Homo-/heterotrinuclear mixed-valent oxo-centered iron/nickel clusters-Mössbauer studies on internal electron-exchange processes.

In a one-pot reaction of N-(5-methylthiazole-2-yl)-thiazole-2-carboxamide HL2 (3) with iron(II) acetate in air, the homotrinuclear heteroleptic mixed-valent oxo-centered iron cluster [Fe(II)Fe(III)O(L2)3(OAc)3] (4) was formed. Exchange of iron(II) in 4 by nickel(II) afforded the heteronuclear cluster [Ni(II)Fe(III)O(L2)3(OAc)3] (6). To obtain crystals suitable for X-ray structure analyses, in 4 and 6, the OAc- co-ligands were exchanged by OBz- ligands to give [Fe(II)Fe2(III)O(L2)3(OBz)3] (5) and [Ni(II)Fe(III)O(L2)3(OBz)3] (7).

Metal- and ligand-directed one-pot syntheses, crystal structures, and properties of novel oxo-centered tetra- and hexametallic clusters.

Starting from closely related metal-ligand combinations, completely different oligomeric metal clusters are synthesized. Whereas, picoline-tetrazolylamide HL(1) (1) and zinc or nickel acetate afforded [2x2] grids [M(4)(L(1))(8)] (2), slightly different N-(2-methylthiazole-5-yl)-thiazole-2-carboxamide HL(2) (5 a) and nickel acetate yielded the monometallic complex [Ni(L(2))(2)(OH(2))(2)] (6). In contrast, reaction of 5 a with zinc acetate produced the tetrametallic zinc cluster [Zn(4)O(L(2))(4)(OAc)(2)] (7).