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The electron deficiency and trans-planar conformation of bithiazole is potentially beneficial for the electron-transport performance of organic semiconductors. However, the incorporation of bithiazole into polymers through a facile synthetic strategy remains a challenge. Herein, 2,2′-bithiazole was synthesized in one step and copolymerized with dithienyldiketopyrrolopyrrole to afford poly(dithienyldiketopyrrolopyrrole-bithiazole), PDBTz . PDBTz exhibited electron mobility reaching 0.3 cm 2 V –1 s –1 in organic field-effect transistor (OFET) configuration; this contrasts with a recently discussed isoelectronic conjugated polymer comprising an electron-rich bithiophene and dithienyldiketopyrrolopyrrole, which displays merely hole-transport characteristics. This inversion of charge-carrier transport characteristics confirms the significant potential for bithiazole in the development of electron-transport semiconducting materials. Branched 5-decylheptacyl side chains were incorporated into PDBTz to enhance polymer solubility, particularly in nonhalogenated, more environmentally compatible solvents. PDBTz cast from a range of nonhalogenated solvents exhibited film morphologies and field-effect electron mobility similar to those cast from halogenated solvents.
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Fu et al. (2015) studied this question.
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