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首页> 外文期刊>Macromolecules >Novel thiophene-phenylene-thiophene fused bislactam-based donor-acceptor type conjugate polymers: Synthesis by direct arylation and properties
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Novel thiophene-phenylene-thiophene fused bislactam-based donor-acceptor type conjugate polymers: Synthesis by direct arylation and properties

机译:新型噻吩-亚苯基-噻吩稠合的双内酰胺基供体-受体型共轭聚合物:直接芳基化合成和性能

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摘要

Three new donor-acceptor copolymers based on thiophene-phenylene-thiophene fused bislactam and various donors (3,4-dodecylthiophene, 4,4'-didodecyl- 2,2'-bithiophene, and ethylenedioxythiophene) were synthesized, characterized, and used in field-effect transistors. Polycondensation was performed using nonactivated thiophene derivatives by employing palladium-catalyzed direct arylation under phosphine-free conditions. This method is superior to traditional cross-coupling polymerization because it requires fewer synthetic operations and does not employ toxic organometallic intermediates. Regioselective polymers can also be generated by using β-substituted thiophene derivatives. The studied polymers were tested in a bottom gate top contact thin film transistor (OTFT) architecture. The best electronic performance was shown by polymer P3, with enhanced π-conjugation due to the appearance of intramolecular attractive interactions.
机译:合成,表征和使用了三种基于噻吩-亚苯基-噻吩稠合双内酰胺的新型供体-受体共聚物(3,4-十二烷基噻吩,4,4'-二癸基-2,2'-联噻吩和乙撑二氧噻吩)场效应晶体管。在无膦条件下,采用钯催化的直接芳基化反应,使用未活化的噻吩衍生物进行缩聚反应。该方法优于传统的交叉偶联聚合,因为它需要较少的合成操作并且不使用有毒的有机金属中间体。区域选择性聚合物也可以通过使用β-取代的噻吩衍生物来产生。在底栅顶部接触薄膜晶体管(OTFT)体系结构中测试了研究的聚合物。聚合物P3表现出最佳的电子性能,由于分子内引诱相互作用的出现,π共轭增强。

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