Search results for "Coupling"

showing 10 items of 1862 documents

Cross-Frequency Coupling in Developmental Perspective

2019

It is generally assumed that different electroencephalogram (EEG) frequency bands are somehow related to different computational modes in the brain. Integration of these computational modes is reflected in the phenomenon of cross-frequency coupling (CFC). On slow temporal scales, CFC may reflect trait-like properties, which posits a question of its developmental trends. This is the first study that explored source-level CFC measures in a developmental perspective using both cross-sectional and longitudinal designs. CFC measures demonstrated good test-retest stability and proved to be higher in adults in cortical areas participating in sensory-motor integration, response inhibition, and atte…

growth curve analysissource-level analysiscross-frequency couplingElectroencephalography050105 experimental psychologylcsh:RC321-57103 medical and health sciencesBehavioral Neuroscience0302 clinical medicineSocial cognitionmedicine0501 psychology and cognitive sciencesEEGAssociation (psychology)lcsh:Neurosciences. Biological psychiatry. NeuropsychiatryBiological PsychiatryOriginal ResearchExtraversion and introversionmedicine.diagnostic_test05 social sciencesPerspective (graphical)Social anxietyAttentional controlCognitionPsychiatry and Mental healthNeuropsychology and Physiological PsychologyNeurologydevelopmental trendsintroversionsocial anxietyPsychology030217 neurology & neurosurgeryCognitive psychologyNeuroscienceFrontiers in Human Neuroscience
researchProduct

IEEE Std. 1459 power quantities ratio approaches for simplified harmonic emissions assessment

2018

The paper investigates the suitability of using power ratio parameters for harmonic emissions assessment at the point of common coupling (PCC). The study is carried out starting from the IEEE Std. 1459-2010 apparent power decomposition, where power factors are defined for evaluating line utilization and harmonic pollution levels. In addition, the study investigates the behavior of new parameters, which are expressed in terms of ratio between IEEE Std. 1459-2010 power quantities. The study is carried out for both single-phase and three-phase case, also considering the presence of capacitors. ? 2018 IEEE.

harmonic sources; IEEE Std. 1459-2010; power definitions; power measurement; power quality020209 energy02 engineering and technologyAC powerAutomotive engineeringlaw.inventionPower (physics)harmonic distortionHarmonic analysisCapacitorHarmonic pollutionlawPower ratio0202 electrical engineering electronic engineering information engineeringHarmonicPoint of common couplingPower measurement harmonic distortion power definitions power quality IEEE Std. 1459-2010 harmonic sourcesSettore ING-INF/07 - Misure Elettriche E ElettronicheMathematics2018 18th International Conference on Harmonics and Quality of Power (ICHQP)
researchProduct

Quantum and classical dynamics of heavy quarks in a quark-gluon plasma

2018

We derive equations for the time evolution of the reduced density matrix of a collection of heavy quarks and antiquarks immersed in a quark gluon plasma. These equations, in their original form, rely on two approximations: the weak coupling between the heavy quarks and the plasma, the fast response of the plasma to the perturbation caused by the heavy quarks. An additional semi-classical approximation is performed. This allows us to recover results previously obtained for the abelian plasma using the influence functional formalism. In the case of QCD, specific features of the color dynamics make the implementation of the semi-classical approximation more involved. We explore two approximate…

heavy quarksheavy ion: scatteringNuclear Theoryapproximation: semiclassicalHigh Energy Physics::LatticeMonte Carlo methoddensity matrix: reducedhiukkasfysiikkaquantum chromodynamics: plasma01 natural sciencesBoltzmann equationLangevin equationHigh Energy Physics - Phenomenology (hep-ph)quarkonium: heavyquantum electrodynamicsQuarkonium suppression[ PHYS.NUCL ] Physics [physics]/Nuclear Theory [nucl-th]quark gluon: plasmaMathematical physics[PHYS]Physics [physics]Quantum chromodynamicsPhysicsquarkonium: suppressionBoltzmann equationquark gluon plasmaLangevin equationHigh Energy Physics - Phenomenologyheavy quark: couplingQuarkNuclear and High Energy Physicsquark-gluon plasma[PHYS.NUCL]Physics [physics]/Nuclear Theory [nucl-th]FOS: Physical sciencesNuclear Theory (nucl-th)quantum chromodynamics0103 physical scienceslcsh:Nuclear and particle physics. Atomic energy. Radioactivityheavy quarkstochastic010306 general physicsplasma: weak couplingta114010308 nuclear & particles physicsHigh Energy Physics::Phenomenologykvarkki-gluoniplasmaTime evolutionPlasmaHeavy Ion Phenomenologyfree energyrecombinationabelian[PHYS.HPHE]Physics [physics]/High Energy Physics - Phenomenology [hep-ph]Quark–gluon plasmalcsh:QC770-798[ PHYS.HPHE ] Physics [physics]/High Energy Physics - Phenomenology [hep-ph]High Energy Physics::ExperimentJournal of High Energy Physics
researchProduct

