Search results for " chiral"

showing 10 items of 80 documents

Modification of Dzyaloshinskii-Moriya-Interaction-Stabilized Domain Wall Chirality by Driving Currents

2018

We measure and analyze the chirality of Dzyaloshinskii-Moriya-interaction (DMI) stabilized spin textures in multilayers of $\mathrm{Ta}|{\mathrm{Co}}_{20}{\mathrm{F}}_{60}{\mathrm{B}}_{20}|\mathrm{MgO}$. The effective DMI is measured experimentally using domain wall motion measurements, both in the presence (using spin-orbit torques) and absence of driving currents (using magnetic fields). We observe that the current-induced domain wall motion yields a change in effective DMI magnitude and opposite domain wall chirality when compared to field-induced domain wall motion (without current). We explore this effect, which we refer to as current-induced DMI, by providing possible explanations for…

Current (mathematics)Current-inducedGeneral Physics and AstronomyFOS: Physical sciencesSpin currents02 engineering and technology-01 natural sciencesMeasure (mathematics)Spin current0103 physical sciencesMesoscale and Nanoscale Physics (cond-mat.mes-hall)ddc:55022 Física010306 general physicsDomain Wall ChiralitySpin-½PhysicsCondensed matter physicsfísicaCondensed Matter - Mesoscale and Nanoscale PhysicsTheoretical predictionsPhysics021001 nanoscience & nanotechnologyMagnetic fieldDomain wall (magnetism)Dzyaloshinskii-Moriya-interaction (DMI)0210 nano-technologyChirality (chemistry)Field-induced domainDzyaloshinskii-Moriya-interaction
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Novel σ1 antagonists designed for tumor therapy: Structure – activity relationships of aminoethyl substituted cyclohexanes

2021

Abstract Depending on the substitution pattern and stereochemistry, 1,3-dioxanes 1 with an aminoethyl moiety in 4-position represent potent σ1 receptor antagonists. In order to increase the stability, a cyclohexane ring first replaced the acetalic 1, 3-dioxane ring of 1. A large set of aminoethyl substituted cyclohexane derivatives was prepared in a six-step synthesis. All enantiomers and diastereomers were separated by chiral HPLC at the stage of the primary alcohol 7, and their absolute configuration was determined by CD spectroscopy. Neither the relative nor the absolute configuration had a large impact on the σ1 affinity. The highest σ1 affinity was found for cis-configured benzylamines…

DU145 tumor cellsCachannelPrimary alcohol01 natural sciencesAminoethylcyclohexanes; Antagonistic activity; Biotransformation; Ca; 2+; influx assay; Calculated free energy of binding; CD spectroscopy; Chiral HPLC; DU145 tumor cells; Inhibition of human prostate tumor cell growth; Lipophilicity; Molecular dynamics simulations; Molecular interactions; per-residue binding free energy; Selectivity; Stereochemistry; Structure affinity relationships; Voltage gated Ca; 2+; channel; σ receptors; σ; 1; receptor affinityInhibition of human prostate tumor cell growthStereochemistryDrug DiscoveryMoietySelectivityBiotransformationσ receptor0303 health sciencesChemistryAminoethylcyclohexanesCD spectroscopyAbsolute configurationAminoethylcyclohexaneMolecular interactionGeneral MedicineAntagonistic activityper-residue binding free energyreceptor affinityLipophilicityVoltage gated CaStereochemistry12+Calculated free energy of bindingRetinal ganglion03 medical and health sciencesσMolecular dynamics simulationChiral HPLCLipophilicityMolecular interactionsStructure affinity relationship030304 developmental biologyPharmacologyDU145 tumor cellinflux assayMolecular dynamics simulations010405 organic chemistryOrganic ChemistryDiastereomer0104 chemical sciencesChiral column chromatographyσ receptorsStructure affinity relationshipsEnantiomerEuropean Journal of Medicinal Chemistry
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πNscattering in relativistic baryon chiral perturbation theory reexamined

2011

We have analyzed pion-nucleon scattering using the manifestly relativistic covariant framework of infrared regularization up to $\mathcal{O}({q}^{3})$ in the chiral expansion, where $q$ is a generic small momentum. We describe the low-energy phase shifts with a similar quality as previously achieved with heavy baryon chiral perturbation theory, $\sqrt{s}\ensuremath{\lesssim}1.14$ GeV. New values are provided for the $\mathcal{O}({q}^{2})$ and $\mathcal{O}({q}^{3})$ low-energy constants, which are compared with previous determinations. This is also the case for the scattering lengths and volumes. Finally, we have unitarized the previous amplitudes and as a result the energy range where data …

Elastic scatteringPhysicsNuclear and High Energy PhysicsParticle physicsChiral perturbation theoryUnitarityHeavy baryon chiral perturbation theory010308 nuclear & particles physicsScatteringHadronScattering length01 natural sciencesBaryon0103 physical sciencesNuclear Experiment010306 general physicsPhysical Review C
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Measurements of the Generalized Electric and Magnetic Polarizabilities of the Proton at LowQ2Using the Virtual-Compton-Scattering Reaction

