End Group Modification of Regioregular Polythiophene through Postpolymerization Functionalization

Abstract

HT-poly(3-hexylthiophenes) (HT-PHT) with H/Br end group composition were prepared via a modified McCullough method using anhydrous ZnCl2 for the transmetalation step. These bromine-terminated HT-PHT can be end group modified at the ω end through a cross-coupling reaction with thienylzinc compounds bearing a THP-protected hydroxy or STABASE-protected amino groups. After deprotection, HT-PHTs with −OH or −NH2 functional groups at the ω end were obtained. In addition, HT-PHT with pure H/H end group composition were also modified by treatment with Vilsmeier reagent and functionalized with formaldehyde groups at both the α and ω chain ends. Reduction of the formaldehyde groups produced the HT-PHT diol. MALDI−TOF is a powerful tool to monitor each step of these end group functionalizations.