Search results for "LANTHANIDE"

showing 10 items of 230 documents

Lanthanide Discrimination with Hydroxyl-Decorated Flexible Metal–Organic Frameworks

2018

We report two new highly crystalline metal-organic frameworks (MOFs), derived from the natural amino acids serine (1) and threonine (2), featuring hexagonal channels densely decorated with hydroxyl groups belonging to the amino acid residues. Both 1 and 2 are capable of discriminating, via solid-phase extraction, a mixture of selected chloride salts of lanthanides on the basis of their size, chemical affinity, and/or the flexibility of the network. In addition, this discrimination follows a completely different trend for 1 and 2 because of the different locations of the hydroxyl groups in each compound, which is evocative of steric complementarity between the substrate and receptor. Last bu…

Steric effectschemistry.chemical_classificationLanthanideSubstrate (chemistry)02 engineering and technologyCrystal structure010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesChloride0104 chemical sciencesAmino acidInorganic ChemistryCrystallographychemistryChemical affinitymedicineMetal-organic frameworkPhysical and Theoretical Chemistry0210 nano-technologymedicine.drugInorganic Chemistry
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Structure and superconductivity in LnNi2B2C: comparison of calculation and experiment

2001

Abstract The experimental relation between the superconducting transition temperature ( T c ) and lattice size for the lanthanide nickel borocarbides is clarified. The electronic density of states (DOS) at the Fermi energy is calculated by the LMTO method for selected non-magnetic lanthanides. The T c and the DOS are both shown to scale in the same way with a structural parameter that characterizes the bond angle in the NiB 4 tetrahedra. The results strongly support arguments that the suppression of superconductivity on going from smaller to larger lanthanides in the quaternary nickel borocarbides is structurally driven. A structure– T c relationship of this type is unusual for intermetalli…

SuperconductivityLanthanideCondensed matter physicsIntermetallicchemistry.chemical_elementFermi energyGeneral ChemistryCondensed Matter PhysicsCondensed Matter::Materials ScienceNickelMolecular geometryTight bindingchemistryCondensed Matter::SuperconductivityMaterials ChemistryTetrahedronCondensed Matter::Strongly Correlated ElectronsSolid State Communications
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Source and Nature of Inhaled Atmospheric Dust from Trace Element Analyses of Human Bronchial Fluids

2011

International audience; Rapid volcanic eruptions quickly ejecting large amounts of dust provoke the accumulation of heavy metals in people living in surrounding areas. Analyses of bronchoalveolar lavage samples (BAL) collected from people exposed to the paroxysmal 2001 Etna eruption revealed a strong enrichment of many toxic heavy metals. Comparing the BAL to the dust composition of southeastern Sicily, we found that only V, Cr, Mn, Fe, Co, and U enrichment could be related to the volcanic event, whereas Ni, Cu, Cd, and Pb contents come from the dissolution of particles of anthropogenic origin. Furthermore, the nature of these inhaled anthropogenic particles was revealed by anomalous La and…

TEPHRA010504 meteorology & atmospheric sciences[SDU.STU]Sciences of the Universe [physics]/Earth Sciences550 - Earth sciencesVolcanic EruptionsPM2.5010501 environmental sciences01 natural sciencesvolcanic eruptionBRONCHOALVEOLAR LAVAGEatmospheric particulatetrace element distributionDISSOLUTIONTRACEREnvironmental ChemistryHumansVOLCANIC ASHTephraDissolutionSicilyERUPTION0105 earth and related environmental sciencesgeographyInhalation Exposuregeography.geographical_feature_categoryChemistryAtmosphereTrace elementDustGeneral ChemistryAtmospheric dustParticulatesReference Standardsatmospheric particulate; trace element distribution; volcanic eruptionTrace ElementsSettore GEO/08 - Geochimica E Vulcanologiarespiratory tract diseasesTrace elements lanthanides medical geochemistry bronchoalveolar lavagesVolcanoSolubility13. Climate actionEnvironmental chemistryBronchoalveolar Lavage FluidVolcanic ashEnvironmental MonitoringASH PARTICLES
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COMPARISON OF THE PHOTOCATALYTIC DEGRADATION OF 2-PROPANOL IN GAS-SOLID AND LIQUID-SOLID SYSTEMS BY USING TiO2 – LnPc2 HYBRID POWDERS

