10025-74-8Relevant articles and documents
Synthesis, characterization and thermal behaviour of solid 2-methoxybenzoates of trivalent metals
Siqueira,Carvalho,Ionashiro,Bannach,Rodrigues,Ionashiro
, p. 945 - 951 (2008)
Solid-state Ln(L)3 compounds, where Ln stands for trivalent Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu and Y and L is 2-methoxybenzoate have been synthesized. Simultaneous thermogravimetry and differential thermal analysis (TG-DTA), differential scanni
Vacancy mediated room temperature ferromagnetism in Co-doped Dy 2O3
Bandyopadhyay,Sutradhar,Sarkar,Deb,Chakrabarti
, (2012)
Nanoparticles of Co doped dysprosium oxide [Dy1.90Co 0.10O3] were prepared by co-precipitating the precursor salts in presence of air and argon gas. Crystallographic phase and substitution of Co-ion in Dy2O3 were confirmed by Rietveld analysis of the x-ray diffraction patterns. Magnetic susceptibility and magnetization as a function of temperature and magnetic field were measured by Faraday and Superconducting quantum inteference device (SQUID) magnetometers, which showed that the sample synthesized in the inert atmosphere is ferromagnetic at room temperature. But no such effect has been observed in the other sample. This observation confirmed that vacancy mediated ferromagnetism can be introduced in the Co-doped dysprosium oxide.
Synthesis, characterisation and thermal behaviour of solid stat compounds of 4-methylbenzylidenepyruvate with heavier trivalent lanthanides and yttrium(III)
Marques,Melios,Ionashiro
, p. 145 - 150 (2002)
Solid state Ln-4-Me-BP compounds, where Ln stands for heavier trivalent lanthanides (gadolinium to lutetium) and yttrium(III) and 4-Me-BP is 4-methylbenzylidenepyruvate (CH3-C6H4-CH=CH-COCOO-), have been synthesized. Eleme
ACETYLACETONIMINATES OF RARE EARTH ELEMENT CHLORIDES
Andrienko, I. V.,Murav'eva, I. A.,Martynenko, L. I.,Spitsyn, V. I.
, (1988)
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Lanthanide(III) halides: Thermodynamic properties and their correlation with crystal structure
Rycerz,Gaune-Escard
, p. 167 - 174 (2008)
Temperatures and enthalpies of phase transitions of 17 lanthanide(III) halides determined experimentally are reported. Correlations were made between temperature of fusion of lanthanide(III) halides, on the one hand, and enthalpy of fusion, on the other, versus atomic number of lanthanide. According to this classification, the lanthanide(III) halides split into groups, as also do the corresponding crystal structures. A correlation between the crystal structure of lanthanide(III) halides and their respective entropy of fusion (or entropy of fusion + entropy of solid-solid phase transition) was inferred from the aforementioned features. Fusion in those halides with hexagonal, UCl3-type and orthorhombic, PuBr3-type, structures entails an entropy of fusion change (or entropy of fusion + entropy of solid-solid phase transition change) by 50 ± 4 J mol-1 K-1. The homologous entropy change within the group of halides having the rhomboedric, FeCl3-type, structure, is smaller and equals 40 ± 4 J mol-1 K-1. Halides with monoclinic, AlCl3-type, crystal structure constitute a third group associated to an even smaller entropy change upon fusion, only 31 ± 4 J mol-1 K-1. The halides with lower entropies of fusion also have a lower S1300 K - S298 K indicating either a higher degree of order in the liquid or a higher entropy in the solid at room temperatures.
2-Methoxybenzylidenepyruvatewith heavier trivalent lanthanides and yttrium(III): Synthesis and characterization
Ionashiro,Bannach,Siqueira,De Carvalho,Rodrigues,Ionashiro
, p. 953 - 959 (2008)
Solid-state Ln(2-MeO-BP) compounds, where Ln stands for trivalent Eu to Lu and Y(III) and 2-MeO-BP (which is 2-methoxybenzylidenepyruvate) have been synthesized. Simultaneous thermogravimetry and differential thermal analysis (TG-DTA), differential scanni
Acceptor doping of Ln2Ti2O7 (Ln = Dy, Ho, Yb) pyrochlores with divalent cations (Mg, Ca, Sr, Zn)
Belov,Shlyakhtina,Stefanovich,Kolbanev,Belousov,Karyagina,Shcherbakova
, p. 1613 - 1620 (2009)
New LANTIOX high-temperature conductors with the pyrochlore structure, (Ln1-xAx)2Ti2O7-δ (Ln = Dy, Ho, Yb; A = Ca, Mg, Zn; x = 0, 0.01, 0.02, 0.04, 0.07, 0.1), have been prepared at 1400-1600 °C usin
Lanthanide contraction and pH value controlled structural change in a series of rare earth complexes with p-aminobenzoic acid
Sun, Hao-Ling,Ye, Chao-Hong,Wang, Xin-Yi,Li, Jun-Ran,Gao, Song,Yu, Kai-Bei
, p. 77 - 83 (2004)
A series of rare earth complexes with p-aminobenzoic acid (HL) have been synthesized: [RE2L6(H2O)2] n [RE=La (1), Ce(2), Pr(3), Sm(4), Eu(5), Tb(6), Dy(7), Er(9)] and [RE2L6(H2O)4]·2H 2O [RE=Tb(6′), Ho(8), Yb(10), Lu(11), Y(12)]. The crystal structures of 1, 2, 6, 6′, 7, 9 and 12 have been determined and the isomorphous relationships of the others have been identified. Their structures change from two-dimensional (2D) array (the coordination number of the metal ions is nine for 1 and eight for 2-7 and 9) to double-nuclear structure (the metal ions are eight-coordinated) for 6′, 8 and 10-12, as controlled by lanthanide contraction. The structural type has been found influenced by the pH value of the reaction mixtures.
