Derivatization of polyoxotungstates in aqueous solution. Exploration of the kinetic stability of cobalt(II)- and cobalt(III) derivatives of lacunary anions with pyridine and pyridine-type ligands

Citation
Jl. Samonte et Mt. Pope, Derivatization of polyoxotungstates in aqueous solution. Exploration of the kinetic stability of cobalt(II)- and cobalt(III) derivatives of lacunary anions with pyridine and pyridine-type ligands, CAN J CHEM, 79(5), 2001, pp. 802-808
Citations number
36
Categorie Soggetti
Chemistry
Journal title
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE
ISSN journal
00084042 → ACNP
Volume
79
Issue
5
Year of publication
2001
Pages
802 - 808
Database
ISI
SICI code
0008-4042(200105)79:5<802:DOPIAS>2.0.ZU;2-P
Abstract
Four complexes of cobalt(II) with lacunary polyoxotungstate ligands, alpha- [PW11O39Co(H2O)](5-), alpha-[SiW11O39Co(H2O)](6-), alpha (1)-, and alpha (2 )-[P2W17O61Co(H2O)](8-) have been examined as potential precursors to subst itutionally inert derivatized polytungstates that are stable in aqueous sol ution at near neutral pH. Replacement of the terminal water ligand by pyrid ine is readily achieved and the rates of exchange between bound and free py ridine were determined from NMR line widths at temperatures between 24 and 48 degreesC. Oxidation to the aquacobalt(III) and pyridinecobalt(III) polyt ungstates occurs at potentials between +0.64 V (for alpha (1)-[P2W17O61Co(p y)](8-)) and +1.00 V (for alpha (2)-[P2W17O61Co(H2O)](8-)). The cobalt(III) complexes (with the exception of alpha-[PW11O39Co(H2O)](4-) which undergoe s slow reduction by the solvent) were prepared by controlled potential elec trolysis and by oxidation with potassium perdisulfate. The rates of pyridin e substitution on the aquacobalt(III) complexes were determined and follow the sequence alpha(1)-[P2W17O61Co(H2O)](7-) (similar to0.5 M-1 s(-1)) >> al pha (2)-[P2W17O61Co(H2O)](7-) similar to alpha-[SiW11O39Co(H2O)](5-). Cesiu m salts of alpha (1)-[P2W17O61CoIII(L)](7-) (L = pyrazine, 4,4'-bipyridine, isonicotinic acid, and the ethyl ester of isonicotinoylglycylglycine) and the "dumbbell" 2:1 complex with bridging 4,4' -bipyridine were isolated and characterized by cyclic voltammetry and H-1 NMR spectroscopy.