Search results for "Metals and Alloy"

showing 10 items of 1341 documents

Violurato complexes of nickel(II). Formation equilibria. Deprotonation equilibria of the coordinated ligands and related stereochemical changes

1986

The formation equilibria of nickel(II) violurato-complexes in water and dimethylsulphoxide-water (80∶20) as well as deprotonation of the coordinated ligands and related stereochemical changes are reported. The stability constants of the Ni2+-H2V− complexes logβ1=5.06, Iogβ2=9.38, logβ3=12.98 as well as the acidity constants of the [Ni(H2V)3]− complex, logβj1= 8.37, logβj2=15.76, logβj3=22.37 are determined at 25 °C and 0.1M NaClO4. A new violurato-complex of Ni2+, Na4[Ni(HV)3]5H2O, is isolated and characterized.

Aqueous solutionChemistryStereochemistryOrganic solventMetals and Alloyschemistry.chemical_elementMedicinal chemistryCatalysisInorganic ChemistryNickelchemistry.chemical_compoundDeprotonationStability constants of complexesMaterials ChemistryHydrateOrganometallic chemistryTransition Metal Chemistry
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Compounds of tungsten(VI) with citric acid: A spectrophotometric, polarimetric and hydrogen-1, carbon-13 N.M.R. study of the formation and interconve…

1986

Tungsten(VI)-citrate complexes, which occur in aqueous solution, were studied by polarimetric and absorbance measurements. The pH of the medium is the principal variable controlling complex formation and interconversion equilibria. At high pH (>6), the stable complexes are monomers with 1∶2 and 1∶1 stoichiometry, depending on the tungsten(VI)-citrate ratio, while at lower pH two different dinuclear complexes are formed. The intervals of existence of these species with the pH, the number of equivalents of acid necessary for their formation, as well as the conditional stability constant, have also been calculated. The structure of these compounds have been investigated by1H and13C-n.m.r. spec…

Aqueous solutionInorganic chemistryMetals and Alloyschemistry.chemical_elementTungstenOxygenCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryStability constants of complexesMaterials ChemistryMoleculeStoichiometryOrganometallic chemistryTransition Metal Chemistry
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Complexes of molybdenum(VI) with organic diacid ligands: The molybdenum(VI)-malonic acid system

1983

Malonic acid (C3O4H4) and MoVI form in aqueous solution two dinuclear dioxo-complexes of which the stability is a function of the pH of the medium. Both complexes have a 1∶1 metal-ligand stoichiometric ratio, and the interconversion may involve a structural rearrangement. Conditional dissociation constants have been determined spectrophotometrically. Saline cryoscopy supports the spectrophotometric results. Salts of [Co(en)3]3+ have been isolated. The ligand behaviour of malonic acid differs partially from that observed for α-polyhydroxy ligands.

Aqueous solutionLigandInorganic chemistryMetals and Alloyschemistry.chemical_elementMalonic acidMedicinal chemistryCatalysisInorganic ChemistryDissociation constantchemistry.chemical_compoundchemistryMolybdenumMaterials ChemistryOrganometallic chemistryStoichiometryTransition Metal Chemistry
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Oxamidato complexes. Part 4. Electrochemical study of the copper(III)/copper(II) couple in monomeric N,N?-bis(substituent)oxamidatocopper(II) complex…

1993

The electrochemical behaviour of a series of monomeric N,N′-bis(substituent)oxamidato copper(II) complexes of formula Na2[Cu(3,5,3′,5′-X4obbz)]·4H2O [X = Cl (1), Br (2), I (3) and obbz = oxamidobis(benzoato)], Na2-[Cu(obbz)]·4H2O (4), Na2[Cu(5,5′-Me2obbz)]·4H2O (5), Na2[Cu(4,5,4,5′-(MeO)4obbz)]·4H2O(6),Na2[Cu(obp)]· 3.5H2O (7) (obp = oxamidobis(propionato)) and Na2[Cu(pba)]·6H2O (8), [pba = propylenebis(oxamate)] has been investigated by cyclic voltammetry, rotating disk electrode and coulometry in water and dimethylsulphoxide (dmso) solutions. NaNO3 (0.1 M) and n-Bu4NPF6 (0.1 M) were used as supporting electrolytes in H2O and dmso respectively, all solutions being thermostatted at 25 °C. I…

Aqueous solutionLigandOxamideInorganic chemistryMetals and AlloysSubstituentchemistry.chemical_elementMedicinal chemistryCopperInorganic Chemistrychemistry.chemical_compoundchemistryMaterials ChemistryRotating disk electrodeCyclic voltammetryOrganometallic chemistryTransition Metal Chemistry
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A new method for fluoride determination by using fluorophores and dyes anchored onto MCM-41Electronic supplementary information (ESI) available: IR s…

2002

A new colourimetric and fluorimetric method for fluoride determination in aqueous samples based on the specific reaction between fluoride and silica has been developed and applied on real samples.

Aqueous solutionMetals and AlloysNanotechnologyGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryMCM-41Materials ChemistryCeramics and CompositesFluorideNuclear chemistryChemical Communications
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Oxidative transformation of aryls using molybdenum pentachloride.

2012

Molybdenum pentachloride combines a strong Lewis acid character with an unusually high oxidation potential creating a powerful reagent for oxidative transformations. Since the oxidative coupling reaction of aryls is induced at an extraordinarily high reaction rate, a variety of labile groups, e.g. iodo, tert-alkyl, etc., are tolerated on the aromatic core. Furthermore, the co-formed molybdenum salts can either be exploited for template effects to obtain uncommon geometries in a preferred manner, or redox-play starts after aqueous workup. Therefore MoCl(5) represents a unique and easily available reagent.

