Search results for "anions"

showing 10 items of 126 documents

Magnetic exchange interactions in the heteropoly complexes [M4(H2O)2(PW9O34)2]10− [M=Co(II) and Cu(II)]

1990

The magnetic properties of the heteropolyanions [M4(H2O)2(PW9O34)2]10− [M=Co(II) and Cu(II)] down to 4 K are reported. Their individual heteropoly molecules contain a rhomblike arrangement formed by four coplanar MO6 octahedra sharing edges. The magnetic properties support an intramolecular ferromagnetic exchange in the Co(II) tetramer, and antiferromagnetic exchange in the Cu(II) tetramer. These behaviors are discussed assuming anisotropic exchange in the Co(II) compound, and Heisenberg exchange in the Cu(II) compound. Carlos.Gomez@uv.es

Magnetic PropertiesExchange InteractionsGeneral Physics and AstronomyCopper ComplexesAntiferromagnetismTetramerVery Low TemperatureAntiferromagnetismMoleculeAnisotropy:FÍSICA::Química física [UNESCO]Cobalt Complexes ; Copper Complexes ; Heteropolyanions ; Magnetic Properties ; Exchange Interactions ; Ferromagnetism ; Antiferromagnetism ; Anisotropy ; Heisenberg Model ; Ultralow Temperature ; Very Low TemperatureCondensed matter physicsChemistryHeisenberg modelUltralow TemperatureUNESCO::FÍSICA::Química físicaCrystallographyOctahedronFerromagnetismIntramolecular forceFerromagnetismHeisenberg ModelAnisotropyCobalt ComplexesHeteropolyanions
researchProduct

Polynitrile anions as ligands: Synthesis, structure and magnetic properties of a new three-dimensional coordination polymer with the 2-dicyanomethyle…

2005

cited By 12; International audience; Reaction between CuCl2 and K2tcpd (tcpd2- = C[C(CN)2]32- = 2-dicyanomethylenc-1,1,3,3-tetracyanopropanediide anion) in presence of the neutral ligand tn (1,3-diaminopropane) in aqueous solution yields the new compound [Cu(tn)(tcpd)] (1) which was characterized by X-ray crystallography. The crystal structure of 1 consists of one [Cu(tn)]2+ unit and one tcpd2- anion, both located on general positions. Each Cu atom presents an essentially octahedral coordination with four nitrogen atoms arising from four polynitrile ligands and two nitrogen atoms from the chelating tn ligand. Despite its six nitrile groups potentially bridging, the tcpd ligand acts with a μ…

NitrileNitrogen atomsCoordination polymerStereochemistryNitrogenCrystal structure010402 general chemistryLigands01 natural scienceschemistry.chemical_compoundAntiferromagnetismTransition metalMaterials Chemistry[CHIM]Chemical SciencesCrystallography010405 organic chemistryLigandChelationMechanical EngineeringCrystal structureMetals and AlloysBridging ligandCondensed Matter PhysicsMagnetic susceptibility0104 chemical sciencesElectronic Optical and Magnetic MaterialsCrystallographyOctahedronchemistryMechanics of MaterialsPolynitrile anions
researchProduct

Long-term expression of the human alpha1-antitrypsin gene in mice employing anionic and cationic liposome vector.

1997

The complete process of gene therapy involves three important steps: targeting, delivery, and gene expression. Since each step can be related to the pharmacological concept of affinity, bioavailability, and intrinsic capacity, this commentary examines, from this perspective, the efficiency of anionic and cationic liposomes as vectors for the in vivo gene transfer of the human alpha1-antitrypsin gene. Small liposomes represent the first generation of liposomes destined for the liver parenchymal cell. Although the final efficiency of gene transfer is low, we found that small liposomes are a kind of high-affinity hepatocyte-destined vector because the dose range for mediating the response is t…

PharmacologyAnionsLiposomeGenetic transferGenetic VectorsGene Transfer TechniquesBiological AvailabilityGene ExpressionGenetic TherapyGene deliveryBiologyVectors in gene therapyBiochemistryGene productMiceBiochemistryCationsalpha 1-AntitrypsinGene expressionLiposomesAnimalsHumansCationic liposomeExpression cassetteBiochemical pharmacology
researchProduct

NMR enantiodifferentiation of triphenylphosphonium salts by chiral hexacoordinated phosphate anions

2003

BINPHAT anion—rather than TRISPHAT—is an efficient NMR chiral shift reagent for triphenylphosphonium salts containing stereogenic centers on the aliphatic side-chain. BINPHAT—rather than TRISPHAT—anion is an efficient NMR (1H and 31P) chiral shift reagent for chiral triphenylphosphonium salts.

