Search results for "Photo"

showing 10 items of 11789 documents

Steering the excited state dynamics of a photoactive yellow protein chromophore analogue with external electric fields

2014

Abstract The first excited state of the Photoactive Yellow Protein chromophore exhibits a strong charge transfer character and the dipole moments of the excited and ground states differ significantly. Furthermore, the excited state charge distribution changes during the isomerization of this chromophore. These observations suggest that external electric fields can be used to control photo-isomerization, providing a new concept for developing photochromic devices, such as e-paper or optical memory. To test this idea, we performed excited state dynamics simulations and static calculations of a PYP chromophore analogue (pCK − ) in an external electric field. By adjusting direction and strength…

010304 chemical physicsField (physics)ChemistryCharge densitySurface hoppingChromophore010402 general chemistryCondensed Matter PhysicsPhotochemistry01 natural sciencesBiochemistryMolecular physics0104 chemical sciencesPhotochromismDipoleElectric fieldExcited state0103 physical sciencesPhysics::Atomic and Molecular ClustersPhysics::Chemical PhysicsPhysical and Theoretical Chemistryta116ComputingMilieux_MISCELLANEOUS
researchProduct

Matrix isolation and quantum chemical studies on the H2O2–SO2complex

2004

Complexation and photochemical reactions of hydrogen peroxide and sulfur dioxide have been studied in solid Ar, Kr and Xe. Complexes between H2O2 and SO2 are characterized using Fourier transform infrared spectroscopy and ab initio calculations. In solid Ar, the H2O2–SO2 complex absorptions are found at wavenumbers of 3572.8, 3518.7, 3511.2, 3504.3, 1340.3, 1280.2 and 1149.9 cm−1. In Kr and Xe matrices, the bonded OH stretching frequencies deviate from the values in Ar, and we propose that the matrix surrounding influences the structure of the H2O2–SO2 complex. UV photolysis of the H2O2–SO2 was also studied in solid Ar, Kr and Xe. This photolysis produces mainly a complex between sulfur tri…

010304 chemical physicsPhotodissociationMatrix isolationGeneral Physics and Astronomy010402 general chemistry7. Clean energy01 natural sciences0104 chemical scienceschemistry.chemical_compoundMatrix (mathematics)chemistryComputational chemistryAb initio quantum chemistry methods0103 physical sciencesSulfur trioxidePhysical chemistryPhysical and Theoretical ChemistryFourier transform infrared spectroscopyHydrogen peroxideSulfur dioxidePhys. Chem. Chem. Phys.
researchProduct

Time-resolved photoisomerization of 1,1′-di-tert-butylstilbene and 1,1′-dicyanostilbene

2016

Abstract Photoisomerization of 1,1′-di-tert-butylstilbene ( 3 ) and 1,1′-dicyanostilbene ( 4 ) is monitored with stationary and broadband transient absorption spectroscopy. The electron affinity of the substituents correlates with the shift of the absorption band. The weak extinction of 3 complicates data interpretation, but comparison with earlier measured 1,1′-dimethylstilbene ( 1 ) and 1,1′-diethylstilbene ( 2 ) helps to assign transient spectra and relaxation paths. For 3 a long-lived perpendicular state P is observed with lifetime τ P  = 134 ps in acetonitrile. For 4 τ P  = 2.1 ps in acetonitrile and 27 ps in n-hexane, the difference indicating a substantial dipole moment (∼3D) of the …

010304 chemical physicsPhotoisomerizationChemistryRelaxation (NMR)Analytical chemistryGeneral Physics and Astronomy010402 general chemistry01 natural sciences0104 chemical sciencesDipolechemistry.chemical_compoundAbsorption bandElectron affinity0103 physical sciencesUltrafast laser spectroscopyPhysical and Theoretical ChemistrySpectroscopyAcetonitrileChemical Physics Letters
researchProduct

Comparaison expérimentale de techniques de caractérisation en intensité et phase d'impulsions optiques ultracourtes

2006

Nous comparons experimentalement les resultats de la caracterisation en intensite et en phase d'impulsions optiques ultracourtes obtenus par differentes techniques employant un montage auto/inter-correlateur en intensite et un analyseur de spectre. Nous employons pour ces tests une impulsion en limite de Fourier, une impulsion affectee par l'auto-modulation de phase et une impulsion similariton.

010309 optics020210 optoelectronics & photonics0103 physical sciences0202 electrical engineering electronic engineering information engineeringGeneral Physics and Astronomy02 engineering and technology01 natural sciencesJournal de Physique IV (Proceedings)
researchProduct

Photoionization cross sections of the 5S1/2 and 5P3/2 states of Rb in simultaneous magneto-optical trapping of Rb and Hg

2018

We report the measurement of the photoionization cross sections of the $5{S}_{1/2}$ and $5{P}_{3/2}$ states of $^{87}\mathrm{Rb}$ in a two-species Hg and Rb magneto-optical trap (MOT) by the cooling laser for Hg. The photoionization cross sections of Rb in the $5{S}_{1/2}$ and $5{P}_{3/2}$ states at 253.7 nm are determined to be ${1}_{\ensuremath{-}1}^{+4.3}\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}20}\phantom{\rule{0.28em}{0ex}}{\text{cm}}^{2}$ and $4.63(30)\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}18}\phantom{\rule{0.28em}{0ex}}{\text{cm}}^{2}$, respectively. To measure the $5{S}_{1/2}$ and $5{P}_{3/2}$ state fractions in the MOT we detected the photoionization rat…

010309 opticsPhysics0103 physical sciencesPhotoionizationTrappingAtomic physics010306 general physics01 natural sciencesMagneto opticalPhysical Review A
researchProduct

Comment on “Thresholded Quantum LIDAR: Exploiting Photon-Number-Resolving Detection”

2020

International audience; The ratio of the SNR with thresholding and with proportional detection for one photon of mean background noise, for a threshold value N from 1 to 4.

