Inherently Chiral Oligomers Based on Indole-Benzothiophene Core

In recent years, transductors of chiral information based on conducting polymers have gained considerable attention. In particular, inherently chiral materials, which allow differentiation between the antipodes of a chiral analyte in terms of energetic variations, are highly desired. In this work, we successfully synthesized a novel inherently chiral oligomer based on an indole-benzothiophene core, namely, 2-([2,2 '-bithiophen]-5-yl)-3-(2-([2,2 '-bithiophen]-5-yl)benzo[b]thiophen-3-yl)-N-methylindole (BTIndT4). The electrochemical characterization evidences a stabilization of electrogenerated radical cations due to the presence of the indole group, which guides the oligomerization, producing well-ordered polymeric matrices. Furthermore, the in situ electrochemical conductance analysis demonstrates a simultaneous intrachain and interchain transfer of charge carriers. Finally, the highly efficient enantiorecognition capabilities of the antipodes of the oligo-BTIndT4 films toward the enantiomers of tryptophan and 3,4-dihydroxyphenylalanine (DOPA), as model chiral analytes, were demonstrated. Synthesis of novel inherently chiral oligomer based on a tailored indole-benzothiophene core for in situ conductance analysis and electroseparation of chiral analytes.image