Search results for "Metallate"

showing 10 items of 11 documents

Exploring the Chemoselectivity towards Cysteine Arylation by Cyclometallated Au III Compounds: New Mechanistic Insights

2020

To gain more insight into the factors controlling the efficient cysteine arylation by cyclometalated Au(III) complexes, the reaction between selected gold compounds and different peptides was investigated by high‐resolution liquid chromatography electrospray ionization mass spectrometry (HR‐LC‐ESI‐MS). The deducted mechanisms of C–S cross‐coupling, also supported by density functional theory (DFT) and quantum mechanics/molecular mechanics (QM/MM) calculations, evidenced the key role of secondary peptidic gold binding sites in favouring the process of reductive elimination.

010405 organic chemistryChemistryElectrospray ionizationOrganic Chemistrycyclometallated gold complexes010402 general chemistryMass spectrometry01 natural sciencesBiochemistryCombinatorial chemistryMolecular mechanicsReductive elimination0104 chemical sciencesddc:cysteine arylationGold CompoundschemoselectivitySettore CHIM/03 - Chimica Generale E InorganicapeptidesMolecular MedicineDensity functional theoryChemoselectivityMolecular BiologyCysteinemass spectrometry
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Physicochemical characterization of metal hexacyanometallate–TiO2composite materials

2015

The paper describes the synthesis and characterization of novel TiO2–metal hexacyanometallates (MHCMs) composite materials. The starting material, TiO2, was modified by addition of cobalt-hexacyanoferrate (CoHCF) or iron-hexacyanocobaltate (FeHCC) at various concentrations. The resulting composites were characterized as follows: cyclic voltammetry (CV) followed the formation of TiO2–MHCM clusters, TEM micrographs studied their morphology, XAS and XPS data indicated that MHCM bonds to TiO2 through the nitrogen atom of its –CN group and modifies the environment of Ti compared to that of pure anatase. As expected, and confirmed by UV-Vis and XP-valence band data, the electronic properties of T…

AnataseX-ray absorption spectroscopyMorphology (linguistics)ChemistryGeneral Chemical EngineeringGeneral ChemistryCharacterization (materials science)MetalX-ray photoelectron spectroscopyvisual_artvisual_art.visual_art_mediumPhotocatalysisCOMPOSITESTiO2metalhexacanometallateComposite materialCyclic voltammetryPhotocatalysis
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White-light phosphorescence emission from a single molecule: application to OLED.

2009

A simple mononuclear cyclometallated iridium(III) complex exhibits white photo- and electro- luminescence in the wavelength range from 440 to 800 nm, which originates from a single emitting excited state of mixed character. Bolink Henk, Henk.Bolink@uv.es ; Coronado Miralles, Eugenio, Eugenio.Coronado@uv.es

DesignLuminescenceUNESCO::QUÍMICAAb initioColorchemistry.chemical_elementEfficiency010402 general chemistryPhotochemistry:QUÍMICA [UNESCO]01 natural sciencesCatalysisCopolymerIridium ComplexesMaterials ChemistryOLEDMoleculeIridiumDiodeEmitting DevicesMononuclear cyclometallated iridiumPhosphorescence010405 organic chemistryChemistrybusiness.industryUNESCO::QUÍMICA::Química analíticaMetals and AlloysAb-InitioGeneral ChemistryDiodes0104 chemical sciences3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBlueOLEDExcited stateGreen:QUÍMICA::Química analítica [UNESCO]Ceramics and CompositesOptoelectronicsMononuclear cyclometallated iridium ; Luminescence ; Phosphorescence ; OLEDLuminescencePhosphorescencebusinessChemical communications (Cambridge, England)
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Mixed Titanium–Hafnium Chloridometallate Complexes

2007

The addition of either NEt 3 BzCl or [Ph 3 PNPPh 3 ]Cl (1 equiv. chloride per metal) to a 1:1 mixture of HfCl 4 and TiCl 3 in SOCl 2 results in Ti oxidation and leads to the corresponding salts of the [TiHfCl 10 ] 2- ion. A solution IR investigation in the v(M-Cl) region indicates that this ion is in equilibrium with the homodimetallic [Ti 2 Cl 10 ] 2- and [Hf 2 Cl 10 ] 2- ions. An X-ray study of the NEt 3 Bz + salt reveals an edge-sharing bioctahedral dianion sitting on a crystallographic inversion centre. The crystal is a solid solution of different species with compositional disorder at the metal site, each metal position having the occupancy Ti 0.685 Hf 0.315 . The M-M and M-Cl distance…

