Search results for "chiral [model]"

showing 10 items of 83 documents

Catalytic enantioselective aza-Reformatsky reaction with seven-membered cyclic imines dibenzo[b,f][1,4]oxazepines

2017

A catalytic enantioselective aza-Reformatsky reaction is reported with cyclic dibenzo[b,f][1,4]oxazepines and ethyl iodoacetate leading to the synthesis of chiral ethyl 2-(10,11-dihydrodibenzo[b,f][1,4]oxazepin-11-yl)acetate derivatives with excellent yields and high enantioselectivities (up to 98% yield and 97 : 3 er) using a readily available diaryl prolinol L4 as the chiral ligand and Me2Zn as the zinc source under an air atmosphere. Furthermore, different transformations were carried out with the corresponding chiral β-amino esters, preserving in all cases the optical purity.

010405 organic chemistryStereochemistryOrganic ChemistryEthyl iodoacetateChiral ligandEnantioselective synthesis010402 general chemistry01 natural sciences0104 chemical sciencesCatalysisProlinolReaccions químiqueschemistry.chemical_compoundchemistryYield (chemistry)Reformatsky reactionEnantiomeric excessQuímica orgànica
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Scattering Studies with Low-Energy Kaon-Proton Femtoscopy in Proton-Proton Collisions at the LHC

2020

The study of the strength and behaviour of the antikaon-nucleon ($\mathrm{\overline{K}N}$) interaction constitutes one of the key focuses of the strangeness sector in low-energy Quantum Chromodynamics (QCD). In this letter a unique high-precision measurement of the strong interaction between kaons and protons, close and above the kinematic threshold, is presented. The femtoscopic measurements of the correlation function at low pair-frame relative momentum of (K$^+$ p $\oplus$ K$^-$ $\overline{\mathrm{p}}$) and (K$^-$ p $\oplus$ K$^+$ $\overline{\mathrm{p}}$) pairs measured in pp collisions at $\sqrt{s}$ = 5, 7 and 13 TeV are reported. A structure observed around a relative momentum of 58 Me…

:Kjerne- og elementærpartikkelfysikk: 431 [VDP]Protonchiral dynamicsGeneral Physics and Astronomyhiukkasfysiikkanucl-ex01 natural sciencesHigh Energy Physics - ExperimentHigh Energy Physics - Experiment (hep-ex)ALICELHC HBTCorrelation functionHBT[PHYS.HEXP]Physics [physics]/High Energy Physics - Experiment [hep-ex]scattering [p p]correlation functionKaon-ProtonNuclear Experiment (nucl-ex)Nuclear ExperimentNuclear ExperimentQuantum chromodynamicsPhysicsLarge Hadron ColliderPhysicsstrong interactionCHIRAL DYNAMICSVDP::Kjerne- og elementærpartikkelfysikk: 431SIGMA-HYPERON PRODUCTIONddc:3. Good healthPRIRODNE ZNANOSTI. Fizika.p interactions:Nuclear and elementary particle physics: 431 [VDP]CERN LHC CollNUCLEON INTERACTIONSVDP::Nuclear and elementary particle physics: 431P INTERACTIONSIsospinLHC5000 GeV-cms/nucleon 7000 GeV-cms/nucleon 13000 GeV-cms/nucleonpp collisionsParticle Physics - Experimentp p: scatteringStrong interactionLAMBDA(1405)Kaon-Proton Femtoscopy pp collisions LHCFOS: Physical sciences[PHYS.NEXP]Physics [physics]/Nuclear Experiment [nucl-ex]Physics and Astronomy(all)Strangenesslambda(1405)114 Physical sciencesALICE; femtoscopyp-pNuclear physicsMomentumALICE LHC High-Energy Physicschiral [model]strangenessnucleon interactionsKaon-Proton ; Femtoscopy ; p-pfemtoscopyquantum chromodynamics0103 physical sciencesNuclear Physics - Experimentddc:530010306 general physicsNuclear Physicsanti-K nucleon: interactionhep-exHigh Energy Physics::PhenomenologySIGMA-HYPERON PRODUCTION; NUCLEON INTERACTIONS; CHIRAL DYNAMICS; P INTERACTIONS; LAMBDA(1405)interaction [anti-K nucleon]mass differenceNATURAL SCIENCES. Physics.Kaon-Proton Femtoscopysigma-hyperon productionHigh Energy Physics::Experimentmodel: chiralexperimental results
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Catalytic Enantioselective Aza-Reformatsky Reaction with Cyclic Imines

