Search results for "coupling [Higgs particle]"

showing 10 items of 443 documents

Electron paramagnetic resonance study of exchange coupled Ce3+ ions in Lu2SiO5 single crystal scintillator

2016

Abstract The Ce 3+ ions incorporation inside lutetium oxyorthosilicate (Lu 2 SiO 5 ) single crystals was studied by electron paramagnetic resonance. Already known Ce1 and Ce2 centers originating from the lattice peculiarity allowing two lutetium sites coordinated by different number of the oxygen ions were detected. Remarkably, for the Ce2 center, the determined g 2 tensor is asymmetric and could not be diagonalized as compared to the Ce1 center, for which the three principal values and corresponding axes orientation have been determined and reported previously. Besides, the much weaker resonance lines found in spectra close to those coming from the Ce1 and Ce2, and following them under cry…

Dimerchemistry.chemical_element02 engineering and technology01 natural sciencesSpectral linelaw.inventionIonchemistry.chemical_compoundlaw0103 physical sciencesExchange coupled ionsLutetium oxyorthosilicateElectron paramagnetic resonanceInstrumentationCoupling constantRadiation010308 nuclear & particles physics021001 nanoscience & nanotechnologyLutetiumMagnetic fieldchemistryScintillatorsElectron paramagnetic resonanceAtomic physicsCerium ions0210 nano-technologySingle crystalRadiation Measurements
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Diquark-diquark correlations in theS01ΛΛpotential

2005

We derive a $\ensuremath{\Lambda}\ensuremath{\Lambda}$ potential from a chiral constituent quark model that has been successful in describing one, two, and three nonstrange baryon systems. The resulting interaction at low energy is attractive at all distances due to the $\ensuremath{\sigma}$ exchange term. The attraction allows for a slightly bound state just below the $\ensuremath{\Lambda}\ensuremath{\Lambda}$ threshold. No short-range repulsive core is found. We extract the diquark-diquark contribution that turns out to be the most attractive and probable at small distances. At large distances the asymptotic behavior of the $\ensuremath{\Lambda}\ensuremath{\Lambda}$ interaction provides a…

DiquarkBaryonPhysicsCoupling constantNuclear and High Energy PhysicsParticle physicsBound stateSigmaConstituent quarkAtomic physicsLambdaLambda baryonPhysical Review D
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From the Golgi-Cajal mapping to the transmitter-based characterization of the neuronal networks leading to two modes of brain communication: Wiring a…

2007

After Golgi-Cajal mapped neural circuits, the discovery and mapping of the central monoamine neurons opened up for a new understanding of interneuronal communication by indicating that another form of communication exists. For instance, it was found that dopamine may be released as a prolactin inhibitory factor from the median eminence, indicating an alternative mode of dopamine communication in the brain. Subsequently, the analysis of the locus coeruleus noradrenaline neurons demonstrated a novel type of lower brainstem neuron that monosynaptically and globally innervated the entire CNS. Furthermore, the ascending raphe serotonin neuron systems were found to globally innervate the forebrai…

DopamineTortuosityBrain functionWiring transmissionSynaptic TransmissionDiffusionDual probe microdialysisMicrofluorimetrychemistry.chemical_compoundCatecholaminesPressure gradientsVolume transmissionHistofluorescenceLocus coeruleusExtracellular spaceNeurological and mental disordersNeurotransmitterNeuronsNeurotransmitter AgentsGeneral NeuroscienceBrain5-HydroxytryptamineAmygdalamedicine.anatomical_structure5-Hydroxytryptamine; Amygdala; Brain function; Brain uncoupling protein-2; Catecholamines; CA turnover; Clearance; Diffusion; Dopamine; Dorsal raphe; Dual probe microdialysis; Extracellular space; Extrasynaptic receptors; Histofluorescence; Local circuits; Locus coeruleus; Mapping of monoamine neurons; Microdensitometry; Microfluorimetry; Neurological and mental disorders; Noradrenaline; Nucleus accumbens; Pressure gradients; Receptor mosaics; Receptor–receptor interactions; Substantia nigra; Thermal gradients; Tortuosity; Transmitter–receptor mismatches; Volume fraction; Volume transmission; Wiring transmissionClearanceNucleus accumbensCA turnoverLocal circuitsReceptor–receptor interactionsSilver StainingMapping of monoamine neuronsModels NeurologicalNeurotransmissionBiologySerotonergicSubstantia nigramedicineBiological neural networkAnimalsHumansThermal gradientsTransmitter–receptor mismatchesVolume fractionExtrasynaptic receptorsMonoamine neurotransmitterchemistryReceptor mosaicsForebrainNoradrenalineLocus coeruleusBrain uncoupling protein-2Neurology (clinical)NeuronNerve NetMicrodensitometry5-Hydroxytryptamine Amygdala Brain function Brain uncoupling protein-2 Catecholamines CA turnover Clearance DiffusionNeuroscienceDorsal raphe
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Forward rapidity isolated photon production in proton-nucleus collisions

