Search results for " complexation"

showing 10 items of 17 documents

Recognition of oxovanadium(V) species and its separation from other metal species through selective complexation by some acyclic ligands

1998

Acyclic molecules possessing –OH (phenoxo and alkoxo type) groups and imine or amine moieties have been developed to sense the specific preference for VO3+ species. These molecules also showed a capability to quantitatively separate oxovanadium(V) species from a reaction mixture containing metal species of V, Mo, U, Fe, and Mn ions in solution. A cascade quantitative separation of VO3+ followed by cis–MoO2+2 followed by trans –UO2+2 species is demonstrated from their mixture. Synthesis and structural details of oxo-species of vanadium molybdenum and uranium are also discussed. Factors influencing the complexation of these molecules towards oxo metal species of V, Mo and U are also addressed.

Absorption SpectraPolyanilineStereochemistryMetal ions in aqueous solutionImineCis-Dioxome(Vi)Vanadiumchemistry.chemical_elementTrans-Dioxoo(Iv)Medicinal chemistryInorganic ChemistryMetalSynthesisTransmetalationchemistry.chemical_compoundOxidationElectronicMaterials ChemistryPolythiophenesMoleculeSelective ComplexationPhysical and Theoretical ChemistryConducting PolymerCis-Dioxov(V)TransmetallationChemistryReactivityChemistryRecognitionMolybdenumvisual_artvisual_art.visual_art_mediumAmine gas treatingCrystallographicPolyhedron
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Specific separation and recovery of phosphate anions by a novel NiFe-LDH/rGO hybrid film based on electroactivity-variable valence

2022

Phosphorus is a non-renewable resource. Supplies are limited and much phosphorus is currently wasted during the production and utilization process, causing concerns about future supplies and widespread environmental problems. To solve these problems, a new type of NiFe-LDH/rGO electrically switched ion-selective (ESIX) film is designed, based on the dominant mechanism of inner-sphere complexation. An ESIX process allows the NiFe-LDH/rGO hybrid film to achieve a controllably selective uptake and release of the phosphate anions. This route involves tuning potential steps to regulate the redox states of the composite film and the variable metal (e.g., Ni, Fe (II)/(III)) in coordination centers…

Adsorption capacityPhosphorusInner-sphere complexationSettore ING-IND/27 - Chimica Industriale E TecnologicaPhosphatesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialsColloid and Surface ChemistryValence state transitionSelective extractionMetalsLayered double hydroxideHydroxidesGraphitePhosphate anion
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A novel thermodynamic approach for the complexation study of toxic metal cations by a landfill leachate

2018

Landfill leachates can contaminate nearby aquifers. The hazards deriving from this contamination also depend on the chemical speciation of various contaminants. A novel approach is proposed here to face this problem from a chemical thermodynamics point of view. The complexing ability of the soluble fraction of a landfill leachate (collected from Bellolampo, Palermo, Italy) towards Pb2+, Cd2+ and Cu2+ has been investigated at T = 298.15 K in NaClaq at I = 0.1 mol dm−3. The soluble fraction of the landfill leachate was first characterized by different analytical techniques. Then, its acid–base properties were studied by ISE-H+ potentiometric titrations and modelled by the so-called diprotic-l…

Aqueous solutionChemistryPotentiometric titrationInorganic chemistry02 engineering and technologyGeneral Chemistry010501 environmental sciences021001 nanoscience & nanotechnology01 natural sciencesCatalysisMetalAnodic stripping voltammetryLandfill leachate sequestering ability complexation toxic metalsChemical thermodynamicsSequestrantvisual_artMaterials Chemistryvisual_art.visual_art_mediumTitrationSettore CHIM/01 - Chimica AnaliticaLeachate0210 nano-technology0105 earth and related environmental sciences
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Sequestration of alkyltin(IV) cations by complexation with amino-polycarboxylic chelating agents

