Search results for "Ryle"

showing 10 items of 138 documents

Ultra-sensitive fluorescence spectroscopy of isolated surface-adsorbed molecules using an optical nanofiber.

2009

The strong radial confinement and the pronounced evanescent field of the guided light in optical nanofibers yield favorable conditions for ultra-sensitive surface spectroscopy of molecules deposited on the fiber. Using the guided mode of the nanofiber for both excitation and fluorescence collection, we present spectroscopic measurements on 3,4,9,10-perylenetetracarboxylic dianhydride molecules (PTCDA) at ambient conditions. Surface coverages as small as 1 per thousand of a compact monolayer still give rise to fluorescence spectra with a good signal to noise ratio. Moreover, we analyze and quantify the self-absorption effects due to reabsorption of the emitted fluorescence light by circumjac…

Optics and PhotonicsMaterials scienceOptical fiberLuminescenceSurface PropertiesFluorescence spectroscopyFluorescencelaw.inventionAnhydridesOpticslawMonolayerFiber Optic TechnologySpectroscopyLaser-induced fluorescencePeryleneOptical FibersTotal internal reflectionbusiness.industryLasersFluorescenceAtomic and Molecular Physics and OpticsSpectrometry FluorescenceAdsorptionLuminescencebusinessOptics express
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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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Synthesis of rigid ethynyl-bridged polytopic picolinate ligands for MOF applications

2015

Abstract Segmented homopolytopic ligands that consist of a rigid central arylene platform, ethynylene spacers, and terminal chelating picolinate subunits have been synthesized in good yields in a two-step procedure involving a Sonogashira-type cross coupling reaction between the ester methyl 5-bromopyridine-2-carboxylate and several arylacetylenes, followed by hydrolysis of the resulting methyl picolinates. A similar strategy has been employed for the preparation of heteroditopic ligands containing picolinate and a second non-chelating pyridine or benzoate unit. The compounds are potential candidates for organic linkers in metal–organic frameworks (MOFs).

Organic ChemistryAryleneSonogashira couplingBiochemistryCombinatorial chemistryCoupling reactionchemistry.chemical_compoundHydrolysischemistryDrug DiscoveryPyridineOrganic chemistryMetal-organic frameworkChelationTetrahedron Letters
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Fast and Efficient Microwave-Assisted Synthesis of Perylenebisimides

2015

Perylene-3,4,9,10-tetracarboxylic acid bisimides have been widely studied as industrial pigments. Lately, these dyes have drawn considerable attention because of applications as photocatalysts and organic semi-conductors. Here, we report a novel method for fast and efficient synthesis of many different perylenebisimides, based on microwave-assisted reactions.

Organic ChemistryDyes/pigmentAmines; Amino acids; Condensation reactions; Dyes/pigments; Microwave chemistry; PerylenebisimidesPerylenebisimidesPerylenebisimideAmino acidMicrowave chemistryCondensation reactionAmino acidsAmines; Amino acids; Condensation reactions; Dyes/pigments; Microwave chemistry; Perylenebisimides; Organic Chemistry; Physical and Theoretical ChemistryDyes/pigmentsAminesPhysical and Theoretical ChemistryCondensation reactionsAmine
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Energy Transfer at the Single-Molecule Level: Synthesis of a Donor-Acceptor Dyad from Perylene and Terrylene Diimides

2013

In 2004, we reported single-pair fluorescence resonance energy transfer (spFRET), based on a perylene diimide (PDI) and terrylene diimide (TDI) dyad (1) that was bridged by a rigid substituted para-terphenyl spacer. Since then, several further single-molecule-level investigations on this specific compound have been performed. Herein, we focus on the synthesis of this dyad and the different approaches that can be employed. An optimized reaction pathway was chosen, considering the solubilities, reactivities, and accessibilities of the building blocks for each individual reaction whilst still using established synthetic techniques, including imidization, Suzuki coupling, and cyclization reacti…

Organic ChemistryGeneral ChemistryChromophorePhotochemistryCatalysischemistry.chemical_compoundFörster resonance energy transferchemistrySuzuki reactionDiimideYield (chemistry)MoleculePeryleneDyadChemistry - A European Journal
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Efficient deep-red light-emitting electrochemical cells based on a perylenediimide-iridium-complex dyad

2009

A two-layer light-emitting electrochemical cell device based on a new perylenediimide-iridium-complex dyad is presented emitting in the deep-red region with high external quantum efficiencies (3.27%). Costa Riquelme, Ruben Dario, Ruben.Costa@uv.es ; Orti Guillen, Enrique, Enrique.Orti@uv.es ; Bolink, Henk, Henk.Bolink@uv.es ; Gierschner, Johannes, Johannes.Gierschner@uv.es

Organic light-emitting devicesMaterials scienceLightUNESCO::QUÍMICALight-emitting electrochemical cellschemistry.chemical_elementImidesIridium:QUÍMICA [UNESCO]CatalysisElectrochemical cellExternal quantum efficienciesElectrochemistryOrganometallic CompoundsMaterials ChemistryLight-emitting electrochemical cells ; Organic light-emitting devices ; Perylenediimide-iridium-complex ; External quantum efficienciesRed lightIridiumPerylenePhotonsLuminescent AgentsMolecular Structurebusiness.industryUNESCO::QUÍMICA::Química analíticaMetals and AlloysGeneral ChemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryLuminescent MeasurementsCeramics and Composites:QUÍMICA::Química analítica [UNESCO]OptoelectronicsPerylenediimide-iridium-complexbusiness
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Generation of white LED light by frequency downconversion using a perylene-based dye

2012

A high efficiency white light emitting diode (LED) was fabricated by generation of frequency down-conversion from a GaN/InGaN blue LED. In place of conventional inorganic phosphors, a perylene-based dye was used for colour conversion. The resulting hybrid structure is analysed by focusing on the visual performance of the realised LEDs employing the most relevant photometric parameters of a light source. Preparation of the organic polymer is described as well. The thermal stability of the dye was investigated and a simple structure which avoids colour degradation is proposed.

