The topological arrangement of the metal centres in the first characterized hexanuclear manganese complexes, [{MnIII3L(O)(O2CMe)(OMe)3}2]·2solv [L =N-(X-Substituted salicylidene)-N′,N′-bis(2-hydroxyethyl)ethyienediamine (X = 5-MeO, 5-Cl, 5-Br) and N-(naphthylidene)-N,N′-bis(2-hydroxyethyl)ethylenediamine, solv = 2H2O or MeOH], is unprecedented and shows that a variety of small bridging ligands including oxo, carboxylato and alkoxo anions may simultaneously cooperate with a dinucleating ancillary ligand to the building up of high-nuclearity manganese assemblies.
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Xia et al. (1995) studied this question.
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