A Triad of Highly Reduced, Linear Iron Nitrosyl Complexes: {FeNO}8–10. (25th August 2016)

• Record Type: Journal Article
• Authors: Chalkley, Matthew J.; Peters, Jonas C.
• Is Part Of: Angewandte Chemie. Volume 128:Number 39(2016)
• Page Start: 12174
• Page End: 12177
• Publication Date: 2016-08-25
• Subjects: Boratrane -- Eisen -- Koordinationschemie -- Metall-Ligand-Kovalenz -- Stickstoffoxide; Chemistry -- Periodicals; 540
• DOI: 10.1002/ange.201605403
• Languages: English
• ISSNs: 0044-8249

Abstract

Abstract: Given the importance of Fe–NO complexes in both human biology and the global nitrogen cycle, there has been interest in understanding their diverse electronic structures. Herein a redox series of isolable iron nitrosyl complexes stabilized by a tris(phosphine)borane (TPB) ligand is described. These structurally characterized iron nitrosyl complexes reside in the following highly reduced Enemark–Feltham numbers: {FeNO} 8, {FeNO} 9, and {FeNO} 10 . These {FeNO} 8–10 compounds are each low‐spin, and feature linear yet strongly activated nitric oxide ligands. Use of Mössbauer, EPR, NMR, UV/Vis, and IR spectroscopy, in conjunction with DFT calculations, provides insight into the electronic structures of this uncommon redox series of iron nitrosyl complexes. In particular, the data collectively suggest that {TPBFeNO} 8–10 are all remarkably covalent. This covalency is likely responsible for the stability of this system across three highly reduced redox states that correlate with unusually high Enemark–Feltham numbers.