Organic polymerMaterials sciencebusiness.industryPhosphordyes light emitting diodes phosphors polymers wide band gap semiconductors GaN-InGaN blue LED colour conversionSettore ING-INF/01 - Elettronicalaw.inventionchemistry.chemical_compoundOpticsLight sourcechemistrylawOptoelectronicsDegradation (geology)Thermal stabilityElectrical and Electronic EngineeringbusinessPeryleneDiodeLight-emitting diode
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Enhanced susceptibility of cholesteryl sulfate-enriched low density lipoproteins to copper-mediated oxidation

1995

AbstractCholesteryl sulfate (CS) is a minor component of cell membranes, also present in lipoproteins, and its exact function is unknown. Since oxidation of low density lipoproteins (LDL) is thought to be an important determinant of atherogenesis, we investigated the influence of CS enrichment on copper-mediated oxidation of LDL. CS was found to act as a pro-oxidant, as measured by lipid oxidation parameters. The results also suggest that these effects were dependent on the sulfate group since pure cholesterol or cholesteryl acetate did not promote Cu2+-mediated oxidation. Our findings imply that CS may affect the oxidizability and hence the potential atherogenicity of LDL.

Oxidized LDLArteriosclerosisBiophysicschemistry.chemical_elementCholesteryl sulfateCholesteryl sulfateBiochemistryThiobarbituric Acid Reactive Substanceschemistry.chemical_compoundStructure-Activity RelationshipLipid oxidationStructural BiologyCholesterylester transfer proteinOxidationGeneticsHumansSulfateMolecular BiologyIntermediate-density lipoproteinbiologyCholesterolCell BiologyCopperLipoproteins LDLMembranechemistryBiochemistrybiology.proteinlipids (amino acids peptides and proteins)Cholesterol EstersLipid PeroxidationCopperFEBS Letters
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Spectroscopic characterization of red perylimide/surfactant nanocomposites

2011

Novel photoluminescent materials formed by some selected surfactants, metal derivatives of bis(2-ethylhexyl) sulfosuccinate (M(AOT)n; M = Na+, Co2+, Er3+ and Yb3+), bis(2-ethylhexyl) amine (BEEA), bis(2-ethylhexy1) phosphoric acid (HDEHP) and a 1:1 BEEA/HDEHP mixture, doped with the red perylimide (ROT-300) have been prepared, and their optical properties have been tested by absorption spectroscopy and steady state and timeresolved fluorescence. Experimental results show spectral shifts of the typical ROT-300 absorption and fluorescence bands with respect to that in apolar solvent medium. Data analysis leads consistently to attribute this feature mainly to the freezing of the diffusive move…

PERYLENEROT ASEMaterials sciencePhotoluminescenceDye laserMICELLESAbsorption spectroscopyDYEMechanical EngineeringAnalytical chemistryDNAFluorescenceMicelleMechanics of MaterialsLiquid crystalGeneral Materials ScienceLASERAbsorption (chemistry)LuminescenceSettore CHIM/02 - Chimica Fisica
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Resource or waste? A perspective of plastics degradation in soil with a focus on end-of-life options.

2018

‘Capable-of-being-shaped’ synthetic compounds are prevailing today over horn, bone, leather, wood, stone, metal, glass, or ceramic in products that were previously left to natural materials. Plastic is, in fact, economical, simple, adaptable, and waterproof. Also, it is durable and resilient to natural degradation (although microbial species capable of degrading plastics do exist). In becoming a waste, plastic accumulation adversely affects ecosystems. The majority of plastic debris pollutes waters, accumulating in oceans. And, the behaviour and the quantity of plastic, which has become waste, are rather well documented in the water, in fact. This review collects existing information on pla…

PLA polylactic acidPS polystyreneETS European Emissions Trading schemePOM polyoxymethyleneHMC heat melt compactor technology02 engineering and technology010501 environmental sciencesNHV net habitable volumeLDPE low-density polyethylene01 natural sciencesPC polycarbonateResin identification codeLCP liquid crystal polymerslcsh:Social sciences (General)PAC pro-oxidant additive containingPET polyethylene terephthalateEPR Extended Producers ResponsibilityMultidisciplinaryWaste managementNatural materials021001 nanoscience & nanotechnologyPU or PUR polyurethaneSettore AGR/02 - Agronomia E Coltivazioni ErbaceeEPS expandable polystyreneRIC resin identification codeSettore AGR/14 - PedologiaPVDF polydifluoroethylenelcsh:H1-990210 nano-technologyBiogeoscienceGPPS Polystyrene (General Purpose)PVC polyvinyl chlorideResource (biology)Polymethyl methacrylatePA polyamidePBT polybutylene terephthalatePSU polyarylsulfonePTFE polytetrafluoroethylenePMMA polymethyl methacrylatePHA polyhydroxyalkanoateMicrobiologyPEEK polyaryletheretherketoneArticleEnvironmental scienceEnvironmental science Biogeoscience Industry MicrobiologyPPA polyphthalamideTPE thermoplastic polyester elastomerNatural degradationIndustryPPS polyphenylene sulphidelcsh:Science (General)ABS acrylonitrile-butadiene-styrene0105 earth and related environmental sciencesbusiness.industryPP polypropyleneHDPE high-density polyethyleneBPA bisphenol AHBCD hexabromocyclododecaneFuture studyAgricultureDOM dissolved organic matterDegradation (geology)Environmental sciencebusinesslcsh:Q1-390Heliyon
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