Synthesis and physico-chemical characterization of a new series of hydroxide ion acetylacetonate lanthanide(III)—ditungsten decacarbonyl hydride complexes

• Published in: Journal of alloys and compounds 2004-07, Vol.374 (1), p.382-386
• Main Authors: Volpe, M, Bombieri, G, Clemente, D.A, Foresti, E, Grillone, M.D
• Format: Article
• Language: English
• Subjects: Clusters; Condensed matter: electronic structure, electrical, magnetic, and optical properties; Crystal structure; Exact sciences and technology; Lanthanides; Magnetic resonances and relaxations in condensed matter, mössbauer effect; Metal carbonyls; Nuclear magnetic resonance and relaxation; Physics; X-ray spectroscopy
• ISSN: 0925-8388; 1873-4669
• DOI: 10.1016/j.jallcom.2003.11.153

A novel series of the heterometallic lanthanide(III) ionic cluster complexes of general formula Ln 9(acac) 16(OH) 10[W 2(CO) 10(μ-H)] with Ln=Sm ( 1a), Eu ( 1b), Gd ( 1c), Dy ( 1d), and Yb ( 1e) was prepared and characterized by FTIR, 1 H NMR spectroscopy and single crystal X-ray analysis. The cluster series was obtained by reaction in ethanol solution of the 2,4-pentanedionate hydrate of lanthanide(III), Ln(acac) 3·3H 2O, with the hydridic ditungsten decacarbonyl, [W 2(CO) 10(μ-H)] −. X-ray analysis showed that the complexes 1a– 1e are isostructural. The complete structural characterization of the Eu derivative ( 1b) shows, similarly to their chromium derivative analogues, a square antiprismatic arrangement of the nona-lanthanide hydroxide ion acetylacetonate cationic cluster where the species [W 2(CO) 10(μ-H)] − plays the role of the anionic counter ion.