Search results for "chiral"

showing 10 items of 752 documents

Photografted methacrylate-based monolithic columns coated with cellulose tris(3,5-dimethylphenylcarbamate) for chiral separation in CEC

2018

A chiral capillary monolithic column for enantiomer separation in capillary electrochromatography was prepared by coating cellulose tris(3,5-dimethylphenylcarbamate) on porous glycidyl methacrylate-co-ethylene dimethacrylate monolith in capillary format grafted with chains of [2(methacryloyloxy)ethyl] trimethylammonium chloride. The surface modification of the monolith by the photografting of [2(methacryloyloxy)ethyl] trimethylammonium chloride monomer as well as the coating conditions of cellulose tris(3,5-dimethylphenylcarbamate) onto the grafted monolithic scaffold were optimized to obtain a stable and reproducible chiral stationary phase for capillary electrochromatography. The effect o…

inorganic chemicalsCHIRAL MONOLITHIC ORGANIC COLUMNSMonolithic HPLC columnFiltration and Separation02 engineering and technology01 natural sciencesEnantioseparationAnalytical Chemistry//purl.org/becyt/ford/1 [https]chemistry.chemical_compoundCapillary electrochromatographyMonolithic hplc columnPhotografting//purl.org/becyt/ford/1.4 [https]AcetonitrileCelluloseMonolithCelluloseAcetonitrileCELLULOSE TRIS(35-DIMETHYLPHENYLCARBAMATE)ChromatographyCapillary electrochromatographygeographyCellulose tris(35-dimethylphenylcarbamate)Chromatographygeography.geographical_feature_categoryCAPILLARY ELECTROCHROMATOGRAPHYEnantiomer010401 analytical chemistryCiencias QuímicasENANTIOSEPARATIONQuímica021001 nanoscience & nanotechnologyChiral monolithic organic columns0104 chemical sciencesMonomerChemistryMonomerchemistryPhotograftingPHOTOGRAFTINGQuímica AnalíticaEnantiomer0210 nano-technologyMonolithCIENCIAS NATURALES Y EXACTAS
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Domain formation in monolayers

1995

For phospholipids at the air/water interface we demonstrate that molecular chirality in some, but not in all, cases influences the domain shapes. In other cases chirality in the head group region can cause a chiral structure considering the tail arrangement. This indicates head group ordering. Minute changes of the molecular structure may change domain morphology from circular to dendritic. This can be related to slight changes of the lattice structure. In case of a dendritic domain the chains are more tilted, the deviation from hexagonal symmetry is more pronounced, and hence the lattice anisotropy is larger. This can be understood also in view of recent simulations considering diffusion-l…

inorganic chemicalsMacromolecular SubstancesSurface PropertiesHigh Energy Physics::LatticeBiophysicsBiophysical PhenomenaDomain formationMonolayerpolycyclic compoundsheterocyclic compoundsMolecular BiologyPhospholipidsPhysics::Atmospheric and Oceanic PhysicsSurface diffusionMolecular StructureChemistryorganic chemicalsHigh Energy Physics::PhenomenologyWaterStereoisomerismCell BiologyCrystallographyMicroscopy FluorescenceDomain (ring theory)health occupationsChirality (chemistry)OilsMolecular Membrane Biology
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Amino-Acid-Based Polymerizable Surfactants for the Synthesis of Chiral Nanoparticles

2016

Amino-acid-based chiral surfactants with polymerizable moieties are synthesized, and a versatile approach to prepare particles thereof with a chiral surface functionality is presented. As an example of an application, the synthesized particles are tested for their ability as nucleating agents in the enantioselective crystallization of amino acid conglomerate systems, taking rac-asparagine as a model system. Particles resulting from chiral surfactants with different tail groups are compared and the results demonstrate that only the chiral nanoparticles made of the polymerizable surfactant are able to act efficiently as nucleation agent in enantioselective crystallization.

