Synthesis and crystal structure of the monoclinic modification of Yb(ReO4)(3)(H2O)(4)
Abstract
Ytterbium(III) tetraaquatris(tetraoxorhenate(VII)), Yb(ReO4)3(H2O)4, was prepared by the reaction of Yb2O3 with concentrated HReO4 at room temperature. The colorless compound crystallizes in the monoclinic space group P21/n (No. 14) with four formula units per unit cell (a=730.5(1)pm, b=1484.1(5)pm, c=1311.7(2)pm, ?=93.69(1)). The main feature of the crystal structure is the formation of chains ?1[Yb(H2O)4(ReO 4)2(ReO4)2/2] running along [100]. This arrangement shows distorted cubic antiprisms of [Yb(H2O)4(ReO4)2(ReO 4)2/2] interconnected via the ReO4- ligands. The chains are held together in the solid by hydrogen bonding. The compound is paramagnetic and follows the Curie-Weiss law with a magnetic moment of 4.0?B at room temperature and ?=-42K. It loses hydration water in two steps at temperatures below 400K; decomposition begins at 850K, forming Yb2O3(Re2O7)2 and is complete at 1350K leading to Yb2O3 as final product. © 2003 Elsevier Science (USA). All rights reserved.
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Título según WOS: | Synthesis and crystal structure of the monoclinic modification of Yb(ReO4)(3)(H2O)(4) |
Título según SCOPUS: | Synthesis and crystal structure of the monoclinic modification of Yb(ReO4)3(H2O)4 |
Título de la Revista: | JOURNAL OF SOLID STATE CHEMISTRY |
Volumen: | 172 |
Número: | 1 |
Editorial: | ACADEMIC PRESS INC ELSEVIER SCIENCE |
Fecha de publicación: | 2003 |
Página de inicio: | 200 |
Página final: | 204 |
Idioma: | English |
URL: | http://linkinghub.elsevier.com/retrieve/pii/S002245960300029X |
DOI: |
10.1016/S0022-4596(03)00029-X |
Notas: | ISI, SCOPUS |