Search results for "Polar"

showing 10 items of 3817 documents

Binding properties of mono-(6-deoxy-6-amino)-β-cyclodextrin towards p-nitroaniline derivatives: a polarimetric study

2009

Abstract Polarimetry was used in order to investigate the formation of supramolecular complexes between mono-6-amino-β-cyclodextrin and various p-nitroaniline derivatives at two different pH values. Comparison with the behaviour of native β-cyclodextrin gave us the opportunity to consider the effect exerted by the presence of charged groups, having different solvation requirements, on the binding equilibrium. Data offer some support to the hypothesis of ‘dynamic co-inclusion’ of solvent molecules within the host–guest complex.

chemistry.chemical_classificationCyclodextrinStereochemistryOrganic ChemistrySupramolecular chemistrySolvationNitro compoundcyclodextrins polarimetric study host-guest complexes stability constantsSettore CHIM/06 - Chimica OrganicaBiochemistryInclusion compoundSolventchemistry.chemical_compoundchemistryDrug DiscoveryMoleculeAmine gas treatingTetrahedron
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Polarimetry as a useful tool for the determination of binding constants between cyclodextrins and organic guest molecules

2006

Binding constants for cyclodextrin inclusion complexes can be easily estimated by means of simple polarimetric measurements. Determinations are as reliable and accurate as those obtained by means of other more sophisticated techniques, and take advantage by the limited waste of material required. Our results are briefly compared with literature values obtained by means of different techniques.

chemistry.chemical_classificationCyclodextrinchemistryComputational chemistryOrganic ChemistryDrug DiscoveryPolarimetryAnalytical chemistryMoleculecyclodextrin polarimetry host-guest interactionsSettore CHIM/06 - Chimica OrganicaBiochemistry
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1992

A structural investigation is described of poly(L-lactic acid) by best fitting of powder X-ray diffraction patterns. The examined sample shows the already known pseudo-orthorhombic α-form, and it was possible to determine the location of the two 103 polymeric helices in the unit cell and the size distribution of the crystallites. Furthermore, a study is reported of the crystallization kinetics of the above cited polymer by light depolarization measurements in an optical microscope. The crystallization kinetic constants in bulk were evaluated in a temperature range (70–165°C) wider than that previously resulting from measurements of radial growth of spherulites.

chemistry.chemical_classificationDiffractionMaterials scienceDepolarizationPolymerAtmospheric temperature rangeKinetic energylaw.inventionCrystallographychemistryOptical microscopeChemical engineeringlawPolymer chemistryCrystalliteCrystallizationDie Makromolekulare Chemie
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Direct surface relief pattering of azo-polymers films via holographic recording

2014

In this work surface relief direct formation during holographic recording in poly (Disperse Red 1 – methacrylate) films was studied. In this material azo-dye Disperse Red 1 is covalently attached to the main polymeric chain making lateral mass transport in the film caused by a presence of light electric field direction modulation very fast and effective. Surface relief grating formation process was induced by 532 nm laser. Read-out was performed by 660 nm diode laser. Diffraction efficiencies kinetics dependence on polarization state of reading and recording beams was studied. Surface relief depth on the films was measured by AFM. Deep surface relief gratings were obtained in Poly (Dispers…

chemistry.chemical_classificationDiffractionPhysicsFabricationbusiness.industryHolographyGeneral Physics and AstronomyPolymerMethacrylateLaserlaw.inventionOpticschemistrylawElectric fieldOptoelectronicsbusinessPolarization (electrochemistry)Canadian Journal of Physics
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Multilayers of CdSe/CdS/ZnCdS Core/Wings/Shell Nanoplatelets Integrated in a Polymer Waveguide

2017

In this work, fabrication of multilayers of colloidal CdSe/CdS/ZnCdS core/wings/shell nanoplatelets (NPls) on solid substrates by layer-by-layer deposition technology is successfully demonstrated for the first time. Integration of multilayers of nanoplatelets into polymeric waveguide resulted in strong dichroism in absorption and polarization effects in photoluminescence with preferable absorption and emission of TE (horizontal) mode that evidences about in-plane orientation of NPls relative to the planar waveguide. The propagation of the excitation and emission light along the waveguide was thoroughly investigated both theoretically and experimentally for different number of NPl layers.

chemistry.chemical_classificationFabricationMaterials sciencePhotoluminescencebusiness.industry02 engineering and technologyPolymerDichroism010402 general chemistry021001 nanoscience & nanotechnologyPolarization (waves)01 natural sciencesWaveguide (optics)Atomic and Molecular Physics and Optics0104 chemical sciencesOpticschemistryNanocrystalOptoelectronicsElectrical and Electronic Engineering0210 nano-technologybusinessExcitationIEEE Journal of Selected Topics in Quantum Electronics
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Restricted and complete-active-space multiconfiguration linear response calculations of the polarizability of formamide and urea

