Search results for "LANTHANIDE"

showing 10 items of 230 documents

Coexistence of long-range antiferromagnetic order and slow relaxation of the magnetization in the first lanthanide complex of a 1,2,4-benzotriazinyl …

2017

The first lanthanide complex of a 1,2,4-benzotriazinyl radical (1), Dy(1)(tbacac)3 (2, tbacac = 2,2,6,6-tetramethyl-3,5-heptane-dionato), was synthesised and found to have an antiferromagnetically ordered ground state with a metamagnetic phase diagram and a critical field of 0.91 T at 1.85 K. The application of a small dc field revealed the single-molecule magnet behaviour of 2, illustrating the coexistence of long-range antiferromagnetic order and slow relaxation of the magnetization. peerReviewed

LanthanideCondensed matter physics010405 organic chemistryChemistryRelaxation (NMR)[CHIM.MATE]Chemical Sciences/Material chemistrykompleksiyhdisteetharvinaiset maametallit010402 general chemistry01 natural sciences3. Good health0104 chemical sciencesInorganic ChemistryMagnetizationMagnetmagnetismAntiferromagnetismcoordination complexesmagnetismiGround staterare earth metalsCritical fieldta116ComputingMilieux_MISCELLANEOUSPhase diagram
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Custom coordination environments for lanthanoids: tripodal ligands achieve near-perfect octahedral coordination for two dysprosium-based molecular na…

2017

Controlling the coordination sphere of lanthanoid complexes is a challenging critical step toward controlling their relaxation properties. Here we present the synthesis of hexacoordinated dysprosium single-molecule magnets, where tripodal ligands achieve a near-perfect octahedral coordination. We perform a complete experimental and theoretical investigation of their magnetic properties, including a full single-crystal magnetic anisotropy analysis. The combination of electrostatic and crystal-field computational tools (SIMPRE and CONDON codes) allows us to explain the static behavior of these systems in detail. NRF-2015R1A2A1A10055658 Grant NRF-2012-0008901 NRF2010-0020209 ERC-CoG-647301 DEC…

LanthanideCoordination sphere010405 organic chemistryUNESCO::QUÍMICARelaxation (NMR)chemistry.chemical_element010402 general chemistry01 natural sciences:QUÍMICA [UNESCO]0104 chemical sciencesInorganic ChemistryMagnetic anisotropychemistryOctahedronComputational chemistryChemical physicsMagnetDysprosiumPhysical and Theoretical ChemistryCoordination geometry
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Coordinatively Unsaturated Lanthanide(III) Helicates: Luminescence Sensors for Adenosine Monophosphate in Aqueous Media

2016

Coordinatively unsaturated double-stranded helicates [(H2 L)2 Eu2 (NO3 )2 (H2 O)4 ](NO3 )4 , [(H2 L)2 Tb2 (H2 O)6 ](NO3 )6 , and [(H2 L)2 Tb2 (H2 O)6 ]Cl6 (H2 L=butanedioicacid-1,4-bis[2-(2-pyridinylmethylene)hydrazide]) are easily obtained by self-assembly from the ligand and the corresponding lanthanide(III) salts. The complexes are characterized by X-ray crystallography showing the helical arrangement of the ligands. Co-ligands at the metal ions can be easily substituted by appropriate anions. A specific luminescence response of AMP in presence of ADP, ATP, and other anions is observed. Specificity is assigned to the perfect size match of AMP to bridge the two metal centers and to replac…

LanthanideCoordination sphereadenosine monophosphateStereochemistryMetal ions in aqueous solutionHydrazide010402 general chemistry01 natural sciencesCatalysisMetalchemistry.chemical_compoundluminescencelanthanidesta116sensingQuenching (fluorescence)ChemistryLigand010405 organic chemistryhelicatesGeneral ChemistryGeneral Medicine0104 chemical sciences3. Good healthCrystallographyvisual_artvisual_art.visual_art_mediumLuminescenceAngewandte Chemie International Edition
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Gas-phase hydrogenation of propionitrile on copper-lanthanide oxides

2009

Abstract The hydrogenation of propionitrile on copper-lanthanide oxide catalysts (2Cu·CeO 2 and 4Cu·Ln 2 O 3 (Ln = La, Pr, Nd)) was studied in the gas phase. The activity of the catalysts varies with the lanthanide in the order 2Cu·CeO 2  > 4Cu·Pr 2 O 3  > 4Cu·La 2 O 3  ≥ 4Cu·Nd 2 O 3 , while the activation energies varies in the opposite order, except for 2Cu·CeO 2 . The main product was the primary amine, n -propylamine. The formation of the unstable imine CH 3 CH 2 N CHCH 3 as a major product over 2Cu·CeO 2 seems to be consistent with the acidity of the catalyst. The catalysts were more selective than conventional copper impregnation catalysts, Cu (10 wt.%) on SiO 2 , La 2 O 3 or CeO 2 ,…

LanthanideCopper oxideInorganic chemistryImineprimary aminechemistry.chemical_element010402 general chemistryHeterogeneous catalysis01 natural sciencesCatalysisCatalysischemistry.chemical_compound[ CHIM.CATA ] Chemical Sciences/Catalysisgas-phase hydrogenationPhysical and Theoretical Chemistrysupported catalystsComputingMilieux_MISCELLANEOUS010405 organic chemistryProcess Chemistry and Technologypropionitrile[CHIM.CATA]Chemical Sciences/CatalysisCopper0104 chemical scienceschemistrycopperAmine gas treatingPropionitrile
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Crystal Structures of Ln2Pd2Pb (Ln: Y, La, Ce, Pr, Nd, Sm, Gd, Tb, Dy, Ho, Er, Tm, and Lu) Compounds.

