Search results for "quench"

showing 10 items of 306 documents

On the zero crossing of the three-gluon vertex

2016

We report on new results on the infrared behaviour of the three-gluon vertex in quenched Quantum Chormodynamics, obtained from large-volume lattice simulations. The main focus of our study is the appearance of the characteristic infrared feature known as 'zero crossing', the origin of which is intimately connected with the nonperturbative masslessness of the Faddeev-Popov ghost. The appearance of this effect is clearly visible in one of the two kinematic configurations analyzed, and its theoretical origin is discussed in the framework of Schwinger-Dyson equations. The effective coupling in the momentum subtraction scheme that corresponds to the three-gluon vertex is constructed, revealing t…

High Energy Physics - TheoryNuclear and High Energy PhysicsLattice simulationsInfraredHigh Energy Physics::LatticeFOS: Physical sciencesThree-gluon vertexKinematicsnonperturbative01 natural sciencesSchwinger–Dyson equations[ PHYS.HTHE ] Physics [physics]/High Energy Physics - Theory [hep-th]High Energy Physics - Phenomenology (hep-ph)High Energy Physics - LatticeQuantum mechanicsLattice (order)0103 physical sciencesddc:530Exact locationquantum chromodynamics: quenching010306 general physicsMathematical physicslatticeQuantum chromodynamicsPhysicsZero crossing010308 nuclear & particles physics[PHYS.HLAT]Physics [physics]/High Energy Physics - Lattice [hep-lat][PHYS.HTHE]Physics [physics]/High Energy Physics - Theory [hep-th]High Energy Physics::PhenomenologyHigh Energy Physics - Lattice (hep-lat)[ PHYS.HLAT ] Physics [physics]/High Energy Physics - Lattice [hep-lat]gluon: vertexcrossingZero crossingghostlcsh:QC1-999GluonDyson-Schwinger equationHigh Energy Physics - PhenomenologyHigh Energy Physics - Theory (hep-th)[PHYS.HPHE]Physics [physics]/High Energy Physics - Phenomenology [hep-ph]infrared[ PHYS.HPHE ] Physics [physics]/High Energy Physics - Phenomenology [hep-ph]lcsh:Physics
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Jet quenching in the strongly-interacting quark–gluon plasma

2009

We propose a hybrid model for medium-induced parton energy loss, in which the hard scales in the process are treated perturbatively, while the soft scales which involve strong coupling dynamics are modeled by AdS/CFT calculations. After fitting a single parameter on R_AA for central Au+Au collisions, we are able to predict different observables like R_AA and I_AA as a function of centrality and reaction plane. We obtain a consistent picture of how jet quenching is modified if the quark-gluon plasma is strongly interacting, and we provide quantitative predictions.

High Energy Physics - TheoryNuclear and High Energy PhysicsParticle physicsNuclear TheoryFOS: Physical sciencesParton7. Clean energy01 natural sciencesNuclear Theory (nucl-th)Nuclear physicsHigh Energy Physics - Phenomenology (hep-ph)0103 physical sciencesNuclear Experiment010306 general physicsJet quenchingPhysics010308 nuclear & particles physicsPlane (geometry)ObservableSingle parameterPlasmaFunction (mathematics)3. Good healthHigh Energy Physics - PhenomenologyHigh Energy Physics - Theory (hep-th)Quark–gluon plasmaPhysics Letters B
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Quenching of gA and its impact in double beta decay

2015

The theory of double beta decay is briefly reviewed. The most recent (2015) results for 0νβ −β − nuclear matrix elements in the interacting boson model (IBM-2) with light and heavy neutrino exchange are given for all nuclei of interest from 48Ca to 238U. The question of quenching of the axial vector coupling constant gA in nuclei is discussed. Possible additional scenarios, such as Majoron emission, and mechanisms, such as sterile neutrino exchanges, are also discussed. nonPeerReviewed

High Energy Physics::Phenomenologyquenchingdouble beta decayNuclear Experiment
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Two-Step Route to Indoles and Analogues from Haloarenes: A Variation on the Fischer Indole Synthesis

2012

In a new variation on the Fischer indole synthesis, readily available haloarenes are converted into a wide range of indoles in just two steps by halogen-magnesium exchange and quenching with di-tert-butyl azodicarboxylate, followed by reaction with aldehydes or ketones under acidic conditions. The protocol, which is readily extended to the preparation of indole isosteres, 4- and 6-azaindoles and thienopyrroles, obviates the need to prepare potentially toxic aryl hydrazines, simultaneously avoiding undesirable anilines such as naphthylamines.

