Search results for "Chela"

showing 10 items of 415 documents

Bachelard, un passeur de traces

2012

International audience

[SHS.PHIL] Humanities and Social Sciences/Philosophy[ SHS.PHIL ] Humanities and Social Sciences/PhilosophyBachelardpasseur[SHS.PHIL]Humanities and Social Sciences/PhilosophytracesComputingMilieux_MISCELLANEOUS
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Cahiers Gaston Bachelard n°13, Imaginaire et interprétation : hommage à Gilbert Durand

2015

International audience

[SHS.PHIL] Humanities and Social Sciences/Philosophy[ SHS.PHIL ] Humanities and Social Sciences/PhilosophyGilbert Durandinterprétation[SHS.PHIL]Humanities and Social Sciences/PhilosophyhommageGaston BachelardComputingMilieux_MISCELLANEOUSImaginaire
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La lecture minkowskienne de Bachelard : la repoétisation de la vie dénudée

2015

International audience

[SHS.PHIL] Humanities and Social Sciences/Philosophy[ SHS.PHIL ] Humanities and Social Sciences/Philosophylecture minkowskienneBachelard[SHS.PHIL]Humanities and Social Sciences/PhilosophyrepoétisationComputingMilieux_MISCELLANEOUSvie dénudée
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Bachelard et Mircea Eliade : les figures de l'alchimiste

2008

International audience

alchimiste[SHS.DROIT]Humanities and Social Sciences/Law[SHS.DROIT] Humanities and Social Sciences/LawMircea EliadeBachelard[ SHS.DROIT ] Humanities and Social Sciences/LawComputingMilieux_MISCELLANEOUS
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Efficient synthesis of new C-functionalized macrocyclic polyamines

2010

A powerful synthetic route for the preparation of new poly-azamacrocycles, valuable precursors of bifunctional chelating agents with applications in nuclear medicine, is reported. The desired functional group was introduced onto the macro-cycle backbone during the cyclization step, thus avoiding the tedious preparation of a C-functionalized synthon. The regioselective reaction of macrocycles bearing an aminomethyl pendant arm with aldehydes is also described.

amines010402 general chemistry01 natural sciencesAldehydeChemical synthesischemistry.chemical_compoundN ligands[ CHIM.ORGA ] Chemical Sciences/Organic chemistryOrganic chemistryChelationPhysical and Theoretical ChemistryBifunctionalComputingMilieux_MISCELLANEOUSchemistry.chemical_classification010405 organic chemistryLigand[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic ChemistrySynthonRegioselectivity0104 chemical sciences3. Good healthmacrocycleschemistryFunctional groupbifunctional chelating agents
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Dipeptides of S-Substituted Dehydrocysteine as Artzyme Building Blocks: Synthesis, Complexing Abilities and Antiproliferative Properties †

2021

Background: Dehydropeptides are analogs of peptides containing at least one conjugate double bond between α,β-carbon atoms. Its presence provides unique structural properties and reaction centre for chemical modification. In this study, the series of new class of dipeptides containing S-substituted dehydrocysteine with variety of heterocyclic moieties was prepared. The compounds were designed as the building blocks for the construction of artificial metalloenzymes (artzymes). Therefore, the complexing properties of representative compounds were also evaluated. Furthermore, the acknowledged biological activity of natural dehydropeptides was the reason to extend the study for antiproliferativ…

antiproliferative activityBALB 3T3 CellsDouble bondPotentiometric titrationSulforhodamine BTriazoleAntineoplastic Agents010402 general chemistry01 natural sciencesCatalysisArticlelcsh:ChemistryInorganic ChemistryMiceStructure-Activity Relationshipchemistry.chemical_compoundElimination reactionCell Line TumorAnimalsHumansChelationCysteinePhysical and Theoretical Chemistrydehydrocysteinelcsh:QH301-705.5Molecular BiologySpectroscopyCell Proliferationchemistry.chemical_classification010405 organic chemistryOrganic ChemistryChemical modificationDipeptidesGeneral MedicineHydrogen-Ion ConcentrationCombinatorial chemistryEnzymes0104 chemical sciencesComputer Science Applicationsdehydropeptideslcsh:Biology (General)lcsh:QD1-999chemistrycomplexing agentaddition-elimination reactionDrug Screening Assays AntitumorCopperConjugateInternational Journal of Molecular Sciences
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A metal-responsive interdigitated bilayer for selective quantification of mercury( ii ) traces by surface plasmon resonance

