Search results for "coupling"

showing 10 items of 1862 documents

Influence of the Nature of Boron‐Doped Diamond Anodes on the Dehydrogenative Phenol‐Phenol Cross‐Coupling

2019

Boron doped diamondCoupling (electronics)chemistry.chemical_compoundMaterials sciencechemistryElectrochemistryPhenolElectrochemistryPhotochemistryCatalysisAnodeChemElectroChem
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Anodic coupling of guaiacol derivatives on boron-doped diamond electrodes.

2011

The anodic treatment of guaiacol derivatives on boron-doped diamond electrodes (BDD) provides a direct access to nonsymmetrical biphenols, which would require a multistep sequence by conventional methods. Despite the destructive nature of BDD anodes they can be exploited for chemical synthesis.

Boron doped diamondchemistry.chemical_compoundchemistryOrganic ChemistryElectrodeInorganic chemistryCoupling (piping)GuaiacolPhysical and Theoretical ChemistryDiamond electrodesBiochemistryChemical synthesisAnodeOrganic letters
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Adiabatic-antiadiabatic crossover in a spin-Peierls chain

2004

We consider an XXZ spin-1/2 chain coupled to optical phonons with non-zero frequency $\omega_0$. In the adiabatic limit (small $\omega_0$), the chain is expected to spontaneously dimerize and open a spin gap, while the phonons become static. In the antiadiabatic limit (large $\omega_0$), phonons are expected to give rise to frustration, so that dimerization and formation of spin-gap are obtained only when the spin-phonon interaction is large enough. We study this crossover using bosonization technique. The effective action is solved both by the Self Consistent Harmonic Approximation (SCHA)and by Renormalization Group (RG) approach starting from a bosonized description. The SCHA allows to an…

Bosonizationmedia_common.quotation_subjectFOS: Physical sciencesFrustrationddc:500.201 natural sciencesOmega010305 fluids & plasmasCondensed Matter - Strongly Correlated ElectronsCondensed Matter::Superconductivity0103 physical sciences[PHYS.COND.CM-SM]Physics [physics]/Condensed Matter [cond-mat]/Statistical Mechanics [cond-mat.stat-mech]010306 general physicsCondensed Matter - Statistical MechanicsSpin-½media_commonCoupling constantPhysicsStrongly Correlated Electrons (cond-mat.str-el)Statistical Mechanics (cond-mat.stat-mech)Condensed matter physicsOrder (ring theory)Renormalization groupCondensed Matter PhysicsCoupling (probability)Electronic Optical and Magnetic Materials75.10.Pq 63.70.+hCondensed Matter::Strongly Correlated Electrons[PHYS.COND.CM-SCE]Physics [physics]/Condensed Matter [cond-mat]/Strongly Correlated Electrons [cond-mat.str-el]
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Measuring High-Order Interactions in Rhythmic Processes Through Multivariate Spectral Information Decomposition

2021

Many complex systems in physics, biology and engineering are modeled as dynamical networks and described using multivariate time series analysis. Recent developments have shown that the emergent dynamics of a network system are significantly affected by interactions involving multiple network nodes which cannot be described using pairwise links. While these higher-order interactions can be probed using information-theoretic measures, a rigorous framework to describe them in the frequency domain is still lacking. This work presents an approach for the spectral decomposition of multivariate information measures, capable of identifying higher-order synergistic and redundant interactions betwee…

Brain modelingMultivariate statisticsTechnology and EngineeringGeneral Computer ScienceTime series analysiComplex systemTIME-SERIESHEART-RATETime series analysisEEG analysisInformation theoryMOTOR IMAGERYMatrix decompositionCouplingFrequency-domain analysiRedundancyelectronic oscillatorsRedundancy (engineering)General Materials ScienceNETWORKTime domainFrequency-domain analysissignal processingTEMPERATUREParametric statisticsinformation theoryPhysicsFEEDBACKGeneral Engineeringclimate dynamicsTime measurementspectral analysisTK1-9971Mathematics and Statisticshigh-order interactionsconnectivityFrequency domainCouplingsElectrical engineering. Electronics. Nuclear engineeringBiological systeminformation dynamicsCoherenceIEEE Access
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Electrochemical Synthesis of 2-Hydroxy-para-terphenyls by Dehydrogenative Anodic C–C Cross-Coupling Reaction

