Search results for " solution"

showing 10 items of 3084 documents

Soft Nanoonions: A Dynamic Overview onto Catanionic Vesicles Temperature-Driven Transition.

2020

Catanionic vesicles are emerging interesting structures for bioapplications. They self-generate by a pairing of oppositely charged ionic surfactants that assemble into hollow structures. Specifically, the anionic-cationic surfactant pair assumes a double-tailed zwitterionic behavior. In this work, the multilamellar-to-unilamellar thermal transition of several mixed aqueous systems, with a slight excess of the anionic one, were investigated. Interestingly, it was found that the anionic counterion underwent a dissociation as a consequence of a temperature increase, leading to the mentioned thermal transition. The present work proposed the spectroscopic techniques, specifically multinuclear NM…

Ionic bonding02 engineering and technology01 natural sciencesDissociation (chemistry)nanoreservoirslcsh:ChemistryDiffusionPulmonary surfactantNanoreservoirlcsh:QH301-705.5SpectroscopyMicelleschemistry.chemical_classificationMicroscopyAqueous solutionMicroscopy ConfocalVesiclediffusionTemperatureSodium Dodecyl SulfateGeneral Medicine021001 nanoscience & nanotechnologyComputer Science ApplicationsChemical physicsDrug deliveryCetrimonium Compoundsmicroscopy0210 nano-technologyAnionsMaterials science010402 general chemistryCatanionic vesicles; Diffusion; Microscopy; Nanoreservoirs; NMRCatalysisPhase TransitionArticleInorganic ChemistrySurface-Active AgentsCationsPhysical and Theoretical ChemistryMolecular BiologyNuclear Magnetic Resonance BiomolecularNanotubes CarbonOrganic ChemistryCatanionic vesicleNMR0104 chemical scienceslcsh:Biology (General)lcsh:QD1-999chemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoPairingcatanionic vesiclesCounterionInternational journal of molecular sciences
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Anomalous and Not-So-Common Behavior in Common Ionic Liquids and Ionic Liquid-Containing Systems

2019

This work highlights unexpected, not so well known responses of ionic liquids and ionic liquid-containing systems, which are reported in a collective manner, as a short review. Examples include: (i) Minima in the temperature dependence of the isobaric thermal expansion coefficient of some ILs; (ii) Viscosity Minima in binary mixtures of IL + Molecular solvents; (iii) Anomalies in the surface tension within a family of ILs; (iv) The constancy among IL substitution of Cp/Vm at and around room temperature; (v) ILs as glass forming liquids; (vi) Alternate odd-even side alkyl chain length effects; (vii) Absolute negative pressures in ILs and IL-containing systems; (viii) Reversed-charged ionic l…

Ionic bondingThermodynamicsReview02 engineering and technology010402 general chemistry01 natural sciencesLower critical solution temperatureodd-even effectsThermal expansionionic liquidslcsh:ChemistrySurface tensionchemistry.chemical_compoundViscosityLCSTsurface tensionAlkylchemistry.chemical_classificationreversed charge ILsunusual behaviorGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesChemistrylcsh:QD1-999chemistrythermal expansion coefficientviscosityIonic liquidIsobaric process0210 nano-technologyFrontiers in Chemistry
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Mössbauer effect study of the electronic ground state of iron(II) in [57FexM1−x(bipy)3](ClO4)2 (M = Mn, Ni, Zn) and [57FexM1−x(phen)3](ClO4)2 (M = Ni…

1980

Earlier work in our laboratory on the effect of metal dilution on the 5T2(Oh ⇌ 1A1(Oh) equilibrium in polycrystalline spin crossover systems of iron(II) has shown that the relative stability of the high spin state, 5T2(Oh), at a given temperature, increases markedly with decreasing iron concentration. These results have initiated the present work. Using 57Fe Mossbauer spectroscopy, we have investigated the electronic ground state of iron(II) in the highly diluted solid solutions [FexM1−xL3] with L = bipy, M = Mn, Ni, Zn, x ≲ 0.005 and L = phen, M = Ni, Zn, x ≲ 0.005. Although the critical field potential (Vc) of the pure iron complexes, which are known to be low spin, is reported to be not …

Ionic radiusSpin statesChemistryInorganic chemistryAnalytical chemistryQuadrupole splittingInorganic ChemistryMetalSpin crossovervisual_artMössbauer spectroscopyMaterials Chemistryvisual_art.visual_art_mediumPhysical and Theoretical ChemistryGround stateSolid solutionInorganica Chimica Acta
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Radiation-Engineered Functional Nanoparticles in Aqueous Systems.

