Search results for " solution"

showing 10 items of 3084 documents

Cyclodextrins in polymer synthesis: photocrosslinkable films via free radical copolymerization of methylated β-cyclodextrin-complexed styrene with so…

2001

The copolymerization of a methylated-β-cyclodextrin (m-β-CD) 1:1 host-guest compound of styrene (1a) with various molar ratios of sodium 4-(acrylamido)-phenyldiazosulfonate (2) is described. The copolymerization of complex 1a with 2 was carried out in water with 2,2′-azobis(N,N′-dimethyleneisobutyramidine)-dihydrochloride as the free radical initiator at 40°C. Depending on the amount of 2 incorporated in the copolymer, water- or DMF-soluble copolymers of high molar mass were obtained. Irradiation of the copolymers with UV light in solution resulted in rapid decomposition of the azo chromophore, and irradiation of the polymers as films led to crosslinking and thus to insolubility.

chemistry.chemical_classificationAqueous solutionMolar massMaterials sciencePolymers and PlasticsGeneral Chemical EngineeringGeneral ChemistryPolymerInclusion compoundStyrenechemistry.chemical_compoundMonomerchemistryPolymer chemistryMaterials ChemistryCopolymerRadical initiatorDesigned Monomers and Polymers
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p-Nitrophenolate: A Probe for Determining Acid Strength in Ionic Liquids

2009

In order to obtain an acidity scale in room-temperature ionic liquid solutions, the protonation equilibrium of sodium p-nitrophenolate in [bm(2)im][NTf(2)] and in [bmpyrr][NTf(2)], at 298 K, has been studied by means of spectrophotometric titration. Carboxylic acids differing in both structure and in water solution strength have been used. Data collected indicate that in the analyzed ionic liquid solutions carboxylic acids are less dissociated than in water solution. Furthermore, by virtue of a mutual interaction, the studied equilibrium seems to be affected by both the nature of the ionic liquids and the carboxylic acids.

chemistry.chemical_classificationAqueous solutionMolecular StructureCarboxylic acidOrganic ChemistryInorganic chemistryCarboxylic AcidsIonic LiquidsWaterProtonationSettore CHIM/06 - Chimica OrganicaHydrogen-Ion ConcentrationNitrophenolsSolutionsAcid strengthNitrophenolchemistry.chemical_compoundchemistryIonic Liquids Carboxylic acids Acidity measurementsIonic liquidMoleculeTitrationThe Journal of Organic Chemistry
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Water-compatible molecularly imprinted polymers obtained via high-throughput synthesis and experimental design.

2003

A technique allowing high-throughput synthesis and evaluation of molecularly imprinted polymer sorbents at a reduced scale (mini-MIPs) was developed and used for the optimization of MIPs for use in pure aqueous environments. The technique incorporated a 4-port liquid-handling robot for the rapid dispensing of monomers, templates, solvents and initiator into the reaction vessels of a 96-well plate. A library of 80 polymers, each ca. 50 mg, could thus be prepared in 24 h. The MIP rebinding capacity and selectivity could be rapidly assessed in the batch mode by quantifying nonbound fractions in parallel using a UV monochromator plate reader. This allowed a complete evaluation of the binding ch…

chemistry.chemical_classificationAqueous solutionMolecularly imprinted polymerNanotechnologyGeneral ChemistryPolymerBiochemistryCatalysischemistry.chemical_compoundColloid and Surface ChemistryTemplateMonomerMolecular recognitionchemistryChemical engineeringMolecular imprintingSelectivityJournal of the American Chemical Society
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Speciation of tin(II) in aqueous solution: thermodynamic and spectroscopic study of simple and mixed hydroxocarboxylate complexes

2013

This contribution reports the results of potentiometric and Mossbauer investigations on the formation, stability, and structure of binary and ternary mono- and binuclear complexes of Sn2+ with three hydroxocarboxylic ligands (namely L = tartrate, malate, and citrate) and chloride at T = 298.15 K in different ionic media and ionic strengths (0.15 and 1.00 mol dm−3 in NaCl(aq) and 1.00 mol dm−3 in NaNO3(aq)). The stability constants of various simple Sn i H j L (2+−) and mixed Sn i H j L k Cl (2+−−) species obtained in the different experimental conditions are reported, and various speciation diagrams of the simple and mixed systems are shown in different conditions. The sequestering ability …

chemistry.chemical_classificationAqueous solutionMössbauer spectroscopyPotentiometric titrationEnthalpyInorganic chemistrySequestrationIonic bondingComputer programGeneral ChemistryChlorideCoordination chemistryCoordination complexTrigonal bipyramidal molecular geometrychemistrySettore CHIM/03 - Chimica Generale E InorganicamedicineMetal complexeSettore CHIM/01 - Chimica AnaliticaStability constantsTernary operationmedicine.drugMonatshefte für Chemie - Chemical Monthly
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Numerical Simulation of the Kinetics of Radical Decay in Single-Pulse High-Energy Electron-Irradiated Polymer Aqueous Solutions