2016

Reusable surface plasmon resonance chips allowing the quantitative and selective detection of mercury(II) ions in water at the 0.01 nM level are reported. The surface-modified gold sensor consists of a rarefied self-assembled monolayer of octanethiol topped with a Langmuir–Blodgett monolayer of an amphiphilic and highly-specific chelator. The interdigitated architecture confers to the bilayer a high packing density, surface coverage, and binding-group accessibility.

aqueous-solutionwaterAnalytical chemistrychemistry.chemical_element02 engineering and technology010402 general chemistry[ CHIM ] Chemical Sciences01 natural sciencesBiochemistryAnalytical ChemistryIonsensoroptical-detectionMonolayerAmphiphilevoltammetric determinationElectrochemistryEnvironmental Chemistry[CHIM]Chemical SciencesChelationSurface plasmon resonanceSpectroscopyimpedance spectroscopyBilayerself-assembled monolayerssprgold021001 nanoscience & nanotechnology0104 chemical sciencesMercury (element)chemistryions0210 nano-technology
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Influence of structural elements on iron(III) chelating properties in a new series of amino acid-derived monohydroxamates

2018

Abstract A series of amino acid-derived monohydroxamate compounds A1 – A7 was synthesized and characterized for their coordination properties of Fe(III). The series varies in their skeletal lengths and compositions; some compounds lack external substituents, others are substituted with external functional amino or carboxylic groups, or alternatively inert methyl. Undertaken investigations allowed the determination of stoichiometry, stability constants and spectroscopic parameters of formed ferric complexes. Incorporation of an external functional group with a dissociable proton affects the coordination behavior; the presence of carboxylic or amino groups hampers the formation of mono-, di- …

chemistry.chemical_classification010405 organic chemistryChemistryStereochemistrySiderophores010402 general chemistry01 natural sciences0104 chemical sciencesAmino acidInorganic Chemistrychemistry.chemical_compoundHydroxamatesFe(III) complexesFunctional groupPolymer chemistryMaterials ChemistrymedicineFerricChelationPhysical and Theoretical ChemistryStoichiometrymedicine.drugInorganica Chimica Acta
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Structural diversity of copper(II) amino alcoholate complexes

2017

Abstract Amino alcohols which carry both amino and hydroxyl groups in the same molecule are good chelating and bridging ligands. They have been broadly used for the preparation of copper(II) amino alcoholate complexes through the self-assembly process, which generally leads to the formation of diverse structures from mononuclear to polynuclear copper(II) clusters. There are three main factors to control the nuclearity of these clusters: (i) the molar ratio of Cu(II) to amino alcohol, (ii) the choice of the counter anions and (iii) the nature of the amino alcohol. These structures can be used as model systems in magnetic studies, allowing a better understanding about the magnetic interaction…

chemistry.chemical_classification010405 organic chemistryChemistryStereochemistrychemistry.chemical_elementAlcoholPolymer010402 general chemistry01 natural sciencesCopper0104 chemical sciencesInorganic ChemistryHydroxylationMetalchemistry.chemical_compoundvisual_artPolymer chemistryMaterials Chemistryvisual_art.visual_art_mediumMoleculeChelationPhysical and Theoretical ChemistryLiterature surveyCoordination Chemistry Reviews
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Copper(II) and nickel(II) complexes of pyridylamido hexadentate ligands: chemical speciation and spectroscopic studies

2003

Abstract Two novel potentially hexadentate ligands, 1,10-(2-bis picolinamide)-4,7-diazadecane (pycdpnen) and 1,8-bis(2-picolinamide)-3,6-dioxaoctane (pycdado) have been synthesised as their hydrochloride salt; its protonation constants and the stability constants of the copper(II) and nickel(II) chelates have been determined by potentiometry. Amide groups deprotonation permits the formation of [MLH −1 ] + species in all cases, while only pycdado gives [MLH −2 ] species. The solid complexes of copper and nickel with the neutral and the deprotonated ligands have been synthesised and characterised by IR, UV–Vis and ESR spectroscopy. The amidic groups are coordinated through the oxygen atoms in…

chemistry.chemical_classification010405 organic chemistryHydrochlorideInorganic chemistrychemistry.chemical_elementSalt (chemistry)Protonation[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesCopper0104 chemical sciencesInorganic ChemistryNickelchemistry.chemical_compoundDeprotonationchemistryAmidePolymer chemistryMaterials ChemistryChelation[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUS
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