Search results for "Metals"

showing 10 items of 2013 documents

[FeIILSCoIIILS]2⇔ [FeIIILSCoIIHS]2 photoinduced conversion in a cyanide-bridged heterobimetallic molecular square

2010

The self-assembly of [Fe(III){B(pz)(4)}(CN)(3)](-) and [Co(II)(bik)(2)(S)(2)](2+) affords the diamagnetic cyanide-bridged [Fe(II)(LS)Co(III)(LS)](2) molecular square which is converted into the corresponding magnetic [Fe(III)(LS)Co(II)(HS)](2) species under light irradiation at relatively low temperatures.

StereochemistryCyanideMetals and AlloysLight irradiationGeneral ChemistryCatalysisSquare (algebra)Surfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundCrystallographychemistryMaterials ChemistryCeramics and CompositesDiamagnetismChemical Communications
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Synthesis and crystal structure of an unprecedented bismuth porphyrin containing ester pendant arms

2000

International audience; An easily prepared porphyrin with pendant arms is shown to form a stable complex with bismuth(III) ion; the complex is eight coordinate with a square antiprismatic coordination geometry; the solid-state structure exhibits the formation of a dimer assembled via mutual coordination of a terminal ester group.

StereochemistryDimerchemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciences[ CHIM ] Chemical SciencesCatalysisBismuthIonchemistry.chemical_compoundMaterials Chemistry[CHIM]Chemical SciencesCoordination geometrySquare antiprismatic molecular geometry010405 organic chemistryChemistryMetals and AlloysGeneral ChemistryPorphyrin0104 chemical sciences3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyCeramics and Composites
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Single chain magnet behaviour in an enantiopure chiral cobalt(II)–copper(II) one-dimensional compound

2010

The self-assembly of an enantiomerically pure, chiral dianionic oxamatocopper(II) complex with cobalt(II) ions leads to neutral oxamato-bridged heterobimetallic chains that combine chirality and slow magnetic relaxation, providing thus the first example of ‘‘chiral single chain magnets (CSCMs). Ruiz Garcia, Rafael, Rafael.Ruiz@uv.es ; Lloret Pastor, Francisco, Francisco.Lloret@uv.es

StereochemistryHigh Energy Physics::LatticeUNESCO::QUÍMICAchemistry.chemical_elementSingle chainComputer Science::Computational Geometry010402 general chemistry01 natural sciences:QUÍMICA [UNESCO]CatalysisIonMagnetic RelaxationMaterials ChemistryMagnetic relaxation[CHIM.COOR]Chemical Sciences/Coordination chemistrySelf-assembly ; Dianionic oxamatocopper ; Cobalt ; Ions ; Magnetic RelaxationComputingMilieux_MISCELLANEOUSIons010405 organic chemistryUNESCO::QUÍMICA::Química inorgánicaHigh Energy Physics::PhenomenologyMetals and AlloysGeneral ChemistrySelf-assemblyCobalt:QUÍMICA::Química inorgánica [UNESCO]Copper3. Good health0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyEnantiopure drugchemistryMagnetCeramics and CompositesDianionic oxamatocopperChirality (chemistry)Cobalt
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Tungsten(VI)-gluconic acid complexes: Polarimetric and13C-N.m.r. Studies in an excess of tungsten(VI)

1986

A polarimetric study of the tungsten (VI)-gluconic acid system in an excess of metal reveals the formation of four stable complexes: two monomers with 1 : 2 and 2: 1 stoichiometries and two dimers of 2:2 composition. The pH ranges of these species, the amount of acid equivalents their formation requires, and their conditional stability constants have also been calculated.

StereochemistryInorganic chemistryMetals and Alloyschemistry.chemical_elementTungstenCatalysisInorganic ChemistryMetalchemistry.chemical_compoundchemistryStability constants of complexesvisual_artAldonic acidMaterials Chemistryvisual_art.visual_art_mediumGluconic acidStoichiometryOrganometallic chemistryTransition Metal Chemistry
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Synthesis and structure of charge transfer salts of tetrathiafulvalene (TTF) and tetramethyl-TTF with 2,4,7-trinitro and 2,4,5,7-tetranitro-9-fluoren…

2009

Charge transfer salts of tetrathiafulvalene (TTF) and tetramethyltetrathiafulvalene (TMTTF) with the organic acceptors 2,4,7-trinitro-9-fluorenone and 2,4,5,7-tetranitro-9-fluorenone have been prepared and characterized. The compounds (TTF)(TENF) (1), (TTF)3(TRNF)2 (2) and (TMTTF)(TRNF) (3) contain mixed stacks of alternating TTF and nitrofluorenone units. Surprisingly, the degree of charge transfer that occurs in these salts is not controlled solely by the redox potentials of the building blocks, but apparently also by the most effective intermolecular interactions in the solid, as determined from the crystal struc- tures obtained. These three compounds exhibit poor electron delocalization…

StereochemistryMechanical EngineeringIntermolecular forceMetals and AlloysElectron delocalizationCharge (physics)Crystal structureCondensed Matter PhysicsRedoxElectronic Optical and Magnetic MaterialsCrystalchemistry.chemical_compoundCrystallographychemistryMechanics of MaterialsMaterials ChemistryDiamagnetismTetrathiafulvaleneSynthetic Metals
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Template synthesis of multi-macrocycles by metathesis reaction.

