A study of the cathodic and anodic doping of polybithiophene and poly-3-phe
nylthiophene in acetonitrile and propylene carbonate demonstrates that the
main fractions of charges of either sign undergo quasireversible redox conv
ersions. Two types of retarded processes reveal themselves. One is associat
ed with conversions of residual portions of positive and negative doping ch
arges trapped in the nonconducting matrix of a neutral polymer at final sta
ges of the undoping process. The other is due to redox conversions of polym
er chemically modified when interacting with solution components.