Journal
POLYHEDRON
Volume 29, Issue 16, Pages 3066-3073Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.poly.2010.08.002
Keywords
Ruthenium; Polyoxometalate; Transition metal-substituted; polyoxotungstate; Trilacunary; Keggin
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Funding
- University of Aveiro
- Portuguese Foundation for the Science and Technology (FCT)
- FCT [SFRH/BPD/11571/2002]
- Fundação para a Ciência e a Tecnologia [SFRH/BPD/11571/2002] Funding Source: FCT
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Novel ruthenium multi-substituted polyoxometalate compounds of general formulae K6Na[SiW9O37Ru4III(H2O)(3)Cl-3]center dot nH(2)O (alpha- and beta-SiW9O34 isomers) were synthesised via the reactions of the trilacunary Keggin alpha- and beta-[SiW9O34](10-) anions with RuCl3 in aqueous solution. Characterisation was performed by analytical, spectroscopic, magnetic, and electrochemical techniques. The results are in accordance with the new polyoxometalates having the trivacant Keggin anion (alpha or beta isomer) linked to a cubane-type Ru4O4 cluster. The co-ordination sphere of ruthenium is completed with water molecules and chloride anions. Magnetic measurements showed that the majority of the molecules have the Ru ions cluster in a compensated configuration constrained to an antiferromagnetic alignment at very low temperature and following a Curie-Weiss like behaviour. For both isomers, cyclic voltammetry revealed quasi-reversible redox processes at the ruthenium centres, namely Ru-IV/III and Ru-III/II, which were found to be pH dependent. The novel polyoxotungstates incorporate the highest content of ruthenium (W:Ru = 2.25:1) ever reported for Keggin-, Dawson or sandwich-type transition metal-substituted polyoxometalates and may find promising applications as oxidative catalysts. (C) 2010 Elsevier Ltd. All rights reserved.
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