Mono- and Di-Lanthanide Derivatives of 22-Tungsto-2-antimonate(III), [Ln(H2O)4Sb2W21O72(OH)]10- and [Ln2(H2O)8Sb2W20O70)]8
. The mono‐lanthanide‐containing [Ln(H2O)4Sb2W21O72(OH)]10– (Ln = Yb (1), Lu (2)), and the di‐lanthanide‐containing [Ln2(H2O)8Sb2W20O70)]8– (Ln = Yb (3), Lu (4), Y (5)) have been synthesized in aqueous‐acidic media and characterized in the solid state. Polyanions 1 and 2 were prepared by reaction of...
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Published in | Zeitschrift für anorganische und allgemeine Chemie (1950) Vol. 639; no. 14; pp. 2510 - 2515 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
WILEY-VCH Verlag
01.11.2013
WILEY‐VCH Verlag Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
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Summary: | . The mono‐lanthanide‐containing [Ln(H2O)4Sb2W21O72(OH)]10– (Ln = Yb (1), Lu (2)), and the di‐lanthanide‐containing [Ln2(H2O)8Sb2W20O70)]8– (Ln = Yb (3), Lu (4), Y (5)) have been synthesized in aqueous‐acidic media and characterized in the solid state. Polyanions 1 and 2 were prepared by reaction of Ln3+ ions with [Sb2W22O74(OH)2]12– (Sb2W22), whereas 3–5 were prepared by using the trilacunary 9‐tungstoantimonate(III) [B‐α‐SbW9O33]9– (SbW9). Polyanions 1–5 crystallized as sodium salts in the triclinic system, space group P$\bar{1}$. All compounds were characterized in the solid state by FTIR, single‐crystal XRD, TGA, and elemental analysis. Polyanions 1–5 contain the lacunary [Sb2W20O70]14– unit (Sb2W20), which is coordinated to either a lanthanide and a tungsten ion, leading to a structure with Cs symmetry in polyanions 1 and 2, or to two lanthanide ions, leading to a structure with idealized C2h symmetry, in polyanions 3–5. |
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Bibliography: | Dedicated to Professor Bernt Krebs on the Occasion of His 75th Birthday Ministry of Higher Education of the Arab Republic of Egypt ark:/67375/WNG-1SKF76Z5-8 istex:4A69CCF36ADB7CCD049970FF645F35B83004FC03 ArticleID:ZAAC201300530 Supporting Information for this article is available on the WWW under http://dx.doi.org/10.1002/zaac.201300530 or from the author. Deutsche Forschungsgemeinschaft - No. KO-2288/8-1 |
ISSN: | 0044-2313 1521-3749 |
DOI: | 10.1002/zaac.201300530 |