010309 opticsPhysics[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]PhotonLidarOpticsbusiness.industry0103 physical sciencesGeneral Physics and Astronomy010306 general physicsbusiness01 natural sciencesQuantumPhysical Review Letters
researchProduct

Effective characterization of the phase and intensity profiles of asymmetrically distorted light pulses in optical fiber systems

2009

International audience; We address the problem of characterization of light pulses that propagate in long-haul high-bit-rate optical communication systems under strongly perturbed conditions. We show that the conventional technique for characterization of the phase and intensity profile of such pulses becomes qualitatively inconsistent when the pulse's profile is asymmetrically distorted with respect to its center of mass. We resolve these inconsistencies by partially reformulating the conventional technique by means of appropriate pulse parameters, which we call upgraded parameters, that allow a fair characterization of the intensity and phase of all types of light pulses, including those …

010309 optics[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistry020210 optoelectronics & photonics0103 physical sciences[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistry0202 electrical engineering electronic engineering information engineeringStatistical and Nonlinear Physics02 engineering and technology190.5530 060.5530 060.2330 060.2360 060.451001 natural sciencesAtomic and Molecular Physics and Optics
researchProduct

Active components for integrated plasmonic circuits

2009

International audience; We present a comprehensive study of highly efficient and compact passive and active components for integrated plasmonic circuit based on dielectric-loaded surface plasmon polariton waveguides.

010309 optics[SPI.OPTI] Engineering Sciences [physics]/Optics / PhotonicComputer science[SPI.NANO] Engineering Sciences [physics]/Micro and nanotechnologies/Microelectronics0103 physical sciences[SPI.OPTI]Engineering Sciences [physics]/Optics / PhotonicPhysics::Atomic and Molecular ClustersPhysics::Optics[ SPI.NANO ] Engineering Sciences [physics]/Micro and nanotechnologies/Microelectronics[ SPI.OPTI ] Engineering Sciences [physics]/Optics / Photonic[SPI.NANO]Engineering Sciences [physics]/Micro and nanotechnologies/Microelectronics010306 general physics01 natural sciences
researchProduct

Sensitive Assays by Nucleophile-Induced Rearrangement of Photoactivated Diarylethenes.

2018

Upon light-induced isomerization, diarylethenes (DAEs) equipped with reactive aldehyde moieties rearrange selectively in the presence of amines, accompanied by decoloration. In a comprehensive study, the probe structure was optimized with regard to its inherent reactivity in the nucleophile-triggered rearrangement reaction. Detailed structure−reactivity relationships could be derived, in particular with regard to the type of integrated (het)aryl moieties as well as the location of the formyl residue, and the probes’ intrinsic reactivity with primary and secondary amines was optimized. Utilizing an ancillary base, the initially formed rearrangement product can engage in a subsequent catalyti…

010402 general chemistry01 natural sciencesBiochemistryAldehydeCatalysischemistry.chemical_compoundPhotochromismColloid and Surface ChemistryNucleophile541 Physikalische ChemieReactivity (chemistry)Rearrangement reactionsensingchemistry.chemical_classification010405 organic chemistryArylGeneral ChemistryphotochromismCombinatorial chemistry0104 chemical sciences540 Chemie und zugeordnete WissenschaftenaminechemistryCatalytic cycleddc:540diaryletheneddc:541547 Organische ChemieIsomerizationddc:547Journal of the American Chemical Society
researchProduct

Gold/Isophorone Interaction Driven by Keto/Enol Tautomerization

2016

The binding behavior of isophorone (C9H14O) to Au adatoms and clusters deposited on MgO/Ag(001) thin films is investigated by scanning tunneling microscopy (STM) and density functional theory (DFT). The STM data reveal the formation of various metal/organic complexes, ranging from Au1/isophorone pairs to larger Au aggregates with molecules bound to their perimeter. DFT calculations find the energetically preferred keto-isophorone to be unreactive toward gold, while the enol-tautomer readily binds to Au monomers and clusters. The interaction is governed by electrostatic forces between the hydroxyl group of the enol and negative excess charges residing on the ad-gold. The activation barrier b…

010402 general chemistryPhotochemistry01 natural sciencesChemical reactionlaw.inventionchemistry.chemical_compoundlawketo-enol tautomerismgold compoundsMoleculePhysical and Theoretical Chemistryta116Isophoroneta114010405 organic chemistryKeto–enol tautomerismEnolTautomer0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsisophoroneGeneral EnergychemistryDensity functional theoryScanning tunneling microscopeJournal of Physical Chemistry C
researchProduct