Search results for "Titration"

showing 10 items of 312 documents

Ion pair recognition by ditopic crown ether based bis-urea and uranyl salophen receptors

2016

ionition pair bindingcrown ethersuranyl salophensureatitraussupramolecular chemistryditopic receptorsionisidosanion bindinguranyylisalofeenitkemialliset sidoksetkruunueetteritsupramolekyylikemia¹H NMR titrationsNMR-spektroskopiaorgaaniset yhdisteetröntgenkristallografiaX-ray crystallography
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Differential regulation of hexameric and dodecameric hemocyanin from A. leptodactylus

2013

The oxygen binding properties of hemocyanins are regulated on a short time scale by effectors such as l-lactate, urate and protons, and on longer time scales by expression of the different types of subunits. For Astacus leptodactylus it was shown previously that acclimation to higher temperatures leads to increased levels of a 6-meric hemocyanin species, whereas at lower temperatures the 12-meric form prevails. Here we show that the temperature dependence of the two forms supports the idea, that the maintenance of high affinity towards oxygen is the driving force for the differential expression of these hemocyanins. Furthermore, the two different types of hemocyanin differ not only in the a…

medicine.medical_treatmentProtein subunitAllosteric regulationBiophysicschemistry.chemical_elementAstacus leptodactylusBiochemistryOxygenAnalytical ChemistryAllosteric RegulationmedicineAnimalsBinding siteMolecular BiologyBinding SitesbiologyChemistryTemperatureIsothermal titration calorimetryHemocyaninbiology.organism_classificationUric AcidOxygenBiochemistryHemocyaninsLactatesBiophysicsAnuraProtein MultimerizationProtonsOxygen bindingBiochimica et Biophysica Acta (BBA) - Proteins and Proteomics
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Inorganic Mercury Sequestration by a Poly(ethylene imine) Dendrimer in Aqueous Solution

2015

The interaction of the G-2 poly(ethylene imine) dendrimer L, derived from ammonia as initiating core, with Hg(II) and HgCl4 2− was studied in aqueous solution by means of potentiometric (pH-metric) measurements. Speciation of these complex systems showed that L is able to form a wide variety of complexes including 1:1, 2:1, 3:1 and 3:2 metal-to-ligand species, of different protonation states, as well as the anion complexes ((H7L)HgCl4) 5+ and ((H8L)HgCl4) 6+ . The stability of the metal complexes is very high, making L an excellent sequestering agent for Hg(II), over a large pH range, and a promising ligand for the preparation of functionalized activated carbons to be employed in the remedi…

mercuryImineInorganic chemistryPotentiometric titrationPharmaceutical Sciencechemistry.chemical_elementProtonationmercury dendrimers sequestration water contamination environmentArticleAnalytical Chemistrydendrimerspoly(ethylene imine)Metallcsh:QD241-441chemistry.chemical_compoundAmmoniacontaminationlcsh:Organic chemistryDendrimerDrug DiscoveryremediationPhysical and Theoretical ChemistryAqueous solutionMolecular StructureOrganic ChemistryMercury (element)chemistryChemistry (miscellaneous)visual_artPotentiometryvisual_art.visual_art_mediumMolecular MedicineEnvironmental PollutantsIminesPolyethylenesMolecules
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Opioid-induced hyperalgesia after rapid titration with intravenous morphine: Switching and re-titration to intravenous methadone.

