Search results for " chirality"

showing 10 items of 24 documents

Dynamic formation of hybrid peptidic capsules by chiral self-sorting and self-assembly.

2014

Owing to their versatility and biocompatibility, peptide-based self-assembled structures constitute valuable targets for complex functional designs. It is now shown that artificial capsules based on β-barrel binding motifs can be obtained by means of dynamic covalent chemistry (DCC) and self-assembly. Short peptides (up to tetrapeptides) are reversibly attached to resorcinarene scaffolds. Peptidic capsules are thus selectively formed in either a heterochiral or a homochiral way by simultaneous and spontaneous processes, involving chiral sorting, tautomerization, diastereoselective induction of inherent chirality, and chiral self-assembly. Self-assembly is shown to direct the regioselectivit…

ChemistryStereochemistryProton Magnetic Resonance SpectroscopySupramolecular chemistryDynamic covalent chemistryRegioselectivityStereoisomerismGeneral ChemistryGeneral MedicineResorcinareneInherent chiralityTautomerCatalysisSelf-assemblyChirality (chemistry)Peptidesta116Angewandte Chemie (International ed. in English)
researchProduct

Induced Chirality in Confined Space on Halogen Gold Complexes

2015

The solubilization of HAuCl4 in toluene within optically active reverse micelles and lamellar structures formed by (1R,2S)-Dodecyl(2-hydroxy-1-methyl-2-phenylethyl)- dimethylammonium bromide (DMEB) has allowed us to evidence the complex phenomenology accompanying the confinement of Au salt within these nanostructures. Together with a chloride/bromide exchange process occurring in the first coordination sphere of an Au ion, UV−vis and electronic circular dichroism (ECD) spectra reveal the appearance of an induced dichroic signal attributable to Au complexes entrapped in the hydrophilic domain of the DMEB chiral nanostructures. Interestingly, change of the effective oxidation state and coordi…

Circular dichroismSupramolecular chiralityCoordination spherechirality confined space DMEBPhotochemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundGeneral EnergychemistryBromideRAY-ABSORPTION SPECTROSCOPY; BODY DISTRIBUTION-FUNCTIONS; NEAR-EDGE STRUCTURE; STABILIZED MICROEMULSIONS; SUPRAMOLECULAR CHIRALITY; CINCHONIDINE ADSORPTION; ELECTRONIC-STRUCTURES; CHIROPTICAL ACTIVITY; UNDECAGOLD CLUSTERS; CONDENSED MATTERPhysical and Theoretical ChemistryAbsorption (chemistry)SpectroscopyChirality (chemistry)Settore CHIM/02 - Chimica FisicaCoordination geometryThe Journal of Physical Chemistry C
researchProduct

Cytotoxic secondary metabolites from the endophytic fungus Aspergillus versicolor KU258497

2018

Abstract Two new isocoumarin dimers (1 and 2) and one new dihydroquinolone derivative (3) were isolated from Aspergillus versicolor, an endophyte derived from leaves of the Egyptian water hyacinth Eichhornia crassipes (Pontederiaceae), together with ten other known metabolites. Chemical structures of the isolated metabolites were determined based on HRESIMS, extensive 1D and 2D NMR spectroscopy. The relative and absolute configurations of the new natural products were established by ROESY and electronic circular dichroism (ECD) spectroscopy, respectively. The axial chirality of the isocoumarin 7,7′-homodimers (1 and 2) was deduced by TDDFT-ECD calculations. All isolated compounds were asses…

Circular dichroismbiology010405 organic chemistryChemistryStereochemistryPlant Sciencebiology.organism_classificationAntimicrobial01 natural sciencesBiochemistryEndophyte0104 chemical sciencesIsocoumarin010404 medicinal & biomolecular chemistrychemistry.chemical_compoundTermészettudományokAxial chiralityPontederiaceaeAspergillus versicolorKémiai tudományokAgronomy and Crop ScienceTwo-dimensional nuclear magnetic resonance spectroscopyBiotechnology
researchProduct

Inherently Chiral Calixarenes

1994

Due to the nonplanarity of the basic 1 n -metacyclophane system, calixarenes and resorcarenes can be transformed into molecules with inherent chirality. Various attempts to achieve this goal are reviewed. Special emphasis is given to derivatives with C n -symmetry, including derivatives of spherand calixarenes and other calixarene-like macrocycles.

Computational chemistryChemistryCalixareneOrganic chemistryMoleculeInherent chiralitySymmetry (physics)
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

Multiwall carbon-nanotube interconnects: radial effects on physical models and resistance calculations for various metal substrates

2010

Based on a model with singular attractive potential of equidistant conductive cylinders, we illustrate an approach to calculate the electron spectrum of metallic multiwall carbon nanotubes (MW CNT) with an arbitrary number of coaxial layers. We compute the number of electrically active channels, N ch , in the ideal case when all MW CNT shells are contacted to the electrodes, starting from the one-electron spectrum. The dependence of N ch on the temperature and on both the innermost and outermost shells radii allows us to discuss the potential performances of MW CNT interconnects, affecting the power dissipation of integrated circuits. Our description improves over the isolated shells model,…

Materials scienceContact resistanceShell (structure)Nanotube ChiralityNanotechnologyRadiusCarbon nanotubeDissipationMolecular physicslaw.inventionCondensed Matter::Materials SciencelawPhysics::Atomic and Molecular ClustersElectric potentialCoaxialCAS 2010 Proceedings (International Semiconductor Conference)
researchProduct

Chiral mesophases of hydrogen-bonded liquid crystals

2020

The chiral induction in hydrogen-bonded liquid crystals is investigated. The experimental study was accompanied by detailed density functional theory calculations and variable-temperature solid-state deuteron NMR measurements indicating that interactions between the linking groups of the hydrogen-bond accepting unit play a key role in the chiral induction.

Materials scienceHydrogenProcess Chemistry and TechnologyBiomedical EngineeringChemieEnergy Engineering and Power Technologychemistry.chemical_element02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesIndustrial and Manufacturing Engineering0104 chemical sciencesCrystallographychemistryDeuteriumChemistry (miscellaneous)Liquid crystalMaterials ChemistryChemical Engineering (miscellaneous)Supramolecular Chemistry Liquid Crystals Chirality Hydrogen Bonding Crystal EngineeringDensity functional theorySettore CHIM/07 - Fondamenti Chimici Delle Tecnologie0210 nano-technologyChiral induction
researchProduct