Search results for "Aqueous medium"

showing 10 items of 33 documents

Dioxouranium(VI) hydrolysis at 75 and 100°C in 3.6 molkg-1 LiClO4

2008

This work concerns the acidic properties of uranyl ion UO22+ at 75 and 100 °C in 3.6 molal (molkg-1 solvent) LiClO4 aqueous medium. The investigation was carried out by a coulometric-potentiometric technique. Direct and reverse acid base titrations were carried out in order to check the achievement of actual equilibrium conditions. Moreover, in order to reveal oversaturation conditions, a further check was carried out on clean saturated hydrolyzed solutions.

Acid-base titrations check of equilibrium conditions hydrolysis in hot LiClO4 aqueous medium.Settore CHIM/01 - Chimica Analitica
researchProduct

Highlights on contemporary recognition and sensing of fluoride anion in solution and in the solid state

2012

The fluoride anion has recently gained well deserved attention among the scientific community for its importance in many fields of human activities, but also for concerns on its effect on health and the environment. Although surprisingly overlooked in systematic studies in the past, fluoride has nowadays become a topical target in the field of anion recognition. A multitude of scientific reports are published every year where the establishment of efficient and specific interaction with fluoride is sought in polar and aqueous media. Here, the emphasis is directed to a detailed description of the most interesting contemporary studies in the field, with a particular focus given to those publis…

AnionsAqueous mediumChemistryMultitudeSolid-stateMolecular ConformationWaterNanotechnologyHydrogen BondingGeneral ChemistryCrystallography X-RaySolutionschemistry.chemical_compoundFluoridesHumansEngineering ethicsFluorideta116Chemical Society Reviews
researchProduct

Beads of Acryloylated Polyaminoacidic Matrices Containing 5-Fluorouracil for Drug Delivery

2002

Spherical polymeric microparticles have been prepared by a reverse phase suspension polymerization technique. The starting polymer was alpha,beta-poly(N-2-hydroxyethyl)-DL-aspartamide (PHEA), partially derivatized with glycidylmethacrylate (GMA). PHEA-GMA copolymer (PHG) was crosslinked in the presence of N,N'-dimethylacrylamide (DMAA) or N,N'-ethylenebisacrylamide (EBA). 5-fluorouracil was incorporated into PHG-DMAA or PHG-EBA beads both during and after the crosslinking process. Swelling studies revealed a high affinity toward aqueous medium, influenced by the presence of 5-fluorouracil. The in vitro release study showed that the release rate depends on the chemical structure of the beads…

Antimetabolites AntineoplasticMaterials scienceChemical structurePharmaceutical Sciencemacromolecular substancesExcipientsDrug Delivery SystemsPhase (matter)Polymer chemistryCopolymermedicineParticle Sizechemistry.chemical_classificationCalorimetry Differential ScanningAqueous mediumdigestive oral and skin physiologytechnology industry and agricultureProteinsHydrogelsGeneral MedicinePolymerHydrogen-Ion ConcentrationMicrospheresMolecular WeightKineticsCross-Linking ReagentsAcrylateschemistryDrug deliveryMicroscopy Electron ScanningIndicators and ReagentsSuspension polymerizationFluorouracilSwellingmedicine.symptomDrug Delivery
researchProduct

Selective and Efficient Removal of Mercury from Aqueous Media with the Highly Flexible Arms of a BioMOF

2016

A robust and water-stable metal-organic framework (MOF), featuring hexagonal channels decorated with methionine residues (1), selectively captures toxic species such as CH3 Hg(+) and Hg(2+) from water. 1 exhibits the largest Hg(2+) uptake capacity ever reported for a MOF, decreasing the [Hg(2+) ] and [CH3 Hg(+) ] concentrations in potable water from highly hazardous 10 ppm to the much safer values of 6 and 27 ppb, respectively. Just like with biological systems, the high-performance metal capture also involves a molecular recognition process. Both CH3 Hg(+) and Hg(2+) are efficiently immobilized by specific conformations adopted by the flexible thioether "claws" decorating the pores of 1. T…

Aqueous medium010405 organic chemistryHexagonal crystal systemChemistryInorganic chemistrychemistry.chemical_elementBiological activityGeneral Medicine02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesMercury (element)Metalchemistry.chemical_compoundPotable waterMolecular recognitionThioethervisual_artvisual_art.visual_art_medium0210 nano-technologyAngewandte Chemie International Edition
researchProduct

Proton coupled electron transfer of ubiquinone Q2 incorporated in a self-assembled monolayer.

2011

We present a complete study of the reduction of ubiquinone Q(2) (UQ(2)) in simpler aqueous medium, over a pH range of 2.5 to 12.5. The short isoprenic chain ubiquinones (UQ(2)) were incorporated in a self-assembled monolayer. Under these conditions, the global 2e(-) electrochemical reaction can be described on the basis of a nine-member square scheme. The thermodynamic constants of the system were determined. The global 2e(-) process is controlled by the uptake of the second electron. The elementary electrochemical rate constants obtained by fitting of the experimental rate constant were k(s4) = 1.5 s(-1) for QH˙(+)(2)↔ QH(2), k(s5) = 1.5 s(-1) for QH˙↔ QH(-) and k(s6) = 1 s(-1) for Q˙(-)↔ …

Aqueous mediumChemistrySurface PropertiesUbiquinoneAnalytical chemistryGeneral Physics and AstronomyWaterSelf-assembled monolayerElectronHydrogen-Ion ConcentrationElectrochemistryElectron TransportReaction rate constantCoenzyme Q – cytochrome c reductaseMonolayerElectrochemistryThermodynamicsGoldPhysical and Theoretical ChemistryProton-coupled electron transferProtonsOxidation-ReductionPhysical chemistry chemical physics : PCCP
researchProduct

Voltammetric behavior of berenil.

