Search results for "Fluorescence"

showing 10 items of 2463 documents

Covalent and non-covalent coupling of a Au102 nanocluster with a fluorophore: energy transfer, quenching and intracellular pH sensing

2021

Interactions between an atomically precise gold nanocluster Au102(p-MBA)44 (p-MBA = para mercaptobenzoic acid) and a fluorescent organic dye molecule (KU, azadioxatriangulenium) are studied. In solution, the constituents form spontaneously a weakly bound complex leading to quenching of fluorescence of the KU dye via energy transfer. The KU can be separated from the complex by lowering pH, leading to recovery of fluorescence, which forms a basis for an optical reversible pH sensor. However, the sensor is not a stable entity, which could be delivered inside cells. For this purpose, a covalently bound hybrid is synthesized by linking the KU dye to the ligand layer of the cluster via an ester b…

Quenching (fluorescence)FluorophoreChemistryLigandIntracellular pHGeneral EngineeringBioengineering02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesFluorescenceAtomic and Molecular Physics and Optics0104 chemical sciencesNanoclusterschemistry.chemical_compoundCovalent bondMoleculeGeneral Materials Science0210 nano-technologyNanoscale Advances
researchProduct

Rotational quenching of monodeuterated water by hydrogen molecules

2011

Cross sections and rate coefficients for low lying rotational transitions in HDO induced by para and ortho-H(2) collisions are presented for the first time. Calculations have been performed at the close-coupling and coupled-states levels with the deuterated variant of the H(2)O-H(2) interaction potential of Valiron et al. [J. Chem. Phys., 2008, 129, 134306]. Rate coefficients are presented for temperatures between 5 and 100 K and are compared to the corresponding rates for H(2)O and D(2)O. Significant differences caused by the isotopic substitution, in particular the C(2v) symmetry breaking, are observed. Finally, our rates are found to be significantly larger (by up to three orders of magn…

Quenching (fluorescence)HydrogenChemistryAbundance (chemistry)Analytical chemistryGeneral Physics and AstronomyRotational transitionchemistry.chemical_elementInteraction potentialDeuteriumOrders of magnitude (time)Computational chemistrySymmetry breakingPhysical and Theoretical ChemistryAstrophysics::Galaxy AstrophysicsPhysical Chemistry Chemical Physics
researchProduct

Photochemistry of 3,6-bis(styryl)pyridazines in solution and in neat liquid crystalline phase—optical switching and imaging techniques

2008

Abstract 3,6-Bis(styryl)pyridazines 1a – f with 2–6 alkoxy groups show on irradiation in solution a stereoisomerization which leads to a photostationary state of ( E , E )- and ( E , Z )-isomer. Sensitizing and quenching experiments reveal that the ( E , E )→( E , Z ) route is a pure triplet process, whereas the ( E , Z )→( E , E ) route can have a minor singlet by-reaction. Hexyloxy or dodecyloxy chains on the terminal benzene rings convey the ( E , E )-isomers of compounds 1a , b , d – f thermotropic liquid crystalline properties. In particular S A , S C , and S F/I phases were studied with regard to their photochemical behavior. Depending on the system, photodegradation of the smectic ph…

Quenching (fluorescence)Liquid crystalChemistryPhotostationary statePhase (matter)Organic ChemistryDrug DiscoveryAlkoxy groupSinglet statePhotodegradationPhotochemistryBiochemistryThermotropic crystalTetrahedron
researchProduct

Oligophenylenevinylenes in Spatially Confined Nanochannels: Monitoring Intermolecular Interactions by UV/Vis and Raman Spectroscopy

2008

Perhydrotriphenylene-based channel-forming inclusion compounds (ICs) and thin films made of polyphenylenevinylene (PPV)-type oligomers with terminal alkoxy groups are investigated and compared in a combined experimental and theoretical approach. Interchromophore interactions and host-guest interactions are elucidated by UV/Vis and Raman spectroscopy. The impact of the local environment of the chromophore on the optical and photophysical properties is discussed in light of quantum-chemical calculations. In stark contrast to thin films where preferential side-by-side orientation leads to quenching of photoluminescence (PL) via non-emissive traps, the ICs are found to be attractive materials f…

Quenching (fluorescence)Materials sciencePhotoluminescenceIntermolecular forceAnalytical chemistryChromophoreCondensed Matter PhysicsPhotochemistryElectronic Optical and Magnetic MaterialsBiomaterialssymbols.namesakeUltraviolet visible spectroscopynanochannels inclusion compoundsElectrochemistryAlkoxy groupsymbolsThin filmRaman spectroscopyFIS/03 - FISICA DELLA MATERIA
researchProduct

Sensitive laser spectroscopy on trapped barium ions by quenching with hydrogen

1983

The sensitivity of laser spectroscopy on barium ions stored in a radio frequency quadrupole trap was drastically increased by using hydrogen for quenching the optically pumped metastable states. The attained fluorescence intensity per ion permits the detection of single ions. The method will be applied to environmental studies on actinides.

Quenching (fluorescence)Materials sciencePhysics and Astronomy (miscellaneous)HydrogenGeneral EngineeringAnalytical chemistryPhysics::OpticsGeneral Physics and Astronomychemistry.chemical_elementBariumActinideIonchemistryRadio-frequency quadrupolePhysics::Plasma PhysicsMetastabilityPhysics::Atomic PhysicsAtomic physicsSpectroscopyApplied Physics B Photophysics and Laser Chemistry
researchProduct

Molecular quenching and relaxation in a plasmonic tunable system

2008

Molecular fluorescence decay is significantly modified when the emitting molecule is located near a plasmonic structure. When the lateral sizes of such structures are reduced to nanometer-scale cross sections, they can be used to accurately control and amplify the emission rate. In this Rapid Communication, we extend Green's dyadic method to quantitatively investigate both radiative and nonradiative decay channels experienced by a single fluorescent molecule confined in an adjustable dielectric-metal nanogap. The technique produces data in excellent agreement with current experimental work.

