Search results for "Stokes shift"

showing 10 items of 16 documents

Effect of molecular Stokes shift on polariton dynamics

2021

When the enhanced electromagnetic field of a confined light mode interacts with photoactive molecules, the system can be driven into the regime of strong coupling, where new hybrid light-matter states, polaritons, are formed. Polaritons, manifested by the Rabi split in the dispersion, have shown potential for controlling the chemistry of the coupled molecules. Here, we show by angle-resolved steady-state experiments accompanied by multi-scale molecular dynamics simulations that the molecular Stokes shift plays a significant role in the relaxation of polaritons formed by organic molecules embedded in a polymer matrix within metallic Fabry-Pérot cavities. Our results suggest that in the case …

010304 chemical physicsScatteringRelaxation (NMR)Physics::OpticsGeneral Physics and Astronomy010402 general chemistry7. Clean energy01 natural sciencesMolecular physics0104 chemical sciencessymbols.namesakeMolecular dynamicsMolecular vibrationStokes shift0103 physical sciencesPolaritonsymbolsRadiative transferPhysical and Theoretical ChemistryExcitationThe Journal of Chemical Physics
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Electronic and Functional Scope of Boronic Acid Derived Salicylidenehydrazone (BASHY) Complexes as Fluorescent Dyes

2017

[EN] A series of boronic acid derived salicylidenehydrazone (BASHY) complexes was prepared and photophysically characterized. The dye platform can be modified by (a) electronic tuning along the cyanine-type axis via modification of the donor-acceptor pair and (b) functional tuning via the boronic acid residue. On the one hand, approach (a) allows the control of photophysical parameters such as Stokes shift, emission color, and two-photon absorption (2PA) cross section. The resulting dyes show emission light-up behavior in nonpolar media and are characterized by high fluorescence quantum yields (ca. 0.5-0.7) and brightness (ca. 35000-40000 M-1 cm(-1)). Moreover, the 2PA cross sections reach …

BrightnessDesignFluorophores010402 general chemistryPhotochemistry01 natural sciencessymbols.namesakechemistry.chemical_compoundResidue (chemistry)ChromophoreMolecular logicStokes shiftMoietyPROYECTOS DE INGENIERIABodipy dyes2-Photon absorptionEnhancement010405 organic chemistryChemistryOrganic ChemistryChromophoreFluorescence0104 chemical sciences3. Good healthsymbolsSurface modificationProbesHighly fluorescentDerivativesBoronic acidThe Journal of Organic Chemistry
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Luminescence of a self-trapped exciton in GeO2 crystal

1993

Abstract The self-trapped exciton (STE) is discovered in the GeO2 crystal. A PL band at 2.5 eV with a strong Stokes shift is excited only in the fundamental absorption range of GeO2 crystal with the quantum yield about 0.4 and the decay time constant 800 ± 5 μs at 80 K. The PL thermal quenching occurs at 200 K with the energy about 0.25 eV and the frequency factor 107. At 4.5 K the PL decay kinetics splits into two components with time constants 270 μs and 8000 μs, which can be due to a triplet state split in the zero magnetic field. The STE in GeO2 is very similar to a STE in SiO2.

Condensed matter physicsChemistryExcitonQuantum yieldGeneral ChemistryCondensed Matter PhysicsCrystalsymbols.namesakeStokes shiftExcited stateMaterials ChemistrysymbolsAtomic physicsTriplet stateAbsorption (electromagnetic radiation)LuminescenceSolid State Communications
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The natural compound chrysosplenol-D is a novel, ultrasensitive optical sensor for detection of Cu(II)

2020

Abstract Herein, we introduce a novel, ultrasensitive optical sensor for determination of Cu(II) ions over the concentration range of 0 to 1 μM Cu(II). The optical sensor is based on the natural molecule chrysosplenol-D (Chp-D) extracted from the flowering plant Chiliadenus montanus (Vahl.) Brullo. Free Chp-D emits fluorescence at 566 nm when excited at 292 nm. Chp-D chelates Cu(II) ions to form a 1:1 (metal:ligand) complex, which quenches the fluorescence emission peak of the free probe at 566 nm. “Turn-off” luminescence could be easily determined and provided distinct proof of the chelation of Cu(II) ions by Chp-D. This novel optical sensor offers a considerable fluorescence mechanism (ch…