1993

Abstract Berenil is reduced on mercury drops electrode in buffered aqueous media. The reduction of —N=N— group is controlled by diffusion. Polarographie waves are of analytical usefulness. The hydrogen discharge is favored by the basic centers of the molecule in Co(ll)/ammonia-buffered media.

Aqueous mediumHydrogenAnalytical chemistryPharmaceutical Sciencechemistry.chemical_elementHydrogen-Ion ConcentrationTrypanocidal AgentsMercury (element)chemistryElectrodeElectrochemistryMoleculeVoltammetryDiminazeneElectrodesOxidation-ReductionPolarographyJournal of pharmaceutical sciences
researchProduct

Interaction between nitroxyl radicals and CdTe quantum dots: Determination of fluorescence-quenching mechanisms in aqueous solution

2019

Abstract The present work characterizes the optical properties of CdTe quantum dots (CdTe QDs) after interaction with nitroxyl radicals based on steady-state and time-resolved fluorescence spectroscopy studies. QDs of different sizes were exposed to 2 different nitroxyl radicals, i.e., TEMPO and 4-amino-TEMPO radicals. A clear dependence of dynamic and static Stern-Volmer constants values, KD and KS, respectively, was observed as a function of the size of QDs used, with a change from a mostly static mechanism (for smaller QD sizes) to a dynamic mechanism predominating as the nanoparticles increase in size. All observed effects are dependent on both the concentration of the radical and the s…

Aqueous solutionAqueous mediumChemistryGeneral Chemical EngineeringRadicalGeneral Physics and AstronomyNanoparticle02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesCadmium telluride photovoltaicsFluorescence spectroscopy0104 chemical sciencesNitroxyl radicalsQuantum dot0210 nano-technologyJournal of Photochemistry and Photobiology A: Chemistry
researchProduct

Micelles of Polysoaps:  The Role of Bridging Interactions

1996

Polysoaps, hydrophilic polymers incorporating amphiphilic monomers, form intrachain micelles in aqueous media. The micelles are similar to those formed by monomeric amphiphiles but are also endowed with a swollen, starlike corona formed by the spacer chains joining the amphiphiles. Long polysoaps form strings comprising many intrachain micelles. Exchange of amphiphiles between such micelles may give rise to bridging attraction, resulting in the adoption of a collapsed configuration in which the swollen micelles are close packed into a spherical globule. Upon addition of free amphiphiles, this structure unravels in a highly nonlinear fashion. Titration by surfactants, and the resulting swell…

Aqueous solutionPolymers and PlasticsAqueous mediumOrganic ChemistryMicelleInorganic Chemistrychemistry.chemical_compoundMonomerHydrophilic polymersChemical engineeringchemistryPulmonary surfactantIntermolecular interactionAmphiphileMaterials ChemistryOrganic chemistryMacromolecules
researchProduct

Spectroscopic, radiochemical, and theoretical studies of the Ga3+-N-2-hydroxyethyl piperazine-N'-2-ethanesulfonic acid (HEPES buffer) system: evidenc…

2013

Recent reports have claimed a superior performance of HEPES buffer in comparison to alternative buffer systems for 67/68 Ga labeling in aqueous media. In this paper we report spectroscopic (1H and 71 Ga NMR), radiochemical, mass spectrometry and theoretical modeling studies on the Ga3+/HEPES system (HEPES = N-2-hydroxyethylpiperazine-N′-2-ethanesulfonic acid) performed with the aim of elucidating a potential contribution of HEPES in the 68/67 Ga radiolabeling process. Our results demonstrate that HEPES acts as a weakly but competitive chelator of Ga3+ and that this interaction depends on the relative Ga3+: HEPES concentration. A by-product formed in the labeling mixture has been identified …

Contrast MediaGallium Radioisotopes010402 general chemistryMass spectrometry01 natural sciencesHepes bufferchemistry.chemical_compoundRadiology Nuclear Medicine and imagingChelationComputer SimulationHEPESChromatographyAqueous medium010405 organic chemistrySpectrum AnalysisMagnetic Resonance Imaging0104 chemical sciences3. Good healthPiperazinechemistryModels ChemicalDrug DesignIsotope LabelingProton NMREthanesulfonic acidRadiopharmaceuticalsHEPESNuclear chemistryContrast mediamolecular imaging
researchProduct

Towards the fluorogenic detection of peroxide explosives through host-guest chemistry

2018

[EN] Two dansyl-modified beta-cyclodextrin derivatives (1 and 2) have been synthesized as host-guest sensory systems for the direct fluorescent detection of the peroxide explosives diacetone diperoxide (DADP) and triacetone triperoxide (TATP) in aqueous media. The sensing is based on the displacement of the dansyl moiety from the cavity of the cyclodextrin by the peroxide guest resulting in a decrease of the intensity of the fluorescence of the dye. Both systems showed similar fluorescent responses and were more sensitive towards TATP than DADP.

Explosive material1002macromolecular substances010402 general chemistryPhotochemistry01 natural sciencesPeroxide178chemistry.chemical_compoundpolycyclic compoundsMoietyhost–guest chemistryFluorescent sensorsHost–guest chemistrylcsh:Sciencechemistry.chemical_classificationCyclodextrinsMultidisciplinarycyclodextrinsCyclodextrinAqueous medium010405 organic chemistryperoxide explosivesFluorescence0104 chemical sciencesChemistrychemistryfluorescent sensorslcsh:QHost-guest chemistryPeroxide explosivesResearch Article
researchProduct