Search results for "tammet"

showing 10 items of 409 documents

Access to Phylogeny from Voltammetric Fingerprints of Seeds: the Apsparagus Case

2016

A methodology for characterizing vegetal taxonomic groups from the voltammetric fingerprints of polyphenolic components of seeds is described. It is based on recording the voltammetric response of microparticulate films deposited on glassy carbon electrodes from seed extracts using different organic solvents. The obtained responses in contact with aqueous electrolytes provided characteristic voltammetric profiles at the level of genera/subgenera and/or families using bivariant and multivariant chemometric methods. The voltammograms of 14 species from 5 different families provided family-characteristic patterns. Analysis of voltammetric responses for a set of 20 species of the Asparagus genu…

MicroextractionChromatographybiologyChemistryAsparagusVoltammetry of microparticles010401 analytical chemistryfood and beverages02 engineering and technologyAqueous electrolyteGlassy carbon021001 nanoscience & nanotechnologybiology.organism_classification01 natural sciences0104 chemical sciencesAnalytical ChemistryChemotaxonomyChemometric techniquesChemotaxonomyPhylogeneticsElectrochemistryMyrsiphyllumAsparagusSubgenus0210 nano-technology
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Electrochemical detection of the 2-isobutyl-3-methoxypyrazine model odorant based on odorant-binding proteins: The proof of concept

2014

Abstract We developed an electrochemical assay for the detection of odorant molecules based on a rat odorant-binding protein (rOBP3). We demonstrated that rOBP3 cavity binds 2-methyl-1,4-naphtoquinone (MNQ), an electrochemical probe, as depicted from the decrease of its electrochemical signal, and deduced the dissociation constant, Kd MNQ  = 0.5(± 0.2) μM. The amount of MNQ displaced from rOBP3 by 2-isobutyl-3-methoxypyrazine (IBMP), a model odorant molecule, was measured using square-wave voltammetry. The release of MNQ by competition led to an increase of the electrochemical response. In addition, this method allowed determination of the dissociation constant of rOBP3 for IBMP, Kd IBMP  =…

Models MolecularIsothermal microcalorimetryOdorant bindingBiophysicsAnalytical chemistryCalorimetryReceptors OdorantElectrochemistryBinding CompetitiveCaffeic AcidsElectrochemistryPhysical and Theoretical ChemistryVoltammetryBinding SitesChemistryVitamin K 3Electrochemical TechniquesGeneral MedicineCombinatorial chemistryFluorescenceRecombinant ProteinsDissociation constantImmobilized ProteinsSpectrometry FluorescencePyrazinesCalibrationTitrationBiosensorBioelectrochemistry
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Cubane-Type Mo3FeS44+,5+ Complexes Containing Outer Diphosphane Ligands: Ligand Substitution Reactions, Spectroscopic Studies, and Electronic Structu…

2012

A general protocol to access Mo(3)FeS(4)(4+) clusters selectively modified at the Fe coordination site is presented starting from the all-chlorine Mo(3)(FeCl)S(4)(dmpe)(3)Cl(3) (1) [dmpe = 1,2-bis(dimethylphosphane-ethane)] cluster and tetrabutylammonium salts (n-Bu(4)NX) (X = CN(-), N(3)(-), and PhS(-)). Clusters Mo(3)(FeX)S(4)(dmpe)(3)Cl(3) [X = CN(-) (2), N(3)(-) (3), and PhS(-) (4)] are prepared in high yield, and comparison of geometric and redox features upon modification of the coordination environment at the Fe site at parity of ligands at the Mo sites is also presented. The existence of the cubane-type Mo(3)FeS(4)(4+,5+) redox couple is demonstrated by cyclic voltammetry and for co…

Models MolecularPhosphinesIronInorganic chemistryMolecular ConformationElectronsInorganic chemicalsLigandsRedoxlaw.inventionInorganic Chemistrychemistry.chemical_compoundlawOrganometallic CompoundsReactionsDiphosphanePhysical and Theoretical ChemistryElectron paramagnetic resonanceMolybdenumLigandMagnetic PhenomenaSpectrum AnalysisDiphosphane ligandsMagnetic susceptibilityCrystallographychemistryCubaneQuantum TheoryDensity functional theoryCyclic voltammetryOxidation-ReductionSulfurInorganic Chemistry
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Exploring the redox reactivity of magnesium porphine. Insight into the origins of electropolymerisation.