2009

Photocatalytic degradation of 2-propanol was carried out as a probe reaction both in gas–solid and in liquid–solid systems in the presence of TiO2 both bare and impregnated with lanthanide (Sm, Gd, Ho) bis-phthalocyanines (LnPc2) used as sensitizers. Continuous and batch photo-reactors, irradiated with an equal flux of photons, were used in gas–solid and in liquid–solid systems, respectively. Propanone and acetaldehyde were the main intermediates found in both systems during 2-propanol oxidation, whereas carbon dioxide and water were the final oxidation products exclusively in the gas–solid regime. The photocatalysts exhibited significantly higher activity in the liquid–solid system than in…

TiO2Settore CHIM/07 - Fondamenti Chimici Delle TecnologieLanthanide bis-phthalocyanines 2-PropanolHeterogeneous photocatalysiLanthanide bis-phthalocyanines2-Propanol Heterogeneous photocatalysisTiO2
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Combination of single-molecule magnet behaviour and luminescence properties in a new series of lanthanide complexes with tris(pyrazolyl)borate and ol…

2020

A series of tris(pyrazolyl)borate mono-, di- and trinuclear complexes, [Tp2Ln]nX (Ln = Eu, Tb, Gd, Dy, Xn− = various mono-, bis- and tris(β-diketonates) has been prepared. The Tb3+ and Dy3+ complexes are luminescent single molecular magnets (SMM) and exhibit luminescence quantum efficiencies up to 73% for the Tb3+ and 4.4% for the Dy3+ compounds. Similar Eu3+ complexes display bright emission only at lower temperatures. The Dy3+ and Tb3+ complexes possess SMM behavior in a non-zero dc field at low temperatures, while the polynuclear Dy3+ complexes also show slow magnetic relaxation even in zero dc field up to 8 K. Ueff-values determined from dynamic magnetic measurements were up to 31 and 6…

TrisLanthanideMaterials scienceRelaxation (NMR)ElectroluminescenceInorganic ChemistryCrystallographychemistry.chemical_compoundsymbols.namesakechemistryIntramolecular forcesymbolsSingle-molecule magnetLuminescenceRaman spectroscopyDalton transactions (Cambridge, England : 2003)
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Rational design and modelling of f-block molecular nanomagnets

2016

Los imanes monomoleculares o moléculas imán, por sus siglas en inglés SMMs, han suscitado una gran atención en los últimos años debido a sus extraordinarias propiedades físicas. Los cristales de este tipo de moléculas se caracterizan por presentar relajación lenta de la magnetización a baja temperatura, así como curvas de histeresis magnética. Estas moléculas se encuentran entre las entidades con comportamiento magnético más complejas, mostrando fenómenos cuánticos tales como efecto túnel en la magnetización, coherencia cuántica o interferencia cuántica. Por esto, se han postulado como candidatos prometedores para el diseño de bits cuánticos (qubits) de espín en computación cuántica. La pri…

UNESCO::FÍSICA::Electromagnetismo ::MagnetismoUNESCO::QUÍMICA::Química inorgánica ::Estructura de los compuestos inorgánicoslanthanides and actinides:FÍSICA::Electromagnetismo ::Magnetismo [UNESCO]:FÍSICA::Física del estado sólido ::Estados electrónicos [UNESCO]:FÍSICA::Física molecular::Moléculas inorgánicas [UNESCO]:QUÍMICA::Química inorgánica ::Estructura de los compuestos inorgánicos [UNESCO]UNESCO::QUÍMICA::Química inorgánica ::Compuestos de coordinaciónUNESCO::FÍSICA::Física molecular::Moléculas inorgánicas:QUÍMICA::Química inorgánica ::Compuestos de coordinación [UNESCO]computational chemistryquantum computingUNESCO::FÍSICA::Física del estado sólido ::Estados electrónicosmolecular nanomagnetism:QUÍMICA::Química inorgánica ::Tierras raras [UNESCO]coordination complexes:QUÍMICA::Química inorgánica ::Compuestos organometálicos [UNESCO]UNESCO::QUÍMICA::Química inorgánica ::Tierras rarasUNESCO::QUÍMICA::Química inorgánica ::Compuestos organometálicoscrystal field
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Linear Coassembly of Upconversion and Perovskite Nanoparticles: Sensitized Upconversion Emission of Perovskites by Lanthanide‐Doped Nanoparticles