2015

Controlled synthesis of nanoscalar and nanostructured materials enables the development of novel functional materials with fine-tuned optical, mechanical, electronic, magnetic, conductive and catalytic properties that are of use in numerous applications. These materials have also found their potential use in medicine as vehicles for drug delivery, in diagnostics or in combinations thereof. In principle, nanoparticles can be divided into two broad categories, organic and inorganic nanoparticles. For both types of nanoparticles there are numerous possible synthetic routes. Considering the large difference in nature of these materials and the elementary reactions involved in the synthetic rout…

Ionizing radiationReaction mechanismAqueous solutionMaterials scienceIonizing Radiation Water Radiolysis Functional NanoparticlesBiomedical EngineeringNanoparticleBioengineeringNanotechnologyGeneral ChemistryRadiation chemistryCondensed Matter PhysicsWater radiolysisNanomaterialsParticleGeneral Materials ScienceReactivity (chemistry)IrradiationSettore CHIM/07 - Fondamenti Chimici Delle TecnologieFunctional nanoparticles.Journal of nanoscience and nanotechnology
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Physico-chemical state influences in vitro release profile of curcumin from pectin beads

2014

International audience; Curcumin is a polyphenolic compound with diverse effects interesting to develop health benefit products but its formulation in functional foods or in food supplement is hampered by its poor water solubility and susceptibility to alkaline conditions, light, oxidation and heat. Encapsulation of curcumin could be a mean to overcome these difficulties. In this paper, curcumin was encapsulated by ionotropic gelation method in low methoxyl pectin beads associated with different surfactants: Solutol®, Transcutol® and sodium caseinate. After encapsulation, physico-chemical properties of encapsulated curcumin such as its solubility, physical state, tautomeric forms and encaps…

Ionotropic gelation methodfood.ingredientCurcuminPectinChemical PhenomenaChemistry Pharmaceutical02 engineering and technologyMicelleFLIM studiesMatrix (chemical analysis)03 medical and health scienceschemistry.chemical_compoundColloid and Surface ChemistryfoodAnimals[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyPhysical and Theoretical ChemistrySolubility030304 developmental biology0303 health sciencesAqueous solutionChromatographyCalorimetry Differential ScanningChemistryStereoisomerismSurfaces and InterfacesGeneral MedicineIn vitro release021001 nanoscience & nanotechnologyMicrospheresBody FluidsRatsSolventKineticsMicroscopy FluorescenceSolubilityPolyphenolCurcuminPectinsEncapsulation0210 nano-technologyPhysico-chemical stateBiotechnology
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Donnan equilibrium of ionic drugs in pH-dependent fixed charge membranes: theoretical modeling.

2002

Abstract We have studied theoretically the partition equilibrium of a cationic drug between an electrolyte solution and a membrane with pH-dependent fixed charges using an extended Donnan formalism. The aqueous solution within the fixed charge membrane is assumed to be in equilibrium with an external aqueous solution containing six ionic species: the cationic drug (DH + ), the salt cations (Na + and Ca 2+ ), the salt anion (Cl − ), and the hydrogen and hydroxide ions. In addition to these mobile species, the membrane solution may also contain four fixed species attached to the membrane chains: strongly acid sulfonic groups (SO 3 − ), weakly acid carboxylic groups in dissociated (COO − ) a…

IonsDonnan potentialAqueous solutionStereochemistryChemistryInorganic chemistryMembranes ArtificialElectrolyteHydrogen-Ion ConcentrationModels TheoreticalPermeabilitySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialsPartition coefficientHydrophobic effectsymbols.namesakeColloid and Surface ChemistryMembranePharmaceutical PreparationsPartition equilibriumsymbolsCalciumSaltsSemipermeable membraneJournal of colloid and interface science
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Self-consistent continuum solvation (SCCS): the case of charged systems.

