Syntheses, crystal structures and characterizations of new vanadium arsenites and arsenates

Systematic explorations in vanadium arsenites and arsenates led to the isolation four new compounds, namely, α-(VIVO)3(AsIIIO3)2 (1), β-(VIVO)3(AsIIIO3)2 (2), (VIVO)[VIVO(H2O)]2(AsVO4)2 (3), VIIIVIVO2(AsVO4) (4). Compounds 1, 2 and 4 were synthesized by standard solid-state reactions, and compound 3...

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Veröffentlicht in:Journal of solid state chemistry 2012-08, Vol.192, p.263-272
Hauptverfasser: Liu, Jun-Hui, He, Zhang-Zhen, Kong, Fang, Xu, Xiang, Sun, Chuan-Fu, Mao, Jiang-Gao
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Sprache:eng
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Zusammenfassung:Systematic explorations in vanadium arsenites and arsenates led to the isolation four new compounds, namely, α-(VIVO)3(AsIIIO3)2 (1), β-(VIVO)3(AsIIIO3)2 (2), (VIVO)[VIVO(H2O)]2(AsVO4)2 (3), VIIIVIVO2(AsVO4) (4). Compounds 1, 2 and 4 were synthesized by standard solid-state reactions, and compound 3 is a vanadium arsenate dihydrate synthesized through hydrothermal reactions. Compounds 1 and 2 are isomers, and they represent the first examples of ternary inorganic vanadium(IV) arsenites. Single crystal X-ray diffraction analysis indicated that the four compounds display four different structural types. Magnetic property measurements for compound 1 indicated that it exhibits ferromagnetism with the Curie temperature Tc=65K. Thermal stability and optical properties for compounds 1 and 3 were also investigated. Hydrothermal or solid state reactions of V2O5 (or VO2) and As2O3 yielded four new ternary compounds with four different types of structures, namely, α-(VO)3(AsO3)2 (1), β-(VO)3(AsO3)2 (2), (VO)[VO(H2O)]2(AsO4)2 (3), (VO)2(AsO4) (4). α-(VO)3(AsO3)2 (1), β-(VO)3(AsO3)2 (2) represent the first examples of ternary inorganic vanadium(IV) arsenites. [Display omitted] ► Hydrothermal or solid state reactions of V2O5 (or VO2) and As2O3 yielded two new arsenites. ► They represent the first examples of ternary vanadium arsenites. ► Two new ternary vanadium arsenates were also obtained. ► They exhibit four different structural types.
ISSN:0022-4596
1095-726X
DOI:10.1016/j.jssc.2012.04.022