1991

Abstract Using the polarized basis sets of Sadlej, we have carried out multiconfiguration linear response (MCLR) calculations of static and dynamic polarizabilities of water, carbon dioxide, formamide and urea. It is found that the polarized basis sets give a good description of the polarizabilities. The uncorrelates (self-consistent field) polarizabilities are in general 10% or more lower than the experimental values. The correlation as introduced in the complete-active-space (CAS) and restricted-active-space (RAS) MCLR calculations recovers the major part of this deviation.

chemistry.chemical_classificationFormamideField (physics)Basis (linear algebra)Triatomic moleculeGeneral Physics and AstronomyMolecular physicschemistry.chemical_compoundchemistryComputational chemistryPolarizabilityUreaPhysics::Atomic PhysicsComplete active spacePhysics::Chemical PhysicsPhysical and Theoretical ChemistryInorganic compoundChemical Physics Letters
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Cyclodextrin-[60]fullerene conjugates: synthesis, characterization, and electrochemical behavior

2006

Three different functionalized β-cyclodextrins (β-CDs) bearing the C60 moiety linked covalently have been prepared in good yields by reaction between the parent β-CD and [60]fullerene via 1,3-dipolar cycloaddition. These compounds have been fully spectroscopically characterized and their electrochemical behavior has been investigated. Surprisingly, the electrochemical properties of the C60 cage remain unaltered even after chemical functionalization, making these systems very appealing as supramolecular hosts for electron-transfer processes.

chemistry.chemical_classificationFullereneCyclodextrinOrganic ChemistrySupramolecular chemistrySettore CHIM/06 - Chimica OrganicaElectrochemistrycyclodextrin fullereneBiochemistryCombinatorial chemistryCycloadditionchemistryCovalent bondDrug Discovery13-Dipolar cycloadditionOrganic chemistryMoiety
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Counterion transport numbers of poly(acrylic acid)-grafted porous ion-exchange membranes as determined from current step measurements

1997

Abstract The effect of an electric current on the concentration polarization of the external bathing solutions and the permselectivity of poly(acrylic acid)-grafted porous ion-exchange membranes has been studied. The experimental approach is based on the transient behavior of the total electric potential drop through the membrane cell when a current step is imposed from external nonpolarizable electrodes. When this voltage drop is recorded as a function of time, a transition time characteristic of each membrane system is obtained. From this time, the counterion transport number for the salt solution (KClH2O) in the membrane can be obtained. The theoretical modeling is based on the time-dep…

chemistry.chemical_classificationGeneral Chemical EngineeringDrop (liquid)chemistry.chemical_compoundMembranechemistryChemical engineeringPolymer chemistryElectrodeElectrochemistryElectric potentialCounterionElectric currentAcrylic acidConcentration polarizationElectrochimica Acta
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Interactions between 2-Aminobenzothiazole and Natural Organic Matter as Evidenced by CPMAS Nitrogen-15 NMR Spectroscopy

2009

Cross-polarization magic angle spinning (CPMAS) 15N nuclear magnetic resonance (NMR) spectroscopy was used to study the interactions between 2-aminobenzothiazole (ABT) and natural organic matter in the presence of the natural enzyme laccase and synthetic air. Through the use of synthesized model compounds, we were able to confirm previous findings by CPMAS 13C NMR spectroscopy that showed the formation of covalent amide bonds. We also provide evidence of the presence of two additional H bonds between ABT and the natural organic matter. Both H bonds involved the amino and thiazole groups of ABT.

chemistry.chemical_classificationHydrogen bondSettore AGR/13 - Chimica AgrariaHASoil Science2-aminobenzothiazolenuclear magnetic resonance.Nuclear magnetic resonance spectroscopyCPMAShumic acidCarbon-13 NMRABTNMRchemistry.chemical_compoundchemistryCovalent bondMagic angle spinningOrganic chemistryOrganic mattercross-polarization magic angle spinningHPLChigh-performance liquid chromatographyThiazoleSpectroscopy
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The ionic liquid effect on the Boulton-Katritzky reaction: a comparison between substrates of different structure

2015

The mononuclear rearrangement of heterocycles, also called Boulton–Katritzky reaction, was studied in ionic liquid solution using N-(5-phenyl-1,2,4-oxadiazol-3-yl)-N′-(4-nitrophenyl)-formamidine as substrate. The investigation was carried out using piperidine as basic catalyst and several ionic liquids differing in both cation and anion structure. Kinetic data collected were compared with the ones previously reported using (Z)-phenylhydrazone of 3-benzoyl-5-phenyl-1,2,4-oxadiazole to have information about the effect due to the different structure of the alkyl chain borne on the substrate. Furthermore, data were analysed on the grounds of polarity, Kamlet–Taft solvent parameters, but taking…

chemistry.chemical_classificationIonic liquids MRH reaction base catalysisPolarity (physics)Organic ChemistryInorganic chemistrySubstrate (chemistry)Settore CHIM/06 - Chimica OrganicaBiochemistryIonCatalysisSolventchemistry.chemical_compoundchemistryDrug DiscoveryIonic liquidPhysical chemistryPiperidineAlkyl
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