Search results for "LANTHANIDE"

The crystal structure of neodymium and europium chromate heptahydrate: Synthesis, infrared spectra, and thermal behavior of lanthanoid chromate hepta…

1991

Abstract The crystal structures of Nd2(CrO4)3 · 7H2O and Eu2(CrO4)3 · 7H2O were determined by the conventional single-crystal X-ray diffraction technique. In addition, unit cell dimensions were measured for La2 (CrO4)3 · 7H2O and Sm2(CrO4)3 · 7H2O. All these compounds are isostructural. Crystals are monoclinic, space group P2 1 c . For Nd2(CrO4)3 · 7H2O, a = 8.052(4) A, b = 19.143(4) A, c = 13.326(6) A, β = 128.15(4)°, Z = 4, Dx = 3.14 Mg · m−3, T = 296(1); and for Eu2(CrO4)3 · 7H2O, a = 7.965(3) A, b = 18.985(4) A, c = 13.185(4) A, β = 128.00(2)°, Z = 4, Dx = 3.29 Mg · m−3, T = 296(1). Ln atoms are nine-coordinated so that the coordination polyhedron is a tricapped trigonal prism for Ln1 a…

Synthesis and X-ray Crystal Structures of (C5HiPr4)Ln(BH4)2(THF)(Ln = Nd and Sm), Versatile Precursors for Polymerization Catalysts

2000

The new half metallocenes [(C5HiPr4)Ln(BH4)2(THF)] [Ln = Sm (1) and Nd (2)], and [(C5HiPr4)U(BH4)3] (3) have been synthesized. The crystal structures of 1 and 2 and of the metallocenes [(C5HiPr4)2Ln(BH4)] [Ln = Sm (4) and Nd (5)] have been determined. The substitution of the BH4 groups of 1 and 2 by a nitrogen-based ligand is possible. In the presence of butyllithium, these complexes show an activity in isoprene and styrene polymerization.

Modification of calix[4]arenes with CMPO-functions at the wide rim. Synthesis, solution behavior, and separation of actinides from lanthanides

2003

Two calix[4]arene tetraethers (Y = C5H11, C14H29) bearing on their wide rim four –N(Me)–CO–CH2–P(O)Ph2 residues were synthesized for the first time. Their ability to extract lanthanides and actinides from an acidic aqueous phase to organic phases (CH2Cl2, NPHE) was studied. In comparison to the corresponding –NH-analogs, they are less efficient extractants, the selectivity for the light over the heavy lanthanides is less pronounced, while there is still an interesting selectivity of Am3+ over Eu3+. Stability constants for selected lanthanide salts were determined also in homogenous phase (methanol, acetonitrile) but do not account for the different extraction results. The complexation of Gd…

Magnetic properties of AgLnSe2 compounds (Ln=Ho, Er, Tm and Yb)

2001

Abstract The heavy lanthanide selenides AgLnSe2 (Ln=Ho–Yb) crystallize in the orthorhombic AgErSe2 type structure (P212121). The lanthanide ions are placed in the centres of slightly distorted octahedra, whereas each of the silver ions is surrounded by four selenide ions forming a strongly distorted tetrahedron. The high field magnetization (up to 14 T) and the magnetic susceptibility were measured on the polycrystalline samples. The crystal field parameters were estimated from the field dependences of the magnetizations, assuming a rhombic distortion of LnSe6 octahedra. The magnetic susceptibilities were also calculated using the same set of the crystal field parameters. None of the compou…

Synthesis and X-ray crystal structure of cationic polynuclear hydroxide acetylacetonate lanthanide(III) clusters with homodinuclear or heterodinuclea…

2006

The synthesis and characterization of new polynuclear lanthanide(III) ionic clusters of general formula [Ln 9 (acac) 16 (OH) 10 ] + [Mo 2 (CO) 10 (μ-H)]- (Ln = Sm, Eu, Gd, Dy, Yb) and [Sm 9 (acac) 16 OH) 10 ] + [CrW(CO) 10 (μ-H)] - is reported. The polynuclear complexes, prepared under pure nitrogen atmosphere by interaction of the hydridic metal carbonyls with the β-dichetonate Ln(acac) 3 ·3H 2 O (Ln=Sm, Eu, Gd, Dy, Yb). The new clusters were characterized by elemental analysis, complexometric titration for Ln, atomic absorption for Cr, W and Mo, gas-volumetric analysis for CO, FTIR spectroscopy and single crystal X-ray structure determination of [Sm 9 (acac) 16 (OH) 10 ][Mo 2 (CO) 10 (μ-H…

Synthesis, structural characterization and electrochemical and magnetic studies of M(hfac)2 (M = CuII, CoII) and Nd(hfac)3 complexes of 4-amino-TEMPO

2020

Three mononuclear complexes [M(hfac)x(ATEMPO)y], where M = Cu (11) and Co (12), x = y = 2; M = Nd (13), x = 4, y = 1, and two polynuclear complexes [{Cu(hfac)2(ATEMPO)}n], where n = 2 (14) and 4 (15), were obtained by the reaction of M(hfac)x (M = CuII, CoII, NdIII; x = 2, 3) with 4-amino-TEMPO (4-amino-2,2,6,6-tetramethylpiperidin-N-oxyl) in good yields and their structural, electrochemical and magnetic properties were examined. In all cases, the radical is coordinated to the metal through the amino group, except 15, and the metal ions have an octahedral geometry, except 13. Different coordination architectures of the copper complexes were obtained as a function of the stoichiometry and so…

ChemInform Abstract: Pressure-Induced Transformations in PrVO4and SmVO4and Isolation of High-Pressure Metastable Phases.

2013

High-pressure phases of PrVO4 and SmVO4 are synthesized from the zircon-structured compounds at 12 GPa and room temperature (24 h).

Lanthanoid Complexes with[(dad)Li] Ligands—New Starting Materials for Organolanthanoid Chemistry

1995

Cs3UP2S8, a Coordination Polymer Containing the Unprecedented [U=S]2+Sulfidouranium(2+) Moiety

2013

Although terminal chalcogeno ligands are well known for the group 5 and 6 transition metals, they are highly unusual for the oxophilic group 4 metals and unknown so far for the lanthanides or actinides. Cs3UP2S8, is the first actinide compound containing a terminal M=S group. It was synthesized by reacting uranium metal, Cs2S, S, and P2S5 in a 4:1:8:3 ratio at 700 °C in an eutectic LiCl/CsCl mixture. The crystal structure was determined by single-crystal X-ray diffraction techniques. Cs3UP2S8 crystallizes in the rhombohedral space group R [a = 15.5217(8) A; c = 35.132(2) A, V = 8305.0(8) A3, Z = 18]. The crystal structure is based on a tetrahedral network type, wherein the uranium atoms are…

Fast preparation and gas-chromatographic separation of lanthanide and actinide hexafluoroacetylacetonates

1986

A fast method for the separation of lanthanide elements by gas chromatography of their hexafluoroacetylacetonates is described. Individual lanthanides can be isolated within a few minutes, and the whole group can be separated in less than 10 min. The hexafluoroacetylacetonates are applied in form of mixed complexes with tri-n-butyl phosphate or trioctylphosphine oxide prepared by fast extraction into quasi-solid solvents. The applicability of this method for the separation of trivalent actinide elements is shown, including the fast preparation of thin counting samples.