A structural study of the hydrated and the dimethylsulfoxide, N, N′-dimethylpropyleneurea, and N, N-dimethylthioformamide solvated iron(II) and iron(III) ions in solution and solid state

Abstract

The structures of the solvated iron(II) and iron(III) ions have been studied in solution and solid state by extended X-ray absorption fine structure (EXAFS) in three oxygen donor solvents, water, dimethylsulfoxide (Me 2SO), N, N′-dimethylpropyleneurea (DMPU), and one sulfur donor solvent, N, N-dimethylthioformamide (DMTF); these solvents have different coordination and solvation properties. In addition, the structure of hexakis(dimethylsulfoxide)iron(III) perchlorate has been determined crystallographically to support the determination of the corresponding solvate in solution. The hydrated, the dimethylsulfoxide and N, N-dimethylthioformamide solvated iron(II) ions show regular octahedral coordination in both solution and solid state with mean Fe–O, Fe–O, and Fe–S bond distances of 2.10, 2.10, and 2.52 Å, respectively, whereas the N, N′-dimethylpropyleneurea iron(II) solvate is five-coordinated, d(Fe–O) = 2.06 Å. The compounds vary in color from light green (hydrate) to dark orange or red (DMPU). The hydrated iron(III) ion in aqueous solution and the dimethylsulfoxide solvated iron(III) ions in solution and solid state show the expected octahedral coordination, the Fe–O bond distances are 2.00 Å for both, whereas the N, N′-dimethylpropyleneurea iron(III) solvate is found to be five-coordinated with a mean Fe–O bond distance of 1.99 Å. The N, N-dimethylthioformamide solvated iron(III) ion in the solid perchlorate salt is tetrahedrally four-coordinated, the mean Fe–S bond distance is 2.20 Å. Iron(III) is reduced with time to iron(II) in N, N-dimethylthioformamide solution. The compounds vary in color from pale yellow (hydrate) to blackish red (DMPU).