Inorganic chemistryChloridometallate complexes010402 general chemistryElectrochemistry01 natural sciencesIonlaw.inventionInorganic ChemistryMetalCrystallaw[CHIM.CRIS]Chemical Sciences/Cristallography[CHIM.COOR]Chemical Sciences/Coordination chemistryCrystallizationTitanium010405 organic chemistryChemistryLigandMixed‐metal complexes0104 chemical sciencesCrystallographyOctahedronvisual_artvisual_art.visual_art_mediumHafniumSolid solution
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Polyoxometalate salts of cationic nitronyl nitroxide free radicals

2008

The cationic nitronyl nitroxide free radical of the N-methylpyridinium type p-MepyNN + has been combined with [Mo 8 0 26 ] 4- and Keggin [SiW 12 0 40 ] 4- polyanions to afford salts ( p-MepyNN) 4 [Mo 8 0 26 ] DMSO (DMSO = dimethylsulfoxide) (1) and (p-MepyNN)4[SiW 12 0 40 ] 6DMF (DMF = dimethylformamide) (2). Herein, their structural and magnetic properties are described.

Nitroxide mediated radical polymerizationChemistryMagnetismRadicalCationic polymerizationGeneral ChemistryCondensed Matter PhysicsPhotochemistrychemistry.chemical_compoundMetallatePolyoxometalatePolymer chemistryDimethylformamideGeneral Materials ScienceGroup 2 organometallic chemistrySolid State Sciences
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TiO2 Impregnated with Polyoxometallate as Photomediator in 2-Propanol Gas-Solid Regime Photocatalytic Degradation

2008

Photocatalysis TiO2 Polyoxometallate 2-Propanol
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TiO2-H3PW12O40 binary solids prepared in different conditions: a comparison of their photocatalytic activity

2010

Settore CHIM/07 - Fondamenti Chimici Delle Tecnologiepolyoxometallates TiO2 photocatalysis H3PW12O40
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Solid-state cis–trans isomerism in bis(oxamato)palladate(ii) complexes: synthesis, structural studies and catalytic activity

2014

A new generation of bis(oxamato)palladate(II) monomeric complexes has been prepared by using N-2,6-dimethylphenyloxamate (2,6-Me2pma) as the ligand. Four alkaline salts of the complex, namely {[Na(H2O)]2trans-[PdII(2,6-Me2pma)2]}n (1a), {[Na4(H2O)2]cis-[PdII(2,6-Me2pma)2]2}n (1b), {[K4(H2O)3]cis-[PdII(2,6-Me2pma)2]2}n (2), {[Rb4(H2O)3]cis-[PdII(2,6-Me2pma)2]2}n (3) and {[Cs6(H2O)7]trans-[PdII(2,6-Me2pma)2]2cis-[PdII(2,6-Me2pma)2]}n·3nH2O (4), were obtained and structurally characterized by single crystal X-ray diffraction. Both the cis and trans stereoisomers of the [PdII(2,6-Me2pma)2]2− complex anion were isolated in the solid state, in a cation-dependent manner. The trans-isomer as the so…

StereochemistryLigandArylIodobenzenechemistry.chemical_elementGeneral ChemistryCondensed Matter PhysicsMedicinal chemistrychemistry.chemical_compoundMetallatechemistrySuzuki reactionGeneral Materials ScienceCis–trans isomerismPalladiumMonoclinic crystal systemCrystEngComm
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Role of the support on the activity of H3PW12O40 supported on SiO2 or TiO2 in Catalytic and Photocatalytic propene hydration: An EPR Study

2016

Catalytic and catalytic photo-assisted hydration of propene to 2-propanol in gas-solid regime at atmospheric pressure and 85°C were carried out by using the Keggin heteropolyacid (HPA) H3PW12O40 (PW12) supported on home prepared SiO2, WO3, TiO2 or N-doped TiO2. The HPA played the key role both in catalytic and photocatalytic reactions; however, the support strongly influenced the binary material performance. The contemporary presence of heat and UV light improved the activity of the (photo)catalysts. EPR (Electron Paramagnetic Resonance) has been used to understand the intimate mechanism underlying the photoactivity of the supported heteropolyacid and the role played by the support.

Supported polyoxometallates propene hydration EPR studySettore CHIM/07 - Fondamenti Chimici Delle Tecnologie
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H3PW12O40 SUPPORTED ON DIFFERENT OXIDES: INFLUENCE OF THE SUPPORT ON THE CATALYTIC AND CATALYTIC PHOTO-ASSISTED PROPENE HYDRATION

2012

polyoxometallates propene hydrationSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie
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