Detection limitChemistryAnalytical chemistry02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsCharge-transfer complex01 natural sciencesFluorescenceBinding constantAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic Materialssymbols.namesakeLinear rangeStokes shiftMaterials ChemistrysymbolsMoleculePhysical and Theoretical Chemistry0210 nano-technologyLuminescenceSpectroscopyJournal of Molecular Liquids
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π-Extended Pyrene-Fused Double [7]Carbohelicene as a Chiral Polycyclic Aromatic Hydrocarbon

2019

A π-extended double [7]carbohelicene 2 with fused pyrene units was synthesized, revealing considerable intra- and intermolecular π–π interactions as confirmed with X-ray crystallography. As compared to the previous double [7]carbohelicene 1, the π-extended homologue 2 demonstrated considerably red-shifted absorption with an onset at 645 nm (1: 550 nm) corresponding to a smaller optical gap of 1.90 eV (1: 2.25 eV). A broad near-infrared emission from 600 to 900 nm with a large Stokes shift of ∼100 nm (2.3 × 103 cm–1) was recorded for 2, implying formation of an intramolecular excimer upon excitation, which was corroborated with femtosecond transient absorption spectroscopy. Moreover, 2 revea…

General Chemistry010402 general chemistry01 natural sciencesBiochemistryArticleCatalysis0104 chemical sciencesChiral column chromatographysymbols.namesakeCrystallographychemistry.chemical_compoundColloid and Surface ChemistrychemistryStokes shiftIntramolecular forceUltrafast laser spectroscopysymbolsPyreneDensity functional theorySpectroscopyIsomerizationJournal of the American Chemical Society
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In situ formation of pyronin dyes for fluorescence protease sensing

2017

International audience; We report a reaction-based strategy for the fluorogenic detection of protease activity. Based on the "covalent-assembly" probe design principle recently put forward by the Yang group for detection of Sarin related threats (J. Am. Chem. Soc., 2014, 136, 6594-6597), we have designed two unusual nonfluorescent caged precursors (mixed bis-aryl ethers) which are readily converted into a fluorescent unsymmetrical pyronin dye through a domino cyclisation-aromatisation reaction triggered by penicillin G acylase (PGA) or leucine aminopeptidase (LAP). Fluorescence-based in vitro assays and HPLCfluorescence/- MS analyses support the claimed activation mechanism whose the furthe…

In situStereochemistrymedicine.medical_treatment010402 general chemistryalkaline-phosphatase activity01 natural sciencesBiochemistryAminopeptidaseFluorescenceMass SpectrometryIn vivo[ CHIM.ORGA ] Chemical Sciences/Organic chemistryhydrogen-sulfidemedicinePyronineturn-on chemodosimeterPhysical and Theoretical ChemistryChromatography High Pressure Liquidlarge stokes shiftFluorescent DyesProteaseMolecular Structure[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryChemistryOrganic ChemistryFluorescence0104 chemical sciences3. Good healthselective detectionPenicillin G Acylasefluorogenic probesplacental leucine aminopeptidasesensitive detectioncascade reactionLeucineliving cellsPeptide Hydrolases
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Transient absorption with a femtosecond tunable excitation pump reveals the emission kinetics of color centers in amorphous silica.

2021

We report a set of femtosecond (fs) transient absorption (TA) measurements following the dynamics of the so-called nonbridging oxygen hole center in silica, a model color center in wide bandgap amorphous solids, characterized by a very large Stokes shift between the UV excitation and its associated red emission at 1.9 eV. The changes in the TA spectrum were probed in the UV-visible range at various delays after photoexcitation and analyzed as a function of the UV excitation energy, in single-photon absorption conditions. The combination of the experiments helps to clarify the defect photocycle, highlighting how TA measurements with tunable UV excitation could represent a powerful tool to in…