2006

Experimental details of a virtual Compton scattering (VCS) experiment performed on the proton at the MIT-Bates out-of-plane scattering facility are presented. The VCS response functions ${P}_{LL}\ensuremath{-}{P}_{TT}/\phantom{{P}_{TT}\ensuremath{\varepsilon}}\ensuremath{\varepsilon}$ and ${P}_{LT}$ have been measured at ${Q}^{2}=0.057\phantom{\rule{0.28em}{0ex}}{\mathrm{GeV}}^{2}/{c}^{2}$. The generalized electric and magnetic polarizabilities, $\ensuremath{\alpha}({Q}^{2})$ and $\ensuremath{\beta}({Q}^{2})$, and the mean-square electric polarizability radius$\ensuremath{\langle}{r}_{\ensuremath{\alpha}}^{2}\ensuremath{\rangle}$ are obtained from a dispersion analysis of the data. The resu…

Elastic scatteringPhysicsNuclear and High Energy PhysicsProtonHeavy baryon chiral perturbation theoryScatteringHadronNuclear TheoryCompton scatteringFOS: Physical sciencesGeneral Physics and AstronomyElementary particleChirality (electromagnetism)BaryonPolarizabilityQuantum electrodynamicsDispersion (optics)Nuclear Experiment (nucl-ex)Perturbation theoryAtomic physicsNucleonNuclear ExperimentNuclear ExperimentPhysical Review Letters
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Aggregati supramolecolari di tensioattivi in fase gassosa: formazione e solubilizzazione di aminoacidi

ElettrospraySpettrometria di massa in mobilità ionicaTensioattivi chiraliAminoacidiInterazione host-guestAggregati supramolecolariSettore CHIM/02 - Chimica Fisica
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A theoretical and experimental study of the racemization process of hexaaza[5]helicenes

2014

A dynamic 1H NMR study, together with DFT calculations, of bis-([1,2,3]triazolo)[1,5-a:5′,1′-k][1,10]phenanthroline 2 has allowed to identify the ring and open forms of a new example of ring/chain tautomerism, as well as their interconversion barriers (ring/ring and ring/open). The barrier of the exchange process between the chain forms and the ring form was found higher than the 'racemization' process in the closed form, so the ring opening does not contribute to the 'racemization'. The di-1,10-methyl and di-1,10-iodo derivatives have been prepared and their properties calculated.

Helical chirality[CHIM.ORGA]Chemical Sciences/Organic chemistryStereochemistryPhenanthrolineOrganic ChemistryRing (chemistry)BiochemistryTautomer3. Good healthRacemization barrierschemistry.chemical_compoundAzahelicenesChain (algebraic topology)chemistryComputational chemistryDrug DiscoveryProton NMRDiazoimine–triazole equilibriumRacemizationTetrahedron
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Enantioselective Strecker Reaction Catalyzed by an Organocatalyst Lacking a Hydrogen-Bond-Donor Function

2007

Hydrogen bondChemistryOrganocatalysisStrecker amino acid synthesisEnantioselective synthesisOrganic chemistryGeneral ChemistryPlanar chiralityCatalysisCatalysisAngewandte Chemie International Edition
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Chiral Self‐Sorting of trans ‐Chelating Chiral Ligands upon Formation of Pd II Complexes (Eur. J. Inorg. Chem. 15/2014)

2014

Inorganic ChemistrySelf sortingchemistryStereochemistryPolymer chemistrySupramolecular chemistrychemistry.chemical_elementChelationSelf-assemblyPlanar chiralityPalladiumEuropean Journal of Inorganic Chemistry
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The importance of supramolecular reaction media in catalysis

Ionic liquids supramolecular gels ionogels chiral catalysts
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Influence of thermally induced structural transformations on the magnetic and luminescence properties of tartrate-based chiral lanthanide organic-fra…

2020

This work reports on the synthesis and characterization of five enantiomeric pairs of isostructural 3D metal-organic frameworks (MOFs) with the general formula {[Ln2(μ4-tar)2(μ-tar)(H2O)2]·xH2O}n [where Ln(iii) = Tb (Tb-L and Tb-D), Dy (Dy-L and Dy-D), Ho (Ho-L and Ho-D), Er (Er-L and Er-D) and Tm (Tm-L and Tm-D); tar = tartrate (d- or l-) and x = 3 or 4 depending on the counterpart], which possess interesting luminescence and magnetic properties. These MOFs undergo progressive and reversible dehydration processes upon controlled heating yielding three crystalline phases (Ln-L′, Ln-L′′ and Ln-L′′′). Alternating current magnetic measurements on Tb, Dy and Er-based compounds exhibit field ind…

LanthanideMaterials sciencePhotoluminescencelanthanide organic-frameworks MOF chiral circular dichroismGeneral ChemistryTartrateCrystallographychemistry.chemical_compoundchemistrySettore CHIM/03 - Chimica Generale E InorganicaMagnetMaterials ChemistryMoleculeIsostructuralEnantiomerLuminescenceJournal of Materials Chemistry C
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