TY - JOUR
T1 - Molecular Engineering of Non-Halogenated Solution-Processable Bithiazole based Electron Transport Polymeric Semiconductors
AU - Fu, Boyi
AU - Wang, Cheng-Yin
AU - Rose, Bradley Daniel
AU - Jiang, Yundi
AU - Chang, Mincheol
AU - Chu, Ping-Hsun
AU - Yuan, Zhibo
AU - Fuentes-Hernandez, Canek
AU - Bernard, Kippelen
AU - Bredas, Jean-Luc
AU - Collard, David M.
AU - Reichmanis, Elsa
N1 - KAUST Repository Item: Exported on 2020-10-01
PY - 2015/4/13
Y1 - 2015/4/13
N2 - 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.
AB - 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.
UR - http://hdl.handle.net/10754/350202
UR - http://pubs.acs.org/doi/abs/10.1021/acs.chemmater.5b00173
UR - http://www.scopus.com/inward/record.url?scp=84928680439&partnerID=8YFLogxK
U2 - 10.1021/acs.chemmater.5b00173
DO - 10.1021/acs.chemmater.5b00173
M3 - Article
SN - 0897-4756
VL - 27
SP - 2928
EP - 2937
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 8
ER -