Search results for "Photophysics"

showing 10 items of 24 documents

Concentration dependence of amplified spontaneous emission in two oligo-(p-phenylenevinylene) derivatives

2005

Amplified spontaneous emission sASEd in optically pumped polystyrene sPSd films doped with two different oligo-sp-phenylenevinylened derivatives sOPVsd, with three s3-OPVd and five s5-OPVd monomer units is reported. It is observed that there is a maximum content of oligomer s25 wt. % for 3-OPV and 20 wt. % for 5-OPVd that can be introduced in the films, due to degradation sin 3-OPVd and ASE quenching sin 5-OPVd. Optimal concentrations swith minimum pump-intensity thresholds for the observation of ASEd of 15 wt. % and 9 wt. % are measured for the trimer and the pentamer, respectively. The concentration dependence of the ASE threshold is discussed in terms of the optical absorption spectra. G…

Amplified spontaneous emissionPhotoluminescenceQuenching (fluorescence)Materials sciencePentamerAnalytical chemistryGeneral Physics and AstronomyTrimerSettore CHIM/06 - Chimica OrganicaOligomerchemistry.chemical_compoundchemistryconjugated oligomersPolystyreneStimulated emissionphotophysics
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Long lived photoinduced charges in donor-acceptor anthraquinone substituted thiophene copolymers

2006

The photoinduced charge-transfer properties of a series of polyalkylthiophene copolymers, carrying anthraquinone substituents covalently linked to the conjugated backbone, have been studied in the solid state by photoinduced absorption (PA) and light-induced electron spin resonance (LESR) spectroscopy. The measurements indicate the formation of metastable charges arising from the photoinduced electron transfer from the polythiophene backbone to the anthraquinone moieties. At low temperatures (below 200 K), long-lived persistent charges are formed, exhibiting lifetimes that extend for several minutes; their recombination kinetics has been studied by following the formation and decay of the P…

ChemistrySettore CHIM/06 - Chimica OrganicaConjugated systemPhotochemistryAcceptorAnthraquinonePhotoinduced electron transferSurfaces Coatings and Filmslaw.inventionPhotoexcitationchemistry.chemical_compoundlawMaterials ChemistryThiopheneconjugated polymersPolythiophenePhysical and Theoretical ChemistryElectron paramagnetic resonancephotophysics
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Ultrafast decay of the excited singlet states of thioxanthone by internal conversion and intersystem crossing.

2010

The experimental ultrafast photophysics of thioxanthone in several aprotic organic solvents at room temperature is presented, measured using femtosecond transient absorption together with high-level ab initio CASPT2 calculations of the singlet- and triplet-state manifolds in the gas phase, including computed state minima and conical intersections, transition energies, oscillator strengths, and spin-orbit coupling terms. The initially populated singlet pi pi* state is shown to decay through internal conversion and intersystem crossing processes via intermediate n pi* singlet and triplet states, respectively. Two easily accessible conical intersections explain the favorable internal conversio…

Conical intersectionsChemistryTransition statesQuantum yieldInternal conversion (chemistry)Atomic and Molecular Physics and OpticsPhotophysicsIntersystem crossingExcited stateddc:540Solvent effectsUltrafast laser spectroscopySinglet fissionAb initio calculationsSinglet statePhysical and Theoretical ChemistryAtomic physicsTriplet stateChemphyschem : a European journal of chemical physics and physical chemistry
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Experimental and theoretical studies on thymine photodimerization mediated by oxidatively generated DNA lesions and epigenetic intermediates.

