Search results for " Coating."

showing 10 items of 2558 documents

Distinct photodynamics of κ-N and κ-C pseudoisomeric iron(ii) complexes

2021

Two closely related FeII complexes with 2,6-bis(1-ethyl-1H-1,2,3-triazol-4yl)pyridine and 2,6-bis(1,2,3-triazol-5-ylidene)pyridine ligands are presented to gain new insights into the photophysics of bis(tridentate) iron(II) complexes. The [Fe(N^N^N)2]2+ pseudoisomer sensitizes singlet oxygen through a MC state with nanosecond lifetime after MLCT excitation, while the bis(tridentate) [Fe(C^N^C)2]2+ pseudoisomer possesses a similar 3MLCT lifetime as the tris(bidentate) [Fe(C^C)2(N^N)]2+ complexes with four mesoionic carbenes. Financial support from the Deutsche Forschungsge-meinschaft [DFG, Priority Program SPP 2102] "Light-controlled reactivity of metal complexes" (BA 4467/7-1, LO 714/11-1, …

TrisDenticitysynthesisPyridinepyridine derivativecarbenoidIron compoundsCatalysisexperimental studychemistry.chemical_compoundPyridineMaterials Chemistryphysical chemistrycontrolled studyChemistrySinglet oxygenPyridine ligandsSinglet oxygenMetals and AlloysMesoionicGeneral ChemistryNanosecondPyridine ligandSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialsunclassified drugCrystallographyPhotophysicsiron complexisomerCeramics and CompositesCarbeneschemical structurephotodynamicsphysicsExcitationchemical parameters
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Hydrogen activation with perfluorinated organoboranes: 1,2,3-tris(pentafluorophenyl)-4,5,6,7-tetrafluoro-1-boraindene

2013

The perfluorinated boraindene was synthesized and fully characterized. Both computational and crystallographic data show that is antiaromatic. Compound was shown to react reversibly with H2 and to catalyse the hydrogenation of cyclohexene. The mechanism of catalysis was probed experimentally and computationally.

TrisHydrogenChemistryMetals and AlloysCyclohexeneCrystallographic datachemistry.chemical_elementGeneral ChemistryPhotochemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysischemistry.chemical_compoundPolymer chemistryMaterials ChemistryCeramics and Compositesta116AntiaromaticityChem. Commun.
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Self-Radiolysis of Tritiated Water Stored in Zeolites 4A: Production and Behavior of H 2 and O 2

2015

International audience; Radiolysis of confined water and self-radiolysis of tritiated water give rise to several unanswered questions. To take into account this double specificity, we studied systems of zeolites 4A containing tritiated water at different water loading ratios. Two tritiated waters were synthesized at the volumetric activities of 27 and 60 TBq L −1. For each one, five samples were prepared, differentiated by their water loading ratios, expressed in percentage, close to 4%, 7%, 11%, 14%, and 19%. The study of the radiolysis in those systems revealed a double role of zeolites 4A: first, they increase the decomposition of water. Then they enhance the recombination of the major s…

Tritiated water02 engineering and technology010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compound[CHIM.ANAL]Chemical Sciences/Analytical chemistryPhysical and Theoretical ChemistryConfined waterElectrolysis of waterChemistryRadiochemistry021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materials[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[ CHIM.POLY ] Chemical Sciences/Polymers[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]General Energy[CHIM.POLY]Chemical Sciences/PolymersRadiolysis[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistry[ CHIM.ANAL ] Chemical Sciences/Analytical chemistryWater loading[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]0210 nano-technology[CHIM.RADIO]Chemical Sciences/Radiochemistry[ CHIM.RADIO ] Chemical Sciences/Radiochemistry
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Supramolecular self-assembly on the B-Si(111)-(√3x√3) R30° surface: From single molecules to multicomponent networks

