Abstract
The title compound, (C 6H 16N)[Fe 3(CH 3CO 2) 8O(H 2O)]·C 7H 8, was serendipitously crystallized from a reaction of disilanol with iron(II) acetate. The trinuclear acetatoferrate(III) anion has a triethyl-ammonium cation as the counterion. The three Fe atoms lie on the vertices of a regular triangle and are octa-hedrally coordinated. The complete coordination of the anion includes shared ligands among the three metal ions: a central tribridging O atom and six bidentate bridging acetyl groups. The six-coordinations of two of the metal ions are completed by a monodentate acetate ligand, whereas that of the third metal ion is completed by a water molecule. The uncoordinated triethyl-ammonium cation is involved in N - H⋯O hydrogen bonding to a singly coordinated acetyl group. The coordinated aqua molecule is involved in bifurcated O - H⋯O hydrogen bonding. C - H⋯O interactions are also observed. The toluene solvent molecule is disordered over two sets of sites in a 0.609 (11):0.391 (11) ratio.
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Burgoyne, A. R., Meijboom, R., Muller, A., & Omondi, B. O. (2011). Triethylammonium hexa-μ- 2-acetato-κ 12 O:O′-diacetato-κ 2O-aqua-μ 3-oxido- triferrate(III) toluene monosolvate. Acta Crystallographica Section E: Structure Reports Online, 67(8). https://doi.org/10.1107/S160053681102616X
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