2013

Abstract The binding capacity of four amino-polycarboxylic ligands (APCs) [nitrilotriacetate (NTA), ethylenediamine- N , N , N′ , N′ -tetraacetate (EDTA), (S,S)-ethylenediamine- N , N ′-disuccinic acid (S,S-EDDS) and diethylenetriamine- N , N , N′ , N″ , N″ -pentaacetate (DTPA)] towards mono-, di- and tri-alkyltin(IV) cations [(CH 3 )Sn 3 + , (CH 3 ) 2 Sn 2 + , (C 2 H 5 ) 2 Sn 2 + , (CH 3 ) 3 Sn + or (C 2 H 5 ) 3 Sn + ] was studied, in aqueous solutions, by ISE-H + potentiometry, at I  = 0.1 mol L − 1 (NaCl) and at T  = 298.15 K. In all the systems R x Sn (4 − x)+  − APC (R = CH 3 or C 2 H 5 ) a strong 1:1 species is formed together with protonated, hydroxo and dinuclear complexes. The valu…

Aqueous solutionComplexation in aqueous solutionStereochemistryLigandEthylenediamineProtonationAlkyltin(IV) cations; Amino-polycarboxylic ligands; Complexation in aqueous solution; Sequestration ability of complexones;Condensed Matter PhysicsMedicinal chemistryAtomic and Molecular Physics and OpticsAlkyltin(IV) cationElectronic Optical and Magnetic MaterialsIonAmino-polycarboxylic ligandchemistry.chemical_compoundSequestration ability of complexoneschemistryDiethylenetriamineMaterials ChemistryChelationSettore CHIM/01 - Chimica AnaliticaPhysical and Theoretical ChemistrySimple correlationSpectroscopy
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Inclusion complexes of Cethyl-2-methylresorcinarene and pyridine N-oxides: breaking the C–I⋯−O–N+ halogen bond by host–guest complexation

2016

C ethyl-2-Methylresorcinarene forms host–guest complexes with aromatic N-oxides through multiple intra- and intermolecular hydrogen bonds and C–H⋯π interactions. The host shows conformational flexibility to accommodate 3-methylpyridine N-oxide, while retaining a crown conformation for 2-methyl- and 4-methoxypyridine N-oxides highlighting the substituent effect of the guest. N-Methylmorpholine N-oxide, a 6-membered ring aliphatic N-oxide with a methyl at the N-oxide nitrogen, is bound by the equatorial −N–CH3 group located deep in the cavity. 2-Iodopyridine N-oxide is the only guest that manifests intermolecular N–O⋯I–C halogen bond interactions, which are broken down by the host resulting i…

Cethyl-2-methylresorcinarenekemialliset sidoksethost–guest complexationsupramolekulaarinen kemiahalogen bondmacromolecular substanceshalogeenisidospyridine N-oxides
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Host-guest complexes of conformationally flexible

2018

Host–guest complexes of C-hexyl-2-bromoresorcinarene (BrC6) with twelve potential aromatic N-oxide guests were studied using single crystal X-ray diffraction analysis and 1H NMR spectroscopy. In the solid state, of the nine obtained X-ray crystal structures, eight were consistent with the formation of BrC6-N-oxide endo complexes. The lone exception was from the association between 4-phenylpyridine N-oxide and BrC6, in that case the host forms a self-inclusion complex. BrC6, as opposed to more rigid previously studied C-ethyl-2-bromoresorcinarene and C-propyl-2-bromoresorcinarene, undergoes remarkable cavity conformational changes to host different N-oxide guests through C–H···π(host) intera…

ChemistryOrganic Chemistryresorcinarenesendo/exo complexationhost–guest chemistryFull Research PaperC–H···π Interactionsditopic receptorsaromatic N-oxidesBeilstein journal of organic chemistry
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Weighting non-covalent forces in the molecular recognition of C60. Relevance of concave–convex complementarity

2008

The relative contributions of several weak intermolecular forces to the overall stability of the complexes formed between structurally related receptors and [60]fullerene are compared, revealing a discernible contribution from concave–convex complementarity. Viruela Martin, Pedro Manuel, Pedro.M.Viruela@uv.es ; Viruela Martin, Rafael, Rafael.Viruela@uv.es ; Orti Guillen, Enrique, Enrique.Orti@uv.es

