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Electropolymerized Polythiophenes Bearing Pendant Nitroxide Radicals

机译:带有侧链氮氧自由基的电聚合聚噻吩

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摘要

We report a facile way to synthesize poly-thiophenes carrying pendant 2,2,6,6-tetramethylpiperidinyl-1-oxyl (TEMPO) radicals, here called PTATs, by electro-polymerization in boron trifluoride diethyl etherate (BFEE). The spacing between the TEMPO radical and the polythiophene backbone is varied by an alkyl spacer (n = 2, 4, 6), and the electronic and electrochemical properties are examined using UV-vis spectroscopy, cyclic voltammetry, and electrochemical impedance spectroscopy. Film morphologies are also studied via scanning electron microscopy (SEM) and atomic force microscopy (AFM), which show that the longer octyl chain placed between thiophene and TEMPO effectively suppresses aggregation. The highest conductivity and electroactivity are observed for n = 4 and n = 6, respectively. Such morphology differences provide an opportunity to better understand the charge transport and energy storage properties in electronic materials.
机译:我们报告了一种通过在三氟化硼二乙醚(BFEE)中进行电聚合来合成带有2,2,6,6-四甲基哌啶基-1-氧基(TEMPO)侧基(此处称为PTAT)的聚噻吩的简便方法。 TEMPO自由基和聚噻吩主链之间的间隔通过烷基间隔基(n = 2、4、6)进行更改,并使用紫外可见光谱,循环伏安法和电化学阻抗谱检查电子和电化学性质。还通过扫描电子显微镜(SEM)和原子力显微镜(AFM)研究了膜的形态,结果表明,噻吩和TEMPO之间较长的辛基链可有效抑制聚集。分别在n = 4和n = 6时观察到最高的电导率和电活性。这种形态差异为更好地了解电子材料中的电荷传输和能量存储特性提供了机会。

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