2013

The recently developed self-consistent continuum solvation model (SCCS) [O. Andreussi, I. Dabo, and N. Marzari, J. Chem. Phys. 136, 064102 (2012)] is applied here to charged species in aqueous solutions. Describing ions in solution represents a great challenge because of the large electrostatic interactions between the solute and the solvent. The SCCS model is tested over 106 monocharged species, both cations and anions, and we demonstrate its flexibility, notwithstanding its much reduced set of parameters, to describe charged species in solution. Remarkably low mean absolute errors are obtained with values of 2.27 and 5.54 kcal/mol for cations and anions, respectively. These results are co…

IonsModels MolecularAqueous solutionChemistryMetal ions in aqueous solutionImplicit solvationStatic ElectricitySolvationGeneral Physics and AstronomyWaterElectrostaticsIonSolventSolvation shellChemical physicsComputational chemistryQuantum TheoryThermodynamicsPhysical and Theoretical ChemistryThe Journal of chemical physics
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Do zwitterionic species exist in the non-enzymatic peptide bond formation?

2012

The use of proper computational methods and models has allowed answering the controversial question of whether zwitterionic species exist in the mechanism of peptide bond synthesis in aqueous solution. In fact, the different conformations of zwitterionic species open the door to different mechanistic paths.

IonsModels MolecularAqueous solutionChemistryMetals and AlloysGeneral ChemistryZwitterionicCombinatorial chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsPeptide bondNon enzymaticMaterials ChemistryCeramics and CompositesQuantum TheoryThermodynamicsPeptide bondOrganic chemistryPeptidesChemical Communications
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Long-ranged and soft interactions between charged colloidal particles induced by multivalent coions

2015

Forces between charged particles in aqueous solutions containing multivalent coions and monovalent counterions are studied by the colloidal probe technique. Here, the multivalent ions have the same charge as the particles, which must be contrasted to the frequently studied case where multivalent ions have the opposite sign as the substrate. In the present case, the forces remain repulsive and are dominated by the interactions of the double layers. The valence of the multivalent coion is found to have a profound influence on the shape of the force curve. While for monovalent coions the force profile is exponential down to separations of a few nanometers, the interaction is much softer and lo…

Ionschemistry.chemical_classificationValence (chemistry)Aqueous solutionLatexSurface PropertiesForce profileChemistryStatic ElectricityGeneral ChemistrySilicon DioxideCondensed Matter PhysicsCharged particleIonColloidal probe techniqueCrystallographyColloidal particleChemical physicsddc:540Colloids[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]CounterionComputingMilieux_MISCELLANEOUS
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Bright Blue Phosphorescence from Cationic Bis-Cyclometalated Iridium(III) Isocyanide Complexes

2012

We report new bis-cyclometalated cationic indium(III) complexes [((CN)-N-boolean AND)(2)Ir(CN-tert-Bu)(2)](CF3SO3) that have tert-butyl isocyanides as neutral auxiliary ligands and 2-phenylpyridine or 2-(4'-fluoropheny1)-R-pyridines (where R is 4-methoxy, 4-tert-butyl, or 5-trifluoromethyl) as (CN)-N-boolean AND ligands. The complexes are white or pale yellow solids that show irreversible reduction and oxidation processes and have a large electrochemical gap of 3.58-3.83 V. They emit blue or bluegreen phosphorescence in liquid/solid solutions from a cyclometalating-ligand-centered excited state. Their emission spectra show vibronic structure with the highest-energy luminescence peak at 440-…

Ir(Iii) ComplexesIsocyanideCationic polymerizationchemistry.chemical_elementEmitting Electrochemical-CellsExcited-State PropertiesElectroluminescent DevicesPhotochemistryAncillary LigandsInorganic Chemistrychemistry.chemical_compoundchemistryExcited stateEfficient BlueIii ComplexesMetal-ComplexesEmission spectrumIridiumPhysical and Theoretical ChemistryPhosphorescenceLuminescenceTurn-On TimesPhotophysical PropertiesSolid solutionInorganic Chemistry
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