Investigation of protonation induced metal-to-metal electron transfer in a cyano-bridged MnIII–FeIII dinuclear complex
Abstract
Reaction of [Mn(salophen)Cl] {salophen2− = o-phenylenediamine bis(salicylidenaminato)} with a tricyano Fe(III) precursor complex, [Fe(bbp)(CN)3]2− {H2bbp = bis(2-benzimidazolyl)pyridine}, affords a dinuclear cyano-bridged heterometallic MnIII-(μ-NC)-FeIII fragment in the complex salt [Mn(salophen)(H2O)2][Mn(salophen)(H2O)(μ-NC)Fe(bbp)(CN)2]·4H2O (1). The title compound shows field-induced slow relaxation of magnetization below 2.8 K. Possibility of a protonation induced metal-to-metal electron transfer (MMET) process in the parent complex is probed by UV-visible, electrochemical, and electron spin resonance studies.