Formation of 1 ∶ 1 and 2 ∶ 2 complexes of Ce(iii) with the heteropolytungstate anion α2-[P2W17O61]10−, and their interaction with proline. The structure of [Ce2(P2W17O61)2(H2O)8]14−†
Abstract
The “1 ∶ 1” complex of Ce3+ and α2-[P2W17O61]10− is formed in an equimolar solution of Ce(NO3)3 and K10[P2W17O61], but attempts to isolate a solid yield salts of the 1 ∶ 2 complexes first described by Peacock and Weakley in 1971. With a 3-fold excess of Ce3+ however, a crystalline ammonium salt (anion 1) could be isolated in 90% yield based on tungstate. Structural analysis of these crystals (monoclinic, C2/c; a
= 46.1124(6); b
= 12.7451(1); c
= 26.4624(2) Å, β
= 93.570(1)°, Z
= 4; 18856 independent reflections, R1 = 0.0799; wR2 = 0.1594) revealed a head-to-head dimeric
anion with each 9-coordinate Ce(III) cation attached to four oxygens that surround the lacuna of one tungstophosphate anion, a terminal O(W) of the second tungstophosphate, and four water molecules. Phosphorus-31 NMR spectra of solutions of 1 revealed two sets of resonances, A and B, the relative intensities of which could be fitted to an equilibrium 2A B, with K
= 1.46 ± 0.04 M−1 at 23 °C. Further NMR analysis suggests a scheme in which 1, which is in rapid exchange with the “monomer” (2), is also in slow exchange with a labile associate of Ce3+ and the 1 ∶ 2 complex. The exchange process between 1 and 2 is responsible for the non-observance of one of the expected
9 lines in the tungsten-183 NMR spectrum and an exchange-broadened P-NMR line. Addition of proline to form a ternary complex [Ce(P2W17O61)(proline)(aq)]7−(Kform
= 4.5 ± 0.1 M−1 from 1H-NMR) restores the missing W-NMR resonance.