Phosphonium saltsBINPHATChiral anionsOrganic ChemistryTRISPHATPhosphateBiochemistryStereocenterchemistry.chemical_compoundNMR enantiodifferentiationTRISPHATchemistryReagentddc:540Drug DiscoveryAmino acids and derivativesOrganic chemistryTetrahedron Letters
researchProduct

N-Alkyl Ammonium Resorcinarene Salts as High-Affinity Tetravalent Chloride Receptors.

2016

N-Alkyl ammonium resorcinarene salts (NARYs, Y=triflate, picrate, nitrate, trifluoroacetates and NARBr) as tetravalent receptors, are shown to have a strong affinity for chlorides. The high affinity for chlorides was confirmed from a multitude of exchange experiments in solution (NMR and UV/Vis), gas phase (mass spectrometry), and solid-state (X-ray crystallography). A new tetra-iodide resorcinarene salt (NARI) was isolated and fully characterized from exchange experiments in the solid-state. Competition experiments with a known monovalent bis-urea receptor (5) with strong affinity for chloride, reveals these receptors to have a much higher affinity for the first two chlorides, a similar af…

PicrateInorganic chemistryta221chemistry.chemical_elementSalt (chemistry)receptors010402 general chemistry01 natural sciencesChlorideMedicinal chemistryCatalysishost-guest systemschemistry.chemical_compoundnoncovalent interactionsChlorinemedicineAmmoniumta116Alkylta218chemistry.chemical_classificationta214ta114010405 organic chemistryOrganic ChemistryGeneral ChemistryResorcinarene0104 chemical scienceschemistrychlorineTrifluoromethanesulfonateanionsmedicine.drugChemistry (Weinheim an der Bergstrasse, Germany)
researchProduct

Effect of deicing salts on urban soils and health status of roadside trees in the Opole region.

2004

This article reports on a study whose aim was to evaluate the impact of snow removal salts on urban soil properties and the health of roadside trees. The evaluation was done by chemical analyses of soil samples and plant matter combined with toxicity testing, performed with a Protoxkit F, a protozoan microbiotest. Samples were collected at 45 locations on three main roads in the town of Opole (Poland). The roads differed in the snow removal technology and amount of chemical substances (mostly NaCI) used on them during the winter. The study showed that when soil was exposed to a high level of NaCI, it tended to be more alkaline and also exhibited increased content of Na + and Cl - . The toxi…

PollutionAnionsSoil testHealth Toxicology and Mutagenesismedia_common.quotation_subjectManagement Monitoring Policy and LawSodium ChlorideToxicologymedicine.disease_causeTetrahymena thermophilaTreesCalcium ChlorideSoilAnimal scienceDry weightCationsmedicineEcotoxicologyAnimalsSoil PollutantsCitiesParticle Sizemedia_commonChlorosisEcologyChemistryurban soil; roadside tree; deicing salt; microbiotest; salinity; toxicity; experimenIceEnvironmental factorGeneral MedicineSalinityPlant LeavesSoil waterSaltsPolandSeasonsEnvironmental MonitoringEnvironmental toxicology
researchProduct

Stability of Prussian Blue films on ITO electrodes: effect of different anions

1993

Abstract Transformation of insoluble newly deposited Prussian Blue (PB) into the soluble structure stabilizes the film and allows its total oxidation to Prussian Yellow. The stability of PB films in electrochemical processes in successive potential cycling experiments and under long-term chemical attack by an electrolyte depends not only on the cation that takes part but also on the nature of the anion present. In aqueous media, the sulphate ion clearly destabilizes the crystalline structure whereas the nitrate ion favours stabilization. Initial changes in the voltammograms recorded immediately after the spectroscopic tests have been detected in all media. During the immersion period water …

