CYCLIC VOLTAMMETRY AND DIFFERENTIAL CYCLIC VOLTABSORPTOMETRY OF SOLUBLE OLIGOTHIOPHENES - EVIDENCE FOR A 4-FOLD CHARGED PI-DIMER IN DUODECITHIOPHENE

Citation
B. Nessakh et al., CYCLIC VOLTAMMETRY AND DIFFERENTIAL CYCLIC VOLTABSORPTOMETRY OF SOLUBLE OLIGOTHIOPHENES - EVIDENCE FOR A 4-FOLD CHARGED PI-DIMER IN DUODECITHIOPHENE, Journal of electroanalytical chemistry [1992], 399(1-2), 1995, pp. 97-103
Citations number
31
Categorie Soggetti
Electrochemistry,"Chemistry Analytical
Journal title
Journal of electroanalytical chemistry [1992]
ISSN journal
15726657 → ACNP
Volume
399
Issue
1-2
Year of publication
1995
Pages
97 - 103
Database
ISI
SICI code
Abstract
Cyclic voltammetry (CV) and differential cyclic voltabsorptometry (DCV A) measurements have been carried out on solutions of alkyl-substitute d oligothiophenes (nT, where n is the number of thiophene rings) with n = 1, 2, 3, 4, 6, 8, and 12. For 4 less than or equal to n less than or equal to 8, the CV curves present two oxidation waves, which are at tributed to the successive formation of the radical cation and the dic ation. The DCVA curve of 6T shows similar behavior. In the case of 12T , the CV curve also presents two irreversible oxidation peaks, whereas only one peak is obtained with DCVA. This last behavior is consistent with previously reported measurements on chemically oxidized 12T. Whe n plotted as a function of the reversed number of rings, the first and second oxidation peak potentials align along two straight lines that tend to merge at n --> infinity. The single oxidation potential of 12T , estimated from DCVA, aligns with the first oxidation potential of sh orter oligothiophenes. By combining these results with previously publ ished optical and ESR measurements on chemically oxidized 6T and 12T, we suggest a model where oxidized 12T molecules condense into four-fol d charged pi-dimers.