2016

A catalytic highly enantioselective aza-Reformatsky reaction with cyclic aldimines and ketimines for the synthesis of chiral b-amino esters with good yields and excellent enantioselectivities is reported.Areadily available diaryl prolinol is used as a chiral ligand, ZnMe2 as a zinc source and ethyl iodoacetate as reagent in the presence of air atmosphere. The reaction with cyclic ketimines generates a quaternary stereocenter with excellent levels of enantioselectivity. Furthermore, five-membered N-sulfonyl ketimines were used as electrophiles with good enantiomeric excesses, under the optimized reaction conditions. Moreover, several chemical transformations were performed with the chiral b-…

AldimineEthyl iodoacetateBeta-amino ester010402 general chemistry01 natural sciencesCatalysisReaccions químiquesStereocenterchemistry.chemical_compoundCatàlisiAsymmetric catalysisOrganic chemistryheterocyclic compoundsReformatsky reactionchemistry.chemical_classification010405 organic chemistryOrganic ChemistryChiral ligandEnantioselective synthesisGeneral Chemistry0104 chemical sciencesProlinolCyclic ketiminesZincchemistryReformatsky reactionFISICA APLICADAReagentQuímica orgànicaChemistry - A European Journal
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Input of P, N-(phosphanyl, amino)-ferrocene hybrid derivatives in late transition metals catalysis

2018

International audience; Unequally functionalized ferrocenes give access to valuable hemilabile reactivity in catalytic reaction. We address the synthesis of hybrid (P, N)-ferrocenyl compounds for which recent catalytic breakthrough applications have been reported, transversely in late transition metals chemistry. Palladium, nickel, rhodium, iridium, and emerging iron and gold catalysis are illustrated from selected examples, which include CC bond formation from cross-coupling and polymerization, allylic substitution, cyanation, hydroformylation, CH arylation and silylation and hydrogenation reactions.

Allylic rearrangementnickel-complexesAminophosphinesethylene oligomerizationchemistry.chemical_elementHomogeneous catalysispbeta-ketoestersCyanation[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryn ligands01 natural sciencesRhodiumCatalysisInorganic ChemistryPolymer chemistryoxazoline-containing ligandsMaterials ChemistryOrganic chemistry[CHIM]Chemical SciencesReactivity (chemistry)Physical and Theoretical ChemistryPolyfunctionalized ligandsferrocenyl ligands010405 organic chemistryasymmetric catalysisHemilabile hybridsHomogeneous catalysischiral ligandssimple ketones0104 chemical scienceschemistrystructural-characterizationFerroceneHydroformylationPalladiumLate transition metals
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On-surface Synthesis of a Chiral Graphene Nanoribbon with Mixed Edge Structure.

2020

Abstract Chiral graphene nanoribbons represent an important class of graphene nanomaterials with varying combinations of armchair and zigzag edges conferring them unique structure‐dependent electronic properties. Here, we describe the on‐surface synthesis of an unprecedented cove‐edge chiral GNR with a benzo‐fused backbone on a Au(111) surface using 2,6‐dibromo‐1,5‐diphenylnaphthalene as precursor. The initial precursor self‐assembly and the formation of the chiral GNRs upon annealing are revealed, along with a relatively small electronic bandgap of approximately 1.6 eV, by scanning tunnelling microscopy and spectroscopy.

Band gapAnnealing (metallurgy)530 Physics010402 general chemistry01 natural sciencesBiochemistrygraphene nanoribbonNanomaterialslaw.inventionlawchiral edge540 Chemistrypolycyclic aromatic hydrocarbonon-surface synthesisSpectroscopyQuantum tunnelling010405 organic chemistryChemistryGraphenescanning tunneling microscopy and spectroscopyCommunicationOrganic ChemistryGeneral ChemistryCommunications0104 chemical sciencesZigzagChemical physics570 Life sciences; biologyGraphene nanoribbonsChemistry, an Asian journal
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Chiral anomalies in even and odd dimensions

1985

Odd dimensional Yang-Mills theories with an extra ‘topological mass” term, defined by the Chern-Simons secondary characteristic, are discussed. It is shown in detail how the topological mass affects the equal time charge commutation relations and how the modified commutation relations are related to non-abelian chiral anomalies in even dimensions. We also study the SU(3) chiral model (Wess-Zumino model) in four dimensions and we show how a gauge invariant interaction with an external SU(3) vector potential can be defined with the help of the Chern-Simons characteristic in five dimensions.

