Influence of the Lanthanide Ion and Solution Conditions on Formation of Lanthanide Wells–Dawson Polyoxotungstates

• Published in: Journal of cluster science 2006-06, Vol.17 (2), p.389-425
• Main Authors: Zhang, Cheng, Bensaid, Laurence, McGregor, Donna, Fang, Xikui, Howell, Robertha C., Burton-Pye, Benjamin, Luo, Qunhui, Todaro, Louis, Francesconi, Lynn C.
• Format: Article
• Language: English
• Subjects: Aqueous solutions; Catalysis; Cations; Cerium; Crystallography; Equilibrium; Lanthanides; Ligands; Polyoxometallates; Stability; Stability constants; Trends
• ISSN: 1040-7278; 1572-8862
• DOI: 10.1007/s10876-006-0066-9

Lanthanide complexes of polyoxometalates, including the α2-P2W17O6110− ligand, have been pioneered by Michael T. Pope, to whom this paper is dedicated. Examination of the solid-state and solution behavior of lanthanide complexes of the α2-P2W17O6110− ligand are reported here to identify trends that will facilitate rational synthesis of hybrid organic lanthanide polyoxometalate complexes. Therefore, combining our data with that obtained by Pope and others a number of trends come into view. It is clear that there are two structural types for the 1:1 or 2:2 [Ln(H2O)X(α2-P2W17O61)]214− species. The early lanthanides show a “cap to cap” structure that allows the Ln ion to be 9 coordinate and accommodates the longer bond lengths. The mid-late lanthanides show a “cap to belt” structure that allows the lanthanides to be 8 coordinate; this structural type is appropriate for the shorter bond lengths of the later lanthanides. The 1:1⇌1:2 equilibrium, that was observed by Pope for the Ce(III) analog is prevalent for the early- mid lanthanides. This equilibrium is slightly dependent on pH; however, cations have a major influence on this equilibrium. Larger, poorly hydrated cations appear to favor the 1:2 species for the early to mid lanthanides. Cations do not appear to influence the equilibrium for the later lanthanides; for all counterions, the 1:1 species was stable with no trace of the 1:2 species. Stability constants, K1 and K2, for the early to mid lanthanides were measured in this study by a competitive method and compared well with other published stability constant determinations. We suggest that the stability constants are not only dependent on the strength of interaction of the Ln with the α2-P2W17O6110− ligand, but are also significantly influenced by the medium. The medium may bias the equilibria of the early-mid lanthanides and later lanthanides. The log K1/log K2 ratios are very close, suggesting that it is difficult to separate the 1:1 and 1:2 Ln: α2-P2W17O6110− species.