Search results for "Triplet"

showing 10 items of 159 documents

Colour tuning by the ring roundabout: [Ir(C^N)2(N^N)]+ emitters with sulfonyl-substituted cyclometallating ligands

2015

A series of cationic bis-cyclometallated iridium(III) complexes [Ir(C^N)2(N^N)]+ is reported. Cyclometallating C^N ligands are based on 2-phenylpyridine with electron-withdrawing sulfone substituents in the phenyl ring: 2-(4-methylsulfonylphenyl)pyridine (H1) and 2-(3-methylsulfonylphenyl)pyridine (H2). 2-(1H-Pyrazol-1-yl)pyridine (pzpy) and 2-(3,5-dimethyl-1H-pyrazol-1-yl)pyridine (dmpzpy) are used as electron-rich ancillary N^N ligands. The complexes have been fully characterized and the single crystal structure of [Ir(2)2(dmpzpy)][PF6]·MeCN has been determined. Depending on the position of the methylsulfonyl group, the complexes are green or blue emitters with vibrationally structured em…

Sulfonylchemistry.chemical_classificationGeneral Chemical Engineeringchemistry.chemical_element02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyRing (chemistry)Photochemistry01 natural sciences0104 chemical sciencesSulfoneCrystallographychemistry.chemical_compoundchemistryPyridineDensity functional theoryIridiumTriplet state0210 nano-technologySingle crystalRSC Advances
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Regioisomerism in cationic sulfonyl-substituted [Ir(C^N)2(N^N)]+ complexes: its influence on photophysical properties and LEC performance

2016

A series of regioisomeric cationic iridium complexes of the type [Ir(C^N)2(bpy)][PF6] (bpy = 2,2'-bipyridine) is reported. The complexes contain 2-phenylpyridine-based cyclometallating ligands with a methylsulfonyl group in either the 3-, 4- or 5-position of the phenyl ring. All the complexes have been fully characterized, including their crystal structures. In acetonitrile solution, all the compounds are green emitters with emission maxima between 493 and 517 nm. Whereas substitution meta to the Ir-C bond leads to vibrationally structured emission profiles and photoluminescence quantum yields of 74 and 77%, placing a sulfone substituent in a para position results in a broad, featureless em…

Sulfonylchemistry.chemical_classificationPhotoluminescenceChemistrySubstituentQuantum yieldchemistry.chemical_element02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciences0104 chemical sciencesSulfoneInorganic Chemistrychemistry.chemical_compoundCrystallographyDensity functional theoryIridiumTriplet state0210 nano-technologyDalton Transactions
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A penetration depth study on the non-centrosymmetric superconductors Li2(Pd1−xPtx)3B

2008

Abstract We study the superconducting order parameter in the non-centrosymmetric compounds Li 2 (Pd 1− x Pt x ) 3 B ( x =0, 0.3, 0.7 and 1) by measuring magnetic penetration depth λ ( T ). The low temperature λ ( T ) shows a linear temperature dependence for x ⩾0.3, but follows exponential-like behavior for lower Pt contents. These findings suggest that a spin-triplet state might gradually develop with increasing x due to the broken inversion symmetry.

SuperconductivityMaterials scienceSpin statesCondensed matter physicsPoint reflectionSymmetry breakingSpin–orbit interactionElectrical and Electronic EngineeringTriplet stateCondensed Matter PhysicsPenetration depthElectronic Optical and Magnetic MaterialsPhysica B: Condensed Matter
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ChemInform Abstract: Relaxation Phenomena of a Triplet Spin Probe in Glassy and Crystalline o-Terphenyl.

2010

The authors used quinoxaline in its photoexcited triplet state as a spin probe in order to measure the spin-lattice relaxation rate in o-terphenyl glass as a function of temperature. They found a power law with an exponent close to 2. Since o-terphenyl can easily be crystallized, they investigated the crystal, too. Below 3.5 K the spin is highly polarized, contrary to the behavior in the glass, where it reaches thermal equilibrium down to the lowest temperatures of their experiment (1.4 K). Around 3.5 K the polarization in the crystal vanishes. Above it appears with opposite sign due to thermal equilibration.

Thermal equilibriumCondensed matter physicsGeneral MedicinePolarization (waves)Condensed Matter::Disordered Systems and Neural NetworksSpin probeCrystalchemistry.chemical_compoundchemistryTerphenylOrganic chemistryTriplet stateLuminescenceSpin (physics)ChemInform
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A study of electron transfer in Ru(dcbpy)2(NCS)2 sensitized nanocrystalline TiO2 and SnO2 films induced by red-wing excitation.

2008

Excited state dynamics and electron transfer from the Ru(dcbpy)2(NCS)2 (RuN3) sensitizer to semiconductor nanoparticles were studied using time-resolved femtosecond absorption spectroscopy. We found that excitation of the red wing of the absorption spectrum of the sensitizer populates the (3)MLCT state directly, both in solution and attached on semiconductor nanoparticle films. Electron injection is slowed down and becomes gradually less efficient as excitation moves towards red from the absorption maximum at 535 nm. At 675 nm the injection is non-exponential and characterized by 5, 30 and 180 ps time constants. The non-exponential electron injection observed is assigned to injection from a…

