Search results for "Chloride"

showing 10 items of 1691 documents

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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Selective recognition of fluoride anion in water by a copper(II) center embedded in a hydrophobic cavity

2014

The ability of a water-soluble pentacationic calix[6]arene-based CuII complex to bind anions in water has been explored. Quite remarkably, the complex exhibits strong and selective fluoride binding in the pH range of 6–7. The binding constant at pH 5.9 was evaluated to be 85 000 M−1, which is one of the highest values ever reported for a fluoride probe in water and at this pH. The complex also binds chloride ions, but 1000 times less efficiently. The combination of the calix[6]arene hydrophobic cavity with the CuII complex, presenting its labile site in the endo position, is the reason for the selective recognition process. The single crystal X-ray structure of the organo-soluble parent com…

Aqueous solutionMolecular modelChemistryInorganic chemistrychemistry.chemical_elementGeneral ChemistryChlorideBinding constantCopperchemistry.chemical_compoundPolymer chemistrymedicineWater clusterSingle crystalFluorideta116medicine.drugChemical Science
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Fractionation of unsubstituted cellulose from solutions in either Ni-tren or (N,N-dimethylacetamide + LiCl)

2000

Starting from solutions of unsubstituted cellulose (Avicel PH101, M w = 30.1 kg/mol and M w /M n = 3 or Solucell 500, M w = 230 kg/mol, M w /M n = 2.8) in either Nitren (0.8 M aqueous solution of the dihydroxotris(2-aminoethly)amine nickel(II) complex) or in a mixed solvent DMAc+LiCl (consisting of N,N-dimethylacetamide plus lithium chloride) it was investigated whether the segregation of a second phase caused by the addition of suitable precipitants leads to polymer fractionation. With Ni-tren the long chains accumulate in the precipitate formed upon the addition of sulfuric acid; as the pH falls below 9, the solution is free of cellulose. Nevertheless this route option for fractionation m…

Aqueous solutionPolymers and PlasticsOrganic ChemistryFractionationCondensed Matter PhysicsDimethylacetamideSolventchemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryAcetoneLithium chloridePhysical and Theoretical ChemistryCellulosePolymer fractionationMacromolecular Chemistry and Physics
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Protonation of Carbonate in Aqueous Tetraalkylammonium Salts at 25°C.

2006

Protonation constants of carbonate were determined in tetramethylammonium chloride (Me4NClaq 0.1≤I/mol kg−1 ≤4) and tetraethylammonium iodide (Et4NIaq 0.1≤I/mol kg−1 ≤1) by potentiometric ([H+]-glass electrode) measurements. Dependence of protonation constants on ionic strength was taken into account by modified specific ion interaction theory (SIT) and by Pitzer models. Literature data on the protonation of carbonate in NaClaq (0.1≤I/mol kg−1 ≤6) were also critically analysed. Both protonation constants of carbonate follow the trend Et4NI>Me4NCl > NaCl. An ion pair formation model designed to take into account the different protonation behaviours of carbonate in different supporting electr…

Aqueous solutionProtonation of carbonateSpecific ion interaction theory (SIT)Ion pair formation modelChemistryInorganic chemistryTetraalkylammonium saltProtonationDependence on ionic strengthElectrolyteIon pairsAnalytical Chemistrychemistry.chemical_compoundIonic strengthTetramethylammonium chlorideAqueous solutionPitzer equationsCarbonateSettore CHIM/01 - Chimica AnaliticaProtonation of carbonate; Dependence on ionic strength; Aqueous solution; Tetraalkylammonium salts; Ion pair formation model; Specific ion interaction theory (SIT); Pitzer equationPitzer equation
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ZrO2SiO2 mixed oxides: surface aspects, photophysical properties and photoreactivity for 4-nitrophenol oxidation in aqueous phase

1996

Abstract Mixed oxides of ZrO2 and SiO2 were synthesized by a sol-gel technique by using zirconyl chloride and commercial silica gel as starting materials. The paper reports some surface features of the powders and the photoreactivity results obtained in the oxidation of 4-nitrophenol in aqueous suspensions of powdered photocatalyst. The optical characterization of the suspension was also performed by measuring the photon flows reflected and absorbed by the reacting system. The photoactivity exhibited by the ZrO2SiO2 samples is very scarce especially if compared with that shown by a TiO2 sample tested at equal experimental conditions. The low photoreactivity can be justified on the basis of…

Aqueous solutionSilica gelProcess Chemistry and TechnologyInorganic chemistryAqueous two-phase systemCatalysisThermogravimetryNitrophenolchemistry.chemical_compoundchemistryPhotocatalysisZirconyl chloridePhysical and Theoretical ChemistrySol-gelJournal of Molecular Catalysis A: Chemical
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Influence of chloride anions on the electrodeposition and electroactivity of the polymer matrix in polypyrrole, poly( N -methylpyrrole) and polypyrro…

