Search results for "Química Inorgánica"

showing 10 items of 84 documents

A new intermediate intercalate in superconducting sodium-doped hafnium nitride chloride

2005

Anew phase has been observed during the sodiumintercalation of hafnium nitride chloride as intermediate between the host β-HfNCl and the already reported Na 0.29 HfNCl with Tc of 24 K; the new intermediate shows interlayer spacings ranging from 9.48 to 9.67 A°, corresponds to a second stage intercalate of HfNCl and is superconducting with a critical temperature of 20 K. Beltran Porter, Daniel, Daniel.Beltran@uv.es

Materials scienceSuperconducter ; Sudium-doped hafniem nitride ; Critical temperatureSodiumUNESCO::QUÍMICAInorganic chemistryIntercalation (chemistry)chemistry.chemical_elementNitrideChloride:QUÍMICA [UNESCO]CatalysisPhase (matter)Materials ChemistrymedicineCritical temperatureSudium-doped hafniem nitrideSuperconductivityUNESCO::QUÍMICA::Química inorgánicaDopingMetals and AlloysGeneral MedicineGeneral Chemistry:QUÍMICA::Química inorgánica [UNESCO]Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsHafniumCrystallographySuperconducterchemistryCeramics and Compositesmedicine.drug
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Very high titanium content mesoporous silicas

2001

Titanium content in mesoporous titanosilicate catalysts has been modulated up to a minimum Si/Ti value of 1.9 by using complexing agents able to coordinate both Si and Ti atoms and harmonize the reactivity of the resulting precursors avoiding subsequent phase segregation and leading to chemically very homogeneous materials. El Haskouri, Jamal, Jamal.Haskouri@uv.es ; Beltran Porter, Aurelio, Aurelio.Beltran@uv.es ; Beltran Porter, Daniel, Daniel.Beltran@uv.es ; Amoros del Toro, Pedro Jose, Pedro.Amoros@uv.es

Materials scienceUNESCO::QUÍMICAInorganic chemistrychemistry.chemical_elementMesoporous:QUÍMICA [UNESCO]CatalysisCatalysisPhase (matter)Materials ChemistryReactivity (chemistry)SilicasTitaniumUNESCO::QUÍMICA::Química inorgánicaSegregationMetals and AlloysTitanium ; Mesoporous ; Titanium ; Silicas ; SegregationGeneral Chemistry:QUÍMICA::Química inorgánica [UNESCO]Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryHomogeneousCeramics and CompositesMesoporous materialTitanium
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Intercalation of decamethylferrocenium cations in bimetallic oxalate-bridged two-dimensional magnets

1997

The structure and magnetic properties of novel hybrid molecule-based magnets formed by combination of two magnetically active sublattices, the bimetallic oxalatobridged honeycomb net [MnIIMIII(ox)3] (MII = Mn, Fe, Co, Cr, Ni, Cu; MIII = Cr, Fe) and the organometallic cation decamethylferrocenium, are reported. Clemente Leon, Miguel, Miguel.Clemente@uv.es ; Coronado Miralles, Eugenio, Eugenio.Coronado@uv.es ; Galan Mascaros, Jose Ramon, Jose.R.Galan@uv.es ; Gomez Garcia, Carlos Jose, Carlos.Gomez@uv.es

Materials scienceUNESCO::QUÍMICAIntercalation (chemistry)Inorganic chemistry:QUÍMICA [UNESCO]CatalysisOxalateDecamethylferrocenium ; Bimetallic ; MagneticalDecamethylferroceniumchemistry.chemical_compoundMaterials ChemistryMoleculeBimetallic stripBimetallicUNESCO::QUÍMICA::Química inorgánicaMetals and AlloysHoneycomb (geometry)General ChemistryMagnetical:QUÍMICA::Química inorgánica [UNESCO]Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographychemistryMagnetCeramics and CompositesChemical Communications
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The first metamagnetic one-dimensional molecular material with nickel(ii) and end-to-end azido bridges

