Synthesis, characterization, and structures of Mn(DMHP)3 x 12H2O and Mn(DMHP)2Cl x 0.5H2O.

This report describes the synthesis, characterization, and X-ray crystal structures of two Mn(III) complexes, Mn-(DMHP) 3 .12H 2 O and Mn(DMHP) 2 Cl.0.5H 2 O (DMHP = 1,2-dimethyl-3-hydroxy-4-pyridinone). Mn(DMHP) 2 Cl was prepared from the reaction of Mn(II) chloride with 2 equiv of DMHP under reflux in the presence of triethylamine. Mn(DMHP) 3 was obtained by reacting Mn(II) acetate with 3 equiv of DMHP in the presence of sodium acetate. Mn(DMHP) 3 could also be prepared by reacting Mn(OAC) 3 .2H 2 O with 3 equiv of DMHP in the presence of triethylamine. Both Mn(III) complexes have been characterized by elemental analysis, infrared spectroscopy, electronic paramagnetic resonance, electrospray ionization spectroscopy, electrochemical method, and X-ray crystallography. The X-ray crystal structure of Mn(DMHP) 2 Cl.0.5H 2 O revealed a rare example of five-coordinated Mn(III) complexes with two bidentate ligands and a square pyramidal coordination geometry. Surprisingly, the average Mn-O (hydroxy) bond distance in Mn(DMHP) 2 Cl.0.5H 2 O is ∼0.025 A longer than that of the average Mn-O (carbonyl) bond, suggesting an extensive delocalization of electrons in the two pyridinone rings. The structure of Mn(DMHP) 3 . 12H 2 O, a rare example of six-coordinate high-spin Mn(III) complexes without Jahn-Teller distortion, is isostructural to M(DMHP) 3 .12H 2 O (M = Al, Ga, Fe, and In). The electrochemical data for Mn(DMHP) 3 suggests that the Mn(III) oxidation state is highly stabilized by three DMHP ligands. DMHP has the potential as a chelator for the removal of excess intracellular Mn and the treatment of chronic Mn toxicity.