Search results for "quenching"

showing 10 items of 275 documents

Hands On: Using Tryptophan Fluorescence Spectroscopy to Study Protein Structure

2019

Fluorescence spectroscopy is well suited to obtain information about the structure and function of proteins. The major advantage of this spectroscopic technique is the pronounced dependence of the fluorescence emission characteristics of fluorophores on their distinct local environment and the rather inexpensive equipment required. In particular, the use of intrinsic tryptophan fluorescence offers the possibility to study structure and function of proteins without the need to modify the protein. While fluorescence spectroscopy is technically not demanding, a number of factors can artificially alter the results. In this article, we systematically describe the most common applications in fluo…

0301 basic medicine030103 biophysicsQuenching (fluorescence)ChemistryTryptophanFluorescenceFluorescence spectroscopy03 medical and health sciences030104 developmental biologyProtein structureTryptophan fluorescenceBiophysicsLocal environmentSpectroscopy
researchProduct

Emerging switchable ultraviolet photoluminescence in dehydrated Zn/Al layered double hydroxide nanoplatelets

2019

AbstractLayered double hydroxides show intriguing physical and chemical properties arising by their intrinsic self-assembled stacking of molecular-thick 2D nanosheets, enhanced active surface area, hosting of guest species by intercalation and anion exchanging capabilities. Here, we report on the unprecedented emerging intense ultraviolet photoluminescence in Zn/Al layered double hydroxide high-aspect-ratio nanoplatelets, which we discovered to be fully activated by drying under vacuum condition and thermal desorption as well. Photoluminescence and its quenching were reproducibly switched by a dehydration–hydration process. Photoluminescence properties were comprehensively evaluated, such a…

0301 basic medicineMaterials sciencePhotoluminescenceCoprecipitationIntercalation (chemistry)Thermal desorptionlcsh:Medicineswitchable ultraviolet photoluminescenceengineering.materialTwo-dimensional materialsArticle03 medical and health scienceschemistry.chemical_compound0302 clinical medicine2D materials Layered Double Hydroxides Photoluminescence Vacuumlcsh:ScienceQuenchingMultidisciplinaryZn/Al layered double hydroxideX-ray Diffractionlcsh:RSettore FIS/01 - Fisica SperimentaleLayered double hydroxidesExfoliation joint030104 developmental biologychemistryChemical engineeringengineeringHydroxidelcsh:Q030217 neurology & neurosurgeryScientific Reports
researchProduct

A systems-wide understanding of photosynthetic acclimation in algae and higher plants

2017

The ability of phototrophs to colonise different environments relies on robust protection against oxidative stress, a critical requirement for the successful evolutionary transition from water to land. Photosynthetic organisms have developed numerous strategies to adapt their photosynthetic apparatus to changing light conditions in order to optimise their photosynthetic yield, which is crucial for life on Earth to exist. Photosynthetic acclimation is an excellent example of the complexity of biological systems, where highly diverse processes, ranging from electron excitation over protein protonation to enzymatic processes coupling ion gradients with biosynthetic activity, interact on drasti…

0301 basic medicine[SDV.BIO]Life Sciences [q-bio]/BiotechnologyPhysiologyAcclimatizationContext (language use)PhD traininginterdisciplinary trainingPlant Science: Biochemistry biophysics & molecular biology [F05] [Life sciences]BiologyacclimationPhotosynthesisAcclimatizationModels Biologicalmodelling03 medical and health sciencesAlgaeChlorophytaapplication industrielle[SDV.BV]Life Sciences [q-bio]/Vegetal Biologymathematical modellingPhotosynthesis: Biochimie biophysique & biologie moléculaire [F05] [Sciences du vivant]biodiversitymodélisationmicro-alguePhototrophphotosynthetic systemEcologyNon-photochemical quenchingSystems Biologyacclimatation photosynthétiquephotosynthetic optimisationPlanktonPlantsanalyse rétrospectivebiology.organism_classificationindustrial applicationEuropean Training Network030104 developmental biologyAcclimation; European Training Network; PhD training; biodiversity; interdisciplinary training; mathematical modelling; microalgal cultivation; non-photochemical quenching; photosynthetic optimisationPhotosynthetic acclimationadaptation à la lumièremicroalgal cultivationappareil photosynthétiqueBiochemical engineeringnon-photochemical quenching
researchProduct

