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showing 10 items of 11789 documents

Theoretical and Experimental Study of Polarization Modulation Instability in All-Normal Dispersion Photonic Crystal Fibers

2018

Experimental observation of polarization modulation instability in all-normal dispersion photonic crystal fibers is reported. Stokes and anti-Stokes sidebands with spectral shift of 40 nm were observed when the fiber was pumped at 1064 nm. Experimental results are baked by a vectorial four-wave mixing model.

symbols.namesakeFour-wave mixingMaterials sciencesymbolsPhysics::OpticsPolarization modulationSpectral shiftSelf-phase modulationPolarization (waves)InstabilityMolecular physicsRaman scatteringPhotonic-crystal fiberLatin America Optics and Photonics Conference
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Theoretical Study of the Electronic Spectrum of trans-Stilbene

1997

The electronic spectrum of trans-stilbene in the energy range up to 6 eV has been studied using multiconfigurational second-order perturbation theory (CASPT2). The study includes a geometry determination of the ground state. In all, 12 singlet and one triplet excited states were studied. The calculated spectrum makes it possible to assign the valence excited singlet states corresponding to the three bands observed in the low-energy region of the one-photon absorption spectrum. The most intense feature of the calculated spectrum corresponds to the 11Ag → 21Bu transition at 4.07 eV. The weakly allowed 11Bu state was found 0.3 eV below 21Bu. Transition to the 31Ag state, computed at 4.95 eV, i…

symbols.namesakeValence (chemistry)PhotoisomerizationAbsorption spectroscopyChemistryExcited stateRydberg formulasymbolsTrans stilbeneSinglet statePhysical and Theoretical ChemistryAtomic physicsGround stateThe Journal of Physical Chemistry A
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Hadronic light-by-light contribution to $(g-2)_\mu$ from lattice QCD with SU(3) flavor symmetry

2020

We perform a lattice QCD calculation of the hadronic light-by-light contribution to $(g-2)_\mu$ at the SU(3) flavor-symmetric point $m_\pi=m_K\simeq 420\,$MeV. The representation used is based on coordinate-space perturbation theory, with all QED elements of the relevant Feynman diagrams implemented in continuum, infinite Euclidean space. As a consequence, the effect of using finite lattices to evaluate the QCD four-point function of the electromagnetic current is exponentially suppressed. Thanks to the SU(3)-flavor symmetry, only two topologies of diagrams contribute, the fully connected and the leading disconnected. We show the equivalence in the continuum limit of two methods of computin…

symmetry: flavorParticle physicstopologymagnetic momentPhysics and Astronomy (miscellaneous)Feynman graphHigh Energy Physics::LatticeLattice field theoryHadronExtrapolationhep-lat01 natural sciencesspace: Euclideansymbols.namesakePionHigh Energy Physics - LatticeLattice (order)quantum chromodynamics0103 physical sciencesquantum electrodynamicsFeynman diagramcontinuum limit010306 general physicsEngineering (miscellaneous)perturbation theorylatticeParticle Physics - PhenomenologyQuantum chromodynamicsPhysicsform factor: transitioncurrent: electromagneticfinite size: effect[PHYS.HLAT]Physics [physics]/High Energy Physics - Lattice [hep-lat]010308 nuclear & particles physicslattice field theoryphoton photon: scatteringhep-phParticle Physics - LatticeLattice QCDsuppressionHigh Energy Physics - Phenomenology[PHYS.HPHE]Physics [physics]/High Energy Physics - Phenomenology [hep-ph]symbolsflavor: SU(3)n-point function: 4
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Synthesis of new hybrid 1,4-thiazinyl-1,2,3-dithiazolyl radicals via Smiles rearrangement

2017

The condensation reaction of 2-aminobenzenethiols and 3-aminopyrazinethiols with 2-amino-6-fluoro-N-methylpyridinium triflate afforded thioether derivatives that were found to undergo Smiles rearrangement and cyclocondensation with sulphur monochloride to yield new hybrid 1,4-thiazine-1,2,3-dithiazolylium cations. The synthesized cations were readily reduced to the corresponding stable neutral radicals with spin densities delocalized over both 1,4-thiazinyl and 1,2,3-dithiazolyl moieties. peerReviewed

synthesis010405 organic chemistryChemistryRadical12010402 general chemistryPhotochemistryCondensation reaction01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundDelocalized electron14-thiazinyl-123-dithiazolyl radicalsThioether4-thiazinyl-1Smiles rearrangementYield (chemistry)Polymer chemistrysynteesiSmiles rearrangementTrifluoromethanesulfonateta1163-dithiazolyl radicalsDalton Transactions
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Fluorinated heterocyclic compounds: an assay on the photochemistry of some fluorinated 1-oxa-2-azoles: an expedient route to fluorinated heterocycles

