Synthesis and crystal structure of the monoclinic modification of Yb(ReO4)(3)(H2O)(4)

Mujica C.; Llanos J.; Sánchez V.; Gomez-Romero, P; Casan-Pastor, N

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