Indole testQuenching (fluorescence)IndolesHalogenationChemistryArylOrganic ChemistryTwo stepFischer synthesiHalogenationGreen Chemistry TechnologyChemistry Techniques SyntheticHydrocarbons AromaticSettore CHIM/08 - Chimica Farmaceuticachemistry.chemical_compoundIndoleFischer indole synthesisOrganic chemistrythienopyrrolesMagnesiumFischer synthesis; Indoles; azaindoles; thienopyrrolesFischer synthesisazaindolesazaindole
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A New ZnIITweezer Pyridine-Naphthalene System - An Off-On-Off System Working in a Biological pH Window

2005

Their basic idea consisted of the connec-tion of an amine to a fluorophoric anthracene unit on oneside and to a pyridine moiety on the other. At acidic pHvalues the amino and the pyridine groups are protonatedand a photoinduced electron transfer (PET) occurs fromthe π-π* excited state of the anthracene to the protonatedpyridinium unit, leading to quenching of the fluorescence.However, at high pH values, where the amino group is notprotonated, PET alternatively takes place from the aminelone pair to the same excited state of the fluorophore, yield-ing the same inhibitory effect on the fluorescence. Betweenthese two pH values, there is a pH window where PET doesnot take place and fluorescence…

Inorganic Chemistrychemistry.chemical_compoundAnthraceneFluorophoreQuenching (fluorescence)chemistryExcited statePyridineAmine gas treatingPhotochemistryFluorescencePhotoinduced electron transfer
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Light-induced charge separation in a donor–chromophore–acceptor nanocomposite poly[TPA-Ru(tpy)2]@ZnO

2013

The synthesis and characterisation of a new donor–chromophore–acceptor system based on poly(vinyltriphenylamine) as the electron donor and a glycine-functionalised bis(2,2′;6′,2′′-terpyridine)ruthenium(II) complex acting both as a chromophore and as an anchor group attached to ZnO nanorods as the electron acceptor are described. The TPA-containing block copolymer was synthesised by Reversible Addition Fragmentation Chain Transfer (RAFT) polymerisation and the ruthenium complex glycine conjugates prepared by Solid Phase Peptide Synthesis (SPPS) were attached via post-polymerisation esterification. GPC, NMR, IR and UV-Visible spectroscopy were used to characterise the multifunctional chromoph…

Kelvin probe force microscopechemistry.chemical_classificationQuenching (fluorescence)Materials sciencechemistry.chemical_elementElectron donorGeneral ChemistryChromophoreElectron acceptorPhotochemistryAcceptorRutheniumchemistry.chemical_compoundchemistryPolymerizationPolymer chemistryMaterials ChemistryJ. Mater. Chem. C
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Stereodifferentiation in the formation and decay of the encounter complex in bimolecular electron transfer with photoactivated acceptors.

2005

Experimental evidence has been obtained for the involvement of encounter complexes between both enantiomers of a π,π* triplet excited ketone and a chiral phenol or indole. Determination of the pre-equilibrium constants (KEC) and the intrinsic decay rate constants (kd) indicates a significant stereodifferentiation in both steps of the quenching process. Perez Prieto, Julia, Julia.Perez@uv.es ; Galian, Raquel Eugenia, Raquel.Galian@uv.es ; Morant Miñana, Maria Carmen, Maica.Morant@uv.es