Materials scienceAbsorption spectroscopytransient absorption02 engineering and technology01 natural sciencesMolecular physics010309 opticssymbols.namesakeOpticsStokes shift0103 physical sciencesUltrafast laser spectroscopyluminescenceAbsorption (electromagnetic radiation)ultra-fast laser spectroscopyComputingMilieux_MISCELLANEOUS[PHYS.PHYS]Physics [physics]/Physics [physics]business.industrypoint defect021001 nanoscience & nanotechnologyAtomic and Molecular Physics and OpticsAmorphous solidPhotoexcitationsilicaFemtosecondsymbols0210 nano-technologybusinessExcitationOptics letters
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Optical properties of ZnMgO films grown by spray pyrolysis and their application to UV photodetection

2015

This work presents a comprehensive optical characterization of Zn1−xMgxO thin films grown by spray pyrolysis (SP). Absorption measurements show the high potential of this technique to tune the bandgap from 3.30 to 4.11 eV by changing the Mg acetate content in the precursor solution, leading to a change of the Mg-content ranging from 0 up to 35%, as measured by transmission electron microscopy-energy dispersive x-ray spectroscopy. The optical emission of the films obtained by cathodoluminescence and photoluminescence spectroscopy shows a blue shift of the peak position from 3.26 to 3.89 eV with increasing Mg incorporation, with a clear excitonic contribution even at high Mg contents. The lin…

Materials sciencePhotoluminescenceBand gapAnalytical chemistryCathodoluminescence02 engineering and technology01 natural sciencessymbols.namesakeStokes shift0103 physical sciencesMaterials ChemistryEmission spectrumElectrical and Electronic EngineeringSpectroscopyAbsorption (electromagnetic radiation)010302 applied physicsTelecomunicacionesbusiness.industry021001 nanoscience & nanotechnologyCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsBlueshiftsymbolsOptoelectronicsElectrónica0210 nano-technologybusiness
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Specific orientation of dipole moments in azocrown cetocyanine dyes determined by electrooptical absorption measurements (EOAM)

2019

Abstract From electrooptical absorption measurements (EOAM) follows that the dipole moments of azacrown ketocyanine dyes 2,5-di{(E)-1-[4-(4,7,10,13-tetraoxa-1-azacyclopentadecyl)phenyl]methylidene}-1-cyclopentanone (Compound 1) and (E)-1-(2-hydroxy-4methoxyphenyl)-3-[4-(4,7,10,13-tetraoxa-1-azacyclopentadecyl)phenyl]-2-propen-1-one (Compound 2) in the equilibrium ground state μg and the change of dipole moments upon transition to the excited Franck–Condon state Δaμ are large. This alteration causes a significant long-wavelength shift of the absorption and emission spectra, as well as large fluorescence Stokes shift with increasing polarity of the solvent. From the DFT calculations follows t…

Materials scienceTransition dipole momentBiophysics02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesBiochemistryFluorescenceAtomic and Molecular Physics and Optics0104 chemical sciencessymbols.namesakeDipoleExcited stateStokes shiftsymbolsPhysical chemistryEmission spectrum0210 nano-technologyGround stateLone pairJournal of Luminescence
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Temperature-Dependence of Solvent-Induced Stokes Shift and Fluorescence Tunability in Carbon Nanodots

2019

We carried out a cryogenic investigation on the optical properties of carbon dots, aiming to better understand their emission mechanism and the role of the solvent. The solvatochromic Stokes shift is quantified by a low temperature approach which allows freezing of the photo-excited state of carbon dots, preventing any solvation relaxation. Moreover, the reduction in temperature helps to identify the dynamical inhomogeneous contribution to the broadening of the emission band; therefore, disentangling the role of solvent from other types of broadening, such as the homogeneous and the static inhomogeneous contributions.

Materials sciencefluorescence tunabilitychemistry.chemical_element02 engineering and technology010402 general chemistry01 natural scienceslcsh:QD241-441symbols.namesakelcsh:Organic chemistrycarbon nanodotCarbon nanodotsStokes shiftcarbon nanodotsSettore FIS/01 - Fisica SperimentaleRelaxation (NMR)SolvatochromismSolvationGeneral Medicine021001 nanoscience & nanotechnologycryogenic optical studyFluorescence0104 chemical sciencesSolventchemistryChemical physicssymbols0210 nano-technologyCarbonC
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