Search results for "LANTHANIDE"

showing 10 items of 230 documents

Adamantylcalixarenes with CMPO groups at the wide rim: synthesis and extraction of lanthanides and actinides

2007

Abstract Starting from p -adamantylcalix[4]- and [6]arenes functionalized with carboxylic acid or ester groups at the adamantane nuclei, carbamoylmethylphosphine oxide (CMPO)-containing ligands of a novel type were synthesized. They were studied as extractants for a series of f-block elements including radioactive 152 Eu(III), 241 Am(III), 233 U(VI), and 239 Pu(IV). Tetrameric ligand 4b in which CMPO residues are connected to adamantane nuclei through methylene groups gave the best extraction results for lanthanides and actinides. For all the ligands the extraction efficiency does not decrease at higher nitric acid concentration. Although the discrimination between trivalent actinides and l…

Lanthanidechemistry.chemical_classificationChemistryLigandCarboxylic acidAdamantaneOrganic ChemistryExtraction (chemistry)ActinideBiochemistrychemistry.chemical_compoundNitric acidDrug DiscoveryMethyleneNuclear chemistryTetrahedron
researchProduct

Trinuclear Lanthanide Coordination Clusters: Single-Molecule-Magnet Behavior and Catalytic Activity in the Friedel-Crafts Alkylation Reaction.

2019

A new multidentate ligand (H3 L) was synthesized by the condensation reaction of 4-tert-butyl-2,6-diformylphenol and 2-amino-4-nitrophenol. The reaction of the ligand with hydrated lanthanide nitrate produced two isostructural trinuclear coordination clusters: [DyLn3 L3 (DMF)3 (H2 O)2 ] ⋅ 3.8DMFLn=Dy (1) and Nd (2) (DMF=N, N-dimethylformamide). Single-crystal X-ray diffraction analysis revealed that there are three lanthanide ions arranged in an almost perfect linear fashion in both complexes. Magnetic studies show single-molecule-magnet (SMM) behavior in the Dy derivative with τ0 =1.7×10-6  s and a thermal energy barrier of 7.0 cm-1 . Both complexes were used as catalysts towards the Fried…

Lanthanidechemistry.chemical_classificationDenticity010405 organic chemistryLigandChemistryGeneral ChemistryAlkylation010402 general chemistryCondensation reaction01 natural sciences0104 chemical sciencesCoordination complexCrystallographyIsostructuralFriedel–Crafts reactionChemPlusChem
researchProduct

Slow magnetic relaxation in carbonato-bridged dinuclear lanthanide(iii) complexes with 2,3-quinoxalinediolate ligands

2012

The coordination chemistry of the 2,3-quinoxalinediolate ligand with different lanthanide(iii) ions in basic media in air affords a new family of carbonato-bridged M 2 III compounds (M = Pr, Gd and Dy), the Dy 2 III analogue exhibiting slow magnetic relaxation behaviour typical of single-molecule magnets. This journal is © 2012 The Royal Society of Chemistry.

Lanthanidechemistry.chemical_classificationLigandChemistryInorganic chemistryMetals and AlloysGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonCoordination complexCrystallographyMagnetMaterials ChemistryCeramics and CompositesMagnetic relaxationChemical Communications
researchProduct

Understanding the Stabilization and Tunability of Divalent Europium 2.2.2B Cryptates

2021

Lanthanides such as europium with more accessible divalent states are useful for studying redox stability afforded by macrocyclic organic ligands. Substituted cryptands, such as 2.2.2B cryptand, that increase the oxidative stability of divalent europium also provide coordination environments that support synthetic alterations of Eu(II) cryptate complexes. Two single crystal structures were obtained containing nine-coordinate Eu(II) 2.2.2B cryptate complexes that differ by a single coordination site, the occupation of which is dictated by changes in reaction conditions. A crystal structure containing a [Eu(2.2.2B)Cl]+ complex is obtained from a methanol-THF solvent mixture, while a methanol-…

Lanthanidechemistry.chemical_classificationLigandCryptandchemistry.chemical_elementCrystal structureDivalentInorganic ChemistryCrystallographychemistryMoleculePhysical and Theoretical ChemistryEuropiumSingle crystalInorganic Chemistry
researchProduct

Group 3 and 4 metal alkyl and hydrido complexes containing a linked amido-cyclopentadienyl ligand: “constrained geometry” polymerization catalysts fo…

2002

Abstract In order to understand the nature of the putative cationic 12-electron species [M(η 5 :η 1 -C 5 R 4 SiMe 2 NR′)R″] + of titanium catalysts supported by a linked amido-cyclopentadienyl ligand, several derivatives with different cyclopentadienyl C 5 R 4 and amido substituents R′ were studied systematically. The use of tridentate variants (C 5 R 4 SiMe 2 NCH 2 CH 2 X) 2− (C 5 R 4 =C 5 Me 4 , C 5 H 4 , C 5 H 3 t Bu ; X=OMe, SMe, NMe 2 ) allowed the NMR spectroscopic observation of the titanium benzyl cations [Ti(η 5 :η 1 -C 5 Me 4 SiMe 2 NCH 2 CH 2 X)(CH 2 Ph)] + . Isoelectronic neutral rare earth metal complexes [Ln(η 5 :η 1 -C 5 R 4 SiMe 2 NR′)R″] can be expected to be active for pol…

Lanthanidechemistry.chemical_classificationLigandHydrideChemistryStereochemistryProcess Chemistry and TechnologyCationic polymerizationHomogeneous catalysisMedicinal chemistryCatalysisCyclopentadienyl complexPolymerizationPhysical and Theoretical ChemistryAlkylJournal of Molecular Catalysis A: Chemical
researchProduct