2019

The anodic C–C cross-coupling reaction provides fast access to a wide range of bi- and terarylic scaffolds by electrochemically mediated arylation reactions. Herein, a metal- and reagent-free electrosynthetic protocol for the synthesis of nonsymmetrical 2-hydroxy-para-teraryl derivatives is presented for the first time. It is scalable, easy to conduct, and allows the use of a broad variety of different functional groups.

C c coupling010405 organic chemistryChemistryOrganic Chemistry010402 general chemistryElectrochemistry01 natural sciencesCombinatorial chemistryCoupling reaction0104 chemical sciencesAnodeSynlett
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Visible-Light Organophotoredox-Catalyzed Synthesis of Precursors for Horner-Type Olefinations

2018

C c coupling010405 organic chemistryChemistryOrganic ChemistryPhysical and Theoretical Chemistry010402 general chemistryPhotochemistry01 natural sciences0104 chemical sciencesVisible spectrumCatalysisEuropean Journal of Organic Chemistry
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Front Cover Picture: SBA‐15/POSS‐Imidazolium Hybrid as Catalytic Nanoreactor: the role of the Support in the Stabilization of Palladium Species for C…

2019

C c couplingFront coverchemistryHeck reactionPolymer chemistrychemistry.chemical_elementGeneral ChemistryNanoreactorHeterogeneous catalysisCoupling reactionPalladiumCatalysisAdvanced Synthesis & Catalysis
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Synthese substituierter 1,4-Divinylbenzole durch doppelte Heck-Reaktion mit Ethen unter Druck

1999

Substituted 1,4-divinylbenzenes 3a–i were synthesized by twofold Heck coupling from the corresponding 1,4-dibromo) (electron withdrawing substituents) or 1,4-di-iododialkoxybenzenes 1a–i and ethene. Oligomerizations could be suppressed by increasing the pressure of ethene to 30 bar, simultaneously improving the yields of the title compounds.

C c couplingchemistry.chemical_compoundchemistryHeck reactionPolymer chemistryPolar effectchemistry.chemical_elementDivinylbenzenePalladiumBar (unit)Journal für praktische Chemie
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MoVReagents in Organic Synthesis (Eur. J. Org. Chem. 11/2016)

2016

C c couplingchemistry.chemical_compoundchemistryMolybdenumReagentOrganic Chemistrychemistry.chemical_elementOrganic chemistryOxidative coupling of methaneOrganic synthesisPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Cobalt−NHC Catalyzed C(sp2)−C(sp3) and C(sp2)−C(sp2) Kumada Cross‐Coupling of Aryl Tosylates with Alkyl and Aryl Grignard Reagents

2021

The first cobalt‐catalyzed cross‐coupling of aryl tosylates with alkyl and aryl Grignard reagents is reported. The catalytic system uses CoF3 and NHCs (NHC=N‐heterocyclic carbene) as ancillary ligands. The reaction proceeds via highly selective C−O bond functionalization, leading to the corresponding products in up to 98 % yield. The employment of alkyl Grignard reagents allows to achieve a rare C(sp2)−C(sp3) cross‐coupling of C−O electrophiles, circumventing isomerization and β‐hydride elimination problems. The use of aryl Grignards leads to the formation of biaryls. The C−O cross‐coupling sets the stage for a sequential cross‐coupling by exploiting the orthogonal selectivity of the cataly…

C(sp2)−C(sp3) cross-couplingcross-couplingC−O activationsustainabilitycobalt catalysisChemcatchem
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