; We report on the photo-thermal activation of dielectric loaded plasmonic switches comprised of gold nanoparticle-doped polymer deposited onto a gold film. The plasmonic switches rely on a multi-mode interferometer design and are fabricated by electron beam lithography applied to a positive resin doped with gold nanoparticles at a volume ratio of 0.52%. A cross-bar switching is obtained at telecom wavelengths by pumping the devices with a visible beam having a frequency within the localized surface plasmon resonance band of the embedded nanoparticles. By comparing the switching performances of doped and undoped devices, we show that for the modest doping level we cons…

Optics and PhotonicsMaterials scienceHot TemperatureLightPolymersFinite Element AnalysisNanoparticleMetal NanoparticlesPhysics::Optics02 engineering and technologyCondensed Matter::Materials Science020210 optoelectronics & photonicsCondensed Matter::Superconductivity0202 electrical engineering electronic engineering information engineeringNanotechnologySurface plasmon resonancePlasmon[PHYS]Physics [physics][ PHYS ] Physics [physics]business.industryDopingSurface plasmonEquipment DesignModels TheoreticalSurface Plasmon Resonance021001 nanoscience & nanotechnologyAtomic and Molecular Physics and OpticsColloidal goldHeat generationTelecommunicationsOptoelectronicsMicrotechnologyCondensed Matter::Strongly Correlated ElectronsGold0210 nano-technologybusinessElectron-beam lithography
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Refractive micro-optical elements for surface plasmons: from classical to gradient index optics.

2010

Controlling the propagation of surface plasmons along a metal-dielectric interface is a key feature for the development of surface plasmon based circuits. We have designed various two-dimensional refractive dielectric optical elements for surface plasmons (SP) and characterized their capacity to route SP, using near- or far-field techniques. We first present basic devices analogous to usual optical components and the associated challenges for SP optics. We then use a metamaterial approach to locally vary the refractive index and fabricate gradient index structures for SP circuitry.

Optics and PhotonicsMaterials sciencePolymersNanophotonicsPhysics::OpticsDielectriclaw.inventionOpticslawMaterials TestingNanotechnologyPolymethyl MethacrylatePlasmonbusiness.industryLasersSurface plasmonMetamaterialEquipment DesignSurface Plasmon ResonanceAtomic and Molecular Physics and OpticsNanostructuresRefractometryMicroscopy Electron ScanningbusinessRefractive indexBeam splitterLocalized surface plasmonOptics express
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Optical experiments on a crystallizing hard-sphere–polymer mixture at coexistence

2010

We report on the crystallization kinetics in an entropically attractive colloidal system using a combination of time resolved scattering methods and microscopy. Hard sphere particles are polystyrene microgels swollen in a good solvent (radius a=380nm, starting volume fraction 0.534) with the short ranged attractions induced by the presence of short polymer chains (radius of gyration rg = 3nm, starting volume fraction 0.0224). After crystallization, stacking faulted face centred cubic crystals coexist with about 5% of melt remaining in the grain boundaries. From the Bragg scattering signal we infer the amount of crystalline material, the average crystallite size and the number density of cry…

Optics and PhotonicsOsmosisMaterials sciencePolymersBiophysicsFOS: Physical sciencesCondensed Matter - Soft Condensed Matterlaw.inventionOpticslawPressureScattering RadiationCrystallizationMicroscopyCondensed matter physicsScatteringbusiness.industryBragg's lawEquipment DesignCondensed Matter::Soft Condensed MatterKineticsVolume fractionRadius of gyrationPolystyrenesSoft Condensed Matter (cond-mat.soft)Grain boundaryCrystalliteSmall-angle scatteringCrystallizationbusinessGelsAlgorithmsPhysical Review E
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Theoretical determination of the geometric and electronic structures of oligorylenes and poli(peri‐naphthalene)

1992

We present a theoretical investigation of the electronic structure of oligorylenes (from perylene to heptarylene, including also the naphthalene molecule) and their corresponding polymer poly(peri‐naphthalene) (PPN) using the nonempirical valence effective (VEH) method. The geometry of the unit cell used to generate the polymer is extrapolated from the PM3‐optimized molecular geometries of the longest oligorylenes. That geometry shows some bond alternation along the perimeter carbon chains and a bond length of ≊1.46 Å is calculated for the peri bonds connecting the naphthalene units. The VEH one‐electron energy level distributions calculated for oligorylenes are used to interpret the experi…

OptimizationChemical BondsBand gapStereochemistryExtrapolationElectric ConductorsGeometryGeneral Physics and AstronomyElectronic structureMolecular physicsEnergy LevelsMolecular orbitalPhysical and Theoretical ChemistryBand Structure:FÍSICA::Química física [UNESCO]Electronic band structurePeryleneFilmsValence (chemistry)Organic PolymersChemistryElectronic Structure ; Perylene ; Naphthalene ; Organic Polymers ; Unit Cell ; Geometry ; Extrapolation ; Optimization ; Chemical Bonds ; Carbon ; Chains ; Energy Levels ; Ionization Potential ; Affinity ; Band Structure ; Electric Conductors ; Films ; PyrolysisUnit CellChainsCarbonUNESCO::FÍSICA::Química físicaBond lengthIonization PotentialMolecular geometryElectronic StructureAffinityIonization energyNaphthalenePyrolysis
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Theoretical study of the effect of substituent and backbone conformation on the electronic properties of symmetrically substituted poly(di‐n‐alkylsil…