Determination of the non-abelian Debye screening mass using classical chromodynamics

2014

Tässä työssä tutkitaan gluonin Debye-massaa, ja sen aika- ja miehityslukudis- tribuutioriippuvuutta käyttäen klassista väridynamiikkaa kahdessa paikkaulot- tuvuudessa. Työssä tutkitaan myös ominaista liikemääräskaalaa ja miehitys- lukudistribuutioita. Gluonin Debye-massa määritetään sovittamalla suora glu- onien dispersiorelaatioon pienellä liikemäärällä. Tuloksia verrataan termisestä kenttäteoriasta johdetun kaavan ennusteisiin. Aluksi tutustutaan raskasionifysiikkaan liittyvään viitekehykseen. Tämän jälkeen kerrataan nopeasti klassinen Yang-Mills teoria jatkumossa ja hilalla. Käydään läpi Fourier kiihdytetty Coulombin mitan kiinnitysmenetelmä yk- sityiskohtaisesti jatkumossa ja hilalla. T…

high energy physics phenomenologygauge theorynon-abelian plasmalattice gauge theorynuclear theoryclassical chromodynamicsfysiikkaweak couplingnon-abelian lattice gauge theoryhigh energy physicsquark gluon plasma
researchProduct

Cross-Linked Imidazolium Salts as Scavengers for Palladium.

2014

Five imidazolium-based materials have been synthesised and used for the first time as palladium scavengers. Radical reactions of suitable bis-vinylimidazolium salts led to a series of insoluble materials through homo-polymerisation, immobilisation with a 3-mercaptopropyl-modified silica gel or co-polymerisation with ethylene glycol dimethylacrylate. These materials were screened as palladium scavengers with a set of palladium(0) and palladium(II) compounds in different solvents and at different starting amounts of palladium. In many cases, residual amounts of palladium were lower than 5 ppm, as requested for the manufacture of active pharmaceutical ingredients and fine chemicals. The applic…

inorganic chemicalsActive ingredientSilica gelchemistry.chemical_elementGeneral ChemistrySettore CHIM/06 - Chimica OrganicaScavenger (chemistry)chemistry.chemical_compoundchemistrySuzuki reactionIonic liquidOrganic chemistryEthylene glycolcross-coupling imidazolium salts ionic liquids palladium supported catalystsPalladiumChemPlusChem
researchProduct

Unprecedented Palladium-Catalyzed Cross-Coupling Reaction of α-Bromo Sulfoxides with Boronic Acids

2003

[reaction: see text] A new Suzuki-type palladium-catalyzed reaction of boronic acids with alpha-bromo sulfoxides has been developed using a protocol similar to the well-documented reaction of boronic acids with aryl halides. Both cross-coupling and homocoupling processes were observed. The best yields in cross-coupling products were obtained when the presence of oxygen was carefully excluded using degassed solvents. The oxidative addition palladium complex intermediate could be isolated and characterized by X-ray single-crystal diffraction.

inorganic chemicalsChemistryArylOrganic Chemistrychemistry.chemical_elementHalideGeneral MedicineBiochemistryOxidative additionOxygenCoupling reactionCatalysischemistry.chemical_compoundSuzuki reactionPolymer chemistryOrganic chemistryPhysical and Theoretical ChemistryPalladiumOrganic Letters
researchProduct

