Search results for "photophysic"

showing 10 items of 39 documents

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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The influence study of the number of substituted heteroaryls at the non-K region of pyrene structure on the photophysical properties based on the exa…

2022

The study of the photophysical properties (thermal - thermogravimetric analysis and optical - absorption, emission in the solution and in powder, quantum efficiency of emission and efficient fluorescence lifetime in the solution) with the focus on the influence of the number of substituted 1-decyl-1H-1,2,3-triazole groups at the non-K region of pyrene structure. To the best of our knowledge, the investigation of the impact of the number of heteroaryl groups at the non-K region of pyrene is reported for the first time. The obtained results for monosubstituted derivative (1) were compared to di- (2, 3) and tetra- (4) analogues previously reported by us in the literature. In addition, theoreti…

Experimental studyPyrene derivativeTriazole motifSubstitution patternPhotophysical propertiesJournal of Molecular Structure
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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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Bright Blue Phosphorescence from Cationic Bis-Cyclometalated Iridium(III) Isocyanide Complexes

2012

We report new bis-cyclometalated cationic indium(III) complexes [((CN)-N-boolean AND)(2)Ir(CN-tert-Bu)(2)](CF3SO3) that have tert-butyl isocyanides as neutral auxiliary ligands and 2-phenylpyridine or 2-(4'-fluoropheny1)-R-pyridines (where R is 4-methoxy, 4-tert-butyl, or 5-trifluoromethyl) as (CN)-N-boolean AND ligands. The complexes are white or pale yellow solids that show irreversible reduction and oxidation processes and have a large electrochemical gap of 3.58-3.83 V. They emit blue or bluegreen phosphorescence in liquid/solid solutions from a cyclometalating-ligand-centered excited state. Their emission spectra show vibronic structure with the highest-energy luminescence peak at 440-…

Ir(Iii) ComplexesIsocyanideCationic polymerizationchemistry.chemical_elementEmitting Electrochemical-CellsExcited-State PropertiesElectroluminescent DevicesPhotochemistryAncillary LigandsInorganic Chemistrychemistry.chemical_compoundchemistryExcited stateEfficient BlueIii ComplexesMetal-ComplexesEmission spectrumIridiumPhysical and Theoretical ChemistryPhosphorescenceLuminescenceTurn-On TimesPhotophysical PropertiesSolid solutionInorganic Chemistry
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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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Multinuclear Cytotoxic Metallodrugs: Physicochemical Characterization and Biological Properties of Novel Heteronuclear Gold-Titanium Complexes

2011

An unprecedented series of titanocene-gold bi- and trimetallic complexes of the general formula [[(η(5)-C(5)H(5))(μ-η(5):κ(1)-C(5)H(4)(CH(2))(n)PPh(2))TiCl(2)](m)AuCl(x)](q+) (n = 0, 2, or 4; m = 1, x = 1, q = 0 or m = 2, x = 0, q = 1) have been prepared and characterized spectroscopically. The luminescence spectroscopy and photophysics of one of the compounds, [[(η(5)-C(5)H(5))(μ-η(5):κ(1)-C(5)H(4)PPh(2))TiCl(2)](2)Au]PF(6), have been investigated in 2MeTHF solution and in the solid state at 77 and 298 K. Evidence for interfragment interactions based on the comparison of electronic band positions and emission lifetimes, namely, triplet energy transfer (ET) from the Au- to the Ti-containing…

Models MolecularSpectrometry Mass Electrospray IonizationLuminescenceMagnetic Resonance SpectroscopyTransfer Excited-StatesCell SurvivalStereochemistryAntineoplastic AgentsCharge-TransferUnsaturated-HydrocarbonsCrystallography X-RayElectronic-StructuresInorganic ChemistryStructure-Activity Relationshipchemistry.chemical_compoundCell Line TumorOrganometallic CompoundsHumansPhysical and Theoretical ChemistrySpectroscopyGroup 2 organometallic chemistryTitaniumArene-Ruthenium ComplexesX-rayTitanocene dichlorideNuclear magnetic resonance spectroscopyChromophoreTitanocene DichlorideCrystallographychemistryHeteronuclear moleculeAnticancer AgentsSpectrophotometry UltravioletGoldLuminescenceGold(Iii) CompoundsPhotophysical Properties
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Multiple Decay Mechanisms and 2D-UV Spectroscopic Fingerprints of Singlet Excited Solvated Adenine-Uracil Monophosphate

2016

The decay channels of singlet excited adenine uracil monophosphate (ApU) in water are studied with CASPT2//CASSCF:MM potential energy calculations and simulation of the 2D-UV spectroscopic fingerprints with the aim of elucidating the role of the different electronic states of the stacked conformer in the excited state dynamics. The adenine 1La state can decay without a barrier to a conical intersection with the ground state. In contrast, the adenine 1Lb and uracil S(U) states have minima that are separated from the intersections by sizeable barriers. Depending on the backbone conformation, the CT state can undergo inter-base hydrogen transfer and decay to the ground state through a conical …

Models Molecularmolecular electronicsChemistry MultidisciplinaryMolecular electronicsphotophysic2-DIMENSIONAL ELECTRONIC SPECTROSCOPYSTATE DYNAMICSBASE-STACKINGPhotochemistry01 natural sciences[CHIM] Chemical SciencesNUCLEIC-ACIDSQuímica quànticaEspectrofotometriaConformational isomerismComputingMilieux_MISCELLANEOUSphotophysics010304 chemical physicsFull PaperHydrogen bondChemistryChemistry (all)Full PapersMolecular spectroscopy[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryChemistryFOURIER-TRANSFORM SPECTROSCOPYSpectrophotometryExcited statePhysical Sciences1ST-PRINCIPLES SIMULATION03 Chemical SciencesGround stateUridine MonophosphateQuantum chemistryEspectroscòpia molecularmolecular electronic010402 general chemistryMolecular physicsCatalysisUltraviolet visible spectroscopy0103 physical sciencesPhotophysics | Hot Paper[CHIM]Chemical SciencesSinglet stateUV/Vis spectroscopyULTRAFAST INTERNAL-CONVERSIONSpectroscopyLIGHT-HARVESTING COMPLEXab initio calculationScience & Technologyab initio calculationsOrganic ChemistryGeneral ChemistryDNAConical intersectionDNA FingerprintingAdenosine Monophosphate0104 chemical sciences[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistryAB-INITIO SIMULATIONSElectrònica molecularMOLECULAR-DYNAMICSSpectrophotometry Ultraviolet
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NHC-Based Iron Sensitizers for DSSCs

2018

International audience; Nanostructured dye-sensitized solar cells (DSSCs) are promising photovoltaic devices because of their low cost and transparency. Ruthenium polypyridine complexes have long been considered as lead sensitizers for DSSCs, allowing them to reach up to 11% conversion efficiency. However, ruthenium suffers from serious drawbacks potentially limiting its widespread applicability, mainly related to its potential toxicity and scarcity. This has motivated continuous research efforts to develop valuable alternatives from cheap earth-abundant metals, and among them, iron is particularly attractive. Making iron complexes applicable in DSSCs is highly challenging due to an ultrafa…

NHC ligands[CHIM.ORGA]Chemical Sciences/Organic chemistry[CHIM.COOR] Chemical Sciences/Coordination chemistry[CHIM.ORGA] Chemical Sciences/Organic chemistrylcsh:QD146-197[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistryiron complexes[CHIM] Chemical Scienceslcsh:Inorganic chemistry[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistryexcited statesCèl·lules fotoelèctriquesphotophysicsFerro
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