1994

We present the results of ab initio 3‐21G∗ geometry optimizations and valence effective Hamiltonian (VEH) band structure calculations aimed at determining the evolution of the geometric and electronic (ionization potential, electron affinities, and band gaps) properties of all‐trans poly(dimethylsilane), poly(diethylsilane), poly(di‐n‐propylsilane), and poly(di‐n‐butylsilane) when increasing the size of the alkyl group. In the latter polymer, we have also studied the 7/3 conformation, in order to analyze the effect of the backbone conformation on the geometric and electronic structure. The VEH ionization potentials of all‐trans poly(di‐n‐alkylsilanes) are almost equal, and as experimental p…

OptimizationEnergy GapPropyl CompoundsBand gapAb initioSubstituentGeometryGeneral Physics and AstronomyElectronic structurechemistry.chemical_compoundAb initio quantum chemistry methodsComputational chemistryMethyl CompoundsConformational ChangesPhysical and Theoretical ChemistryBand Structure:FÍSICA::Química física [UNESCO]Electronic band structureAlkyl Compounds ; Silanes ; Organic Polymers ; Conformational Changes ; Ab Initio Calculations ; Geometry ; Optimization ; Band Structure ; Affinity ; Ionization Potential ; Energy Gap ; Methyl Compounds ; Ethyl Compounds ; Propyl CompoundsDimethylsilaneOrganic PolymersSilanesUNESCO::FÍSICA::Química físicaCrystallographyAlkyl CompoundsIonization PotentialAffinitychemistryEthyl CompoundsIonization energyAb Initio Calculations
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Effect of Lithium Perchlorate on the Kinetics of the Anionic Polymerization of Methyl Methacrylate in Tetrahydrofuran

1999

The kinetics of the anionic polymerization of methyl methacrylate in the presence of lithium perchlorate (LiClO 4 ) are investigated in THF using 1,1-diphenylhexyllithium as initiator in a flow-tube reactor between -30 and 0 °C. The rate constants of propagation determined in the presence of LiClO 4 are lower than those obtained in the absence of the salt, similar to the effect observed for LiCl. For propagation, the reaction order with respect to active center concentration is found to be 0.5 in both cases, which indicates that LiClO 4 does not effectively perturb the aggregation of the enolate ion pair. The formation of various mixed aggregates is proposed. The polydispersity index of the…

Order of reactionPolymers and PlasticsOrganic ChemistryInorganic chemistryKineticsSolution polymerizationLithium perchlorateInorganic Chemistrychemistry.chemical_compoundAnionic addition polymerizationReaction rate constantchemistryMaterials ChemistryMethyl methacrylateTetrahydrofuranMacromolecules
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Synthesis, characterization and thermal degradation of 8-hydroxyquinoline–guanidine–formaldehyde terpolymer

2007

Abstract Terpolymer (8-HQGF) has been synthesized using the monomers 8-hydroxyquinoline, guanidine, formaldehyde in 1:1:2 molar proportions. The structure of 8-HQGF terpolymer has been elucidated on the basis of elemental analysis and various physicochemical techniques, i.e. UV–Visible, FTIR–ATR and 1 H NMR spectroscopy. Detailed thermal degradation study of the new terpolymer has been carried out to ascertain its thermal stability. Thermal degradation curve is discussed which shows two decomposition steps (265–475 °C and 540–715 °C). Sharp–Wentworth and Freeman–Carroll methods have been used to calculate activation energies and thermal stability. The activation energy ( E a ) calculated by…

Order of reactionPolymers and PlasticssynthesisFormaldehydeGeneral Physics and Astronomy02 engineering and technologyActivation energy010402 general chemistry7. Clean energy01 natural scienceschemistry.chemical_compoundsymbols.namesakeSharp-Wentworth methodPolymer chemistryMaterials ChemistryThermal stabilitythermal degradationGuanidineSpectroscopyComputingMilieux_MISCELLANEOUSOrganic Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesGibbs free energyFreeman-Carroll method[ CHIM.POLY ] Chemical Sciences/Polymers[CHIM.POLY]Chemical Sciences/Polymerschemistryspectroscopic characterizationProton NMRsymbolsPhysical chemistry0210 nano-technology8-HQGF terpolymer
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Nanoscale control in organic bulk heterojunctions of new set of materials for photovoltaic applications

2008

Organic PhotovoltaicScanning Force Microscopy (SFM)Solar EnergyConductive Polymers
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Boramers for Photovoltaic Applications

2008

Organic PhotovoltaicScanning Force Microscopy (SFM)Solar EnergyConductive Polymers
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