Search results for "laser"

showing 10 items of 3161 documents

Three-dimensional orientational colocalization of individual donor--acceptor pairs.

2004

We report on the determination of the three-dimensional orientation of the donor and acceptor transition dipoles in individual fluorescence resonance energy transfer (FRET) pairs by means of scanning optical microscopy with annular illumination. Knowledge of the mutual orientation of the donor and acceptor dipole is mandatory for reliable distance determination based on FRET efficiency measurements. In our model system perylenediimide as the donor and terryelenediimide as the acceptor are coupled via a stiff p-terphenyl linker. The absorption dipoles of the donor and acceptor are selectively addressed by the 488 nm and 647 line of an Ar/Kr mixed gas laser, respectively. A clear deviation fr…

ChemistryGeneral Physics and AstronomyLaserFluorescenceAcceptorMolecular physicslaw.inventionDipoleCrystallographyFörster resonance energy transferOptical microscopelawPhysical and Theoretical ChemistryAbsorption (electromagnetic radiation)LinkerThe Journal of chemical physics
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Intense laser effects on donor impurity in a cylindrical single and vertically coupled quantum dots under combined effects of hydrostatic pressure an…

2010

WOS: 000280235800010

ChemistryHydrostatic pressureBinding energyGeneral Physics and AstronomySurfaces and InterfacesGeneral ChemistryCondensed Matter::Mesoscopic Systems and Quantum Hall EffectCondensed Matter PhysicsSurfaces Coatings and FilmsEffective mass (solid-state physics)Quantum wellsImpurityQuantum dotIntense laser effectsElectric fieldElectric fieldRectangular potential barrierAtomic physicsHydrostatic pressureImpurityQuantum well
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Femtosecond Transient Absorption Study of the Dynamics of Acrylodan in Solution and Attached to Human Serum Albumin

2003

The excited-state relaxation dynamics of the protein-labeling dye acrylodan in solution and attached to human serum albumin has been studied by femtosecond transient absorption spectroscopy. Time-resolved spectra and kinetics of stimulated emission and excited-state absorption in the wavelength region from 400 to 800 nm were studied in ethanol and dimethylformamide. The excited-state solvation dynamics is characterized by multiexponential behavior in both solvents. In ethanol solution, the time dependence of the transient spectra is interpreted in terms of fast solvent relaxation followed by excited-state isomerization of the dye. Acrylodan attached to the protein shows a relaxation compone…

ChemistryKineticsSolvationAnalytical chemistryHuman serum albuminPhotochemistryFluorescenceSurfaces Coatings and FilmsFemtosecondUltrafast laser spectroscopyMaterials ChemistrymedicineRelaxation (physics)Physical and Theoretical ChemistryAbsorption (chemistry)medicine.drugThe Journal of Physical Chemistry B
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Atomic Radiative Lifetimes Measured by Pulsed Laser Spectroscopy in the Uv/Vuv Spectral Region

1998

Abstract Experimental lifetime measurements on free atoms and ions performed by using pulsed laser excitation in the ultraviolet and vacuum-ultraviolet spectral regions are presented. Different methods of laser pulse generation, atomization and light detection are described. A short summary of results obtained is also given. Future possibilities in determination of lifetimes and transition probabilities in the short wavelengths region are discussed.

ChemistryLasermedicine.disease_causeIonlaw.inventionPulse (physics)WavelengthlawmedicineRadiative transferPhysics::Atomic PhysicsAtomic physicsSpectroscopyExcitationUltraviolet
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Photophysical Properties of Oligo(phenylene ethynylene) Iridium(III) Complexes Functionalized with Metal-Anchoring Groups

2016

[EN] The electrochemical and photophysical properties of a family of conjugated ligands and their iridium(III) cyclometallated complexes are described. They consist of a series of monocationic Ir-III bis-2-phenylpyridine complexes with p-phenylethynyl-1,10-phenanthroline ligands of different length. The structure of these ligands includes terminal acetylthiol or pyridine groups, which can provide good electrical contacts between metal electrodes. Cyclic voltammetry, absorption and emission spectroscopy, laser flash photolysis and density functional theory calculations reveal that the high conjugation of the diimine ligand affords small energy gaps between the frontier orbitals. Nevertheless…

ChemistryLigandLaser flash photolysischemistry.chemical_element02 engineering and technologyConjugated system010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesFluorescence0104 chemical sciencesMLCTLLCTInorganic ChemistryIr complexesQUIMICA ORGANICAExcited stateFlash photolysisDensity functional theoryIridium0210 nano-technologyHOMO/LUMODiimine
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Determination of the first ionization potential of einsteinium by resonance ionization mass spectroscopy (RIMS)