2010

International audience; Magnesium(II) porphine, MgP (1), was synthesised according to the Lindsey procedure allowing to isolate and crystallise 1-formyldipyrromethane (2) as a synthetic intermediate. Unprecedented Xray diffraction studies revealed multiple intermolecular associations in the crystal between neighbouring units of 2, namely hydrogen bond and CH … π. The electrochemical behaviour of 1 was examined by means of cyclic voltammetry. In oxydation, two well-defined and distinct steps are assigned to macrocycle concerned electron transfers yielding initially the π-cation radical and π dication, respectively. The highly reactive dication condenses neutral magnesium porphine to form a d…

Models MolecularPorphyrinsInorganic chemistrychemistry.chemical_element010402 general chemistryElectrochemistryCrystallography X-Ray01 natural sciencesRedoxOligomerInorganic Chemistrychemistry.chemical_compound[CHIM.ANAL]Chemical Sciences/Analytical chemistryPolymer chemistryElectrochemistryOrganometallic Compounds[CHIM.COOR]Chemical Sciences/Coordination chemistryReactivity (chemistry)Magnesium[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryHydrogen bondChemistryMagnesiumHydrogen Bonding[CHIM.MATE]Chemical Sciences/Material chemistry0104 chemical sciencesDicationCyclic voltammetryOxidation-ReductionDalton transactions (Cambridge, England : 2003)
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Unusual Formation of a Stable 2D Copper Porphyrin Network

2013

Copper(II) 5,15-bis(diethoxyphosphoryl)-10,20-diphenylporphyrin was obtained and characterized by means of cyclic voltammetry, electron paramagnetic resonance, Fourier transform infrared, and UV-visible spectroscopy. Three crystalline forms were grown and studied by means of X-ray diffraction methods (single crystal and powder). The highly electron-withdrawing effect of phosphoryl groups attached directly to the porphyrin macrocycle results in a self-assembling process, with formation of a stable 2D coordination network, which is unusual for copper(II) porphyrins. The resulting 2D structure is a rare example of an assembly based on copper(II) porphyrins where the copper(II) central metal io…

Models MolecularPorphyrinschemistry.chemical_element010402 general chemistryPhotochemistry01 natural scienceslaw.inventionInorganic ChemistryMetalchemistry.chemical_compoundlawMolecule[CHIM]Chemical SciencesPhysical and Theoretical ChemistryPhosphorylationElectron paramagnetic resonanceSpectroscopyComputingMilieux_MISCELLANEOUS010405 organic chemistryElectron Spin Resonance SpectroscopyPorphyrinCopper0104 chemical sciencesCrystallographychemistryvisual_artvisual_art.visual_art_mediumCyclic voltammetrySingle crystalCopper
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Detection of Hypoxanthine from Inosine and Unusual Hydrolysis of Immunosuppressive Drug Azathioprine through the Formation of a Diruthenium(III) Syst…

2021

Hypoxanthine (hpx) is an important molecule for both biochemistry research and biomedical applications. It is involved in several biological processes associated to energy and purine metabolism and has been proposed as a biomarker for a variety of disease states. Consequently, the discovery and development of systems suitable for the detection of hypoxanthine is pretty appealing in this research field. Thus, we have obtained a stable diruthenium (III) compound in its dehydrated and hydrated forms with formula [{Ru(&micro

Models MolecularPurinelcsh:BiotechnologyClinical BiochemistryMolecular Conformationchemistry.chemical_elementinosine02 engineering and technology010402 general chemistry01 natural sciencesArticleHydrolysischemistry.chemical_compoundX-Ray DiffractionLimit of Detectionlcsh:TP248.13-248.65medicineMolecule6-mercaptopurinerutheniumInosinePurine metabolismHypoxanthineazathioprineHydrolysisGeneral Medicine021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical sciencesRutheniumchemistryPurineshypoxanthineMicroscopy Electron ScanningbiomarkerCyclic voltammetry0210 nano-technologyImmunosuppressive Agentsmedicine.drugBiosensors
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Ferrocenyl glycopeptides as electrochemical probes to detect autoantibodies in multiple sclerosis patients' será

2008

Abstract Glycopeptide analogues of CSF114(Glc), modified at N-terminus with new ferrocenyl carboxylic acid and a new ferrocenyl-thiphosphino amino acid, were used to implement a new electrochemical biosensor for autoantibody detection in multiple sclerosis. The ferrocenyl moiety of these "electrochemical probes" did not affect autoantibody recognition both in SP-ELISA and in inhibition experiments. By electrochemical monitoring the interactions of the modified peptides Fc-CSF114(Glc) and 4-FcPhP(S)Abu-CSF114(Glc) with the autoantibodies, we demonstrated that autoantibodies could be detected with a sensitivity comparable to ELISA method. The new electrochemical probes can be proposed to char…