2020

[EN] Interaction of nucleic acids with light is a scientific question of paramount relevance not only in the understanding of life functioning and evolution, but also in the insurgence of diseases such as malignant skin cancer and in the development of biomarkers and novel light-assisted therapeutic tools. This work shows that the UVA portion of sunlight, not absorbed by canonical DNA nucleobases, can be absorbed by 5-formyluracil (ForU) and 5-formylcytosine (ForC), two ubiquitous oxidatively generated lesions and epigenetic intermediates present in living beings in natural conditions. We measure the strong propensity of these molecules to populate triplet excited states able to transfer th…

DNA damagePhotochemistryUltraviolet RaysBasesGeneral Physics and AstronomyPyrimidine dimer010402 general chemistry01 natural sciencesNucleobaseEpigenesis Geneticchemistry.chemical_compoundTriplet energy-transferCytosineQUIMICA ORGANICAMoleculeEpigeneticsPhysical and Theoretical ChemistryUracil010405 organic chemistryDimer formation0104 chemical sciencesThymineDynamicsDamagePhotophysicschemistryBiophysicsNucleic acidSunlightMechanismPhotosensitizationDimerizationOxidation-ReductionDNAThymineDNA DamagePhysical chemistry chemical physics : PCCP
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Photoluminescence in Carborane–Stilbene Triads : A Structural, Spectroscopic, and Computational Study

2016

A set of triads in which o- and m-carborane clusters are bonded to two stilbene units through Ccluster -CH2 bonds was synthesized, and their structures were confirmed by X-ray diffraction. A study on the influence of the o- and m- isomers on the absorption and photoluminescence properties of the stilbene units in solution revealed no charge-transfer contributions in the lowest excited state, as confirmed by (TD)DFT calculations. The presence of one or two B-I groups in m-carborane derivatives does not affect the emission properties of the stilbenes in solution, probably due to the rather large distance between the iodo substituents and the fluorophore. Nevertheless, a significant redshift o…

DiffractionFluorophorePhotoluminescencecarboranesalkenes010405 organic chemistryOrganic ChemistryGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundchemistryExcited statedensity functional calculationsluminescenceCarboraneAbsorption (chemistry)Thin filmLuminescenceta116photophysicsChemistry: A European Journal
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The photophysics and photochemistry of cofacial free base and metallated bisporphyrins held together by covalent architectures

2007

Abstract This review focuses on the photophysical properties of bisporphyrin systems held in a face-to-face configuration by covalent bonds via flexible or rigid spacers and metal–metal bonds. The cofacial arrangement induces intramolecular bismacrocycle interactions promoting basic photophysical events such as excitonic interactions and energy and electron transfers. These events are relevant to mimic light harvesting and reactor devices known for photosynthesis in plants, and can be monitored by luminescence and flash photolysis methods.

Exciton010402 general chemistryPhotochemistryporphyrins01 natural sciencesInorganic Chemistry[ CHIM.OTHE ] Chemical Sciences/OtheremissionMaterials ChemistryluminescencePhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUSphotophysicsexciton010405 organic chemistryChemistryelectron and energy transferFree base0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryphosphorescenceCovalent bondIntramolecular force[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistryFlash photolysisfluorescenceLuminescencePhosphorescence[CHIM.OTHE]Chemical Sciences/Other
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Topological effects of a rigid chiral spacer on the electronic interactions in donor-acceptor ensembles

2005

Two triads (donor-spacer-acceptor), etTTF-BN-C 6 0 (6) and ZnP-BN-C 6 0 (7), in which electron donors (i.e., exTTF or ZnP) are covalently linked to C 6 0 through a chiral binaphthyl bridge (BN), have been prepared in a multistep synthetic procedure starting from a highly soluble enantiomerically pure binaphthyl building block (1). Unlike other oligomeric bridges, with hinaphthyl bridges, the conjugation between the donor and the acceptor units is broken and geometric conformational changes are facilitated. Consequently, distances and electronic interactions between the donor and C 6 0 are drastically changed. Both donor-spacer-acceptor (D-s-A) systems (i.e., 6 and 7) exhibit redox processes…