2004

LanthanideCrystallographyChemistryGeneral MedicineCrystal structureChemInform
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X-ray powder diffraction data for five lanthanoid chromates [Ln2(CrO4)3(H2O)5]·2H2O (Ln=La,Pr,Nd,Sm,Eu)

1994

X-ray powder diffraction data are reported for a series of isomorphous compounds of [Ln2(CrO4)3(H2O)5]·2H2O, where Ln=La, Pr, Nd, Sm, or Eu. The compounds crystallize in monoclinic space group P21/c (No: 14) with Z=4. Refined unit cell parameters and indexed powder diffraction patterns are given.

LanthanideCrystallographyRadiationMaterials scienceX-rayGeneral Materials ScienceCondensed Matter PhysicsInstrumentationPowder diffractionMonoclinic crystal systemPowder Diffraction
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Fast volatilization of some lanthanide and actinide elements from titanium surfaces

1989

The ad- and desorption of trace quantities of the lanthanide elements lanthanum, praseodymium, neodymium, samarium, europium, gadolinium, dysprosium, and ytterbium and of the actinide elements americium and curium were investigated by thermochromatographic and isothermal measurements with hot titanium columns. The adsorption enthalpies deduced from the experimental data are in reasonable agreement with calculated values which indicate considerable variations in volatility under such conditions. More volatile elements can quickly be separated from less volatile elements by heating the mixture on titanium in high vacuum.

LanthanideCuriumChemistryPraseodymiumClinical BiochemistryInorganic chemistrychemistry.chemical_elementAmericiumGeneral MedicineActinideBiochemistryAnalytical ChemistrySamariumLanthanumGeneral Materials ScienceEuropiumFresenius' Zeitschrift f�r Analytische Chemie
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Production and Radiochemical Separation of the Auger Electron Emitter140Nd

2000

Among the Auger electron emitters, the radiolanthanide 140Nd has some unique nuclear properties with potential for endoradiotherapeutic applications. In the present study, 140Nd was produced via the 140Ce(3He,3n) nuclear process at the FZ Julich CV28 cyclotron, irradiating CeO2 with 3He particles of 36 MeV primary energy. Yields of about 5 MBq 140Nd per microAh were experimentally obtained. Batch yields of > 100 MBq 140Nd were reached. 140Nd was separated in 75 +/- 5% radiochemical yield using a two-step process, first by extracting the bulk of the target material according to a Ce(IV)/Nd(III) separation, then by final ion exchange purification.

LanthanideCyclotronElectronsElectronlaw.inventionPhysical PhenomenalawPhysical phenomenaMedicineRadiology Nuclear Medicine and imagingNeodymiumRadioisotopesAuger electron spectroscopyRadiochemistryIon exchangebusiness.industryPhysicsRadiochemistryAuger electron emitterHematologyGeneral MedicineOncologyYield (chemistry)RadiopharmaceuticalsNuclear medicinebusinessActa Oncologica
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New 3d–4f supramolecular systems constructed by [Fe(bipy)(CN)4]− and partially blocked lanthanide cations

2009

Abstract The reaction of acetonitrile (1–5) and mixed acetonitrile/water 1:1 (6–9) solutions containing the cyanide-bearing [Fe(bipy)(CN)4]− building block (bipy = 2,2′-bipyridine) and the partially blocked [Ln(bpym)]3+ cation (Ln = lanthanide trivalent cation and bpym = 2,2′-bipyrimidine) has afforded two new families of 3d–4f supramolecular assemblies of formula [Ln(bpym)(NO3)2(H2O)3][Fe(bipy)(CN)4] · H2O · CH3CN [Ln = Sm (1), Gd (2), Tb (3), Dy (4) and Ho (5)] and [Ln(bpym)(NO3)2(H2O)4][Fe(bipy)(CN)4] [Ln = Pr (6), Nd (7), Sm (8), Gd (9)]. They crystallize in the P21/c (1–5) and P2/c (6–9) space groups and their structures are made up of [Fe(bipy)(CN)4]− anions (1–9) and [Ln(bpym)(NO3)2(…

LanthanideDenticityHydrogen bondChemistrySupramolecular chemistrySpace groupInorganic ChemistryCrystallographychemistry.chemical_compoundOctahedronMaterials ChemistryMoleculePhysical and Theoretical ChemistryAcetonitrilePolyhedron
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[Fe(phen)(CN)4]−: a suitable metalloligand unit to build 3d–4f heterobimetallic complexes with mixed bpym-cyano bridges (phen = 1,10-phenantroline, b…

2010

The synthesis, crystal structure and magnetic properties of a new series of mixed 3d–4f complexes with the formula [{FeIII(phen)(CN)3(μ-CN)}4Ln2III(NO3)2(H2O)6(μ-bpym)]·nH2O [Ln = Eu (1), Gd (2), Dy (3) and Ho (4); n = 8 (1, 3 and 4) and 11 (2); phen = 1,10-phenantroline; bpym = 2,2′-bipyrimidine] are discussed here. Compounds 1–4 are centrosymmetric hexanuclear species whose structure is made up of two cyano-bridged {Fe2IIILnIII} heterobimetallic moieties which are connected through a bis-bidentate bpym molecule between the two rare-earth centers. The values of the iron–lanthanide distance across the single cyano-bridge are Fe(1)⋯Eu(1) = 5.5587(8) and Fe(2)⋯Eu(1) = 5.4908(8) A (1), Fe(1)⋯G…

LanthanideDenticityStereochemistryChemistryHydrogen bondGeneral ChemistryCrystal structureCondensed Matter PhysicsSquare antiprismCrystallographyOctahedronIntramolecular forceMoleculeGeneral Materials ScienceCrystEngComm
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