| Abstrakt: |
Abstract Reaction of 2-acetylpyridine, hydrazine, and an iron(II) salt gives a low-spin binuclear iron(II) complex, [Fe2(pmk)3]4+, in which three tetradentate Schiff base ligands span the two metal centres to give a complex of helical geometry. We report solubilities of the iodide and perchlorate salts, in H2O, in aqueous MeOH, and in aqueous DMSO (perchlorate only), up to 60% by vol of organic cosolvent. Transfer chemical potentials for the complex cation from H2O into the respective mixed solvents have been derived from these solubilities, to give a picture of solvation of this complex in the media studied. Kinetics of base hydrolysis of [Fe2(pmk)3]4+ have been established, in H2O and in 40% MeOH, 20 and 40% i -PrOH, and 20 and 40% DMSO, at 298.2 K. The reactivity of [Fe2(pmk)3]4+ is discussed in relation to reactivities of a selection of iron(II)-diimine complexes, ranging from [Fe(bipy)3]2+ and [Fe(phen)3]2+ to ligand-encapsulated cage complexes. |
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