Prussian blueAqueous solutionChemistryGeneral Chemical EngineeringInorganic chemistryCrystal structureElectrolyteElectrochemistryRedoxAnalytical ChemistryIonchemistry.chemical_compoundPrussian BlueElectrochemistryanionsDissolutionJournal of Electroanalytical Chemistry
researchProduct

Unexpected Reaction of the Unsaturated Cluster Host and Catalyst [Pd3(3-CO)(dppm)3]2+ with the Hydroxide Ion: Spectroscopic and Kinetic Evidence of a…

2006

The title cluster, [Pd(3)(mu(3)-CO)(dppm)(3)](2+) (dppm=bis(diphenylphosphino)methane), reacts with one equivalent of hydroxide anions (OH(-)), from tetrabutylammonium hydroxide (Bu(4)NOH), to give the paramagnetic [Pd(3)(mu(3)-CO)(dppm)(3)](+) species. Reaction with another equivalent of OH(-) leads to the zero-valent compound [Pd(3)(mu(3)-CO)(dppm)(3)](0). From electron paramagnetic resonance analysis of the reaction medium using the spin-trap agent 5,5-dimethyl-1-pyrroline-N-oxide (DMPO), the 2-tetrahydrofuryl or methyl radicals, deriving from the tetrahydrofuran (THF) or dimethyl sulfoxide (DMSO) solvent, respectively, were detected. For both [Pd(3)(mu(3)-CO)(dppm)(3)](2+) and [Pd(3)(mu…

RadicalInner sphere electron transfersolvent effects[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryPhotochemistry01 natural sciencesMedicinal chemistryCatalysislaw.inventionAdductchemistry.chemical_compoundlawElectron paramagnetic resonancehydroxide anionsTetrahydrofuranComputingMilieux_MISCELLANEOUS010405 organic chemistryTetrabutylammonium hydroxideOrganic Chemistry[ CHIM.INOR ] Chemical Sciences/Inorganic chemistryGeneral Chemistrypalladium0104 chemical scienceschemistrydensity functional calculationsHydroxidecluster compoundsSolvent effects
researchProduct

Design of carborane molecular architectures with electronic structure computations: From endohedral and polyradical systems to multidimensional netwo…

2009

11 pags, 6 figs. -- 19th International Conference on Physical Organic Chemistry (ICPOC-19) 13–18 July 2008, Santiago de Compostela, Spain

SingletComputational chemistryIcosahedral symmetryChemistryCASPT2General Chemical EngineeringComputationQuantum chemical computationsMolecular architectureGeneral ChemistryElectronic structureCASSCFDFTElectronic structuresTripletBiradicalsDianionsComputational chemistryAtomCarboraneSinglet stateDimersCarboranes
researchProduct

Synthesis, structure and reaction chemistry of a nucleophilic aluminyl anion.

2018

The reactivity of aluminium compounds is dominated by their electron deficiency and consequent electrophilicity; these compounds are archetypal Lewis acids (electron-pair acceptors). The main industrial roles of aluminium, and classical methods of synthesizing aluminium–element bonds (for example, hydroalumination and metathesis), draw on the electron deficiency of species of the type AlR3 and AlCl31,2. Whereas aluminates, [AlR4]−, are well known, the idea of reversing polarity and using an aluminium reagent as the nucleophilic partner in bond-forming substitution reactions is unprecedented, owing to the fact that low-valent aluminium anions analogous to nitrogen-, carbon- and boron-centred…

Substitution reactionkemiallinen synteesiMultidisciplinaryanionit010405 organic chemistryaluminiumNacNacElectron deficiencyorganometalliyhdisteet010402 general chemistry01 natural sciencesOxidative additionMedicinal chemistry0104 chemical scienceschemistry.chemical_compoundNucleophilechemistryElectrophileorganometallic compoundsReactivity (chemistry)Lewis acids and basesalumiinianionschemical synthesisNature
researchProduct