Influence of the exchange and correlation functional on the structure of amorphous InSb and In3SbTe2 compounds

2016

We have investigated the structural, vibrational, and electronic properties of the amorphous phase of InSb and In3SbTe2 compounds of interest for applications in phase change non-volatile memories. Models of the amorphous phase have been generated by quenching from the melt by molecular dynamics simulations based on density functional theory. In particular, we have studied the dependence of the structural properties on the choice of the exchange-correlation functional. It turns out that the use of the Becke-Lee-Yang-Parr functional provides models with a much larger fraction of In atoms in a tetrahedral bonding geometry with respect to previous results obtained with the most commonly used P…

10120 Department of Chemistrynon-volatile memoryYield (engineering)Theory of Condensed MatterGeneral Physics and Astronomy02 engineering and technologyElectronic structure01 natural sciencesMolecular dynamicsComputational chemistry540 Chemistry0103 physical sciencesPhysical and Theoretical Chemistry010306 general physicsamorphous materialFIS/03 - FISICA DELLA MATERIAQuenchingChemistry021001 nanoscience & nanotechnologyelectronic structure3100 General Physics and AstronomyAmorphous solidab-initio simulationChemical physicsMolecular vibrationTetrahedronDensity functional theory1606 Physical and Theoretical Chemistry0210 nano-technologyphase change material
researchProduct

Quenching of gA deduced from the β-spectrum shape of 113Cd measured with the COBRA experiment

2020

A dedicated study of the quenching of the weak axial-vector coupling strength gA in nuclear processes has been performed by the COBRA collaboration. This investigation is driven by nuclear model calculations which show that the β-spectrum shape of the fourfold forbidden non-unique decay of 113Cd strongly depends on the effective value of gA. Using an array of CdZnTe semiconductor detectors, 45 independent 113Cd spectra were obtained and interpreted in the context of three nuclear models. The resulting effective mean values are g‾A(ISM)=0.915±0.007, g‾A(MQPM)=0.911±0.013 and g‾A(IBFM-2)=0.955±0.022. These values agree well within the determined uncertainties and deviate significantly from th…

113Cd beta-decayaxial-vector couplingspectrum-shape methodCdZnTegA quenchinghiukkasfysiikkaydinfysiikkaCOBRA
researchProduct

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
researchProduct

Nitroanilines as Quenchers of Pyrene Fluorescence

2012

The quenching of pyrene and 1‐methylpyrene fluorescence by nitroanilines (NAs), such as 2‐, 3‐, and 4‐nitroaniline (2‐NA, 3‐NA, and 4‐NA, respectively), 4‐methyl‐3‐nitroaniline (4‐M‐3‐NA), 2‐methyl‐4‐nitroaniline (2‐M‐4‐NA), and 4‐methyl‐3,5‐dinitroaniline (4‐M‐3,5‐DNA), are studied in toluene and 1,4‐dioxane. Steady‐state fluorescence data show the higher efficiency of the 4‐NAs as quenchers and fit with a sphere‐of‐action model. This suggests a 4‐NA tendency of being in close proximity to the fluorophore, which could be connected with their high polarity/hyperpolarizability. In addition, emission and excitation spectra evidence the formation of emissive pyrene—NA ground‐state complexes in…

