Search results for " photostability"

showing 3 items of 3 documents

Frequency-Downconversion Stability of PMMA Coatings in Hybrid White Light-Emitting Diodes

2015

We report on the properties of a poly(methyl methacrylate)-based coating used as a host for an organic dye in hybrid white light-emitting diodes. The device is composed by a pump source, which is a standard inorganic GaN/InGaN blue light-emitting diode (LED) emitting at around 450 nm, and a spin-coated conversion layer making use of Lumogen® F Yellow 083. Under prolonged irradiation, the coating exhibits significant bleaching, thus degrading the color rendering performance of the LED. We present experimental results that confirm that the local temperature rise of the operating diode does not affect the conversion layer. It is also proven that, during the test, the photostability of the orga…

Materials scienceInfraredSettore AGR/13 - Chimica Agraria02 engineering and technologyengineering.materialSettore ING-INF/01 - Elettronica01 natural sciencesCoating0103 physical sciencesMaterials ChemistryElectrical and Electronic EngineeringPhotodegradationDiode010302 applied physicschemistry.chemical_classificationSpin coatingbusiness.industryPMMA hybrid LEDs Lumogen polymer degradation photostability spin coatingPolymer021001 nanoscience & nanotechnologyCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsColor rendering indexchemistryengineeringOptoelectronics0210 nano-technologybusinessLayer (electronics)Journal of Electronic Materials
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Novel Lipophilic Lanthanide Bis-Phthalocyanines Functionalized by Pentadecylphenoxy Groups: Synthesis, Characterization and UV-Photostability

2012

Novel sandwich-type phthalocyanines containing a rare earth metal core (Pr, Nd, Eu-Lu) and macrocycles peripherally substituted by pentadecylphenoxy groups were synthesized using a cardanol-based phthalonitrile precursor and the respective lanthanide acetate. Additionally, the metal free-base analog compound was studied for comparison. The purified reaction products were all found to be thick and viscous substances at room temperature, showing liquid crystalline behavior with a distinct increase in fluidity at ca. 40 ° C. The complexes are readily soluble in chloroalkyl solvents and dissolve fairly well in DMF with some tendency to form aggregates. Besides they are strongly hydrophobic and …

LanthanideIndolesMagnetic Resonance SpectroscopyUltraviolet Rayslanthanide bis-phthalocyaninePharmaceutical ScienceIsoindolesPhotochemistryphotostabilityLanthanoid Series ElementsArticleAnalytical Chemistrylcsh:QD241-441Phthalonitrilechemistry.chemical_compoundUltraviolet visible spectroscopylcsh:Organic chemistrylanthanide bis-phthalocyanines; cardanol; UV-Vis spectroscopy; photostabilityDrug DiscoverycardanolPhysical and Theoretical ChemistryPhotodegradationlanthanide bis-phthalocyaninesDichloromethaneCardanolPhotolysisMolecular StructureOrganic ChemistryUV-Vis spectroscopychemistryChemistry (miscellaneous)Molecular MedicineDimethylformamideAbsorption (chemistry)Molecules
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Assessment of the Potential Energy Hypersurfaces in Thymine within Multiconfigurational Theory: CASSCF vs. CASPT2

2016

The present study provides new insights into the topography of the potential energy hypersurfaces (PEHs) of the thymine nucleobase in order to rationalize its main ultrafast photochemical decay paths by employing two methodologies based on the complete active space self-consistent field (CASSCF) and the complete active space second-order perturbation theory (CASPT2) methods: (i) CASSCF optimized structures and energies corrected with the CASPT2 method at the CASSCF geometries and (ii) CASPT2 optimized geometries and energies. A direct comparison between these strategies is drawn, yielding qualitatively similar results within a static framework. A number of analyses are performed to assess t…

Chemistry Multidisciplinary2-DIMENSIONAL ELECTRONIC SPECTROSCOPYPharmaceutical Sciencephotostability0305 Organic Chemistry01 natural sciencesLOWEST TRIPLET-STATEAnalytical ChemistryInterpretation (model theory)Molecular dynamicschemistry.chemical_compoundComputational chemistryDrug DiscoveryComplete active spacePerturbation theoryRETINAL CHROMOPHORE MODELComputingMilieux_MISCELLANEOUSAB-INITIOphotochemistry010304 chemical physicsBasis (linear algebra)ChemistryCOUPLED-CLUSTER METHODSPhotochemical ProcessesPotential energy[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryChemistryChemistry (miscellaneous)2ND-ORDER PERTURBATION-THEORYPhysical SciencesANO BASIS-SETSCASSCF/CASPT2Molecular MedicineThermodynamicsLife Sciences & BiomedicineBiochemistry & Molecular BiologyField (physics)INITIO MOLECULAR-DYNAMICSMolecular Dynamics Simulation010402 general chemistryMolecular physicsArticlelcsh:QD241-441lcsh:Organic chemistryCASSCF/CASPT2; photochemistry; DNA; thymine; photostability0103 physical sciencesthyminePhysical and Theoretical ChemistryULTRAFAST INTERNAL-CONVERSIONScience & TechnologyOrganic ChemistryDNAEXCITED-STATE DYNAMICS0104 chemical sciencesThymineModels ChemicalMolecules; Volume 21; Issue 12; Pages: 1666
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