inorganic chemicalsMaterials sciencePolymers and PlasticsPolymersNucleationNanoparticleModel system02 engineering and technology010402 general chemistry01 natural sciencesPolymerizationlaw.inventionSurface-Active AgentsPulmonary surfactantlawMaterials ChemistryOrganic chemistryAmino AcidsCrystallizationchemistry.chemical_classificationMolecular Structureorganic chemicalsOrganic Chemistrytechnology industry and agricultureEnantioselective synthesisStereoisomerism021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical sciencesAmino acidchemistryNanoparticles0210 nano-technologyChirality (chemistry)Macromolecular Rapid Communications
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Prediction of properties of chiral compounds by molecular topology

1998

Abstract A common assumption in chemistry is that chiral behavior is associated with 3-D geometry. However, chiral information is related to symmetry, which allows the topological handling of chiral atoms by weighted graphs and the calculation of new descriptors that give a weight to the corresponding entry in the main diagonal of the topological matrix. In this study, it is demonstrated that, operating in this way, chiral topological indices are obtained that can differentiate the pharmacological activity between pairs of enantiomers. The 50% inhibitory concentration (IC50) values of the D2 dopamine receptor and the σ receptor for a group of 3-hydroxy phenyl piperidines are specifically pr…

inorganic chemicalsStereochemistryIn Vitro TechniquesMain diagonalStructure-Activity RelationshipMatrix (mathematics)PiperidinesComputational chemistryMaterials ChemistryAnimalsHypnotics and SedativesReceptors sigmaheterocyclic compoundsPhysical and Theoretical ChemistrySpectroscopyGroup (mathematics)Chemistryorganic chemicalsStereoisomerismComputer Graphics and Computer-Aided DesignDopamine D2 Receptor AntagonistsCharacter (mathematics)Models ChemicalDrug DesignCentral Nervous System StimulantsMolecular topologyEnantiomerSymmetry (geometry)Chirality (chemistry)Journal of Molecular Graphics and Modelling
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Enantioselective transport of amino acid through supported chiral liquid membranes

1993

Abstract Two chiral alcohols, nopol and (2S)-(−)-methyl-1-butanol, immobilized in the pores of a polyethylene film were used for the anantioselective transport of amino acid hydrochloride. The degree of stereoselectivity of the permeation process varied from 0.39 to 1.52 depending on both the type of the chiral membrane phase and the properties of the amino acid. The evaluation of the membrane ability to separate stereoisomers was performed by the step-by-step analysis by considering the effect of amino acids' hydrophobicity, polarity and degree of chirality. For the purpose of this paper, the chirality measure was introduced. It was demonstrated that the enantioselectivity was affected mai…

inorganic chemicalschemistry.chemical_classificationamino acidschiral discriminationStereochemistryHydrochlorideorganic chemicalsEnantioselective synthesisFiltration and SeparationPermeationBiochemistryAmino acidsupported liquid membraneschemistry.chemical_compoundMembranechemistryPhase (matter)Organic chemistryheterocyclic compoundsGeneral Materials ScienceStereoselectivityPhysical and Theoretical ChemistryChirality (chemistry)Journal of Membrane Science
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Chiral Magneto-Electrochemistry

2018

Magneto-electrochemistry (MEC) is a unique paradigm in science, where electrochemical experiments are carried out as a function of an applied magnetic field, creating a new horizon of potential scientific interest and technological applications. Over time, detailed understanding of this research domain was developed to identify and rationalize the possible effects exerted by a magnetic field on the various microscopic processes occurring in an electrochemical system. Notably, until a few years ago, the role of spin was not taken into account in the field of magneto-electrochemistry. Remarkably, recent experimental studies reveal that electron transmission through chiral molecules is spin se…

magneto-electrochemistryMaterials scienceField (physics)chirality02 engineering and technology010402 general chemistryElectrochemistryspin01 natural scienceslcsh:ChemistryMaterials Chemistrymagneto-electrochemistry; CISS; spin; chirality; spin-dependent electrochemistryPhysics::Chemical PhysicsMagnetoSpin-½Condensed matter physicsHorizon021001 nanoscience & nanotechnology0104 chemical sciencesElectronic Optical and Magnetic MaterialsMagnetic fieldlcsh:QD1-999FerromagnetismChemistry (miscellaneous)spin-dependent electrochemistryElectrode0210 nano-technologyCISS
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Characterization of the synthetic cannabinoid MDMB-CHMCZCA