3,4′,5,5′-Tetramethoxy-2′-methylbiphenyl-4-ol

2019

The asymmetric unit of the title compound, C17H20O5, contains two independent molecules, A and B, with similar geometries [dihedral angles between the phenyl rings = 56.19 (8) and 54.98 (7)°, respectively]. Intramolecular O—H...O hydrogen bonds occur in both molecules. In the crystal, the A molecules form [1\overline{1}0] chains linked by O—H...O hydrogen bonds from the hydroxyl group to one of the methoxy O atoms. The B molecules form O—H...O hydrogen bonds to the hydroxyl O atoms of the A molecules and thus act as fixed spacers between the chains of molecule A. Some weak C—H...O contacts are also present.

inorganic chemicalsbiaryl systemcrystal structurebiology010405 organic chemistryHydrogen bondMeth-Crystal structureDihedral angle010402 general chemistrybiology.organism_classification01 natural scienceshumanities0104 chemical sciencesCrystalchemistry.chemical_compoundCrystallographychemistryGroup (periodic table)cross-couplinglcsh:QD901-999Tetralcsh:CrystallographyPhysics::Chemical PhysicsIUCrData
researchProduct

Thieme Chemistry Journals Awardees – Where Are They Now? Molybdenum(V)-Mediated Synthesis of Nonsymmetric Diaryl and Aryl Alkyl Chalcogenides

2017

Oxidative chalcogenation reaction using molybdenum(V) reagents provides fast access to a wide range of nonsymmetric aryl sulfides and selenides. The established protocol is tolerated by a variety of labile functions, protecting groups, and aromatic heterocycles. In particular, when labile moieties are present, the use of molybdenum(V) reagents provides superior yields compared to other oxidants.

inorganic chemicalschemistry.chemical_classificationmolybdenum pentachloridedisulfides010405 organic chemistryArylOrganic Chemistrychemistry.chemical_elementMolybdenum pentachloride010402 general chemistryoxidative coupling01 natural sciences0104 chemical scienceschemistry.chemical_compoundchemistryMolybdenumReagentcross-couplingOrganic chemistryOxidative coupling of methaneC–S bond formationAlkylSynlett
researchProduct

Novel oxybispyridylboronic acids: synthesis and study of their reactivity in Suzuki-type cross-coupling reactions

2007

Abstract This paper sets forth the synthesis of novel oxybispyridylboronic acids, which are prepared from the corresponding halo-oxybispyridines via halogen–metal exchange using n-butyllithium and treatment with triisopropylborate. A range of efficient cross-coupling reactions of these novel boronic acids with selected aryl halides is described. This strategy produces novel pyridylethers of interest in cholinergic medicinal chemistry.

inorganic chemicalschemistry.chemical_compoundchemistryArylOrganic ChemistryDrug DiscoveryOrganic chemistryHalideReactivity (chemistry)General MedicineBiochemistryCombinatorial chemistryCoupling reactionTetrahedron
researchProduct

Direct arylation of heteroaromatic compounds with congested, functionalised aryl bromides at low palladium/triphosphane catalyst loading.

2011

International audience; A new ferrocenyl triphosphane ligand associated to palladium was found to be an efficient catalyst for the direct coupling of highly congested, functionalised aryl bromides with a variety of heteroarenes. These coupling reactions can generally be performed by using a low-loading (0.1-0.5 mol%) of the catalyst. The present protocol tolerates important and useful functional groups, which allows for further elaboration into more sophisticated heterocyclic molecules. The straightforward arylation of heteroaromatic compounds with congested ortho-substituted aryl bromides may permit further convergent syntheses of diverse ligands, biologically active molecules and molecula…

inorganic chemicalschemistry.chemical_element010402 general chemistry01 natural sciencesCatalysisCoupling reactionCatalysis[ CHIM.CATA ] Chemical Sciences/Catalysischemistry.chemical_compoundMoleculeOrganic chemistryEfficient catalystaryl bromidesheterocycles010405 organic chemistryChemistryLigandArylOrganic Chemistryferrocenyl polyphosphaneGeneral Chemistry[CHIM.CATA]Chemical Sciences/Catalysispalladium0104 chemical sciencesC[BOND]H activationTriphosphanePalladium
researchProduct