2001

A novel single azido bridged one-dimensional Ni(II) chain, which represents the first metamagnetic one-dimensional metal–azido system with only end-to-end azido bridges, has been synthesised and characterised by a low temperature magnetic study. Lloret Pastor, Francisco, Francisco.Lloret@uv.es

Metamagnetic ; Nickel ; Azido bridges ; SynthesisedSynthesisedMaterials scienceUNESCO::QUÍMICAchemistry.chemical_elementPhotochemistry:QUÍMICA [UNESCO]CatalysisChain (algebraic topology)NickelPolymer chemistryMaterials ChemistryMagnetic studyMolecular materialsazide ligandAzido bridgesUNESCO::QUÍMICA::Química inorgánicaMetals and AlloysGeneral Chemistry:QUÍMICA::Química inorgánica [UNESCO]Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsNickelchemistryCeramics and CompositesMetamagnetic
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Expanding the 2, 2’-bipyrimidine bridged 1D homonuclear coordination polymers family: [MIIbpymCl2] (M=Fe, Co) magnetic and structural characterization

2013

One pot reaction of hydrated chloride salts of Fe(II) and Co(II) with stoichiometric amounts of 2, 2’-bipyrimidine (bpym) in a methanol/ acetonitrile mixture afforded the corresponding 1D homonuclear coordination polymers, [μ-(bpym)MCl2]n. Crystal structures of both complexes are isomorphous in the highly symmetric orthorhombic space group Fddd. The 1D coordination polymers are composed of almost orthogonal alternating bipyrimidine bridges linking the {MCl2} units. The magnetic behaviour of the Fe(II)compound can be well understood as a uniform S=2 chain with antiferromagnetic exchange interaction between metal ion sites. In the case of the Co(II) ion, also an antiferromagnetic interaction …

Models MolecularPolymersStereochemistryIronCrystal structureQuímica Inorgánica y NuclearHomonuclear moleculeIonInorganic ChemistryMetalCiencias Naturales y ExactasOrganometallic CompoundsAntiferromagnetismMolecular StructureChemistryMagnetic PhenomenaExchange interactionCiencias QuímicasCobaltCrystallographyPyrimidinesvisual_artvisual_art.visual_art_mediumOrthorhombic crystal systemno correspondeSpin canting
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A catalytic highly enantioselective direct synthesis of 2-bromo-2-nitroalkan-1-ols through a Henry reaction.

2008

Highly enantiomerically enriched 2-bromo-2-nitroalkan-1-ols are prepared by direct condensation of aliphatic and aromatic aldehydes with bromonitromethane in the presence of a catalytic amount of copper(II) acetate and a C1-symmetric camphorderived amino pyridine ligand. Blay Llinares, Gonzalo, Gonzalo.Blay@uv.es ; Hernandez Olmos, Victor, Victor.Hernandez@uv.es ; Pedro Llinares, Jose Ramon, Jose.R.Pedro@uv.es

Nitroaldol reactionEnrichedCondensationPyridinesBromonitromethaneUNESCO::QUÍMICACatalytic ; Synthesis ; Henry reaction ; Enriched ; CondensationMolecular Conformationchemistry.chemical_elementAcetatesLigands:QUÍMICA [UNESCO]CatalysisCatalysisSynthesisMaterials ChemistryOrganic chemistryCatalyticAldehydesEthaneChemistryUNESCO::QUÍMICA::Química inorgánicaCondensationMetals and AlloysEnantioselective synthesisStereoisomerismGeneral Chemistry:QUÍMICA::Química inorgánica [UNESCO]Nitro CompoundsCopperPyridine ligandSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAlcoholsCeramics and CompositesHenry reactionCopperChemical communications (Cambridge, England)
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Organometallic Chemistry of the Transition Metals

2018

Este documento ha sido elaborado en el marco de un proyecto de Renovación de Metodologías Docentes concedido por el Servicio de Formación Permanente de la Universitat de Valencia. (UV-SFPIE_RMD17-725369) Este documento forma parte de la asignatura Química Inorgánica Avanzada impartida en el Master Universitario en Química This document forms part of the course Advance Inorganic Chemistry belonging to the Master in Chemistry