Crystal growth and structural remarks on malonate-based lanthanide coordination polymers

2016

The synthesis, structural characterization and thermal study of new coordination polymers (CPs) of formula [Ln2(mal)3(H2O)5]·2H2O [Ln = Ho (1·2H2O), Tb (1a), Dy (1b), Er (1c) and Yb (1d); mal = malonate], [Ln2(mal)3(H2O)6] [Ln = Sm (2) and Ce (2a)], [Ce2(mal)3(H2O)6]·2H2O (3·2H2O) and [Ce2(mal)3(H2O)3]·2H2O (4·2H2O) are presented. Complexes 1–4 have been also characterized by single crystal X-ray diffraction. The structure of 2 was previously reported (Elsegood, M. R. J., Husain, S., Private Communication, 2014) and it is very close to that of 3. In the light of these results and those previously reported in the literature for malonate-containing lanthanide(III) complexes, a detailed overvi…

Lanthanidechemistry.chemical_classificationMaterials science010405 organic chemistryHydrogen bondSupramolecular chemistryCrystal growthGeneral ChemistryCrystal structurePolymer010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical scienceschemistry.chemical_compoundCrystallographyMalonatechemistryGeneral Materials ScienceSingle crystalCrystEngComm
researchProduct

Effect of the remaining lanthanide catalysts on the hydrolytic and enzymatic degradation of poly-(ε-caprolactone)

2003

Poly-(e-caprolactone) is a biodegradable polymer, which can be used for both medical and environmental applications. Due to its multiple applications the synthesis of such a polymer has been attracting an increasing attention in the past few decades. In our work, the polymers were synthesised by bulk polymerisation, using different lanthanide halides as initiators. The lanthanide derivatives are known as very active catalysts in the ring-opening polymerisation of cyclic esters. Moreover, they are not toxic in comparison of catalysts, which are usually used for this synthesis. In this paper, the influence of the lanthanides on both the hydrolytic and enzymatic degradation of the PCL obtained…

Lanthanidechemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic Chemistrychemistry.chemical_elementPolymerCondensed Matter PhysicsChlorideBiodegradable polymerSamariumchemistry.chemical_compoundPolymerizationchemistryLanthanide trifluoromethanesulfonatesMaterials ChemistrymedicineOrganic chemistryCaprolactonemedicine.drugMacromolecular Symposia
researchProduct

Single ion magnets based on lanthanoid polyoxomolybdate complexes

2016

Polyoxometalate (POM) chemistry has recently offered excellent examples of single ion magnets (SIMs) and molecular spin qubits. Compared with conventional coordination compounds, POMs provide rigid and highly symmetric coordination sites. However, all POM-based SIMs reported to date exhibit a very limited range of possibilities for chemical processability. We present herein two new families of POM-based SIMs which are soluble in organic solvents: [Ln(β-Mo8O26)2]5− {LnIII = Tb, Dy, Ho, Er, Tm and Yb} and the functionalised POMs [Ln{Mo5O13(OMe)4NNC6H4-p-NO2}2]3− {LnIII = Tb, Dy, Ho, Er, Yb and Nd}. In addition, these two families represent the first SIMs based on polyoxomolybdates. A magneto-…

Lanthanidechemistry.chemical_classificationSingle ionChemistryUNESCO::QUÍMICAInorganic chemistry02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences:QUÍMICA [UNESCO]0104 chemical sciencesCoordination complexInorganic ChemistryCrystalCrystallographyMagnetPolyoxometalate[CHIM]Chemical Sciences0210 nano-technology
researchProduct

Neutral and cationic trimethylsilylmethyl complexes of the rare earth metals supported by a crown ether: synthesis and structural characterization

2003

The synthesis of a series of thermally robust, isolable trimethylsilylmethyl complexes of the rare earth metals stabilized by 12-crown-4 [Ln(CH2SiMe3)3(12-crown-4)] (Ln = Sc, Y, Sm, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu) is reported. The crystallographically characterized yttrium and lutetium complexes [Ln(CH2SiMe3)3(12-crown-4)] exhibit facial coordination of the crown ether at the neutral lanthanide trialkyl unit. The coordination geometry can be derived from a capped octahedron. VT NMR spectroscopic studies revealed a labile coordination of the crown ether in thf solution. Reaction of the diamagnetic derivatives with triethylammonium tetraphenylborate in thf results in the clean formation of th…

Lanthanidechemistry.chemical_classificationTetraphenylborateStereochemistryCationic polymerizationchemistry.chemical_elementYttriumLutetiumInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryOctahedronCrown etherCoordination geometryDalton Transactions
researchProduct

Carbamoylmethylphosphinoxide derivatives based on the triphenylmethane skeleton. Synthesis and extraction properties.

2005

Two different strategies were used to synthesize tri(2-alkoxy-5-nitrophenyl)methanes 6a,b. The X-ray structures of 6a and its precursor 5 show the molecules in a conformation with a syn-orientation of the nitro and alkoxy groups. Hydrogenation and acylation by the appropriate active ester gave the corresponding tri-CMPO derivatives 4a,b. Their ability to complex lanthanide ions was studied by NMR spectroscopy and by nuclear magnetic relaxation dispersion and further characterized by quantum mechanical calculations. Extraction experiments from acidic solution to dichloromethane reveal a reasonable selectivity of Am(III) over Eu(III), but in contrast to similar tetra-CMPOs derivatives of cali…

Lanthanidechemistry.chemical_classificationTriphenylmethaneOrganic ChemistryNitro compoundNuclear magnetic resonance spectroscopyAcylationchemistry.chemical_compoundchemistryComputational chemistryAlkoxy groupOrganic chemistryMoleculeSelectivityThe Journal of organic chemistry
researchProduct