2017

Abstract Understanding the physical and chemical processes in which local interactions lead to ordered structures is of particular relevance to the realization of supramolecular architectures on surfaces. While spectacular patterns have been demonstrated on metal surfaces, there have been fewer studies of the spontaneous organization of supramolecular networks on semiconductor surfaces, where the formation of covalent bonds between organics and adatoms usually hamper the diffusion of molecules and their subsequent interactions with each other. However, the saturation of the dangling bonds at a semiconductor surface is known to make them inert and offers a unique way for the engineering of m…

Two-dimensional molecular networkSupramolecular chemistryNanotechnology02 engineering and technology010402 general chemistry01 natural sciencesLondon dispersion forcelaw.invention[SPI.MAT]Engineering Sciences [physics]/MaterialsMultiscale modellinglawMaterials ChemistryMolecule[SPI.NANO]Engineering Sciences [physics]/Micro and nanotechnologies/MicroelectronicsScanning tunneling microscopyTopology (chemistry)[SPI.ACOU]Engineering Sciences [physics]/Acoustics [physics.class-ph]ChemistryIntermolecular forceSemiconductor surfacesMetals and AlloysDangling bondSurfaces and InterfacesGeneral ChemistrySelf-assembly Intermolecular forces021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSelf-assemblyScanning tunneling microscope0210 nano-technology
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Hybrid materials with nanoscopic anion-binding pockets for the colorimetric sensing of phosphate in water using displacement assays

2008

Mesoporous amino-functionalised solids containing certain dyes have been used as suitable anion hosts in displacement assays for the colorimetric signalling of phosphate in water. Amoros del Toro, Pedro Jose, Pedro.Amoros@uv.es

UNESCO::QUÍMICAInorganic chemistryAnionNanotechnologyPhosphateHybrid materials ; Anion ; Colorimetry ; Phosphate:QUÍMICA [UNESCO]CatalysisIonchemistry.chemical_compoundMaterials ChemistryAnion bindingColorimetryNanoscopic scaleUNESCO::QUÍMICA::Química inorgánicaMetals and AlloysGeneral ChemistryPhosphate:QUÍMICA::Química inorgánica [UNESCO]Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryCeramics and CompositesColorimetryHybrid materialsMesoporous materialHybrid materialDisplacement (fluid)
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Reduction of tris(benzene-1,2-dithiolate)molybdenum(VI) by hydroxide ions in dry tetrahydrofuran solution.

2001

Tris(benzene-1,2-dithiolate)molybdenum(VI) reacts rapidly and quantitatively with tetrabutylammonium hydroxide to yield the corresponding Mo(V) and Mo(IV) complexes and hydrogen peroxide; the reaction has been executed in dry tetrahydrofuran where the reaction rate shows a fair dependence on complex and OH2 concentrations. Cervilla Avalos, Antonio, Antonio.Cervilla@uv.es ; Perez Pla, Francisco, Francisco.Perez@uv.es ; Llopis Jover, Elisa, Elisa.Llopis@uv.es

UNESCO::QUÍMICAInorganic chemistrychemistry.chemical_element:QUÍMICA [UNESCO]CatalysisReaction ratechemistry.chemical_compoundMaterials ChemistryReduction ; Hydroxide ions ; Tetrahydrofuran solution ; Hydrogen peroxide ; OH2Hydrogen peroxideBenzeneTetrahydrofuranReductionUNESCO::QUÍMICA::Química inorgánicaTetrabutylammonium hydroxideMetals and AlloysGeneral ChemistryHydrogen peroxide:QUÍMICA::Química inorgánica [UNESCO]Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsHydroxide ionschemistryOH2MolybdenumYield (chemistry)Ceramics and CompositesHydroxideTetrahydrofuran solutionChemical communications (Cambridge, England)
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The selective oxidative dehydrogenation of ethane over hydrothermally synthesised MoVTeNb catalysts

2002

Mo–V–Te–Nb metal oxide catalysts prepared by hydrothermal synthesis and heat-treated in N2 at high temperatures (600–700 °C) show high activity and selectivity for the oxidative dehydrogenation of ethane to ethene. Yields of ethene of 75% have been obtained at 400 °C on the best catalysts. Dejoz Garcia, Ana Maria, Ana.M.Dejoz@uv.es

