A Mixed-Valence VIV/VV Alkoxo-polyoxovanadium Cluster Series [V6O8(OCH3)11]n+/−: Exploring the Influence of a μ-Oxo Ligand in a Spin Frustrated Structure

Autor: Hans Hartl, Charles Daniel
Rok vydání: 2009
Předmět:
Zdroj: Journal of the American Chemical Society. 131:5101-5114
ISSN: 1520-5126
0002-7863
DOI: 10.1021/ja8073648
Popis: The synthesis and structural characterization of the neutral mixed-valence methoxo-polyoxovanadium cluster [V(6)O(8)(OCH(3))(11)] (1) and its single oxidation product in the hexachloroantimonate salt [V(6)O(8)(OCH(3))(11)][SbCl(6)] (2) are presented here. The cluster comprises a hexauclear polyoxovanadate core of the Lindqvist structure, of which all but one of the mu-bridging oxo ligands are substituted by methoxo. As revealed by cyclic voltammetry, the cluster is highly redox active, displaying several further thermodynamically stable V(IV)/V(V) mixed-valence redox derivatives. Furthermore, valence sum calculations performed on the X-ray structural data as well as results from IR and UV-vis spectrometry characterize them as class II mixed-valence compounds. In the present article, we equally present results from cyclic voltammetry, UV-vis spectrometry, and magnetic measurements obtained for members of the previously reported [V(6)O(7)(OCH(3))(12)] cluster series, which, as opposed to 1 and its derivatives, contain exclusively methoxo ligands as mu-bridging moieties. Magnetic measurements performed on the highly reduced cluster species [V(IV)(5)V(V)(1)O(7)(OCH(3))(12)](-) and [V(IV)(6)O(7)(OCH(3))(12)](2-) reveal net antiferromagnetic exchange interactions between the d-electrons, which at lower temperatures are in part suppressed for reasons attributed to geometric spin frustration. Among the present results, the comparison of the cyclic voltammograms of 1 and [V(6)O(7)(OCH(3))(12)] has proven to be of considerable interest, showing an unexpectedly pronounced discrepancy in all but one of their corresponding redox potentials. In particular, a detailed analysis of the electrochemical conversions indicates that the observed shift is almost entirely the result of a different degree of d-electron spin-spin interactions in corresponding mixed valence species of the cluster series.
Databáze: OpenAIRE
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