2020

Sensitized emission of lead halide perovskite nanoparticles (LHPNPs) can be achieved by near‐infrared (NIR) excitation of nearby lanthanide‐doped upconversion nanoparticles (UCNPs) by using a low‐cost diode laser. Here, the first preparation of linear assemblies of core and core–shell NPs, as well as linear coassemblies of LHPNPs and UCNPs, within an open peapod‐like lead sulfate shell are reported. UCNPs with a NaYF4 matrix doped with ytterbium and thulium or erbium, and with an inert shell of NaYF4 in the case of core‐shell, and all‐inorganic CsPbX3 NPs (X = halide) are chosen for these studies. Interestingly, the lead sulfate shell enhances the luminescence of the core/core– shell UCNPs …

YtterbiumLanthanideMaterials sciencechemistry.chemical_elementNanoparticle02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesPhoton upconversion0104 chemical sciencesElectronic Optical and Magnetic MaterialsBiomaterialsErbiumThuliumchemistryChemical engineeringElectrochemistry0210 nano-technologyLuminescencePerovskite (structure)Advanced Functional Materials
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On the development of a new approach to the design of lanthanide-based materials for solution-processed OLEDs

2019

The targeted design of lanthanide-based emitters for solution-processed organic light-emitting diodes (OLEDs) resulted in obtaining an NIR OLED with one of the highest efficiencies among ytterbium-based solution-processed OLEDs (30 μW W-1). The design was aimed at the combination of high luminescence efficiency with solubility and charge carrier mobility. The latter was achieved thanks to the introduction of the purposefully selected neutral ligands, which combine electron mobility and the ability to sensitize lanthanide luminescence. Besides, the HOMO and LUMO energies and charge carrier mobility of solution-processed thin films of coordination compounds were measured experimentally for th…

YtterbiumLanthanidechemistry.chemical_classificationElectron mobilityMaterials science010405 organic chemistrybusiness.industrychemistry.chemical_element010402 general chemistry01 natural sciences0104 chemical sciencesCoordination complexInorganic ChemistrychemistryOLEDOptoelectronicsLuminescenceEuropiumbusinessHOMO/LUMODalton Transactions
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Chemistry of lanthanide–metal carbonyl systems: the ytterbium–chromium carbonyls interaction

2001

Abstract The interaction of the chromium carbonyl hydrides HCr2(CO)10− or HCr(CO)5− with Yb(acac)3·3H2O has been investigated, and the experimental conditions leading to the isolation of ytterbium–chromium carbonyl complex species are reported. Formulation of the coordination compounds produced by such interactions has been proposed on the basis of analytical data and IR spectroscopy.

YtterbiumLanthanidechemistry.chemical_classificationMechanical EngineeringAcetylacetoneInorganic chemistryMetals and Alloyschemistry.chemical_elementInfrared spectroscopyMetal carbonylChemical synthesisCoordination complexchemistry.chemical_compoundChromiumchemistryMechanics of MaterialsMaterials ChemistryJournal of Alloys and Compounds
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Actinide and lanthanide thin-layer developments using a drop-on-demand printing system

2023

Actinide and lanthanide thin layers with specific requirements regarding thickness, homogeneity, chemical purity, mechanical stability, and backing properties are applied in a multitude of physics and chemistry experiments. A novel target preparation method, the so-called “Drop-on-Demand” (DoD) technique, based on a commercial nanoliter (nL) dispenser is applied since a few years in the Nuclear Chemistry unit at Johannes Gutenberg University Mainz. The wetting behaviour of the nL droplets on the substrate’s surface is a key parameter determining the spatial distribution of the deposited material after evaporation. By switching from aqueous to organic solvents as well as by substrate surface…

aktinoidit lantanoiditactinideslanthanidesdrop-on-demand printing systemharvinaiset maametallit
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