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POTENTIAL-DEPENDENT NUCLEOPHILICITY OF POLYANILINE

机译:聚苯胺的潜在依赖核

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The reaction of electrode-confined polyaniline with trifluoroacetic anhydride in acidified acetonitrile giving insulating and electroinactive trifluoroacetylated polyaniline has been studied by electrochemistry, reflectance IR, and microelectrochemistry. Variation of electrochemical. potential from 0.2 V (reduced, most reactive) to 0.6 V (oxidized by 0.5 electron per repeat unit, unreactive) vs SCE allows control of the reaction rate. Reaction of trifluoroacetic anhydride with aniline oligomers N-phenylphenylenediamine and N,N'-diphenylphenylenediamine gave N-trifluoroacetylation products exclusively, exhibiting positive shifts in oligomer oxidation potential of >0.5 V, with terminal amines reacting considerably faster than internal amines. Reflectance IR following the potential-dependent growth of CO and CS peaks for macroelectrode films of polyaniline treated with trifluoroacetic anhydride showed similar potential dependence of reactivity as conductivity measurements during trifluoroacetylation of polyaniline-derivatized microelectrode arrays. Polyaniline trifluoroacetylation was accompanied by narrowing but no shifting of the potential window of electroactivity and conductivity, and eventual elimination of all conductivity. Trifluoroacetylation of polyaniline terminal amines, rapid at all potentials, does not detectably affect conductivity. Also examined by electrochemistry were the reactions of polyaniline with other anhydrides resulting in the reactivity order (F3CCO)(2)O > (Cl3CCO)(2)O > (H2ClCCO)(2)O > (HCl2CCO)(2)O (H3CCO)(2)O. IR through polyaniline electrodeposited onto optically transparent Au electrodes shows that essentially complete loss of polyaniline electroactivity occurs when approximate to 25% of nitrogens are trifluoroacetylated. Electroactivity and conductivity of trifluoroacetylated polyaniline may be recovered by hydrolysis in K2CO3/CH3OH/O-2 solution to regenerate polyaniline. Use of the reversible trifluoroacetylation of polyaniline provides a proof-of-concept for a new approach to an erasable-programmable-read-only-memory device. [References: 67]
机译:通过电化学,反射红外和微电化学研究了电极约束的聚苯胺与三氟乙酸酐在酸化的乙腈中的反应,从而产生绝缘和电惰性的三氟乙酰化聚苯胺。电化学变化。与SCE相比,从0.2 V(还原的,最具反应性的)电势到0.6 V(每个重复单元被0.5电子氧化,无反应性)的电势可以控制反应速率。三氟乙酸酐与苯胺低聚物N-苯基苯二胺和N,N'-二苯基苯二胺的反应仅产生N-三氟乙酰化产物,低聚物氧化电位的正位移大于0.5 V,末端胺的反应明显快于内部胺。在用三氟乙酸酐处理的聚苯胺大电极膜的聚苯胺大电极膜上,随着CO和CS峰的电位依赖性增长而产生的反射IR与电导率测量结果类似,反映了对苯胺衍生的微电极阵列进行三氟乙酰化时的反应活性。聚苯胺三氟乙酰化伴随着电活性和电导率的潜在窗口变窄但没有移动,并最终消除了所有电导率。在所有电位下,聚苯胺末端胺的三氟乙酰化作用均未检测到影响电导率。还通过电化学检查了聚苯胺与其他酸酐的反应,其反应顺序为(F3CCO)(2)O>(Cl3CCO)(2)O>(H2ClCCO)(2)O>(HCl2CCO)(2)O (H3CCO)(2)O。通过电沉积到光学透明的Au电极上的聚苯胺的IR显示,当大约25%的氮被三氟乙酰化时,聚苯胺电活性基本上完全丧失。通过在K2CO3 / CH3OH / O-2溶液中水解以再生聚苯胺,可以回收三氟乙酰化聚苯胺的电活性和电导率。聚苯胺的可逆三氟乙酰化的使用为可擦除可编程只读存储器设备的新方法提供了概念验证。 [参考:67]

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