2004

Selective heterodimerisation of tetraurea calix[4]arenes containing four or eight ω-alkenyl groups with a tetratosyl urea calix[4]arene has been effectively used to synthesize multi-macrocycles via metathesis reaction.

StereochemistryMetals and AlloysGeneral ChemistryTemplate synthesisCombinatorial chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryMaterials ChemistryCeramics and CompositesSalt metathesis reactionUreaChemical communications (Cambridge, England)
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Two- and one-step cooperative spin transitions in Hofmann-like clathrates with enhanced loading capacity

2014

Structural, magnetic, calorimetric and Mo¨ssbauer studies of the cooperative spin crossover naphthalene and nitrobenzene clathrates of the novel FeII Hofmann-like porous metal–organic framework {Fe(bpb)[Pt(CN)4]}2Guest are described (bpb = bis(4-pyridyl)butadiyne).

StereochemistryMetals and AlloysOne-StepGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsNitrobenzeneCrystallographychemistry.chemical_compoundchemistrySpin crossoverFISICA APLICADAMössbauer spectroscopyMaterials ChemistryCeramics and CompositesSpin (physics)NaphthaleneChem. Commun.
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Synthesis, spectroscopic characterization and electrochemical behaviour of nickel(II) complexes with C-meso-5,5,7,12,12,14-hexamethylcyclotetradecane…

1993

A series of complexes of formula {Ni(Me6[14]aneN4)X2| (Me6[14]aneN4) = C-meso-5,5,7,12,12,14-hexamethyl-1,4,-8,11-tetraazacyclotetradecane and X = N3(1), NCO (2), NCS (3), AcO (4) or I (5) has been synthesized. The crystal structure of (5) has been determined by X-ray diffraction methods. The nickel atom is surrounded by a square-planar array of nitrogen atoms, giving a low-spin complex. The macrocyclic ligand shows the most stable conformation, the six-membered rings exhibiting the chair form while the gauche conformation is adopted by the five-membered rings. Spectroscopic and magnetic data for (1)–(4) are consistent with octahedral coordination around the nickel atom, which is achieved b…

StereochemistryMetals and Alloyschemistry.chemical_elementCrystal structureInorganic Chemistrychemistry.chemical_compoundNickelCrystallographyOctahedronchemistryX-ray crystallographyMaterials ChemistryMoleculeMacrocyclic ligandCyclic voltammetryOrganometallic chemistryTransition Metal Chemistry
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Modular functionalized polyphosphines for supported materials: previously unobserved (31)P-NMR «through-space» ABCD spin systems and heterogeneous pa…

2014

The modular design of polyphosphines, diversely functionalized for facile immobilization on virtually any kind of support, is reported. Previously unobserved ABCD (31)P NMR spin-spin systems evidence the control exercised on the polyphosphines conformation. We illustrate the catalytic performance at low Pd loading of the recyclable immobilized polyphosphines in C-C bond formation reactions.

StereochemistryMetals and Alloyschemistry.chemical_elementGeneral ChemistryBond formationCombinatorial chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysischemistryMaterials ChemistryCeramics and CompositesSpin (physics)PalladiumChemical communications (Cambridge, England)
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Polyamines containing naphthyl groups as pH-regulated molecular machines driven by light

2001

A series of compounds made up by linking methylnaphthalene fragments at both ends of different polyamine chains have shown to behave as pH-regulated molecular machines driven by light and fluorescence emission studies have proved the formation of an excimer between the two naphthalene units whose appearance, fluorescence intensity and decay times depend on the pH value of the media. Albelda Gimeno, Maria Teresa, Teresa.Albelda@uv.es ; Garcia-España Monsonis, Enrique, Enrique.Garcia-Es@uv.es ; Soriano Soto, Concepción, Concepcion.Soriano@uv.es

StereochemistryPHUNESCO::QUÍMICAPhotochemistryExcimerNaphthyl:QUÍMICA [UNESCO]CatalysisFluorescencechemistry.chemical_compoundMaterials ChemistryPolyaminesUNESCO::QUÍMICA::Química orgánicaMethylnaphthaleneNaphthalene:QUÍMICA::Química orgánica [UNESCO]Metals and AlloysGeneral ChemistryFluorescenceMolecular machineSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsFluorescence intensitychemistryPolyamines ; Naphthyl ; Methylnaphthalene ; PH ; FluorescenceCeramics and CompositesPolyamine
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