A unique cobalt-gold coordination system, in which the oxidation states of the cobalt centers are closely correlated with the multinuclear molecular structures, is reported. This system contains a CoII3AuI6 nonanuclear structure in [Co 3{Au3(tdme)(D-pen-N,O,S)3}2] ([2]) and a CoIIIAuI3 tetranuclear structure in [Co{Au3(tdme)(D-pen-N,S)3}] ([3]) [tdme = 1,1,1-tris(diphenylphosphinomethyl)ethane, D-pen = D-penicillamininate], which are stereoselectively prepared from the reaction of a tripod-type trigold(I) metalloligand [Au3(tdme)(D-pen)3]3- ([1] 3-) with Co2+ and Co3+, respectively. The anomalous stability of the +II oxidation state of each octahedral cobalt center in [2], despite the coordination of two aliphatic amine and two aliphatic thiolato groups that commonly provide a strong ligand field, is notable. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
CITATION STYLE
Hashimoto, Y., Yoshinari, N., Matsushita, N., & Konno, T. (2014). Close correlation between metal oxidation states and molecular structures in a cobalt-gold multinuclear coordination system with mixed D-penicillaminate and tripodal triphosphine. European Journal of Inorganic Chemistry, (22), 3474–3478. https://doi.org/10.1002/ejic.201402531
Mendeley helps you to discover research relevant for your work.