The crystal structure of the organic-inorganic title salt, [Mn(C 18 H 18 N 2 O 4 )-(H 2 O) 2 ]ClO 4 , has been redetermined at 100 K. In contrast to the crystal structure determinations at room temperature [Akitsu et al. (2005). Acta Cryst. C61, m324-m328; Bermejo et al. (2007). Eur. J. Inorg. Chem. pp. 3789-3797], positional disorder of the ethylene bridge in the Schiff base ligand and the perchlorate anion is not observed at 100 K. The Mn III ion is six-coordinated with the tetradentate Schiff base chelate ligand N,N 0 -bis(3-methoxy-2-oxybenzylidene)ethylenediamine occupying coordination sites in the equatorial plane and the aqua ligands residing in the two axial positions. The octahedral coordination sphere of the Mn III ion exhibits an axial elongation due to the Jahn-Teller effect, which is characteristic of a d 4 high-spin electronic configuration.
Structure descriptionTransition metal complexes of Schiff bases show an interesting chemistry, including various aspects of organometallic and bioinorganic chemistry (Yamada, 1999). Schiff base complexes find application in a variety of catalytic transformations as they have the ability to coordinate to metal ions and stabilize unusual oxidation states. Metal complexes containing salen-type Schiff bases are important owing to their resemblance to metallopropyrins with respect to their electronic structure and catalytic activities in the way that they mimic enzymatic oxidations (Groves, 2005). Interest in the coordination chemistry of manganese complexes in high oxidation states is largely centred on the