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The interplay of inverted redox potentials and aromaticity in the oxidized states of new pi-electron donors: 9-(1,3-dithiol-2-ylidene)fluorene and 9-(1,3-dithiol-2-ylidene)thioxanthene derivatives.

Amriou, S.; Wang, C.S.; Batsanov, A.S.; Bryce, M.R.; Perepichka, D.F.; Orti, E.; Viruela, R.; Vidal-Gancedo, J.; Rovira, C.

Authors

S. Amriou

C.S. Wang

D.F. Perepichka

E. Orti

R. Viruela

J. Vidal-Gancedo

C. Rovira



Abstract

Derivatives of 9-(1,3-dithiol-2-ylidene)fluorene (9) and 9-(1,3-dithiol-2-ylidene)thioxanthene (10) have been synthesised using Horner–Wadsworth–Emmons reactions of (1,3-dithiol-2-yl)phosphonate reagents with fluorenone and thioxanthen-9-one. X-ray crystallography, solution electrochemistry, optical spectroscopy, spectroelectrochemistry and simultaneous electrochemistry and electron paramagnetic resonance (SEEPR), combined with theoretical calculations performed at the B3P86/6-31G** level, elucidate the interplay of the electronic and structural properties in these molecules. These compounds are strong two-electron donors, and the oxidation potentials depend on the electronic structure of the oxidised state. Two, single-electron oxidations (equation imageequation image) resulting in a single, two-electron oxidation process. The latter is due to the aromatic structure of the thioxanthenium cation (formed on the loss of a second electron), which stabilises the dication state (102+) compared with the radical cation. This contrasts with the nonaromatic structure of the fluorenium cation of system 9. The two-electron oxidation wave in the thioxanthene derivatives is split into two separate one-electron waves in the corresponding sulfoxide and sulfone derivatives 27–29 owing to destabilisation of the dication state.

Citation

Amriou, S., Wang, C., Batsanov, A., Bryce, M., Perepichka, D., Orti, E., …Rovira, C. (2006). The interplay of inverted redox potentials and aromaticity in the oxidized states of new pi-electron donors: 9-(1,3-dithiol-2-ylidene)fluorene and 9-(1,3-dithiol-2-ylidene)thioxanthene derivatives. Chemistry - A European Journal, 12(12), 3389-3400. https://doi.org/10.1002/chem.200501326

Journal Article Type Article
Publication Date 2006-04
Journal Chemistry - A European Journal
Print ISSN 0947-6539
Electronic ISSN 1521-3765
Publisher Wiley
Peer Reviewed Peer Reviewed
Volume 12
Issue 12
Pages 3389-3400
DOI https://doi.org/10.1002/chem.200501326
Keywords Aromaticity, Electron donors, Fluorene, Redox chemistry, Thioxanthene.
Public URL https://durham-repository.worktribe.com/output/1541665