Chiral anomalyPhysicsHigh Energy Physics::Lattice53C80Statistical and Nonlinear PhysicsCharge (physics)Gauge (firearms)58G25Wess–Zumino modelHigh Energy Physics::TheoryChiral modelInvariant (mathematics)81E20Mathematical PhysicsGauge anomalyMathematical physicsVector potential
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Total Synthesis of (±)-Oxalicumone C and Chiral Resolution and Elucidation of Its Absolute Configuration

2014

The racemic total synthesis, the chiral resolution, and the elucidation of the absolute configuration of the natural product oxalicumone C were investigated. The goal was achieved by a synthetic strategy beginning with the synthesis of a 5-hydroxy-7-methylchromone precursor. Further modification possibilities were achieved by introduction of a vinyl moiety into the chromone, which was based on a selective iodination step in the 3-position. Further transformations furnished the racemic natural product. To determinate the absolute configuration of naturally occurring oxalicumone C, both enantiomers were separated by chiral HPLC. Comparison of the calculated and experimental vibrational circul…

Chiral column chromatographyCircular dichroismChemistryStereochemistryOrganic ChemistryVibrational circular dichroismAbsolute configurationTotal synthesisPhysical and Theoretical ChemistryEnantiomerChiral derivatizing agentChiral resolutionEuropean Journal of Organic Chemistry
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Ligands P-stéréogéniques dérivés du calix[4]arène. Synthèses et applications en catalyse asymétrique

2010

We were interested in synthesis of P-stereogenic ligands derived from calix[4]arene and in their application in asymmetric catalysis. Mono et diphosphines were prepared on the upper rim of the macrocyle starting from the mono or dianion of the calix[4]arene and chlorophosphines borane or the oxazaphospholidine borane complex. The best selectivity was obtained by reaction of the dianion with the oxazaphospholidine borane complex leading to a bisaminophosphine borane. After acidolysis with HCl giving the corresponding bischlorophosphine and reaction with organolithium reagents, diphosphines diborane were obtained with good yields (40 à 60 %). X-ray structures of the prepared ligands confirmed…

Chiral ligandsStereoselective synthesisAsymetric Catalysis[ PHYS.COND.CM-GEN ] Physics [physics]/Condensed Matter [cond-mat]/Other [cond-mat.other]Synthèses stéréosélectivesCalix[4]areneMacrocyclePhosphines P-stéréogéniquesCatalyse asymétrique[CHIM.OTHE] Chemical Sciences/Other[PHYS.COND.CM-GEN] Physics [physics]/Condensed Matter [cond-mat]/Other [cond-mat.other][PHYS.COND.CM-GEN]Physics [physics]/Condensed Matter [cond-mat]/Other [cond-mat.other][ CHIM.OTHE ] Chemical Sciences/OtherP-stereogeniques PhosphinesLigands chiraux[CHIM.OTHE]Chemical Sciences/Other
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Implementation of local chiral interactions in the hyperspherical harmonics formalism

2021

With the goal of using chiral interactions at various orders to explore properties of the few-body nuclear systems, we write the recently developed local chiral interactions as spherical irreducible tensors and implement them in the hyperspherical harmonics expansion method. We devote particular attention to three-body forces at next-to-next-to leading order, which play an important role in reproducing experimental data. We check our implementation by benchmarking the ground-state properties of $^3$H, $^3$He and $^4$He against the available Monte Carlo calculations. We then confirm their order-by-order truncation error estimates and further investigate uncertainties in the charge radii obta…

Chiral perturbation theoryNuclear TheoryTruncation error (numerical integration)Formalism (philosophy)Materials Science (miscellaneous)QC1-999Monte Carlo methodBiophysicsGeneral Physics and AstronomyFOS: Physical sciences01 natural scienceschiral effective field theoryNuclear Theory (nucl-th)Theoretical physics0103 physical sciencesPhysical and Theoretical Chemistry010306 general physicsMathematical PhysicsExotic atomPhysics010308 nuclear & particles physicsPhysicsOrder (ring theory)light nucleiCharge (physics)Harmonicshyperspherical harmonicsnuclear interactionsab-initio theory
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Synthesis, Chirality, and Magnetic Properties of Bimetallic Cyanide-Bridged Two-Dimensional Ferromagnets

2006

The assembly of hexacyanoferrate(III) anions and nickel(II) bis-diamino complexes of the chiral ligand trans-cyclohexane-1,2-diamine (trans-chxn) yields cyanide-bridged two-dimensional ferromagnets of the general formula [Ni(trans-chxn)2]3[Fe(CN)6]2‚2H2O. Their crystal structure is built from cyanide-bridged bimetallic planes separated by the bulky chxn ligands, giving rise to a large interlayer distance ( d ) 11.7 A). These materials order ferromagnetically at the Curie temperature TC ) 14 K. AC susceptibility measurements evidence an unusual magnetic behavior below TC, with a marked frequency dependence. A thorough magnetic analysis demonstrates that this complex behavior is due to the pi…

CrystallographyMagnetic anisotropyDomain wall (magnetism)FerromagnetismChemistryGeneral Chemical EngineeringChiral ligandMaterials ChemistryCurie temperatureGeneral ChemistryCrystal structureChirality (chemistry)Bimetallic stripChemistry of Materials
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