2012

Rapid titration with intravenous morphine (IV-MO) provides fast and efficient pain relief in cancer patients with severe-excruciating pain. However, some patients, after an initially favourable response, can develop an hyperexcitated state unrelieved or worsened by further dose increments.Eighty-one patients admitted on emergency basis titrated with IV-MO were assessed.12 patients were unsuccessfully titrated with IV-MO. Switching to intravenous methadone (IV-ME) and titrating the doses proved to be successfully.In escalating opioid doses rapidly a recognition of the development of hyperalgesia should be suspected. Increasing doses of opioids may stimulate rather than inhibiting the central…

opioid switchingCancer painopioid-induced hyperalgesiaSettore MED/42 - Igiene Generale E Applicataopioid titrationAnnals of palliative medicine
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Complex technological and biological research of solutions for peritoneal dialysis

2018

Objective : The purpose of our work was to conduct technological, analytical, and biological investigations and stability studies of peritoneal dialysis (PD) solutions containing glucose and sodium lactate in single-chamber containers. Methods : Different formulations of PD solutions were prepared and sterilized at a temperature of 121 °C during 15 m. UV-spectrophotometric determination was performed using purified water as a blank. The spectra of the solutions were run in the range of 220 to 400 nm for the identification of an absorption maximum (λ max ) and measuring the absorbance at 228-230 nm and λ max before and after heat sterilization. λ max of the most PD solutions after sterilizat…

prodution5-hydroxymethylfurfuralNeutral red3kidneys cellsPotentiometric titrationSulforhodamine BPharmaceutical Sciencevero cellsSterilization (microbiology)Purified waterChlorideAbsorbancechemistry.chemical_compoundchemistryperitoneal dialysisBromidemedicine4-dideoxyglucoson-3-enPharmacology Toxicology and Pharmaceutics (miscellaneous)cell viabilityNuclear chemistrymedicine.drugInternational Journal of Applied Pharmaceutics
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High-affinity and selective detection of pyrophosphate in water by a resorcinarene salt receptor

2017

N-Alkyl ammonium resorcinarenes selectively bind pyrophosphate in pure water with an exceptionally high binding constant of up to 1.60 × 107 M–1, three orders of magnitude higher than ATP.

pyrophosphatereceptors010402 general chemistryMass spectrometry01 natural sciencesPyrophosphateChloridemolecular diagnosticschemistry.chemical_compoundmedicineresorcinarenesta116Biochemistry Biophysics and Structural Biologyta114010405 organic chemistryIsothermal titration calorimetryGeneral ChemistryResorcinarenePhosphateCombinatorial chemistryOrders of magnitude (mass)0104 chemical sciencesChemistrychemistrySelectivitymedicine.drug
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Polysubstituted ferrocenes as tunable redox mediators

2018

A series of four ferrocenyl ester compounds, 1-methoxycarbonyl- (1), 1,1’-bis(methoxycarbonyl)- (2), 1,1’,3-tris(methoxycarbonyl)- (3) and 1,1’,3,3’-tetrakis(methoxycarbonyl)ferrocene (4), has been studied with respect to their potential use as redox mediators. The impact of the number and position of ester groups present in 1–4 on the electrochemical potential E1/2 is correlated with the sum of Hammett constants. The 1/1+–4/4+ redox couples are chemically stable under the conditions of electrolysis as demonstrated by IR and UV–vis spectroelectrochemical methods. The energies of the C=O stretching vibrations of the ester moieties and the energies of the UV–vis absorptions of 1–4 and 1+–4+ c…

redox mediator010402 general chemistryElectrosynthesis01 natural sciencesMedicinal chemistryRedoxFull Research Paperlcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryRedox titrationparamagnetic NMR spectroscopylcsh:ScienceElectrochemical potential010405 organic chemistryChemistryChemical shiftOrganic Chemistryferrocenespectroelectrochemistrycyclic voltammetry0104 chemical sciencesChemistryFerroceneProton NMRlcsh:QCyclic voltammetryBeilstein Journal of Organic Chemistry
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Thermodynamic and spectroscopic study of the binding of dimethyltin(IV) by citrate at 25°C