Quenching (fluorescence)Materials sciencebusiness.industryRelaxation (NMR)Condensed Matter PhysicsMolecular physicsFluorescenceElectronic Optical and Magnetic MaterialsOpticsQuasiparticleRadiative transferPolaritonMoleculebusinessPlasmonPhysical Review B
researchProduct

Aza–oxa macrocyclic ligands functionalised with naphthylmethyl fluorescent groups

2000

Abstract Compounds L 1 and L 2 were obtained by reaction of 2-(bromomethyl)naphthalene with 1,4,10-trioxa-7,13-diazacyclopentadecane and 1,4,7-trioxa-10-azacyclododecane, respectively. These receptors contain aza–oxa crowns attached covalently to fluorescent groups. The protonation and coordination behaviour of L 1 and L 2 against metal ions has been studied in dioxane:water (70:30 v/v, 25°C, 0.1 M potassium nitrate) using potentiometric methods. All metal ions studied form complexes with L 1 and L 2 with the logarithm of the formation constants L+M 2+ =[M(L)] 2+ in the sequence Cd 2+ ≅Pb 2+ , Zn 2+ 2+ for L 1 and Zn 2+ 2+ 2+ 2+ 2+ for L 2 . The fluorescent behaviour of L 1 and L 2 was stud…

Quenching (fluorescence)Metal ions in aqueous solutionPotentiometric titrationInorganic chemistryProtonationMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundchemistryStability constants of complexesBromideMaterials ChemistryQualitative inorganic analysisPhysical and Theoretical ChemistryAcetonitrilePolyhedron
researchProduct

Zeaxanthin Dependent and Zeaxanthin Independent Changes in Nonphotochemical Energy Dissipation

1994

Summary The influence of zeaxanthin on high-energy-state quenching (qE) of room temperature chlorophyll fluorescence and on the quantum yield of oxygen evolution(ФO2) has been studied with isolated spinach thylakoids. A set of three different pretreatments was tested which all led to thylakoids with high contents of zeaxanthin. Depending on the presence of light the pretreatments differed strongly with respect to their effect on nonphotochemical fluorescence quenching. Independently from the extent of changes in nonphotochemical energy dissipation in the membrane energized state as reflected by nonphotochemical quenching the light pretreatments caused also changes in nonphotochemical energy…

Quenching (fluorescence)biologyPhysiologyChemistryOxygen evolutionfood and beveragesQuantum yieldPlant Sciencebiology.organism_classificationPhotochemistryZeaxanthinchemistry.chemical_compoundChlorophyllThylakoidSpinachAgronomy and Crop ScienceChlorophyll fluorescenceJournal of Plant Physiology
researchProduct

Interactions entre la beta-lactoglobuline et les arômes : impact au niveau moléculaire

2008

Interactions between β-lactoglobulin (BLG) and aroma compounds were investigated by complementary techniques for a better knowledge of binding mechanisms between proteins and aroma compounds at a molecular scale. Two binding sites have been defined for the monomeric BLG, one internal site within the central calyx, and one external site between the calyx and the α helix. In a first step, a relation between the ligand structure and its binding behaviour was established from the study of impact of a wide range of aroma compounds on the structure of native BLG. We evidenced at least two binding behaviours as a function of the chemical class, the hydrophobicity, or the structure of the ligands. …

REARRANGEMENT DE LA STRUCTURESURFACE HYDROPHOBICITY[SPI.GPROC] Engineering Sciences [physics]/Chemical and Process EngineeringRPSSPRINTERACTIONSBETA-LACTOGLOBULINEDCTHERMAL TREATMENTIRTFSITE D'INTERACTIONAROMA COMPOUND[SDV.IDA]Life Sciences [q-bio]/Food engineering[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process EngineeringFLUORESCENCESTRUCTURAL REARRANGEMENTTRAITEMENT THERMIQUE[SDV.IDA] Life Sciences [q-bio]/Food engineeringITCβ-LACTOGLOBULINNMRETAT GLOBULAIRE FONDURMNCDFTIRHYDROPHOBIE DE SURFACEBINDING SITEMOLTEN GLOBULE STATE
researchProduct

Spectroscopy of an optical excited Ga doped SiO2 surface

2007

Abstract We present the first spectroscopical analysis of the Ga/SiO2 surface interaction in hot environment. This interaction gives rise to inclusions of Ga atoms inside the silica matrix that produce structural changes and modify the SiO2 optical characteristics. This paper discusses both the time- and the frequency-resolved spectra of the fluorescence emission following UV pulsed laser excitation of the so “doped” silica in the range 15,000–28,000 cm−1. The investigation is completed by the electron paramagnetic resonance (EPR) spectra of two high-purity synthetic silica samples of commercial origin after thermal treatment in presence and in absence of a Ga atmosphere.

RadiationMaterials scienceDopingAnalytical chemistryPhysics::Opticschemistry.chemical_elementThermal treatmentSpectroscopy gallium atomFluorescenceSpectral linelaw.inventionchemistrylawExcited stateGalliumSpectroscopyElectron paramagnetic resonanceRadiation Physics and Chemistry
researchProduct