FULLERENESUNESCO::QUÍMICANon covalentBUILDING-BLOCK12-TETRACYANO-9:QUÍMICA [UNESCO]CatalysisMolecular recognitionCHEMISTRYSYSTEMSMaterials ChemistryUNESCO::QUÍMICA::Química orgánicaCARBON NANORINGSChemistryCARBON NANORINGS; BUILDING-BLOCK; FULLERENES; 11111212-TETRACYANO-910-ANTHRAQUINODIMETHANE; COMPLEXATION; DERIVATIVES; RECEPTORS; CHEMISTRY; SYSTEMSCOMPLEXATIONDERIVATIVESIntermolecular force:QUÍMICA::Química orgánica [UNESCO]Metals and AlloysRegular polygonMolecular recognition ; Concave-convex ; Stability ; C60 ; Intermolecular forcesGeneral ChemistrySettore CHIM/06 - Chimica Organica11Intermolecular forcesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsWeighting12Concave-convexbody regionsRECEPTORSC60CrystallographyChemical physicsComplementarity (molecular biology)10-ANTHRAQUINODIMETHANECeramics and CompositesMolecular recognitionStability
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Effect of high methoxyl pectin on pea protein in aqueous solution and at oil/water interface

2010

International audience; The effect of the addition of high methoxyl pectin on the stability of pea protein isolate emulsions was investigated. Except for low pectin concentrations at acidic pHs where bridging flocculation occurred the addition of pectin improved emulsion stability to pH changes and depletion flocculation induced by maltodextrin addition. The mechanism of pectin induced stability was probed by measuring protein-pectin complex formation in solution, zeta potential of the emulsions droplets and the change in surface viscoelasticity on pectin addition. The phase diagrams of pectin-pea protein isolate in solution and pectin-pea protein-stabilized emulsions were established based…

Flocculationanimal structuresfood.ingredientPolymers and PlasticsPectinEmulsion stabilitymacromolecular substancescomplex mixtureschemistry.chemical_compoundfood[SDV.IDA]Life Sciences [q-bio]/Food engineeringMaterials ChemistryZeta potential[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process EngineeringAqueous solutionChromatographyInterfacial complexationPea proteindigestive oral and skin physiologyOrganic Chemistryfood and beveragesComplex formationMaltodextrinPectinPhase diagramInterfacial elasticitychemistryChemical engineeringPlant proteinPea proteinEmulsionCarbohydrate Polymers
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Distribution of Lanthanides in Mediterranean Coastal waters

2007

Distribution and behaviour of the whole lanthanide series and yttrium in both seawater column and suspended particulate matter were investigated in coastal water located in the Central Mediterranean Sea. An area characterized by high anthropic pressure, atmospheric fallout and river input due to drainage of little local watersheds was selected. Water masses were discriminated with respect to both surrounding and depth and in relation to the processes occurring at the solid-liquid interface. We found that yttrium and Rare Earth Elements in the labile fraction of the suspended particulates result from the mixing between lithogenic material from the Sicilian basin and detrital material of Saha…

Metals Chemical speciation and complexation GeochemistrySettore GEO/08 - Geochimica E Vulcanologia
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Substitution of carcinogenic solvent dichloromethane for the extraction of volatile compounds in a fat-free model food system

2016

International audience; Dichloromethane is known as a very efficient solvent, but, as other halogenated solvents, is recognized as a hazardous product (CMR substance). The objective of the present work is to propose substitution solvent for the extraction of volatile compounds. The most important physico-chemical parameters in the choice of an appropriate extraction solvent of volatile compounds are reviewed. Various solvents are selected on this basis and on their hazard characteristics. The selected solvents, safer than dichloromethane, are compared using the extraction efficiency of volatile compounds from a model food product able to interact with volatile compounds. Volatile compounds …

MicroextractionEthyl acetate02 engineering and technologyAcetates01 natural sciencesBiochemistryAnalytical Chemistrychemistry.chemical_compound[SDV.IDA]Life Sciences [q-bio]/Food engineeringOrganic chemistrySolubilityCyclopentaneChemistry Physical[ SDV.IDA ] Life Sciences [q-bio]/Food engineeringStarchGeneral Medicine021001 nanoscience & nanotechnologySolventVolatile compounds0210 nano-technologyEthyl acetateCyclopentanesSubstitution of CMRAcetonePolysaccharidesAzeotropeDichloromethaneCyclopentaneAzeotropeAssisted extractionMethylene ChlorideVolatile Organic CompoundsEthanolChromatographyEthanolGreen extraction010401 analytical chemistryOrganic ChemistryExtraction (chemistry)Amylose complexation0104 chemical scienceschemistrySolubilityAroma compoundsCarcinogensSolventsRosemaryAmyloseMicrowaveFood AnalysisMulticriteria decision-analysis
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