Anion-Controlled Assembly of Four Manganese Ions: Structural, Magnetic, and Electrochemical Properties of Tetramanganese Complexes Stabilized by Xanthene-Bridged Schiff Base Ligands

Abstract

The reaction of manganese­(II) acetate with a xanthene-bridged bis­[3-(salicylideneamino)-1-propanol] ligand, H<sub>4</sub>L, afforded the tetramanganese­(II,II,III,III) complex [Mn<sub>4</sub>(L)<sub>2</sub>(μ-OAc)<sub>2</sub>], which has an incomplete double-cubane structure. The corresponding reaction using manganese­(II) chloride in the presence of a base gave the tetramanganese­(III,III,III,III) complex [Mn<sub>4</sub>(L)<sub>2</sub>Cl<sub>3</sub>(μ<sub>4</sub>-Cl)­(OH<sub>2</sub>)], in which four Mn ions are bridged by a Cl<sup>–</sup> ion. A pair of L ligands has a propensity to incorporate four Mn ions, the arrangement and oxidation states of which are dependent on the coexistent anions

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