UNESCO::QUÍMICAOxideOxidative phosphorylation:QUÍMICA [UNESCO]CatalysisCatalysisMetalchemistry.chemical_compoundMaterials ChemistryHydrothermal synthesisOrganic chemistryHigh activityHydrothermal synthesisDehydrogenationEthaneCatalystsUNESCO::QUÍMICA::Química inorgánicaChemistryMetals and AlloysGeneral Chemistry:QUÍMICA::Química inorgánica [UNESCO]Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsOxidative dehydrogenation ; Hydrothermal synthesis ; Ethane ; Catalystsvisual_artCeramics and Compositesvisual_art.visual_art_mediumSelectivityOxidative dehydrogenationChem. Commun.
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[Fe(sal2-trien)][Ni(dmit)2]: towards switchable spin crossover molecular conductors

2004

A cooperative spin transition behaviour with a wide hysteresis loop (30 K) around 240 K has been observed, for the first time, in a salt based on the redox active [Ni(dmit)2]¯, anion and the [Fe(sal2-trien)]+ spin crossover cation. Real Cabezos, Jose Antonio, Jose.A.Real@uv.es

UNESCO::QUÍMICASpin transitionSalt (chemistry)Mineralogy:QUÍMICA [UNESCO]Fe(sal2-trien)][Ni(dmit)2CatalysisIonSpin crossoverMaterials ChemistryRedox activeElectrical conductorchemistry.chemical_classificationMolecular conductorsUNESCO::QUÍMICA::Química inorgánicaMolecular conductors ; Spin transition ; Salt based ; Fe(sal2-trien)][Ni(dmit)2Metals and AlloysSpin transitionSalt basedGeneral Chemistry:QUÍMICA::Química inorgánica [UNESCO]Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographychemistryCeramics and CompositesChemical Communications
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Coexistence of ferro- and antiferromagnetic interactions in a metal-organic radical-based (6,3)-helical network with large channels.

2005

A metal–organic open-framework with an unprecedented (6,3)-helical topology, large channels and mixed ferro- and antiferromagnetic interactions has been synthesized using a three-connecting tricarboxylic polychlorotriphenylmethyl radical and Co(II) ions. Lloret Pastor, Francisco, Francisco.Lloret@uv.es

UNESCO::QUÍMICA::Química inorgánicaChemistryUNESCO::QUÍMICAMetals and AlloysMetal-organicMineralogyGeneral Chemistry:QUÍMICA::Química inorgánica [UNESCO]:QUÍMICA [UNESCO]CatalysisSintetitzationFerro and antiferromagnetic ; Metal-organic ; Coexistence ; Tricarboxylic polychlorotriphenylmethyl radical ; SintetitzationSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonChemical physicsMaterials ChemistryCeramics and CompositesAntiferromagnetismCondensed Matter::Strongly Correlated ElectronsTricarboxylic polychlorotriphenylmethyl radicalFerro and antiferromagneticTopology (chemistry)CoexistenceChemical communications (Cambridge, England)
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UV photoexcitation of a dissolved metalloid Ge9 cluster compound and its extensive ultrafast response.

2015

Femtosecond pump-probe absorption spectroscopy in tetrahydrofuran solution has been used to investigate the dynamics of a metalloid cluster compound {Ge9[Si(SiMe3)3]3}(-). Upon UV photoexcitation, the transients in the near-infrared spectral region showed signatures reminiscent of excess electrons in THF (bound or quasi-free) whereas in the visible part excited state dynamics of the cluster complex dominates.

UV photoexcitationgermanium clustersAbsorption spectroscopyMetals and AlloysGeneral ChemistryElectronPhotochemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsPhotoexcitationchemistry.chemical_compoundchemistryExcited stateFemtosecondMaterials ChemistryCeramics and CompositesCluster (physics)Metalloidta116TetrahydrofuranChemical communications (Cambridge, England)
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