KetoneFormation and decayUNESCO::QUÍMICAPhotochemistry:QUÍMICA [UNESCO]Catalysischemistry.chemical_compoundElectron transferBimolecular electronReaction rate constantMaterials ChemistryPhenolUNESCO::QUÍMICA::Química orgánicaStereodifferentiatioPhotoactivated acceptorschemistry.chemical_classificationIndole testQuenching (fluorescence):QUÍMICA::Química orgánica [UNESCO]Metals and AlloysGeneral ChemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryExcited statePhotoactivated acceptors ; Bimolecular electron ; Stereodifferentiatio ; Formation and decayCeramics and CompositesEnantiomerChemical communications (Cambridge, England)
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Regio- and stereo-selectivity in the intramolecular quenching of the excited benzoylthiophene chromophore by tryptophan

2000

Laser flash photolysis studies on the photobehaviour of a series of bichromophoric derivatives bearing benzoylthiophene and tryptophan groups have shown that the efficiency of the intramolecular quenching process depends on both the stereochemistry of the chiral centers and the relative ketone versus tryptophan orientation. Perez Prieto, Julia, Julia.Perez@uv.es

KetoneUNESCO::QUÍMICAStereo-selectivityPhotochemistry:QUÍMICA [UNESCO]CatalysisTrytophanStereochemistryMaterials ChemistryRegio-selectivitychemistry.chemical_classificationQuenching (fluorescence)UNESCO::QUÍMICA::Química analíticaMetals and AlloysTryptophanGeneral ChemistryChromophoreRegio-selectivity ; Stereo-selectivity ; Benzoylthiophene chromophore ; Stereochemistry ; TrytophanSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBenzoylthiophene chromophorechemistryExcited stateIntramolecular force:QUÍMICA::Química analítica [UNESCO]Ceramics and CompositesFlash photolysisSelectivityChemical Communications
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Coordinatively Unsaturated Lanthanide(III) Helicates: Luminescence Sensors for Adenosine Monophosphate in Aqueous Media

2016

Coordinatively unsaturated double-stranded helicates [(H2 L)2 Eu2 (NO3 )2 (H2 O)4 ](NO3 )4 , [(H2 L)2 Tb2 (H2 O)6 ](NO3 )6 , and [(H2 L)2 Tb2 (H2 O)6 ]Cl6 (H2 L=butanedioicacid-1,4-bis[2-(2-pyridinylmethylene)hydrazide]) are easily obtained by self-assembly from the ligand and the corresponding lanthanide(III) salts. The complexes are characterized by X-ray crystallography showing the helical arrangement of the ligands. Co-ligands at the metal ions can be easily substituted by appropriate anions. A specific luminescence response of AMP in presence of ADP, ATP, and other anions is observed. Specificity is assigned to the perfect size match of AMP to bridge the two metal centers and to replac…

LanthanideCoordination sphereadenosine monophosphateStereochemistryMetal ions in aqueous solutionHydrazide010402 general chemistry01 natural sciencesCatalysisMetalchemistry.chemical_compoundluminescencelanthanidesta116sensingQuenching (fluorescence)ChemistryLigand010405 organic chemistryhelicatesGeneral ChemistryGeneral Medicine0104 chemical sciences3. Good healthCrystallographyvisual_artvisual_art.visual_art_mediumLuminescenceAngewandte Chemie International Edition
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Time resolved confocal luminescence investigations on reverse proton exchange Nd : LiNbO3 channel waveguides

2009

In this work we report on the time and spatial resolved fluorescence of Neodymium ions in LiNbO(3) channel waveguides fabricated by Reverse Proton Exchange. The analysis of the fluorescence decay curves obtained with a sub-micrometric resolution has evidenced the presence of a relevant fluorescence quenching inside the channel waveguide. From the comparison between diffusion simulations and the spatial dependence of the (4)F(3/2) fluorescence decay rate we have concluded that the observed fluorescence quenching can be unequivocally related to the presence of H+ ions in the LiNbO(3) lattice. Nevertheless, it turns out that Reverse Proton Exchange guarantees a fluorescence quenching level sig…

Laser materialsQuenching (fluorescence)Materials scienceLITHIUM-NIOBATE CRYSTALSbusiness.industryFísicaPhysics::Opticschemistry.chemical_elementFluorescence correlation spectroscopyLithium niobateNeodymiumFluorescenceLINBO3Atomic and Molecular Physics and OpticsOpticschemistryFluorescence cross-correlation spectroscopyLaser-induced fluorescenceSpectroscopyLuminescencebusiness
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