Search results for " solution"

showing 10 items of 3084 documents

Azacoronands and Azacyclophanes

2012

Azacycloalkanes and azacyclophanes are among the first macrocyclic ligands developed in the field of supramolecular chemistry. Since they are polyamines, they show dual nature in the coordination of both metal cations, when they are in the free-base form, and anionic species, when they are protonated. As a matter of fact, they played a key role in the birth of macrocyclic chemistry of transition metal complexes and anion coordination chemistry. Furthermore, azacyclophanes fostered also the birth of apolar complexation in aqueous solution, since their aromatic units act as binding sites for apolar substrates. Keywords: azacycloalkanes; azacyclophanes; metal complexes; anion complexes; apolar…

chemistry.chemical_classificationAqueous solutionChemistryStereochemistrySupramolecular chemistryProtonationCoordination complexMetalTransition metalvisual_artPolymer chemistryvisual_art.visual_art_mediumMoleculeBinding site
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Thermodynamics ofN,N,N-octylpentyldimethyl-ammonium chloride in water-urea mixtures

1997

Specific conductivities, densities, heat capacities, and enthalpies of dilution at 25‡C were measured forN,N,N-octylpentyldimethylammonium chloride (OPAC) in water-urea mixtures at various urea concentrations mu as functions of the surfactant concentration ms. From conductivity data, the cmc and the degree of the counterion dissociation Β of the OPAC micelles were calculated. The cmc increases linearly with increasingm u while Βvs. mu is a smooth concave curve. From the experimental thermodynamic data, the apparentY Φ and partialY 2 molar properties (volumes, heat capacities, and relative enthalpies) are derived as functions of mu andm s . The effect of urea on the dependences of the differ…

chemistry.chemical_classificationAqueous solutionChemistryThermodynamics of micellizationEnthalpyBiophysicsThermodynamicsBiochemistryChlorideHeat capacityDissociation (chemistry)chemistry.chemical_compoundmedicineUreaPhysical and Theoretical ChemistryCounterionMolecular Biologymedicine.drugJournal of Solution Chemistry
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Rod-Length Dependent Aggregation in a Series of Oligo(p-benzamide)-Block-Poly(ethylene glycol) Rod-Coil Copolymers

2005

The synthesis of a series of rod-coil diblock copolymers with flexible poly(ethylene oxide) chains (M n = 5 000 g mol -1 ) and rod blocks consisting of monodisperse oligo(p-benzamide)s is described. The formation of defined supramolecular aggregates in solution as well as the solid state has been analyzed. The length of the oligo(p-benzamide)s has been systematically varied from n = 1 to 7 units. The influence of n on aggregation in chloroform and aqueous solution was investigated by GPC as well as UV-vis spectroscopy. A critical aggregation length was found for chloroform (n = 5) and water (n = 4), below which no aggregation is observed under otherwise identical experimental conditions. Ag…

chemistry.chemical_classificationAqueous solutionChloroformPolymers and PlasticsEthylene oxideImidoyl chlorideOrganic ChemistryDispersityChemical modificationPolymerCondensed Matter Physicschemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryCopolymerPhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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Solution properties of polyelectrolytes

1993

Abstract Aqueous size-exclusion chromatography was used to analyse the elution behaviour of several standard ionic polymers, including poly( l -glutamic acid), sodium poly(styrene sulphonate) and poly(acrylic acid), different in nature and chain flexibility, as a function of the pH and ionic strength of the eluent. Two organic-based hydrophilic packings, Spherogel TSK PW4000 and Ultrahydrogel 250, were tested in order to select the optimal conditions of macromolecular separation, and the results obtained for each column were compared. A set of calibration graphs for the above polyions as a function of eluent pH and ionic strength were obtained and compared with those obtained for uncharged …

chemistry.chemical_classificationAqueous solutionChromatographyChemistryElutionOrganic ChemistrySize-exclusion chromatographyIonic bondingPolymerGeneral MedicineElectrostaticsBiochemistryPolyelectrolyteAnalytical ChemistryGel permeation chromatographychemistry.chemical_compoundColumn chromatographyIonic strengthSurface chargeAcrylic acidJournal of Chromatography A
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Calorimetric study on the solubilization of some primary alcohols by reversed AOT micelles

1989

A calorimetric method to evaluate, at the same time, the distribution constant and the standard enthalpy of transfer of a solute partitioned between organic phase and reversed micelles is proposed. The method was applied to the partition of methanol, 1-propanol and 1-pentanol between n-heptane and AOT reversed micelles containing water at 25°C. The results show that the distribution constant decreases as the alcohol alkyl chain length increases and that the solubilization site can change as the water content of reversed AOT micelles increases. In particular, at sufficiently high water content, methanol seems to be preferably solubilized in the aqueous pseudophase whereas 1-pentanol prefers …

chemistry.chemical_classificationAqueous solutionChromatographyChemistryEnthalpyDistribution constantInorganic chemistryBiophysicsPrimary alcoholBiochemistryMicellePartition coefficientchemistry.chemical_compoundMethanolPhysical and Theoretical ChemistryMolecular BiologyAlkylJournal of Solution Chemistry
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Chromatographic and mass spectrometric characterization of the structures of the polypeptide antibiotics samarosporin and stilbellin and identity wit…

