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Molecular Engineering of Nonhalogenated Solution-Processable Bithiazole-Based Electron-Transport Polymeric Semiconductors
Author(s) -
Boyi Fu,
Cheng-Yin Wang,
Bradley D. Rose,
Yundi Jiang,
Mincheol Chang,
PingHsun Chu,
Zhibo Yuan,
Canek Fuentes-Hernández,
Bernard Kippelen,
JeanLuc Brédas,
David M. Collard,
Elsa Reichmanis
Publication year - 2015
Publication title -
chemistry of materials
Language(s) - English
Resource type - Journals
eISSN - 1520-5002
pISSN - 0897-4756
DOI - 10.1021/acs.chemmater.5b00173
Subject(s) - electron mobility , materials science , polymer , conjugated system , organic semiconductor , organic field effect transistor , solubility , semiconductor , electron , polymer chemistry , transistor , chemistry , field effect transistor , organic chemistry , optoelectronics , physics , composite material , quantum mechanics , voltage
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 cm2V-1s-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 non-halogenated, more environmentally compatible solvents. PDBTz cast from a range of non-halogenated solvents exhibited film morphologies and field-effect electron mobility similar to those cast from halogenated solvents

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