Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1306160 | Inorganica Chimica Acta | 2011 | 5 Pages |
We successfully obtained [Ln(α-XW11O39)2]11− (Ln = La and Ce) anions with an approximate cubic LnIIIO8 geometry for the first time in [Me4N]10H[La(α-PW11O39)2]·21H2O (1) and [Me4N]10H[Ce(α-PW11O39)2]·19H2O (2) ([Me4N]+ = tetramethylammonium). The anion is spherically surrounded by [Me4N]+ cations in highly symmetric arrangement. The resulting approximate C2h symmetry of the anion is more stable than C2v, which is explained in terms of lower steric hindrance between the two [PW11O39]7− moieties. 31P NMR spectroscopy of 1 and 2 revealed that [Ln(α-XW11O39)2]11− anions in aqueous solutions partially dissociate into [Ln(H2O)n(PW11O39)]4− and [PW11O39]7− species.
Graphical abstractWe successfully prepared [LnIII(α-PW11O39)2]11− (Ln = La and Ce) anion with a pseudo-cubic LnIIIO8 site by crystallization with [Me4N]+ cation.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► We isolated a lanthanide(Ln)-polyoxotungstate anion with a ∼C2h symmetry. ► A LnO8 (Ln = La and Ce) center of the anion has a rare pseudo-cubic geometry. ► C2h is the most stable form because of a steric effect within the anion. ► 31P NMR revealed a dissociation of the anions in aqueous solutions.