Search results for "element"

showing 10 items of 13601 documents

The role of lithium, perchlorate and water during electrochemical processes in poly(3,4-ethylenedioxythiophene) films in LiClO4 aqueous solutions

2021

Abstract Thin films of poly(3,4-ethylendioxythiophene) (PEDOT) were electrochemically deposited on gold electrodes in aqueous media. The role of perchlorate, lithium, and water during the charge/discharge of PEDOT films was investigated by cyclic voltammetry together with EQCM, vis − NIR spectroscopy, and acoustic impedance, also by means of ac-electrogravimetry in a 0.1 M LiCl O 4 aqueous solutions. In this way, it has been possible to correlate the electrical, mass, color and electromechanical properties changes during the electrochemical reactions of this polymer. Both, hydrated lithium cations and perchlorate anions can act as counterions during the electrochemical reactions, however, a…

Aqueous solutionChemistryGeneral Chemical EngineeringInorganic chemistrychemistry.chemical_elementElectrochemistryLithium perchlorateAnalytical ChemistryPerchloratechemistry.chemical_compoundPEDOT:PSSElectrochemistryLithiumsense organsCyclic voltammetryPoly(34-ethylenedioxythiophene)Journal of Electroanalytical Chemistry
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An electromechanical perspective on the metal/solution interfacial region during the metallic zinc electrodeposition

2009

The difficulty of studying the metal/solution interfacial region makes the use of non-conventional measurement techniques indispensable. In this way, a careful in situ study by means of acoustic impedance techniques coupled with nano-electrogravimetric techniques allowed this interface to be monitored during the metallic zinc electrodeposition process. This paper proves the formation of a viscoelastic layer consisting of ultra-hydrated Zn(II)/Zn(I) salts as a key step in the metallic zinc electrodeposition mechanism in sulfate aqueous solutions. Surprisingly, this layer is located in the metal/solution interfacial region and not on the reaction substrate. The chloride ions effect on the met…

Aqueous solutionChemistryGeneral Chemical EngineeringInorganic chemistrychemistry.chemical_elementZincElectrochemistryMetalchemistry.chemical_compoundTransition metalvisual_artElectrogravimetrySodium sulfateElectrochemistryvisual_art.visual_art_mediumLayer (electronics)Electrochimica Acta
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Synthesis, solid state and solution studies of cobalt(II) complexes with 2-hydroxyiminopropanoic acid

2013

Abstract This paper describes the synthesis of the Zn(II) complex with H2L = 2-hydroxyiminopropanoic acid. The final structure incorporated two linear dimeric anions with two Zn2+ atoms, which are linked by a carbonate anion into a tetranuclear unit. In each dinuclear unit, the two Zn(II) ions are coordinated by three molecules of the doubly deprotonated ligand in two different coordination modes. This result is confirmed both by X-ray crystallography and by ESI-MS investigations of the crystals dissolved in water. Equilibrium studies of the zinc(II) complexes formed by H2L in aqueous solution based on independent pH-metric titrations and zinc ion-selective electrode (ISE) titrations indica…

Aqueous solutionChemistryHydrogen bondLigandInorganic chemistrychemistry.chemical_elementProtonationZincInorganic ChemistryCrystallographyDeprotonationMaterials ChemistryMoleculeTitrationPhysical and Theoretical Chemistryta116Polyhedron
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A study of dimethyltin(IV)-L-cysteinate in aqueous solution

1988

The in vivo activity of some R2Sn-L-cysteinate complexes (R = Me, Et, n-Bu) against murine P-388 leukaemia has been tested. Only the Et2Sn(IV) complex showed a marginal positive effect. Trigonal bipyramidal tin environments with two carbon (R) atoms and the sulfur atom in the equatorial plane and oxygen (carboxylate) and nitrogen (NH2) in apical positions have been proposed for the solid compexes (R = Me, Et, n-Bu, Ph) on the basis of experimental Mossbauer parameters and infrared (IR) data. Aqueous solutions of the Me2SnL-cysteinate have been studied by IR, 1H NMR and 119Sn Mossbauer spectroscopy (in frozen solution) at different pH values to identify the Me2Sn(IV) species present. At pH >…

Aqueous solutionChemistryInorganic chemistryInfrared spectroscopychemistry.chemical_elementGeneral ChemistryNuclear magnetic resonance spectroscopyInorganic ChemistryNMR spectra databaseCrystallographychemistry.chemical_compoundTrigonal bipyramidal molecular geometryDeprotonationCarboxylateTinApplied Organometallic Chemistry
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Thermodynamic study of the interaction of long open-chain polyazaalkanes with cobalt(II) and nickel(II) ions

1993

Complexation equilibria between the open-chain terminally methylated polyamines 1,14-bis(methylamino)-3,6,9,12- tetraazatetradecane (L1), 1,17-bis(methylamino)-3,6,9,12,15-pentaazaheptadecane (L2), 1,20-bis(methylamino)- 3,6,9,12,15,18-hexaazaicosane (L3) and 1,23-bis(methylamino)-3,6,9,12,15,18,21-heptaazatricosane (L4) with Co2+ and Ni2+ have been studied by means of potentiometric and spectrophotometric methods in 0.15 mol dm−3 NaClO4 aqueous solution at 298.15 K The stability constants for the complexes formed have been determined from e.m.f, data. All these ligands form mononuclear ML2+ complexes of similar stability with Co2+ and Ni2+. Binuclear Co2L44+, Ni2L34+ and Ni2L44+ are also f…

