Electronegative Oligothiophenes Fully Annelated with Hexafluorocyclopentene: Synthesis, Properties, and Intrinsic Electron Mobility

Abstract

Synthesis of hexafluorocyclopenta[c]thiophene-repeated oligothiophenes up to 6-mer has been accomplished. The photophysical and electrochemical properties of these oligomers unambiguously exemplify marked electronegative character without disrupting the effective conjugation. The combination of time-resolved microwave conductivity and transient optical spectroscopy measurements of the 6-mer revealed the intrinsic electron mobility to be as high as 2.0 x 10(-1) cm(2) V(-1) s(-1).