Multiple SclerosisMetallocenesCarboxylic acidBiophysics010402 general chemistry01 natural sciencesBiochemistryBiomaterialsImmunoenzyme Techniques[ CHIM.CATA ] Chemical Sciences/CatalysismedicineElectroanalytical methodElectrochemistryMoietyHumansFerrous CompoundsAntigensComputingMilieux_MISCELLANEOUSAutoantibodieschemistry.chemical_classification010405 organic chemistryChemistryMultiple sclerosisOrganic ChemistryAutoantibodyGlycopeptidesGeneral Medicine[CHIM.CATA]Chemical Sciences/Catalysismedicine.diseaseGlycopeptide0104 chemical sciences3. Good healthAmino acidSolutionsBiochemistryMolecular ProbesGoldCyclic voltammetryChromatography Liquid
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Evaluation of adsorption ability of Cyclodextrin-Calixarene Nanosponges towards Pb2+ ion in aqueous solution

2021

Abstract Different cyclodextrin-calixarene nanosponges (CyCaNSs) have been characterized by means of FFC-NMR relaxometry, and used as sorbents to remove Pb2+ ions from aqueous solutions. Considering that the removal treatments may involve polluted waters with different characteristics, the adsorption experiments were performed on solutions without and with the addition of background salts, under different operational conditions. The adsorption abilities and affinities of the nanosponges towards Pb2+ ions were investigated by measuring the metal ion concentration by means of Inductively Coupled Plasma Emission Spectroscopy (ICP-OES) and Differential Pulse Anodic Stripping Voltammetry (DP-ASV…

NanospongesPolymers and PlasticsEnvironmental remediationSpeciationInorganic chemistryRemediation02 engineering and technology010402 general chemistry01 natural sciencesIonMetalAdsorptionCalixareneMaterials ChemistrySettore CHIM/01 - Chimica Analiticachemistry.chemical_classificationAqueous solutionCyclodextrinOrganic ChemistrySettore CHIM/06 - Chimica Organica021001 nanoscience & nanotechnologyAdsorption; FFC-NMR relaxometry; Lead; Nanosponges; Remediation; Speciation0104 chemical sciencesAnodic stripping voltammetrychemistryFFC-NMR relaxometryLeadvisual_artvisual_art.visual_art_mediumAdsorption0210 nano-technology
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Preparation of Graphene Nanoribbons (GNRs) as an Electronic Component with the Multi-walled Carbon Nanotubes (MWCNTs)

2015

Abstract Carbon nanotubes (CNTs) have a well-defined nanostructure to exhibit high electrical conductivity and chemical stability, and have been used as an advanced material to make electrodes of super-capacitor. Graphene nanoribbons (GNRs), as manufactured by unzipping the CNTs, have more flexible adjustable electrical properties than CNTs, and are regarded an even more promising material for super-capacitor electrodes. This paper presented a series of attempts to prepare GNRs by chemically treating multi-walled carbon nanotubes (MWCNTs); this is, an Oxidation-Reduction method was tried to make GNRs by unzipping MWCNTs longitudinally. Efforts were made in various trials to find conditions …

NanostructureMaterials scienceScanning electron microscopeNanotechnologyMulti-walled carbon nanotubesGraphene nanoribbons (GNRs)General MedicineCarbon nanotubeElectrochemical performanceCharacterization (materials science)law.inventionTransmission electron microscopylawElectrodeCyclic voltammetryPreparation methodEngineering(all)Graphene nanoribbonsProcedia Engineering
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Electrochemical tomato (Solanum lycopersicum L.) characterisation using contact probe in situ voltammetr

2015

[EN] An in situ electrochemical contact probe methodology for characterising tomato samples is proposed. It is based on the record of the voltammetric response of antioxidant compounds when glassy carbon electrodes are inserted into the pericarp of fresh tomato specimens cut in half. The absence of pretreatment and in situ sampling avoid sample contamination and the oxidation of air-sensitive compounds thus increasing the representativity of the analytical data relative to conventional electrochemical analysis. Characteristic voltammetric responses recorded for such compounds, including rutin, chlorogenic acid, naringenin, naringenin chalcone and ascorbic acid have been obtained. A positive…

NaringeninIn situ electrochemistryTECNOLOGIA DE ALIMENTOSAnalytical chemistryAscorbic AcidGlassy carbonAntioxidantsAnalytical ChemistryRutinchemistry.chemical_compoundChlorogenic acidSolanum lycopersicumPhenolsVoltammetryNaringenin chalconeChromatographybiologyfood and beveragesGeneral MedicineElectrochemical TechniquesAscorbic acidbiology.organism_classificationTomato varietieschemistrySolanumFood SciencePolyphenolic compounds
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