Aqueous solutionChemistryInorganic chemistryPotentiometric titrationchemistry.chemical_elementMedicinal chemistryInorganic ChemistryNickelMaterials ChemistryChemical stabilityAmine gas treatingPhysical and Theoretical ChemistryAliphatic compoundCobaltEquilibrium constantInorganica Chimica Acta
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Stabilities and coordination modes of histidine in copper(II) mixed-ligand complexes with ethylenediamine, diethylenetriamine or N,N,N′,N″,N″-pentame…

2008

Abstract Solution equilibrium studies on the Cu(II)–polyamine–methionine ternary systems (polyamine: ethylenediamine (en), diethylenetriamine (dien), N,N,N′,N′′,N′′-pentamethyldiethylenetriamine (Me5dien)) have been performed by pH-potentiometry, UV–Vis spectrophotometry and EPR methods. The obtained results suggest the formation of the mixed-ligand complexes with [Cu(A)(Met)]+ stoichiometry in all studied systems. Our spectroscopic results indicate the tetragonal geometry for [Cu(en)(Met)]+, the geometry slightly deviated from square pyramidal for [Cu(dien)(Met)]+ and strongly deviated from square pyramidal towards trigonal bipyramidal for the [Cu(Me5dien)(Met)]+ species. The coordination …

Aqueous solutionChemistryInorganic chemistrychemistry.chemical_elementEthylenediamineCopperSquare pyramidal molecular geometrylaw.inventionInorganic ChemistryTrigonal bipyramidal molecular geometrychemistry.chemical_compoundCrystallographylawDiethylenetriamineMaterials ChemistryPhysical and Theoretical ChemistryElectron paramagnetic resonanceTernary operationPolyhedron
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Complexation of the potassium ion by diaza crown compounds in aqueous solutions

1988

The conductance behavior of potassium nitrate in water with and without 1,7,10,16-tetraoxa-4,13-diazacyclooctandecane[2.2] and 4,7,13,16,21,24-hexaoxa-1,10-diazabicyclo-8.8.8-exacosane[2.2.2] macrocyclic ligands have been studied in order to analyze the complexation behavior of potassium cations in water. The absence of the complexation found in the [2.2] system is discussed in terms of the ligand structural features (presence of hydrogen bond donor and acceptor sites). The ion pair association constant of potassium cryptate as obtained from conductance measurements is also reported and discussed.

Aqueous solutionChemistryLigandHydrogen bondPotassiumInorganic chemistryBiophysicsConductancechemistry.chemical_elementPotassium nitrateBiochemistryCrown Compoundschemistry.chemical_compoundStability constants of complexesPhysical and Theoretical ChemistryMolecular BiologyJournal of Solution Chemistry
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INTERACTIONS OF ORGANOTIN(IV) HALIDES WITH REDUCED GLUTATHIONE IN AQUEOUS-SOLUTION

1993

Abstract Glutathione (GSH) is a compound extremely common among many living organisms in which it plays a fundamental role in the processes of detoxification. Also, organotin(IV) derivatives are more and more commonly used in technological processes or as antitumor drugs. So it seemed interesting to investigate the possible interactions between GSH and organotin compounds in water. Particularly, it has been studied because of its role in the organic radicals linked to the tin center on the stoichiometry and the structure of the adducts. Information was obtained following the reaction between Me n SnCl 4-n (n = 1 to 3) and GSH by Mossbauer and NMR spectroscopies on the assumption that change…

Aqueous solutionChemistryRadicalInorganic chemistrychemistry.chemical_elementQuadrupole splittingBiochemistryMedicinal chemistryInorganic ChemistryTrigonal bipyramidal molecular geometryMössbauer spectroscopyProton NMRTinCoordination geometry
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Determination of organic fluorine in aqueous samples with neutron activation analysis in comparison with the DIN method

1996

Neutron activation analysis (NAA) has been used as detection technique for adsorbable organic fluorine in aqueous samples. The results have been compared with the standardized DIN method which uses a fluoride-ion-selective electrode (ISE).

Aqueous solutionChemistryRadiochemistryElectrodeFluorinechemistry.chemical_elementNeutron activation analysisBiochemistryAnalytical ChemistryNeutron activationAnalytical and Bioanalytical Chemistry
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Complexes of Tungsten(VI) with Mucic Acid: a Spectrophotometric and Polarimetric Study in Aqueous Solution

1986

Abstract Spectrophotometric work on mucic acid-W(VI) system shows the formation of three different oxoanion complexes in aqueous solution; their stability is dependent upon pH. One of the complexes is monomeric tungstodimucate and the other two are 2/2 species. An anomalous cryoscopic behaviour, similar to that of W(VI) tartaric system, has been observed for the dimeric complex formed at higher pH. The stoichiometries and conditional dissociation constants have been polarimetrically determined by means of competitive reactions between the mucic and tartaric ligands. 1 H and 13 C NMR spectra have been interpreted for the similar complex species of both mucic and tartaric acids.

Aqueous solutionChemistryStereochemistryInorganic chemistrychemistry.chemical_elementMucic acidCarbon-13 NMRTungstenInorganic ChemistryDissociation constantchemistry.chemical_compoundMonomerMaterials ChemistryPhysical and Theoretical ChemistryStoichiometryInorganica Chimica Acta
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