4.6 Article

A study on the electro-oxidation and electropolymerization of a new OPE linear molecule by EQCM and in situ FTIR spectroelectrochemistry

期刊

ELECTROCHIMICA ACTA
卷 56, 期 1, 页码 454-462

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2010.09.026

关键词

In situ FTIR spectroelectrochemistry; EQCM; Sonogashira reaction; Oxidation mechanism; 1,4-Bis(4-aminophenylethynyl)benzene)

资金

  1. National Natural Science Foundation of China [21075037, 20975037, 20905025]
  2. Hunan Provincial Science and Technology Departments [09JJ3019, 07JJ3024]

向作者/读者索取更多资源

A novel symmetric conjugated oligo(phenylene-ethynylene) COPE) linear molecule (1,4-bis(4-aminophenylethynyl)benzene): BAB) was synthesized by Sonogashira cross-coupling reactions. The structure and purity of the compound were confirmed by (1)H NMR, (13)C NMR and infrared (IR) and mass spectrometry (MS). The electrochemical oxidation process and mechanism of BAB were investigated via in situ Fourier transform infrared (FTIR) spectroelectrochemistry and electrochemical quartz crystal microbalance (EQCM). The electrochemical oxidation mechanism of BAB was proposed. The studies revealed that the BAB concentration and oxidation potential had a significant influence on the growth of the polymer film. A densely packed polymer film, which exhibited nonelectroactivity, was formed when a high monomer concentration and a high oxidation potential were used. When the electropolymerization of BAB was conducted at a lower concentration, a new pair of redox peaks appeared, and the resultant thin film had better electroactivity. The in situ FTIR studies confirmed that BAR could be electro-oxidized into radical cations and then electropolymerized via para (N-N) and/or ortho (N-C) coupling reactions to form polymers with a larger conjugated pi-electron system. The surface morphology of the poly-BAB was also investigated with atomic force microscopy (AFM) and scanning electron microscopy (SEM). (C) 2010 Elsevier Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据