1998

Abstract The first ionization potential of einsteinium (IP Es ) was determined by resonance ionization mass spectroscopy (RIMS) using samples with ≤10 12 atoms of 254 Es ( T 1/2 =276 days). This method is based on the measurement of photoionization thresholds as a function of applied electric field strength, followed by extrapolation to zero field strength to yield IP Es . An atomic beam of Es was created by heating a filament on which einsteinium was electrodeposited from an aqueous solution onto a tantalum backing and covered with titanium metal. Es atoms were ionized via a three-step excitation scheme, and the ions mass-selectively detected in a time-of-flight (TOF) mass spectrometer. Th…

ChemistryMechanical EngineeringMetals and AlloysAnalytical chemistryThermal ionizationPhotoionizationMass spectrometryAtmospheric-pressure laser ionizationMechanics of MaterialsIonizationMaterials ChemistryAtomic physicsIonization energyElectron ionizationAmbient ionizationJournal of Alloys and Compounds
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Determination of the first ionization potential of nine actinide elements by resonance ionization mass spectroscopy (RIMS)

1998

The high sensitivity of RIMS enables the precise determination of the first ionization potential of actinide elements with a sample size of ≤1012 atoms. By multiple resonant laser excitation, the actinide atoms under investigation are ionized in the presence of an electric field, and the ions are mass-selectively detected in a time-of-flight spectrometer. The first ionization potential is obtained by scanning the wavelength of the laser used for the last excitation step across the ionization threshold Wth—indicated by a sudden increase of the ion count rate—at various electric field strengths. Extrapolation of Wth to electric field strength zero leads directly to the first ionization potent…

ChemistryMechanical EngineeringMetals and AlloysThermal ionizationPhotoionizationMolar ionization energies of the elementsIon sourceAtmospheric-pressure laser ionizationMechanics of MaterialsIonizationMaterials ChemistryAtomic physicsElectron ionizationAmbient ionizationJournal of Alloys and Compounds
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Molecular structure of p -methylaniline and its van der Waals complexes with CF 3 H, CH 4 and CF 4 studied by laser induced fluorescence spectroscopy…

2002

The UV fluorescence excitation and dispersed fluorescence spectra of jet-cooled p-methylaniline have been obtained for the S1←S0 transition. The main spectral bands have been assigned by comparison with those of other relevant substituted benzenes and with the help of computed vibrational frequencies. The structure of p-methylaniline in both the S0 and S1 states has been studied at ab initio quantum chemical calculations at MP2 and CIS levels of theory using the 6-31+G∗ basis sets. Both low- and high-resolution laser induced fluorescence spectra of p-methylaniline van der Waals complexes with CF3H, CH4 and CF4 have been characterised following jet-expansion investigations. The equilibrium g…

ChemistryOrganic ChemistryAb initioMethylanilineFluorescenceAnalytical ChemistryInorganic Chemistrysymbols.namesakeComputational chemistryAb initio quantum chemistry methodssymbolsMoleculePhysical chemistryvan der Waals forceLaser-induced fluorescenceGround stateSpectroscopyJournal of Molecular Structure
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Impact of the synergistic collaboration of oligothiophene bridges and ruthenium complexes on the optical properties of dumbbell-shaped compounds.

2012

The linear and non-linear optical properties of a family of dumbbell-shaped dinuclear complexes, in which an oligothiophene chain with various numbers of rings (1, 3, and 6) acts as a bridge between two homoleptic tris(2,2'-bipyridine)ruthenium(II) complexes, have been fully investigated by using a range of spectroscopic techniques (absorption and luminescence, transient absorption, Raman, and non-linear absorption), together with density functional theory calculations. Our results shed light on the impact of the synergistic collaboration between the electronic structures of the two chemical moieties on the optical properties of these materials. Experiments on the linear optical properties …

ChemistryOrganic Chemistrychemistry.chemical_elementGeneral ChemistryThiophenesConjugated systemPhotochemistryLigandsSpectrum Analysis RamanCatalysisRutheniumRutheniumchemistry.chemical_compoundBipyridineCoordination ComplexesUltrafast laser spectroscopyThiopheneQuantum TheoryThermodynamicsHomolepticAbsorption (electromagnetic radiation)LuminescenceChemistry (Weinheim an der Bergstrasse, Germany)
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Spatial separation of atomic states in a laser cooled ion crystal

1999

A laser cooled ion crystal containing several hundred Ca+ ions has been stored in a linear Paul trap. Cooling is provided by a red detund laser at the 4S1/2−4P1/2 resonance transition. A second laser serves for repumping of those ions which decay from the excited 4P1/2 level to the metastable 3D3/2 state. The ions can be additionally excited by a third laser to a long lived metastable 3D5/2 energy level which decouples them from the cooling laser radiation. The light pressure acting upon the laser cooled ions pushes them into the direction of the laser beam. The ions in the metastable 3D5/2 state, however, do not experience any light pressure force and diffuse to the crystal side which poin…

ChemistryPhysics::OpticsResonanceLaserlaw.inventionIonCrystalRadiation pressurePhysics::Plasma PhysicslawExcited stateMetastabilityPhysics::Atomic PhysicsIon trapAtomic physicsAIP Conference Proceedings
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