COORDINATION (HYDRATION) OF RARE-EARTH IONS IN AQUEOUS CHLORIDE SOLUTIONS FROM X-RAY-DIFFRACTION .2. LACL3, PRCL3, AND NDCL3

被引:289
作者
HABENSCHUSS, A
SPEDDING, FH
机构
[1] IOWA STATE UNIV SCI & TECHNOL,DEPT CHEM,AMES,IA 50011
[2] IOWA STATE UNIV SCI & TECHNOL,DEPT PHYS,AMES,IA 50011
关键词
D O I
10.1063/1.437928
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The inner sphere water coordination of the rare earth ions La3+, Pr3+, and Nd3+ in concentrated (3.4 to 3.8 m) aqueous chloride solutions have been determined from x-ray diffraction measurements. In each solution the rare earth ion exists as the [RE(H2O) 9]3+ aquo complex as determined from the quantitative resolution of the radial distribution functions. The average RE 3+-H2O distances are 2.580, 2.539, and 2.513 Å for LaCI3, PrCI3, and NdCI3, respectively. The average RE3+⋯CI- ion pair distances are near 5.0 Å. These results, together with the octaaquo complex, [RE(H 2O)8]3+, found previously for the heavy rare earth ions, Tb3+ through Lu3+, establish that the inner sphere water coordination of the rare earth ions in aqueous solutions decreases from nine to eight between Nd3+ and Tb3+. © 1979 American Institute of Physics.
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页码:3758 / 3763
页数:6
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