Crystal structure of new complexes of arsenitotungstates with triangular sulfido bridged clusters: Cs5.6K4.4[{Mo3S4(H2O)5}(H2AsW9O33)2]·19.15H2O and K6.35(NH4)2.65[{W3S4(H2O)5}(H2AsW9O33)(HAsW9O33AsOH)]·23.7H2O
Autor: | Vladimir P. Fedin, Elena V. Chubarova, Eugenia V. Peresypkina, I. V. Kalinina, Maxim N. Sokolov |
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Rok vydání: | 2010 |
Předmět: | |
Zdroj: | Journal of Structural Chemistry. 51:303-307 |
ISSN: | 1573-8779 0022-4766 |
DOI: | 10.1007/s10947-010-0046-7 |
Popis: | The reaction of lacunary arsenitotungstate [AsW9O33]9− with [M3S4(H2O)9]4+ in aqueous solution leads to the formation of the complex [{Mo3S4(H2O)5}(H2AsW9O33)2]10−. X-ray crystal structure analysis of its cesium salt of the composition Cs5.6K4.4[{Mo3S4(H2O)5}(H2AsW9O33)2]·19.15H2O (1) is reported. Similarly, the reaction of [AsW9O33]9− with [W3S4(H2O)9]4+ and NaAsO2 yields [{W3S4(H2O)5}(H2AsW9O33)(HAsW9O33AsOH)]9−. For K6.35(NH4)2.65[{W3S4(H2O)5}(H2AsW9O33)×(HAsW9O33AsOH)]·23.7H2O (2) the crystal structure is determined. In both compounds, the {M3S4}4+ cluster cores coordinate one polyoxometalate ion, which functions as a bridging ligand between two metal atoms, and one bidentate polyoxometalate. The other five coordination sites at the cluster core are occupied by water molecules. The complex anions form dimeric associates held together by hydrogen bonds and S...S contacts. |
Databáze: | OpenAIRE |
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