2006

Thermodynamic (potentiometric and calorimetric) and spectroscopic ( 1 H NMR, 119 Sn Mossbauer) studies were performed in aqueous solution in order to characterize the interaction of dimethyltin(IV) cation with citrate ligand. Six species {(CH 3 ) 2 Sn(cit) - ; [(CH 3 ) 2 Sn] 2 (cit) 2 2- ; (CH 3 ) 2 Sn(cit)H 0 ; (CH 3 ) 2 Sn(cit)OH 2- ; [(CH 3 ) 2 Sn] 2 (cit)OH 0 ; [(CH 3 ) 2 Sn] 2 (cit)(OH) 2 - } were found. All the species formed in this system are quite stable and formation percentages are fairly high. For example, at pH = 7.5 and C (CH3)2Sn = C cit = 10 mmol l -1 , E% for [(CH 3 ) 2 Sn] 2 (cit)(OH) 2 - and (CH 3 ) 2 Sn(cit)OH 2- species reaches 65%. Overall thermodynamic parameters obta…

spectroscopyAqueous solutionthermodynamic propertiesdimethyltin(IV) complexesChemistryLigandStereochemistryPotentiometric titrationthermodynamic propertiethermodynamic properties; calorimetry; spectroscopy; potentiometry; dimethyltin(IV) complexesGeneral ChemistryTricarboxylateInorganic ChemistryMetalOctahedronpotentiometryvisual_artMössbauer spectroscopyvisual_art.visual_art_mediumProton NMRPhysical chemistrySettore CHIM/01 - Chimica Analiticacalorimetry
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Calcium mediated polyelectrolyte adsorption on like-charged surfaces.

2011

International audience; Monte Carlo simulations within the primitive model of calcium-mediated adsorption of linear and comb polyelectrolytes onto like-charged surfaces are described, focusing on the effect of calcium and polyion concentrations as well as on the ion pairing between polymers and calcium ions. We use a combination of Monte Carlo simulations and experimental data from titration and calcium binding to quantify the ion pairing. The polymer adsorption is shown to occur as a result of surface overcharging by Ca2+ and ion pairing between charged monomers and Ca2+. In agreement with experimental observations, the simulations predict that the polymer adsorption isotherm goes through …

titrationInorganic chemistrychemistry.chemical_element02 engineering and technologyCalcium010402 general chemistry01 natural sciencesIonQuantitative Biology::Cell BehaviorQuantitative Biology::Subcellular ProcessesinterfacesAdsorptionElectrochemistryGeneral Materials ScienceSpectroscopypolyelectrolytechemistry.chemical_classificationQuantitative Biology::BiomoleculesQuantitative Biology::Neurons and CognitionSurface Chemistry and ColloidsSurfaces and InterfacesPolymerPolymer adsorption021001 nanoscience & nanotechnologyCondensed Matter PhysicsPolyelectrolyte0104 chemical sciencesCondensed Matter::Soft Condensed Matter[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]chemistryPolyelectrolyte adsorptionChemical physicsadsorptionMonte Carlo SimulationsTitration[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]0210 nano-technologyLangmuir : the ACS journal of surfaces and colloids
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Implementation of Computer Assisted Experimental Work in Analytical Chemistry Laboratory Teaching

2019

[EN] Computer-Assisted Experimental Work (CAEW) consists in the incorporation of computer-connected apparatus in the laboratory. This is a new insight into teaching of Classical Analytical Chemistry, wherein the experiments are usually manually conducted. However, it does not represent a complete break with traditional methodology, as the design and goal of the experiment are essentially the same. In this work, we present the implementation of CAEW to a practical included in the Laboratory part of “Analytical Chemistry IV”, taught at the fourth academic year of the Degree in Chemistry: “Potentiometric titration of a mixture of iodure and chlorure with silver”. Three couples of students used…

titrationUniversityTeachingPotentiometric titrationAnalytical chemistryEducational systemsAnalytical Chemistry (journal)PrecipitationprecipitationHigher EducationchemistryteachingChemistryTitrationuniversitycomputer-assistedLearningExperimental workComputer-assistedTranscription (software)Educational systems
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