2004

We report electrochemical studies on the influence of a small concentration of chloride ions on the electroactivity of the polymer matrix of polypyrrole (PPy), poly(N-methylpyrrole) [p(N-MePy)] and a poly(titanocene-propyl-pyrrole) derivative, p(Tc3Py) [Tc(CH2)3NC4H4; Tc=CpCp′TiCl2; Cp=C5H5; Cp′=C5H4] in acetonitrile (AN), tetrahydrofuran (THF) and N,N-dimethylformamide (DMF). The polymer films were obtained on Pt disc electrodes from AN solutions of the monomers containing 0.1 M tetrabutylammonium hexafluorophosphate (TBAPF6) as the supporting electrolyte and then transferred to the corresponding monomer-free solution. Studies in Cl−-containing solutions have shown that the p(Tc3Py) matrix…

Aqueous solutionSupporting electrolyteInorganic chemistryCondensed Matter PhysicsElectrochemistryPolypyrroleChloridechemistry.chemical_compoundMonomerchemistryTetrabutylammonium hexafluorophosphatePolymer chemistryElectrochemistrymedicineGeneral Materials ScienceElectrical and Electronic EngineeringAcetonitrilemedicine.drugJournal of Solid State Electrochemistry
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Synthesis, characterization and thermal behavior of nine new -type quaternary ammonium tetrafluoroborate or hexafluorophosphate salts prepared by met…

2008

Abstract Nine new quaternary ammonium tetrafluoroborate or hexafluoroborate salts were prepared from analogous bromide or chloride salts using anion exchange reaction in which the corresponding bromide or chloride salt was treated with HBF4 or HPF6 acid in aqueous solutions. The characterizations were performed by 1H NMR and 13C NMR spectroscopy as well as by elemental analysis. The single crystals of three tetrafluoroborate and two hexafluorophosphate salts were obtained by slow evaporation from a methanol/ethyl acetate solution and the crystal structures were determined by X-ray single crystal diffraction. Four of the compounds crystallized in the orthorhombic and one in the monoclinic cr…

Aqueous solutionTetrafluoroborateOrganic ChemistryInorganic chemistryHalideCrystal structureChlorideAnalytical ChemistryInorganic Chemistrychemistry.chemical_compoundchemistryBromideHexafluorophosphatemedicineSpectroscopymedicine.drugMonoclinic crystal systemJournal of Molecular Structure
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Arsenic(III) Removal at Low Concentrations by Biosorption usingPhanerochaete chrysosporiumPellets

2013

As(III) removal from dilute aqueous solutions by biosorption onto pellets of the white rot fungus Phanerochaete chrysosporium was investigated. The As(III) uptake capacity was evaluated at low initial concentrations (0.2–1 mg/L) which revealed that the P. chrysosporium pellets were only slightly less efficient than the well studied adsorbent granular ferric hydroxide. Moreover, its performance was much more superior compared to anaerobic granular sludge, another cheaply available bacterial biosorbent. In the studied pH (5–9) and biomass concentration (0.25–1.5 g/L wet weight basis) ranges, no large differences in As(III) removal efficiency were observed. The influence of different ions, com…

Aqueous solutionbiologyProcess Chemistry and TechnologyGeneral Chemical EngineeringBiosorptionPelletschemistry.chemical_elementFiltration and SeparationGeneral Chemistrybiology.organism_classificationChloridechemistry.chemical_compoundchemistrymedicinePhanerochaeteFluorideArsenicChrysosporiummedicine.drugNuclear chemistrySeparation Science and Technology
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A fluorescent chemosensor based on a ruthenium(II)-terpyridine core containing peripheral amino groups that selectively sense ATP in an aqueous envir…

2000

The selective sensing of the ATP anion in an aqueous environment over phosphate, sulfate, and chloride using a fluorescence chemosensor based on Ru(tpy)22+ cores attached to polyammonium groups is reported.

Aqueous solutionchemistry.chemical_elementPhosphatePhotochemistryFluorescenceChlorideRutheniumInorganic Chemistrychemistry.chemical_compoundchemistryparasitic diseasesSense (molecular biology)Polymer chemistryMaterials ChemistrymedicinePhysical and Theoretical ChemistrySulfateTerpyridinemedicine.drugInorganic Chemistry Communications
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Thermodynamics of titanium and vanadium reduction in non-aqueous environment calculated at various levels of theory.

2012

Reduction of titanium and vanadium compounds is a process accompanying the activation of coordinative olefin polymerization catalysts. Four density functional theory (DFT) functionals, coupled cluster with single, double, and perturbative triple excitations method CCSD(T) as well as complete active-space second-order perturbation theory method CASPT2 with a complete active-space self-consistent field CASSCF reference wave function were applied to investigate the thermodynamics of titanium and vanadium reduction. The performance of these theoretical methods was assessed and compared with experimental values. The calculations indicate that vanadium(IV) chloride is more easily reduced by trime…

Aqueous solutionchemistry.chemical_elementThermodynamicsVanadiumChlorideCatalysisMetalCoupled clusterchemistryvisual_artmedicinevisual_art.visual_art_mediumPhysical chemistryDensity functional theoryPhysical and Theoretical ChemistryTitaniummedicine.drugThe journal of physical chemistry. A
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