2004

Abstract Photoinduced heterocyclic rearrangements of ON bond-containing azoles have been claimed in the synthesis of target fluorinated heterocyclic compounds. In this context, the photochemical behavior of some fluorinated 1,2,4-oxadiazoles has been investigated. Irradiations of 3-amino-5-perfluoroalkyl-1,2,4-oxadiazoles at λ =313 nm in methanol gave open-chain products arising from a reaction of the nucleophilic solvent with either the first formed ring-photolytic species or with a nitrilimine moiety generated from it. Differently, irradiations in methanol with the presence of triethylamine (TEA) followed competing phototransposition pathways leading to the ring-isomers 2-amino-5-perfluo…

synthesisFluorinated heterocyclic compounds Oxadiazoles Synthesis Photochemistry Molecular rearrangementsfluorinated heterocyclic compounds;oxadiazoles;synthesis;photochemistry;molecular rearrangementsmolecular rearrangementsContext (language use)PhotochemistryBiochemistryInorganic Chemistrychemistry.chemical_compoundNucleophileEnvironmental ChemistryMoietySettore CHIM/01 - Chimica AnaliticaPhysical and Theoretical ChemistryTriethylaminephotochemistryNitrilimineOrganic ChemistryoxadiazolesSettore CHIM/06 - Chimica OrganicaGeneral MedicineSolventchemistryfluorinated heterocyclic compoundsMethanolSolvolysis
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Synthesis and selected properties of metallo and metal-free 2,3,9,10,16,17,23,24-octacarboxyphthalocyanines

2015

This review article reports methods of synthe sis and selected physicochemical properties of metallo and metal-free 2,3,9,10,16,17,23,24–octacarboxyphthalocyanines. The most frequently used methods of synthesis for this class of co mpounds are described in this article. Moreover, aggregation, catalytic and photocatalytic properties of these complexes are presented. Potential applications of metallo and metal-free 2,3,9,10,16,17,23,24–octacarboxyphthalocyanines are also given.

synthesisabsorption spectraapplicationsChemistry3Organic Chemistryaggregation1724-octacarboxyphthalocyanines16Combinatorial chemistry10Catalysis23catalytic and photocatalytic activitylcsh:QD241-441Metal freelcsh:Organic chemistryPhotocatalysismetallo and metal-free 29ARKIVOC : Archive for Organic Chemistry
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High speed microfluidic prototyping by programmable proximity aperture MeV ion beam lithography

2013

Abstract Microfluidics refers to the science and technology for controlling and manipulating fluids that flow along microchannels. For the development of complex prototypes, many microfluidic test structures are required first. Normally, these devices are fabricated via photolithography. This technique requires a photomask for transferring a pattern to photoresists by exposing with UV light. However, this method can be slow when a new structure is required to change. This is because a series of photomasks are needed, which is time consuming and costly. Here, we present a programmable proximity aperture lithography (PPAL) technique for the development of microfluidic prototype in poly(methyl…

ta113Nuclear and High Energy PhysicsMaterials scienceFabricationApertureMicrofluidicsProcess (computing)NanotechnologyIon beam lithographylaw.inventionlawta318PhotomaskPhotolithographyInstrumentationLithographyNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
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Isophorone on Au/MgO/Ag(001) : Physisorption with Electrostatic Site Selection

2017

We report a computational study of isophorone C9H14O adsorption on a Ag(001)-supported ultrathin MgO film with Au adatoms and clusters employing density functional theory calculations. The calculations show that the keto form of isophorone is more stable than the enol tautomers both in gas phase and on the MgO/Ag(001) surface. The interaction between the keto isophorone and step and terrace sites of MgO/Ag(001) displays long interaction distances, relatively weakly exothermic adsorption energies, lack of charge transfer, and minor changes in the density of states, all of which indicate that the molecule merely physisorbs on the surface. The step sites are energetically preferred adsorption …

ta114Chemistry02 engineering and technology021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesTautomerEnolSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundCrystallographyGeneral EnergyAdsorptionPhysisorptionisophorone adsorption0103 physical sciencesDensity of statesMoleculeDensity functional theoryPhysical and Theoretical Chemistry010306 general physics0210 nano-technologyta116IsophoroneJournal of Physical Chemistry C
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Molecule-like photodynamics of Au102(pMBA)44 nanocluster.

2015

Photophysical properties of a water-soluble cluster Au102(pMBA)44 (pMBA = para-mercaptobenzoic acid) are studied by ultrafast time-resolved mid-IR spectroscopy and density functional theory calculations in order to distinguish between molecular and metallic behavior. In the mid-IR transient absorption studies, visible or near-infrared light is used to electronically excite the sample, and the subsequent relaxation is monitored by studying the transient absorption of a vibrational mode in the ligands. Based on these studies, a complete picture of energy relaxation dynamics is obtained: (1) 0.5-1.5 ps electronic relaxation, (2) 6.8 ps vibrational cooling, (3) intersystem crossing from the low…

ta114ChemistryRelaxation (NMR)General EngineeringGeneral Physics and Astronomytransient absorptionInternal conversion (chemistry)PhotochemistryMolecular physicselectronic relaxationvibrational spectroscopyIntersystem crossinggold nanoclusterUltrafast laser spectroscopyGeneral Materials ScienceDensity functional theoryTriplet stateSpectroscopyGround stateta116femtosecondACS nano
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One-pot synthesis and characterization of subnanometre-size benzotriazolate protected copper clusters

2012

A simple one-pot method for the preparation of subnanometre-size benzotriazolate (BTA) protected copper clusters, Cu(n)BTA(m), is reported. The clusters were analyzed by optical and infrared spectroscopy, mass spectrometry and transmission electron microscopy together with computational methods. We suggest a structural motif where the copper core of the Cu(n)BTA(m) clusters is protected by BTA-Cu(i)-BTA units.

ta114Inorganic chemistryOne-pot synthesischemistry.chemical_elementInfrared spectroscopyTriazolesMass spectrometryCopperCharacterization (materials science)CrystallographychemistryCoordination ComplexesTransmission electron microscopyQuantum TheorySpectrophotometry UltravioletGeneral Materials ScienceStructural motifta116CopperNanoscale
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