Aqueous solutionMetals and Alloyschemistry.chemical_elementGeneral ChemistryOxidative phosphorylationMolybdenum pentachlorideCombinatorial chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsReaction ratechemistryMolybdenumReagentMaterials ChemistryCeramics and CompositesOrganic chemistryOxidative coupling of methaneLewis acids and bases
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In-situ characterisation of organosilane films formation on aluminium alloys by electrochemical quartz crystal microbalance and in-situ ellipsometry

2005

Abstract Organosilane pre-treatments have been studied intensively during the last years in order to replace hexavalent chromium conversion treatments. The aim of this study is to follow in-situ the formation of this organosilane layer in solution. Two in-situ techniques, spectroscopic ellipsometry and electrochemical quartz crystal microbalance, were used to investigate the mechanism and the kinetics of this protective film formation. In-situ measurements highlight that the organosilane film observed after the drying process is not formed into the solution, but during the emersion and drying step. Hence, it has been possible to characterise the presence of a very thin organosilane layer in…

Aqueous solutionMetals and Alloyschemistry.chemical_elementMineralogySurfaces and InterfacesQuartz crystal microbalanceSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryX-ray photoelectron spectroscopyChemical engineeringAluminiumEllipsometryMonolayerMaterials ChemistryThin filmLayer (electronics)
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Structural and Vibrational Study of a New Mixed Dipotassium Hydrogenselenate Dihydrogenphosphate K2(HSeO4)1.5 (H2PO4)0.5.

2006

Abstract Ongoing studies of the KHSeO4–KH2PO4 system, aimed at developing novel proton conducting solids, resulted in the new compound K2(HSeO4)1.5(H2PO4)0.5 (dipotassium hydrogenselenate dihydrogenphosphate). The crystals have been prepared by slow evaporation of an aqueous solution at room temperature. The structural properties of the crystals were characterized by X-ray single analysis (performed at room temperature), which revealed that K2(HSeO4)1.5(H2PO4)0.5 (KHSeP) crystallizes in space group P 1 ¯ with lattice parameters: a = 7.417(3) A, b = 7.668(2) A, c = 7.744(5) A, α = 71.59(3)°, β = 87.71(4)° and γ = 86.04(6)°. The compound has a unit cell volume 416.8(3) A3 and two formula unit…

Aqueous solutionProtonHydrogenInfraredHydrogen bondChemistryMechanical EngineeringInorganic chemistryMetals and AlloysEvaporationSpace groupInfrared spectroscopychemistry.chemical_elementGeneral MedicineCrystal structureCrystallographyChemical bondMechanics of MaterialsMaterials ChemistryTetrahedronChemInform
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Comparison of global responses to mild deficiency and excess copper levels in Arabidopsis seedlings

2013

[EN] Copper is an essential micronutrient in higher plants, but it is toxic in excess. The fine adjustments required to fit copper nutritional demands for optimal growth are illustrated by the diverse, severe symptoms resulting from copper deficiency and excess. Here, a differential transcriptomic analysis was done between Arabidopsis thaliana plants suffering from mild copper deficiency and those with a slight copper excess. The effects on the genes encoding cuproproteins or copper homeostasis factors were included in a CuAt database, which was organised to collect additional information and connections to other databases. The categories overrepresented under copper deficiency and copper e…

ArabidopsisBiophysicsFunctional homologchemistry.chemical_elementCircadian clockTransporterBiochemistryBiomaterialsTranscriptomeSuperoxide dismutaseStomatal closureGene Expression Regulation PlantIron homeostasisArabidopsisThalianamedicineHomeostasisArabidopsis thalianaGeneOligonucleotide Array Sequence AnalysisGeneticsDose-Response Relationship DrugbiologyArabidopsis ProteinsReverse Transcriptase Polymerase Chain ReactionSuperoxide DismutaseProteinMetals and AlloysBindingMicronutrientbiology.organism_classificationmedicine.diseaseCopperDNA-Binding ProteinschemistryBiochemistrySeedlingsChemistry (miscellaneous)biology.proteinFeedback loopTranscription factorTranscriptomeCopper deficiencyCopperTranscription FactorsMetallomics
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Efficient ultraviolet-light energy dissipation by an aromatic ketone.

2010

Experimental evidence on the efficiency of 2,2'4,4'-tetramethoxybenzil for UV-light energy dissipation is provided. This non-phenolic aromatic ketone has a low energy triplet which quickly decays to the ketone ground state, thus avoiding the generation of undesirable reactive species. El Moncef, Abdelkarim, elmonab@alumni.uv.es ; Cuquerella Alabort, Maria Consuelo, Chelo.Cuquerella@uv.es ; Zaballos Garcia, Elena, Elena.Zaballos@uv.es ; Ramirez de Arellano Sanchez, Maria del Carmen, Carmen.Ramirezdearellano@uv.es ; Stiriba, Salah Eddine, Salah.Stiriba@uv.es ; Perez Prieto, Julia, Julia.Perez@uv.es

Aromatic ketoneKetoneUltraviolet RaysUNESCO::QUÍMICAUV-lightPhotochemistry:QUÍMICA [UNESCO]CatalysisLow energyMaterials ChemistryUltraviolet lightTetramethoxybenzil ; UV-light ; Reactive ; Aromatic KetoneAromatic Ketonechemistry.chemical_classificationMolecular StructureUNESCO::QUÍMICA::Química analíticaMetals and AlloysGeneral ChemistryDissipationKetonesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryReactiveCeramics and Composites:QUÍMICA::Química analítica [UNESCO]TetramethoxybenzilGround stateChemical communications (Cambridge, England)
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