2018

We calculate isolated photon production at forward rapidities in proton-nucleus collisions in the Color Glass Condensate framework. Our calculation uses dipole cross sections solved from the running coupling Balitsky-Kovchegov equation with an initial condition fit to deep inelastic scattering data and extended to nuclei with an optical Glauber procedure that introduces no additional parameters beyond the basic nuclear geometry. We present predictions for future forward RHIC and LHC measurements. The predictions are also compared to updated results for the nuclear modification factors for pion production, Drell-Yan dileptons and $J/\psi$ mesons in the same forward kinematics, consistently c…

Drell-Yan processPhotongeometryProtonNuclear TheoryNuclear Theorypi: productionhiukkasfysiikka01 natural sciencesColor-glass condensateHigh Energy Physics - Phenomenology (hep-ph)coupling constant: energy dependenceopticalNuclear ExperimentBrookhaven RHIC CollPhysicsphoton: productionenergy: highhigher-order: 0higher-order: 1suppressionBalitsky-Kovchegov equationHigh Energy Physics - PhenomenologyCERN LHC CollkinematicsNuclear and High Energy PhysicsMeson[PHYS.NUCL]Physics [physics]/Nuclear Theory [nucl-th]FOS: Physical sciencesGlaubermeson114 Physical sciencesdileptonNuclear physicsNuclear Theory (nucl-th)Piondeep inelastic scattering0103 physical sciencesRapidityproton-nucleus collisions010306 general physicsta114010308 nuclear & particles physicsnucleusphoton productionDeep inelastic scatteringboundary condition* Automatic Keywords *rapidity[PHYS.HPHE]Physics [physics]/High Energy Physics - Phenomenology [hep-ph]color glass condensatecross section: dipolep nucleusGlauber
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Inclusive pion-nucleus double charge exchange.

1989

Inclusive double charge exchange reaction is studied by using a model which combines a microscopic many-body calculation of reaction probabilities with a Monte Carlo simulation procedure. Comparison with present experimental results requires that the (\ensuremath{\pi},2\ensuremath{\pi}) reaction be included and a proper evaluation of this latter reaction is also done. The combined results compare favorably with experiment, giving extra support to this model of the pion-nucleus interaction which was previously shown to provide a good description of all other inclusive reactions and elastic scattering.

Elastic scatteringNuclear reactionCoupling constantPhysicsNuclear and High Energy PhysicsParticle physicsMonte Carlo methodMany-body problemNuclear physicsPionmedicine.anatomical_structuremedicineNuclear ExperimentNucleusCharge exchangePhysical review. C, Nuclear physics
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Synthesis ofmeta-Terphenyl-2,2′′-diols by Anodic C−C Cross-Coupling Reactions

2016

The anodic C-C cross-coupling reaction is a versatile synthetic approach to symmetric and non-symmetric biphenols and arylated phenols. We herein present a metal-free electrosynthetic method that provides access to symmetric and non-symmetric meta-terphenyl-2,2''-diols in good yields and high selectivity. Symmetric derivatives can be obtained by direct electrolysis in an undivided cell. The synthesis of non-symmetric meta-terphenyl-2,2''-diols required two electrochemical steps. The reactions are easy to conduct and scalable. The method also features a broad substrate scope, and a large variety of functional groups are tolerated. The target molecules may serve as [OCO](3-) pincer ligands.