Analytical chemistryHyperpolarizabilityPhotochemistryFluorescenceFluorescence spectroscopyAbsorptionDioxaneschemistry.chemical_compoundFOTOQUIMICAANILINASUltrafast laser spectroscopySinglet statePhysical and Theoretical ChemistryFluorescent DyesAniline CompoundsPyrenesQuenching (fluorescence)ChemistryOtras Ciencias QuímicasCiencias QuímicasFluorescenceAtomic and Molecular Physics and OpticsPIRENODESACTIVACIONEnergy TransferExcited statePyreneCIENCIAS NATURALES Y EXACTASTolueneChemPhysChem
researchProduct

Anthracene Fluorescence Quenching by a Tetrakis (Ketocarboxamide) Cavitand

2014

Quenching of both fluorescence lifetime and fluorescence intensity of anthracene was investigated in the presence of a newly derived tetrakis (ketocarboxamide) cavitand at various concentrations. Time-correlated single photon counting method was applied for the lifetime measurements. A clear correlation between the fluorescence lifetime of anthracene as a function of cavitand concentration in dimethylformamide solution was observed. The bimolecular collisional quenching constant was derived from the decrease of lifetime. Fluorescence intensity was measured in the emission wavelength region around 400 nm as a result of excitation at 280 nm. Effective quenching was observed in the presence of…

AnthraceneQuenching (fluorescence)Article SubjectChemistryAnalytical chemistryCavitandPhotochemistryseoksetFluorescenceAtomic and Molecular Physics and OpticsPhoton countingcarbon-tetrachlorideAnalytical Chemistrychemistry.chemical_compoundWavelengthlcsh:QC350-467Dimethylformamideta116stern-volmer plotslcsh:Optics. LightSpectroscopyExcitationJournal of Spectroscopy
researchProduct

Fine tuning of the photophysical properties of cofacial diporphyrins via the use of different spacers

2002

The crystal and molecular structures of two unmetallated diporphyrin species using the biphenylene and dibenzofuran spacers, H4(DPB) and H4(DPO), respectively (DPB 4 − =1,8-bis[5-(2,8,13,17-tetraethyl-3,7,12,18-tetramethylporphyrinyl)]biphenylene; DPO 4 − =4,6-bis[5-(2,8,13,17-tetraethyl-3,7,12,18-tetramethylporphyrinyl)]dibenzofuran), are reported. These data are compared to their literature metallated analogs, stressing on the properties related to the flexibility of the ligands, ··· and M···M interactions. In addition, the lowest energy fluorescence properties of these non-phosphorescent diporphyrin compounds as well as three other related species, H4(DPA), H4(DPX), and H4(DPS) (DPA 4 − …

AnthraceneQuenching (fluorescence)Organic ChemistryBiphenylenePhotochemistryBiochemistryFluorescenceInorganic ChemistryDibenzofuranchemistry.chemical_compoundCrystallographyReaction rate constantMolecular geometrychemistryMaterials ChemistryPhysical and Theoretical ChemistryLuminescenceJournal of Organometallic Chemistry
researchProduct

Potentiometric, NMR, and Fluorescence-Emission Studies on the Binding of Adenosine 5′-Triphosphate (ATP) by Open-Chain Polyamine Receptors Containing…

2003

The interaction in aqueous solution of adenosine 5′-triphosphate (ATP) with a series of open-chain polyamines linked at one or both ends to anthrylmethyl or naphthylmethyl fragments was followed by potentiometric titration, 1H-, 13C-, and 31P-NMR spectroscopy, and by steady-state fluorescence measurements. The results revealed greater stabilities for the compounds containing one anthracene moiety than for those with one naphthalene moiety, the stabilities of the compounds with both ends N-substituted with naphthylmethyl groups being close to those containing just one anthrylmethyl unit. The 1H-NMR spectra showed that in all systems, there is involvement of π-π stacking interactions in the s…

AnthraceneQuenching (fluorescence)StereochemistryOrganic ChemistryPotentiometric titrationProtonationBiochemistryMedicinal chemistryFluorescenceCatalysisAdductInorganic Chemistrychemistry.chemical_compoundchemistryDrug DiscoveryMoietyTitrationPhysical and Theoretical ChemistryHelvetica Chimica Acta
researchProduct