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Functionalized Poly(3-hexylthiophene)s via Lithium–BromineExchange

机译:通过锂-溴官能化的聚(3-己基噻吩)交换

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摘要

Poly(3-hexylthiophene) (P3HT) is one of the most extensively investigated conjugated polymers and has been employed as the active material in many devices including field-effect transistors, organic photovoltaics and sensors. As a result, methods to further tune the properties of P3HT are desirable for specific applications. Herein, we report a facile postpolymerization modification strategy to functionalize the 4-position of commercially available P3HT in two simple steps–bromination of the 4-position of P3HT (Br–P3HT) followed by lithium−bromine exchange and quenching with an electrophile. We achieved near quantitative lithium–bromine exchange with Br–P3HT, which requires over 100 thienyl lithiates to be present on a single polymer chain. The lithiated-P3HT is readily combined with functional electrophiles, resulting in P3HT derivatives with ketones, secondary alcohols, trimethylsilyl (TMS) group, fluorine, or an azide at the 4-position. We demonstrated that the azide-modified P3HT could undergo Cu-catalyzed or Cu-free click chemistry, significantly expanding the complexity of the structuresthat can be appended to P3HT using this method.
机译:聚(3-己基噻吩)(P3HT)是研究最广泛的共轭聚合物之一,已被用作许多器件的活性材料,包括场效应晶体管,有机光伏器件和传感器。结果,对于特定应用而言,需要进一步调节P3HT的性质的方法。在此,我们报告了一种简便的后聚合修饰策略,可通过两个简单的步骤将市售P3HT的4位功能化:溴化P3HT的4位(Br-P3HT),然后进行溴溴化锂交换并用亲电试剂淬灭。我们用Br-P3HT实现了近乎定量的锂-溴交换,这要求在一条聚合物链上存在100多种噻吩基锂。锂化的P3HT容易与功能性亲电试剂结合,生成在4位带有酮,仲醇,三甲基甲硅烷基(TMS),氟或叠氮化物的P3HT衍生物。我们证明了叠氮化物修饰的P3HT可能会经历Cu催化或无Cu的点击化学反应,从而大大扩展了结构的复杂性可以使用此方法将其附加到P3HT。

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