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On the Question of Site-Selective Ligand Exchange in Carboxylate-Substituted Metal Oxo Clusters
Johannes Kreutzer1, Matthias Czakler1, Michael Puchberger1
1Institute of Materials Chemistry, Vienna University of Technology Getreidemarkt 9, 1060 Vienna, Austria E-mail: Ulrich.Schubert@tuwien.ac.at http://www.imc.tuwien.ac.at.
Abstract:
Reaction of [Ti4Zr4O6(OBu)4(OMc)16] (OMc = methacrylate) with acetylacetone (acacH) resulted in dissection of the cluster and formation of [Ti(OBu)2(acac)2] and the smaller cluster [Ti2Zr4O4(OMc)16]. In contrast, the same reaction with [Zr6O4(OH)4(OOCR)12]2·6RCOOH (R = Et, CH2CH=CH2) led to site-selective substitution of two carboxylate ligands and formation of isostructural [Zr6O4(OH)4(OOCR)12- (acac) ]2·6RCOOH (x ≤ 1).
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