2016

The synthetic cannabinoid MDMB-CHMCZCA was characterized by various spectroscopic techniques including NMR spectroscopy and tandem mass spectrometry. The synthetic sample was found to be of S-configuration by VCD spectroscopy and comparison of the data with DFT calculations, while ECD spectroscopy was found to be inconclusive in this case. The enantiomeric purity of samples from test purchases and police seizures was assessed by a self-developed chiral HPLC method.

medicine.medical_treatmentNPS010402 general chemistryTandem mass spectrometry01 natural sciencesFull Research Paperlcsh:QD241-441lcsh:Organic chemistrymedicinelcsh:Sciencechiral HPLCSpectroscopyChromatographyChemistry010401 analytical chemistryOrganic ChemistryNuclear magnetic resonance spectroscopy0104 chemical sciencesCharacterization (materials science)Chiral column chromatographyChemistryVCD spectroscopyECD spectroscopylcsh:QCannabinoidEnantiomersynthetic cannabinoidsBeilstein Journal of Organic Chemistry
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From Symmetry Breaking to Unraveling the Origin of the Chirality of Ligated Au13Cu2 Nanoclusters

2018

A general method, using mixed ligands (here diphosphines and thiolates) is devised to turn an achiral metal cluster, Au13Cu2, into an enantiomeric pair by breaking (lowering) the overall molecular symmetry with the ligands. Using an achiral diphosphine, a racemic [Au13Cu2(DPPP)3(SPy)6]+ was prepared which crystallizes in centrosymmetric space groups. Using chiral diphosphines, enantioselective synthesis of an optically pure, enantiomeric pair of [Au13Cu2((2r,4r)/(2s,4s)‐BDPP)3(SPy)6]+ was achieved in one pot. Their circular dichroism (CD) spectra give perfect mirror images in the range of 250–500 nm with maximum anisotropy factors of 1.2×10−3. DFT calculations provided good correlations wit…

nanoclusterschiralitynanohiukkaset
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Two component chiral gels: a study of properties and behavior as recognition systems

organogels diimidazolium salts chiral recognitionSettore CHIM/06 - Chimica Organica
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[60]Fullerene l -Amino Acids and Peptides: Synthesis under Phase-Transfer Catalysis Using a Phosphine–Borane Linker. Electrochemical Behavior

2017

International audience; A new method to link amino acid and peptide derivatives to [60]fullerene is described. It uses hydrophosphination with a secondary phosphine borane. First, the stereoselective synthesis of secondary phosphine borane amino acid derivatives was achieved by alkylation of phenylphosphine borane with gamma-iodo-alpha-amino ester reagents under phase transfer catalysis (PTC). Second, a sec-phosphine borane amino ester was saponified and coupled with alpha,gamma-diamino esters to afford the corresponding dipeptide derivatives in good yields. Finally, the hydrophosphination reaction of [60]fullerene by the sec-phosphine borane compounds was performed under PTC to obtain C-60…

p-chiral phosphiniteshiv-1 proteaseBoraneAlkylation010402 general chemistrychemistry01 natural scienceschemistry.chemical_compoundc60[ CHIM.ORGA ] Chemical Sciences/Organic chemistryredox propertiesOrganic chemistrytertiary phosphinesRacemizationchemistry.chemical_classificationAddition reactionbond activationDipeptide010405 organic chemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic ChemistrybuckminsterfullereneCombinatorial chemistryfullerene c-600104 chemical sciencesAmino acidchemistryPhenylphosphinederivativesPhosphine
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