FullereneStereochemistryOrganic ChemistryTriad (anatomy)Donor-Acceptor EnsemblesGeneral ChemistrySettore CHIM/06 - Chimica OrganicaFluorescenceAcceptorRedoxCatalysischemistry.chemical_compoundmedicine.anatomical_structurePhotophysicschemistryFullereneCovalent bondUltrafast laser spectroscopymedicineTetrathiafulvalene
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An Ester-Substituted Iridium Complex for Efficient Vacuum-Processed Organic Light-Emitting Diodes

2009

An orange-red-emitting iridium complex (N958) was prepared, and its photophysical and device-based characteristics were investigated. Despite N958 displaying quite poor photophysical properties in solution (acetonitrile), organic light-emitting diode (OLED) devices based on the complex exhibit an efficiency close to 10%.

LuminescenceMaterials scienceLightGeneral Chemical Engineeringchemistry.chemical_elementEstersIridiumPhotochemistryEnergy conversionOrganic light-emitting diodesAbsorptionchemistry.chemical_compoundPhotophysicsGeneral EnergychemistryOrganometallic CompoundsOLEDEnvironmental ChemistryEnergy transformationGeneral Materials ScienceIridiumAcetonitrileElectrodesDiodeChemSusChem
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Tuning the Ultrafast Response of Fano Resonances in Halide Perovskite Nanoparticles

2020

International audience; The full control of the fundamental photophysics of nanosystems at frequencies as high as few THz is key for tunable and ultrafast nanophotonic devices and metamaterials. Here we combine geometrical and ultrafast control of the optical properties of halide perovskite nanoparticles, which constitute a prominent platform for nanophotonics. The pulsed photoinjection of free carriers across the semiconducting gap leads to a subpicosecond modification of the far-field electromagnetic properties that is fully controlled by the geometry of the system. When the nanoparticle size is tuned so as to achieve the overlap between the narrowband excitons and the geometry-controlled…

Materials scienceTerahertz radiationNanophotonicsFOS: Physical sciencesGeneral Physics and AstronomyPhysics::Optics02 engineering and technology010402 general chemistrySettore FIS/03 - FISICA DELLA MATERIA01 natural sciencesOptical switchhalide perovskites nanoparticles[SPI]Engineering Sciences [physics]Fano resonance; halide perovskites nanoparticles; ultrafast photophysics; nanophotonics; Mie resonancesPhysics::Atomic and Molecular Clusters[CHIM]Chemical SciencesGeneral Materials ScienceThin filmPhysics::Chemical PhysicsPerovskite (structure)[PHYS]Physics [physics]Condensed Matter - Materials Sciencebusiness.industryMie resonancesGeneral EngineeringMaterials Science (cond-mat.mtrl-sci)Fano resonanceMetamaterialSettore ING-INF/02 - Campi Elettromagnetici021001 nanoscience & nanotechnology0104 chemical sciencesOptoelectronicsFano resonancenanophotonics0210 nano-technologybusinessultrafast photophysicsUltrashort pulseOptics (physics.optics)Physics - Optics
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Crossed 2D versus Slipped 1D π-Stacking in Polymorphs of Crystalline Organic Thin Films

2019

Polymorphs of organic semiconductors are of great interest as they shed light to structure-property relationships. The full X-ray thin film structure analysis of two polymorphs (B, G) of an important n-type semiconducting dicyano-distyrylbenzene based small molecule (CN-TFPA) is reported. Drastically different structures of the monotropic phases are revealed, that is an uncommon 2D crossed π-stacked arrangement for the B-phase versus a 1D slipped π-stack for G. Both phases exhibit a layered structure in the (100) plane with high structural integrity, driven by the hydrophobic contacts of the terminal CF3 groups; as (100) coincides with the film surface, this allows for exfoliation by scotch…

Materials scienceorganic semiconductorStackingAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsOrganic semiconductorthin film polymorphismCrystallographyorganic optoelectronicsFluorescent materialsfluorescent materialsThin filmtwo-dimensional (2D) charge transportphotophysicsAdvanced Optical Materials
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