Redox and EPR spectral behaviour of radical cations of dibenzothiophene and some of its derivatives

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Abstract

The radical cations of dibenzothiophene 1 and its 2,8-[2H2]-isotopomer (2), a series of methylated dibenzothiophenes, viz. 2,8- (3), 3,7- (4) and 4,6-dimethyldibenzothiophene (5), and 2,4,6,8-tetramethyldibenzothiophene (6), as well as 2,2′- (7) and 4,4′-bidibenzothiophene (8) have been generated in 1,1,1,3,3,3-hexafluoropropan-2-ol, mostly by TlIII trifluoroacetate or 4-tolyl-TlIII trifluoroacetate oxidation. From the hyperfine coupling constants obtained, it is concluded that the 2- and 4-positions of 1.+ are the carbon atoms possessing the highest spin density. This assignment agrees with results of high-level quantum-chemical calculations, placing the 2B1 state as the lowest energy level of 1.+. © Acta Chemica Scandinavica 1997.

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Eberson, L., Hartshorn, M. P., Persson, O., & Radner, F. (1997). Redox and EPR spectral behaviour of radical cations of dibenzothiophene and some of its derivatives. Acta Chemica Scandinavica, 51(4), 492–500. https://doi.org/10.3891/acta.chem.scand.51-0492

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