首页> 外文期刊>Electrochimica Acta >Electrochemical synthesis of polyaniline in the presence of poly(amidosulfonic acid)s with different rigidity of polymer backbone and characterization of the films obtained
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Electrochemical synthesis of polyaniline in the presence of poly(amidosulfonic acid)s with different rigidity of polymer backbone and characterization of the films obtained

机译:在具有不同聚合物骨架刚性的聚(酰胺磺酸)存在下电化学合成聚苯胺和表征所获得的薄膜

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摘要

We have studied electrochemical matrix polymerization of aniline in the presence of poly(amidosulfonic acid)s of different nature: poly(2-acrylamido-2-methyl-1-propanosulfonic acid) (PAMPSA, flexible backbone); poly(p,p'-(2,2'-disulfoacid)-diphenylene-iso-phthalamid) (i-PASA, semi-rigid backbone); poly(p, p'-(2,2'-disulfoacid)-diphelylene-tere-phthalamid) (t-PASA, rigid backbone). Also, we have investigated spectral and electrochemical properties of the films obtained, as well as their surface morphology. The matrix polymerization results in the formation of interpolymer complexes of polyaniline (PANI) and the above-cited polyacids. The acceleration of aniline electropolymerization in the presence of poly(amidosulfonic acid)s was observed due to association of aniline molecules to sulfonic groups of the polyacid and higher local concentration of protons near the polyacid backbone. The rigid-chain polyacids interfere with the normal course of the electropolymerization, which manifests itself in the changes of the shape of time dependences of absorbance and charge. Cyclic voltammetry and spectroelectrochemical experiments showed that the formation of interpolymer complex with rigid-chain polyacids distorts spectroelectrochemical characteristics of PANI. This evidently results from steric hindrances in the formation of quinoid units.
机译:我们已经研究了在不同性质的聚(酰胺基磺酸)存在下苯胺的电化学基体聚合反应:聚(2-丙烯酰胺基-2-甲基-1-丙磺酸)(PAMPSA,柔性骨架);聚(p,p'-(2,2'-二磺酸)-二亚苯基-异邻苯二甲酰胺)(i-PASA,半刚性骨架);聚(p,p'-(2,2'-二磺酸)-二亚戊基-对苯二甲酰胺)(t-PASA,刚性骨架)。另外,我们研究了所得膜的光谱和电化学性质,以及它们的表面形态。基质聚合导致聚苯胺(PANI)和上述多元酸的互聚物络合物的形成。由于存在苯胺分子与多元酸的磺酸基团以及多元酸主链附近质子的较高局部浓度,因此在聚(酰胺基磺酸)存在下,苯胺电聚合反应加速。刚性链多元酸会干扰电聚合反应的正常过程,这在吸收和电荷的时间依赖性形状变化中表现出来。循环伏安法和光谱电化学实验表明,具有刚性链多元酸的共聚体配合物的形成扭曲了PANI的光谱电化学特性。这显然是由于醌型单元形成中的位阻。

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