A. Gigante, Danilo José Coura Gomes, L. S. Lima, F. Caires, O. Treu Filho, M. Ionashiro
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引用次数: 3
Abstract
Characterization, thermal stability and thermal decomposition of heavy trivalent lanthanide mandelates Ln(C 6 H 5 CH(OH)CO 2 ) 3 ·2H 2 O (Ln = Tb to Lu and Y) were investigated employing simultaneous thermogravimetry and differential thermal analysis (TG-DTA), differential scanning calorimetry (DSC), experimental and theoretical infrared spectroscopy, X-ray diffractometry, complexometry and TG-DSC coupled to FTIR. The dehydration of the compounds occurs in a single step and the thermal decomposition of the anhydrous ones occurs in two, three, four or five consecutive steps, with formation of the respective oxides Tb 4 O 7 and Ln 2 O 3 (Ln = Dy to Lu and Y) as final residues. The results also provided information concerning the composition, thermal behavior and gaseous products evolved during the thermal decomposition of these compounds. The theoretical and experimental spectroscopic data suggest the possible modes of coordination of the ligand with the heavy lanthanides. Theoretical 3D structure of Y(L)3•2H2O: (a), (c) and (d) isomers (less stable); (b) yttrium(III) mandelate coordinated by hydroxyl and carboxylate groups (the most stable compound).
采用热重-差热分析(TG-DTA)、差示扫描量热分析(DSC)、实验和理论红外光谱、x射线衍射、络合测量以及TG-DSC耦合FTIR等方法研究了重三价镧系酸盐Ln(c6h5ch (OH)CO 2) 3·2h2o (Ln = Tb to Lu and Y)的表征、热稳定性和热分解。化合物的脱水在一个步骤中发生,无水化合物的热分解在两个,三个,四个或五个连续的步骤中发生,形成各自的氧化物Tb 4o 7和l2o 3 (Ln = Dy to Lu和Y)作为最终残留物。结果还提供了有关这些化合物在热分解过程中的组成、热行为和气态产物的信息。理论和实验光谱数据提示了该配体与重镧系元素可能的配位模式。Y(L)3•2H2O的理论三维结构:(a)、(c)和(d)异构体(不太稳定);(b)由羟基和羧酸基配位的扁桃酸钇(III)(最稳定的化合物)。