Electrolysis010405 organic chemistrySubstrate (chemistry)General Chemistry010402 general chemistryElectrochemistry01 natural sciencesCombinatorial chemistryCatalysisCoupling reaction0104 chemical scienceslaw.inventionPincer movementAnodechemistry.chemical_compoundchemistrylawTerphenylOrganic chemistryMoleculeAngewandte Chemie International Edition
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About the selectivity and reactivity of active nickel electrodes in C–C coupling reactions

2020

Active anodes which are operating in highly stable protic media such as 1,1,1,3,3,3-hexafluoroisopropanol are rare. Nickel forms, within this unique solvent, a non-sacrificial active anode at constant current conditions, which is superior to the reported powerful molybdenum system. The reactivity for dehydrogenative coupling reactions of this novel active anode increases when the electrolyte is not stirred during electrolysis. Besides the aryl-aryl coupling, a dehydrogenative arylation reaction of benzylic nitriles was found while stirring the mixture providing quick access to synthetically useful building blocks.

ElectrolysisChemistryGeneral Chemical Engineeringchemistry.chemical_elementGeneral ChemistryElectrolyteCombinatorial chemistryCoupling reactionAnodelaw.inventionSolventNickellawReactivity (chemistry)SelectivityRSC Advances
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Metal- and reagent-free highly selective anodic cross-coupling reaction of phenols.

2014

The direct oxidative cross-coupling of phenols is a very challenging transformation, as homo-coupling is usually strongly preferred. Electrochemical methods circumvent the use of oxidizing reagents or metal catalysts and are therefore highly attractive. Employing electrolytes with a high capacity for hydrogen bonding, such as methanol with formic acid or 1,1,1,3,3,3-hexafluoro-2-propanol, a direct electrolysis in an undivided cell provides mixed 2,2′-biphenols with high selectivity. This mild method tolerates a variety of moieties, for example, tert-butyl groups, which are not compatible with other strong electrophilic media but vital for later catalytic applications of the formed products.

ElectrolysisFormic acidInorganic chemistryGeneral ChemistryCatalysisCoupling reactionCatalysislaw.inventionchemistry.chemical_compoundchemistryPhenolslawMetalsReagentOxidizing agentOxidative coupling of methaneIndicators and ReagentsMethanolElectrodesAngewandte Chemie (International ed. in English)
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Solvent Control in Electro-Organic Synthesis

2018

Exploiting the solvent control within electro-organic conversions is a far underestimated parameter in prep-scale electrolysis. The beneficial application in several transformations is outlined and in particular discussed for the dehydrogenative coupling of arenes and heteroarenes. This simple electrolytic strategy in fluorinated solvents allows the modulation of the substrate’s nucleophilicity and the stabilization of the intermediates as well as of the final product from over-oxidation.1 Introduction2 Solvent Effects in Kolbe Electrolysis and Anodic Fluorination3 Unique Solvent Effects of 1,1,1,3,3,3-Hexafluoropropan-2-ol (HFIP)4 Anodic Dehydrogenative Coupling Reactions with Use of HFIP …

ElectrolysisKolbe electrolysis010405 organic chemistryChemistryOrganic Chemistry010402 general chemistryElectrosynthesis01 natural sciencesCombinatorial chemistryCoupling reactionElectrochemical fluorination0104 chemical scienceslaw.inventionSolventchemistry.chemical_compoundlawOrganic synthesisSolvent effectsSynlett
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Reaction Condition Screening by Using Electrochemical Microreactor: Application to Anodic Phenol-arene C,C Cross-Coupling Reaction in High Acceptor N…

2013

The anodic phenol-arene C,C cross-coupling reaction was achieved in inexpensive and sustainable media such as methanol, acetic acid, and formic acid by using an electrochemical microreactor which can provide a better performance to screen reaction conditions than in standard beaker-type electrolysis cells. Especially, formic acid as a reaction medium showed good performance. The total amount of cross-coupling product and homo-coupling products as a by-product was clearly increased as the solvent acceptor number increased. To control the selective oxidation of phenol, addition of methanol was effective.

ElectrolysisRenewable Energy Sustainability and the EnvironmentFormic acidInorganic chemistryCondensed Matter PhysicsAcceptorCoupling reactionSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionchemistry.chemical_compoundAcetic acidchemistrylawMaterials ChemistryElectrochemistryPhenolMethanolMicroreactorJournal of The Electrochemical Society
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