Organometallic Transition MetalsUNESCO::QUÍMICAUNESCO::QUÍMICA::Química inorgánica ::Compuestos organometálicos
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Hybrid magnetic materials based on layered double hydroxides: from the chemistry towards the applications

2014

Layered double hydroxides (LDHs) are the leitmotiv of this dissertation. Contradicting the assertion that “any past was better”, LDHs have been continuously revisited from the middle of the twentieth century, and represent an excellent example of the never-ending beauty of Chemistry. New synthetic perspectives are giving a new impetus to LDH chemistry, which among hybrid materials, are finding their heyday. This is resulting in novel materials and also paving the way for new fundamental and practical insights. This dissertation is focused on magnetic LDHs, and for the sake of clarity it is organized in three main parts: we will move from basic synthetic and physical aspects of LDHs, through…

Oxygen Evolution ReactionMagnetoresistanceUNESCO::QUÍMICA::Química inorgánicaUNESCO::QUÍMICAMagnetism:QUÍMICA::Química inorgánica [UNESCO]:QUÍMICA [UNESCO]UNESCO::FÍSICA::Química físicaNanosheetsAnionic claysPhotoisomerizationSupercapacitorsHybrid materialsAnion exchangeGraphene:FÍSICA::Química física [UNESCO]Layered Double Hydroxides
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Confined Pt-1(1+) Water Clusters in a MOF Catalyze the Low-Temperature Water-Gas Shift Reaction with both CO2 Oxygen Atoms Coming from Water

2018

[EN] The synthesis and reactivity of single metal atoms in a low-valence state bound to just water, rather than to organic ligands or surfaces, is a major experimental challenge. Herein, we show a gram-scale wet synthesis of Pt-1(1+) stabilized in a confined space by a crystallographically well-defined first water sphere, and with a second coordination sphere linked to a metal-organic framework (MOF) through electrostatic and H-bonding interactions. The role of the water cluster is not only isolating and stabilizing the Pt atoms, but also regulating the charge of the metal and the adsorption of reactants. This is shown for the low-temperature water-gas shift reaction (WGSR: CO + H2O CO2 + H…

PhysicsWater–gas shift reactionQuímica Inorgánicabiology010405 organic chemistryWater-gas shift reactionSingle atom catalystGeneral MedicineGeneral ChemistryMetal-organic frameworks010402 general chemistrybiology.organism_classification01 natural sciencesCatalysisWater-gas shift reactionSingle-atom catalyst0104 chemical sciencesOxygen atomWater clustersPhysical chemistryValenciaMetal-organic frameworks (MOFs)Platinum
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Dopamine interaction with a polyamine cryptand of 1H-pyrazole in the absence and in the presence of Cu(II) ions. Crystal structure of [Cu2(H21L](ClO4…

2000

The crystal structure of the binuclear Cu2+ complex [Cu2(H21L)](ClO4)3·2H2O of the cryptand L = 1,4,7,8,11,14,17,20,21,24,29,32,33,36-tetradecaazapentacyclo[12.12.12.1^(6,9).1^(19,22),1,^31,34]hentetraconta-6,9(41),19(40), 21,31,34(39)-hexaene is presented; evidence for the formation in solution of binary L–dopamine and ternary Cu2+–L– dopamine complexes is presented. Escarti Alemany, Francisco, Francisco.Escarti@uv.es ; Garcia-España Monsonis, Enrique, Enrique.Garcia-Es@uv.es ; Latorre Saborit, Julio, Julio.Latorre@uv.es

PolyamineTernaryUNESCO::QUÍMICA::Química inorgánicaDopamineCrystal structureUNESCO::QUÍMICABinary:QUÍMICA::Química inorgánica [UNESCO]:QUÍMICA [UNESCO]CuDopamine ; Polyamine ; Cu ; Crystal structure ; Binary ; Ternary
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