Time FactorsAbsorption spectroscopyPhotochemistrySurface PropertiesAnalytical chemistryGeneral Physics and AstronomyElectronsSensitivity and SpecificityRutheniumElectron transferOrganometallic CompoundsPhysical and Theoretical ChemistryTriplet stateAbsorption (electromagnetic radiation)Coloring AgentsTitaniumChemistrybusiness.industryLasersSpectrum AnalysisTin CompoundsMembranes ArtificialNanocrystalline materialNanostructuresKineticsSemiconductorSemiconductorsExcited stateFemtosecondbusinessThiocyanatesPhysical chemistry chemical physics : PCCP
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Theoretical study of the electronic spectrum of p-benzoquinone

1999

The electronic excited states of p-benzoquinone have been studied using multiconfigurational second-order perturbation theory (CASPT2) and extended atomic natural orbital (ANO) basis sets. The calculation of the singlet–singlet and singlet–triplet transition energies comprises 19 valence singlet excited states, 4 valence triplet states, and the singlet 3s,3p, and 3d members of the Rydberg series converging to the first four ionization limits. The computed vertical excitation energies are found to be in agreement with the available experimental data. Conclusive assignments to both valence and Rydberg states have been performed. The main features of the electronic spectrum correspond to the π…

Valence (chemistry)ChemistryExcited statesGeneral Physics and AstronomyPerturbation theoryTriplet stateRydberg statesSpectral lineUNESCO::FÍSICA::Química físicaOrbital calculationssymbols.namesakeOrganic compounds Spectra ; Excited states ; Perturbation theory ; Triplet state ; Rydberg states ; Orbital calculationsOrganic compounds SpectraExcited stateIonizationRydberg formulasymbolsSinglet statePhysical and Theoretical ChemistryAtomic physicsTriplet state:FÍSICA::Química física [UNESCO]Excitation
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Metric Learning in Histopathological Image Classification: Opening the Black Box

2023

The application of machine learning techniques to histopathology images enables advances in the field, providing valuable tools that can speed up and facilitate the diagnosis process. The classification of these images is a relevant aid for physicians who have to process a large number of images in long and repetitive tasks. This work proposes the adoption of metric learning that, beyond the task of classifying images, can provide additional information able to support the decision of the classification system. In particular, triplet networks have been employed to create a representation in the embedding space that gathers together images of the same class while tending to separate images w…

WSItriplet networksembeddingSettore INF/01 - Informaticapatient level accuracymetric learningbreast cancer imagingBreakHisclassification interpretabilityvisualization
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Estudio del proceso de abstracción de hidrógeno en derivados fotoactivos del colesterol

2016

La peroxidación lipídica (PL) es un proceso mediante el cual diversas especies reactivas atacan los lípidos de la membrana celular, promoviendo su degradación oxidativa. En diferentes estudios se ha demostrado que la PL puede producirse por radiación ultravioleta de tipo A en combinación con agentes fotosensibilizantes, los cuales al absorber luz pueden inducir una alteración física o química en otra entidad molecular. Entre estos agentes se encuentran algunos fármacos fotoactivos como los antiinflamatorios no esteroideos (AINEs) del grupo de los ácidos 2-arilpropiónicos, tales como el ketoprofeno (KP), el ácido tiaprofénico (TPA) y el suprofeno (SP). Estos fármacos poseen un grupo cromófor…

abstracción de hidrógenoUNESCO::QUÍMICAfotoproductosestado excitado tripletecolesterolperoxidación lipídica:QUÍMICA [UNESCO]
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Interligand Electron Transfer Determines Triplet Excited State Electron Injection in RuN3−Sensitized TiO2 Films

2004

Electron injection from the transition metal complex Ru(dcbpy)(2)(NCS)(2) (dcbpy = 2,2'-bipyridine-4,4'-dicarboxylate) into a titanium dioxide nanoparticle film occurs along two pathways. The dominating part of the electron injection proceeds from the initially excited singlet state of the sensitizer into the conduction band of the semiconductor on the sub-hundred-femtosecond time scale. The slower part of the injection occurs from the thermalized triplet excited state on the picosecond time scale in a nonexponential fashion, as was shown in a previous study (Benko, G.; et al. J. Am. Chem. Soc. 2002, 124, 489). Here we show that the slower channel of injection is the result of the excited s…

business.industryChemistryLigandElectronPhotochemistrySurfaces Coatings and FilmsElectron transferSemiconductorPicosecondExcited stateSinglet fissionMaterials ChemistryPhysical and Theoretical ChemistryTriplet statebusinessThe Journal of Physical Chemistry B
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Effects of ligand substitution on the excited state dynamics of the Ru(dcbpy)(CO)2I2 complex

2003

Abstract Spectroscopic evidence suggest [PCCP 3 (2001) 1992] that illumination with visible light of the [trans-I-Ru(dcbpy)(CO)2I2] (dcbpy= 4,4′-dicarboxy-2,2′-bipyridine) complex in solution induces dissociation of a CO group followed by reorganization of the ligands and attachment of a solvent molecule. In the present study, we report results on excited state dynamics of this ruthenium complex and its photoproduct. Femtosecond transient absorption measurements reveal dominance of excited state absorption of the reactant and the photoproduct [cis-I-Ru(dcbpy)(CO)(Sol)I2] (Sol=ethanol or acetonitrile) in the visible spectral region. The time-resolved measurements for the reactant at 77 K ind…

chemistryExcited stateUltrafast laser spectroscopyGeneral Physics and Astronomychemistry.chemical_elementMoleculeZINDOPhysical and Theoretical ChemistryTriplet stateGround statePhotochemistryDissociation (chemistry)RutheniumChemical Physics
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