Miller, J. F.,Miller, S. E.,Himes, R. C.
, p. 4449 - 4451 (1959)
Electrogenerated luminescence of chosen lanthanide complexes at stationary oxide-covered aluminium electrode
Staninski, Krzysztof,Lis, Stefan
, p. 81 - 83 (2008)
The electrochemiluminescence (ECL) of aqueous solutions of Tb3+, Dy3+, and Eu3+ complexes having a variety of ligand groups was studied using an oxide-covered aluminium electrode. The ligand groups, under study, were the aromatic acids (salicylic, phthalic), the chelatic ligands (ethylenediamine dl(o-hydroxy-phenylacetic acid), EDDHA and ethylenediamine tetraacetic acid, EDTA), as well as Schiff bases: 1,10-disalicylidene-4,7-diaza-1,10-decyldiamine and 2-salicylideneamine-2-hydroxymethyl-1,3-propanediol. The results show that the generated emissions were mainly the result of energy transfer from the ligands to the metals. The best ECL properties were observed in the case of the complexes Tb(III)-EDDHA, Dy(III)-EDDHA, and Dy(III)-salicylic acid. In the ternary systems: Schiff base-Tb(III)-Eu(III) energy transfer to the emitting level of the Eu(III) ion was observed.
Self-assembled light lanthanide oxalate architecture with controlled morphology, characterization, growing mechanism and optical property
He, Hongmei,Zhang, Youjin,Zhu, Wei,Zheng, Ao
, p. 1546 - 1552 (2011/10/01)
Flower-like Sm2(C2O4)3· 10H2O had been synthesized by a facile complex agent assisted precipitation method. The flower-like Sm2(C2O 4)3·10H2O was characterized by X-ray diffraction, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, field-emission scanning electron microscopy, thermogravimetry- differential thermal analysis and photoluminescence. The possible growth mechanism of the flower-like Sm2(C2O4) 3·10H2O was proposed. To extend this method, other Ln2(C2O4)3·nH2O (Ln = Gd, Dy, Lu, Y) with different morphologies also had been prepared by adjusting different rare earth precursors. Further studies revealed that besides the reaction conditions and the additive amount of complex agents, the morphologies of the as-synthesised lanthanide oxalates were also determined by the rare earth ions. The Sm2(C2O4) 3·10H2O and Sm2O3 samples exhibited different photoluminescence spectra, which was relevant to Sm 3+ energy level structure of 4f electrons. The method may be applied in the synthesis of other lanthanide compounds, and the work could explore the potential optical materials.
Lanthanide carbonates
Janicki, Rafal,Starynowicz, Przemyslaw,Mondry, Anna
, p. 3601 - 3616 (2011/10/11)
The crystal and molecular structures of the rare earth carbonates with the general formulae [C(NH2)]3 [Ln(CO3)4 (H2O)]·2H2O (where Ln = Pr3+,Nd 3+,Sm3+,Eu3+,Gd3+,Tb 3+)and [C(NH2)]3 [Ln(CO3) 4]·2H2O (where Ln = Y3+,Dy 3+,Ho3+,Er3+, Tm3+,Yb 3+,Lu3+) were determined. The crystals consist of monomeric [Ln(CO3)4 (H2O)] 5-or [Ln(CO3)4] 5-complex anions in which the carbonate ligands coordinate to the Ln3+ion in a bidentate manner. The spectroscopic (UV/Vis/NIR and IR) properties of the crystalline lanthanide carbonates, as well as their aqueous solutions, were determined. Correlation between the spectroscopic and the structural data enabled us to conclude that the [Ln(CO3)4 (OH)]6-and [Ln-(CO 3)4]5- species predominate in the light and heavy lanthanide solutions, respectively. The nature of the Ln-O interaction was also discussed. The experimental data, as well as the theoretical calculations, indicated that the Ln-O(CO3 2-) bond is more covalent than the Ln-O(OH2) bond. Moreover, the covalency degree is larger for the heavy lanthanide ions. Inspection of the NBO results revealed that the oxygen hybrids, with the approximate composition sp4, form strongly polarized bonds with the 6s6p5d4 hybrids of lutetium. 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
