Jump to main content
Jump to site search

Issue 6, 2018
Previous Article Next Article

Ferrocenyl-sulfonium ionic liquids – synthesis, characterization and electrochemistry

Author affiliations


New ferrocenylsulfonium cation based ionic liquids were prepared by direct alkylation of the corresponding ferrocenyl-based thioethers with N-alkylbis(trifluoromethanesulfonyl)imides (R′TFSI). This convenient direct access to organometallic sulfonium bis(trifluoromethanesulfonyl)imide (TFSI) salts without the need for ion exchange was chosen in order to obtain highly pure and reversibly redox active room temperature ILs in many cases. In other cases the anion cation interaction in the solid state was studied by XRD analyses. Moreover a diferrocenylmethylsulfonium tetrafluoroborate with two redox active centers was synthesized. The redox chemistry of these sulfonium salts was investigated via cyclic voltammetry. Furthermore, UV-Vis spectra and thermoanalytical data are discussed. The electron-withdrawing sulfonium group is directly bonded to the ferrocenyl unit, therefore this cationic group influences the potential of these ionic liquids in a more pronounced way than being anchored to the ferrocenyl unit via an organic spacer. With their low absorbance in the visible light and reversible, tunable redox potential, these room temperature ILs open perspectives as redox mediators in dye sensitized solar cells (DSSCs), as redox electrolytes in supercapacitors or as overcharge protection additives in batteries.

Graphical abstract: Ferrocenyl-sulfonium ionic liquids – synthesis, characterization and electrochemistry

Back to tab navigation

Supplementary files

Publication details

The article was received on 02 Nov 2017, accepted on 20 Dec 2017 and first published on 20 Dec 2017

Article type: Paper
DOI: 10.1039/C7DT04139J
Citation: Dalton Trans., 2018,47, 1933-1941
  •   Request permissions

    Ferrocenyl-sulfonium ionic liquids – synthesis, characterization and electrochemistry

    A. Venker, T. Vollgraff and J. Sundermeyer, Dalton Trans., 2018, 47, 1933
    DOI: 10.1039/C7DT04139J

Search articles by author