2019

A new method for the numerical simulation of the radiation chemistry of aqueous polymer solutions is introduced. The method makes use of a deterministic approach combining the conventional homogeneous radiation chemistry of water with the chemistry of polymer radicals and other macromolecular species. The method is applied on single-pulse irradiations of aqueous polymer solutions. The speciation of macromolecular species accounts for the variations in the number of alkyl radicals per chain, molecular weight, and number of internal loops (as a consequence of an intramolecular radical-radical combination). In the simulations, the initial polymer molecular weight, polymer concentration, and do…

chemistry.chemical_classificationAqueous solutionNanogels synthesi010304 chemical physicsComputer simulationKineticsPOLY(ETHYLENE OXIDE); SYNTHETIC-POLYMERS; RADIOLYSIS; NANOGELS; DEGRADATIONSingle pulseElectronPolymerRadiation chemistry010402 general chemistry01 natural sciencesradiation chemistry0104 chemical sciencesCondensed Matter::Soft Condensed MatterchemistryChemical physicsnumerical simulation0103 physical sciencesebeam irradiationSettore CHIM/07 - Fondamenti Chimici Delle TecnologieIrradiationPhysical and Theoretical ChemistryThe Journal of Physical Chemistry A
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Improvement of solubility and biocompatibility of MnO based nanoparticles in aqueous solutions

2011

ABSTRACTMnO nanoparticles were surface modified using two different multifunctional polymers. By introducing a PEG group, the long term stability, MRI applicability and sterile filtration could be greatly improved. Furthermore, PEGylated MnO NPs were less toxic compared to non-PEGylated NPs. The results suggest that these nanoparticles are suitable for in vivo applications.

chemistry.chemical_classificationAqueous solutionNanostructureMaterials scienceChemical engineeringchemistryBiocompatibilitySurface modifiedPEG ratioNanoparticlePolymerSolubilityMRS Proceedings
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Nanoparticle Vesicles Through Self Assembly of Cyclodextrin- and Adamantyl-Modified Silica

2010

Stable nanoparticle vesicles were for the first time prepared from adamantyl- and cyclodextrin (CD)-modified silica nanoparticles forming host-guest interactions in aqueous solution. Adamantyl-functionalized nanoparticles were obtained from thiol-isocyanate reaction of thiol-modified nanoparticles with 1-adamantyl isocyanate. The CD modified silica particles were isolated from a reaction of mono-6-para-toluenesulfonyl-β-cyclodextrin with the thiol functionalized silica under microwave conditions in basic media. The obtained particles were characterized in respect of agglomeration and self-assembly behavior in aqueous solution by dynamic light scattering and transmission electron microscopy.…

chemistry.chemical_classificationAqueous solutionNanostructureMaterials sciencePolymers and PlasticsCyclodextrinVesicleOrganic ChemistryNanoparticleInclusion compoundchemistry.chemical_compoundDynamic light scatteringchemistryChemical engineeringPolymer chemistryMaterials ChemistrySelf-assemblyMacromolecular Rapid Communications
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Free energy of transfer ofn-nitroalkanes fromn-octane to water at 25�C

1983

Calorimetric determinations of the thermodynamics of transfer of nitromethane, nitroethane, 1-nitrobutane, 1-nitropentane, and 1-nitrohexane from n-octane to water at 25°C have been made. Transfer free energies calculated by four different models agree reasonably well with observations. Calculations indicate that the dipolar part of the transfer free energy depends only on the dipole moment and size of the-C−NO2 group and is independent of the length of the alkyl chain in nitroalkanes.

chemistry.chemical_classificationAqueous solutionNitromethaneBiophysicsBiochemistryDipoleTransfer (group theory)chemistry.chemical_compoundchemistryMoment (physics)NitroethanePhysical chemistryPhysical and Theoretical ChemistryMolecular BiologyAlkylOctaneJournal of Solution Chemistry
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Water-soluble, cyclodextrin-functionalized semiconductor nanocrystals: Preparation and pH-dependent aggregation and emission properties

2009

Abstract Using peramino-functionalized β-cyclodextrin molecules for phase.transfer of hydrophobic CdSe multishell nanocrystals into water, we obtained hydrophilic nanoparticles with high quantum yield (up to 50%). At pH > 9, the aqueous solution of these nanocrystals remained stable for several months. The nanoparticles showed a strong influence of the pH of the aqueous solution on the emission of the nanocrystals: the quantum yield varied reversible from ∼10% at pH=6 to ∼50% at pH=14, an effect which according to particle size characterization by dynamic light-scattering and asymmetric flow field-flow fractionation has mainly been attributed to reversible partial aggregation of the hydroph…

chemistry.chemical_classificationAqueous solutionPhotoluminescenceCyclodextrinInorganic chemistryBiophysicsQuantum yieldNanoparticleGeneral ChemistryCondensed Matter PhysicsBiochemistryAtomic and Molecular Physics and OpticschemistryNanocrystalChemical engineeringMoleculeParticle sizeJournal of Luminescence
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Metachromatic behavior of methylorange in the presence of ionenes

1994

The addition of different ionenes, polycations with defined structure and charge distances, to methylorange1 in very dilute solutions of water resulted in an observable shift of the absorption maxima from 464 nm to shorter wavelengths. The extent of this so-called metachromasy effect was found to be dependent on the nature of the hydrophobic unit of the polymer backbone. The comparison of UV/VIS spectra's of these solutions with the absorption of a film of a model substance — a dication with methylorange as counteranion — lead to the conclusion that ionenes undergo an exchange of the counteranions when added to a dilute solution of methylorange. Precipitation is slowed down, but the absorpt…

chemistry.chemical_classificationAqueous solutionPolymers and PlasticsAbsorption spectroscopyConcentration effectPolymerPhotochemistryPolyelectrolyteIonDicationColloid and Surface ChemistrychemistryMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryAbsorption (chemistry)Colloid & Polymer Science
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