1983

The structural identity of the polypeptide antibiotics, samarosporin I(II) and stilbellin I(II) with emerimicin IV(III) has been established by thin-layer chromatography, quantitative amino acid analysis by ion-exchange chromatography, gas-liquid chromatography of the N-pentafluoropropionyl amino acid n-propyl esters and N,O-bis-pentafluoropropionyl phenylalaninol with quartz capillaries coated with the chiral stationary phase N-propionyl-L-valine-tert-butylamide, and determination of the relative molecular masses and sequence-specific fragments by field desorption fast atom bombardment mass spectrometry. The separation of closely related sequence analogues of the above polypeptides could b…

chemistry.chemical_classificationAqueous solutionChromatographyChemistryOrganic ChemistryClinical BiochemistryPeptaibolFast atom bombardmentMass spectrometryBiochemistryAnalytical ChemistryAmino acidchemistry.chemical_compoundColumn chromatographyIsovalineMoleculeOrganic chemistryChromatographia
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Influence of dissolved humic material and ionic strength on C8 extraction of pesticides from water

1995

A mixture of twelve intermediate polarity pesticides, mostly carbamate-type, have been chromatographied on an octadecyl-silica bonded-phase column using acetonitrile-water gradient mobile phase and UV detection. Pesticides were extracted from aqueous matrix by solid-phase extraction. The extraction system consisted of a glass microcolumn containing octyl-silica solidphase conditioned with methanol and water. The elution was by acetonitrile-dichloromethane (50:50). Studies of extraction factors like volume of sample, addition of 10% sodium chloride and presence of dissolved humic material are investigated.

chemistry.chemical_classificationAqueous solutionChromatographyElutionChemistrySodiumOrganic ChemistryClinical BiochemistryExtraction (chemistry)chemistry.chemical_elementBiochemistryAnalytical ChemistryMatrix (chemical analysis)Ionic strengthHumic acidSolid phase extractionChromatographia
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Solution properties of polyelectrolytes XII. Semi-quantitative approach to mixed electrostatic and hydrophobic polymer-gel interactions

1996

Abstract Aqueous size-exclusion chromatography of polyanions, where secondary effects affect the total separation mechanism, was investigated. For elution of polyelectrolytes on inorganic silica-based supports, the electrostatic polymer-gel repulsive interactions were evaluated through the values for a hypothetical repulsion layer, X e , according to the model developed by other workers. Using a similar procedure, the existence of an effective barrier defined as X e − X h is proposed for those systems in which electrostatic repulsion and hydrophobic interactions take place simultaneously as secondary mechanisms. X h can be viewed as a measure of the “enlargement” of the geometrical pore rad…

chemistry.chemical_classificationAqueous solutionChromatographyElutionOrganic ChemistryGeneral MedicinePolymerFlory–Huggins solution theoryElectrostaticsBiochemistryPolyelectrolyteAnalytical ChemistryHydrophobic effectchemistryIonic strengthJournal of Chromatography A
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Quasi-elastic light scattering in polymer-containing microemulsion

1996

Abstract Quasi-elastic light scattering (QELS) was performed in dilute water in oil microemulsion stabilized by AOT surfactant. The water-soluble polyethylene oxide (PEO) with low molecular weight (8000) added to the microemulsion seems to be confined within the aqueous microphase, since PEO is insoluble in oil (n-heptane). The measurements by QELS of diffusion coefficient, at dilute concentrations, allow determination of the size of the droplets. The phase diagram of the microemulsion undergoes remarkable changes on addition of the polymer. The results show that at fixed R ( water surfactant ratio) the droplets decrease their size as the concentration of polymer increases. This occurrence …

chemistry.chemical_classificationAqueous solutionChromatographyHydrodynamic radiusDiffusionOrganic Chemistrytechnology industry and agriculturePolymerLight scatteringAnalytical ChemistryInorganic ChemistryReduced propertieschemistryPulmonary surfactantChemical engineeringMicroemulsionSpectroscopyJournal of Molecular Structure
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Microwave-assisted distillation of iodine for the indirect atomic absorption spectrometric determination of iodide in milk samples

2001

To complete these microwave distillation studies, a method for iodide determination in milk-type samples is proposed. The iodide contained in the sample is oxidized to iodine, which is distilled by means of microwave energy and reduced back to iodide. This iodide is combined with Hg(II) and 2,2′-dipyridyl to give an ion pair, which is selectively extracted into IBMK. Mercury is determined in the extract by ETAAS in order to determine iodide. The yield of the distillation process (100%) was evaluated using the Sandell–Kolthoff reaction. In addition, for the solvent extraction, no buffer was needed; 3/5 was the best phase ratio (organic/aqueous); 30 s was the shaking time and the extracts wer…

chemistry.chemical_classificationAqueous solutionChromatographyIodideAnalytical chemistrychemistry.chemical_elementIodineAnalytical Chemistrylaw.inventionLinear rangechemistryAshinglawStandard additionAtomic absorption spectroscopyDistillationSpectroscopyJ. Anal. At. Spectrom.
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