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Molecular Engineering of Non-Halogenated Solution-Processable Bithiazole based Electron Transport Polymeric Semiconductors

机译:非卤代溶液可处理的噻唑基电子传输聚合物的分子工程

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摘要

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.
机译:噻唑的电子缺乏和反平面构象可能有益于有机半导体的电子传输性能。然而,通过简便的合成策略将噻唑并入聚合物仍然是一个挑战。在此,一步合成2,2’-联噻唑并与二噻吩二酮二吡咯并吡咯共聚,得到聚(二噻吩二酮二吡咯并吡咯-吡唑)PDBTz。 PDBTz在有机场效应晶体管(OFET)配置中显示出的电子迁移率达到0.3 cm2V-1s-1;这与最近讨论的包含富电子的联噻吩和二噻吩基二酮基吡咯并吡咯的等电子共轭聚合物相反,后者仅显示空穴传输特性。电荷载流子传输特性的这种反转证实了在电子传输半导体材料的开发中,联苯唑具有巨大的潜力。将支链的5-癸基庚酰基侧链并入PDBTz中,以增强聚合物的溶解性,特别是在非卤代,与环境更相容的溶剂中。用多种非卤代溶剂浇铸的PDBTz表现出薄膜形态和场效应电子迁移率,类似于用卤代溶剂浇铸的PDBTz。

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