Experimental charge density in an oxidized trinuclear iron complex using 15 K synchrotron and 100 K conventional single-crystal X-ray diffraction

• Published in: Dalton transactions : an international journal of inorganic chemistry 2009-01 (4), p.664-671
• Main Authors: Overgaard, Jacob, Larsen, Finn K, Timcob, Grigore A, Iversen, Bo B
• Format: Article
• Language: English
• ISSN: 1477-9226; 1477-9234
• DOI: 10.1039/b811576a

The experimental electron density distribution in a crystal consisting of the simplest conceivable trinuclear carboxylate-bridged iron-mu3-oxo dianion with two alpha-picolinium cations has been determined using both synchrotron (15 K) and conventional (100 K) X-ray diffraction data. The constituent trinuclear oxo-centered molecule consists of six mu2-bridging formate groups between the iron pairs, while the axial ligand for all iron atoms is another formate group. The compound {[FeO(HCOO)5(HCOO)3]2-.H2O.2(alpha-CH3NC5H5)}, (1) crystallizes in the monoclinic space group P2(1)/m with charge assisted hydrogen bonds linking the alpha-picolinium cations to the trinuclear groups. The chemical bonding in the weakly asymmetric Fe3O-core of 1 has been examined through the use of the quantum theory of atoms in molecules, and in combination with experimental d-orbital populations, a significant electron sharing is observed between the Fe atoms and the central oxygen. The central oxygen exhibits clear sp2 hybridization, and the iron atoms have valence shell charge concentrations in all metal-ligand bond directions. The relative bond strengths are evaluated based upon the charge density distribution and found to be in accordance with the geometrical results. Integrated group charges follow expectations from formal chemical valences.