The unusual redox properties of fluoroferrocenes revealed through a comprehensive study of the haloferrocenes

M.S. Inkpen, S. Du, M. Hildebrand, A.J.P. White, N.M. Harrison, T. Albrecht, N.J. Long

Research output: Contribution to journalArticlepeer-review

17 Citations (Scopus)

Abstract

We report the synthesis and full characterization of the entire haloferrocene (FcX) and 1,1′-dihaloferrocene (fcX2) series (X = I, Br, Cl, F; Fc = ferrocenyl, fc = ferrocene-1,1′-diyl). Finalization of this simple, yet intriguing set of compounds has been delayed by synthetic challenges associated with the incorporation of fluorine substituents. Successful preparation of fluoroferrocene (FcF) and 1,1′-difluoroferrocene (fcF2) were ultimately achieved using reactions between the appropriate lithiated ferrocene species and N-fluorobenzenesulfonimide (NFSI). The crude reaction products, in addition to those resulting from analogous preparations of chloroferrocene (FcCl) and 1,1′-dichloroferrocene (fcCl2), were utilized as model systems to probe the limits of a previously reported “oxidative purification” methodology. From this investigation and careful solution voltammetry studies, we find that the fluorinated derivatives exhibit the lowest redox potentials of each of the FcX and fcX2 series. This counterintuitive result is discussed with reference to the spectroscopic, structural, and first-principles calculations of these and related materials.
Original languageEnglish
Pages (from-to)5461-5469
Number of pages9
JournalOrganometallics
Volume34
Issue number22
Early online date2 Nov 2015
DOIs
Publication statusPublished - 23 Nov 2015

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