Synthesis of Polythiophene-Silver Nanocomposites in Ionic Liquid for Catalytic Applications

被引:2
作者
Tavares, Flavia [1 ]
Oliveira, Larissa V. F. [2 ]
Hajjar-Garreau, Samar [3 ,4 ]
Camilo, Fernanda F. [1 ]
机构
[1] Univ Fed Sao Paulo, Inst Environm Chem & Pharmaceut Sci, Chem Dept, BR-09913030 Diadema, SP, Brazil
[2] Fed Univ ABC, Ctr Nat Sci & Humanities, BR-09210580 Santo Andre, Brazil
[3] Univ Haute Alsace, Inst Sci Mat Mulhouse, CNRS, UMR 7361, F-68100 Mulhouse, France
[4] Univ Strasbourg, F-67081 Strasbourg, France
基金
巴西圣保罗研究基金会;
关键词
polythiophene; nanocomposites; silver nanoparticles; ionic liquids; catalyst; ONE-POT SYNTHESIS; HIGH ELECTRICAL-CONDUCTIVITY; ONE-STEP SYNTHESIS; OXIDATIVE POLYMERIZATION; POLYANILINE; NANOPARTICLES; POLYPYRROLE; COMPOSITES; REDUCTION; FACILE;
D O I
10.1021/acsapm.3c02987
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
This study presents an approach to synthesizing a nanocomposite of polythiophene and silver nanoparticles (PBT/Ag), which addresses the challenge of AgNP aggregation and its impact on the catalytic efficiency. The reaction was performed under mild conditions using an ionic liquid, specifically bis(trifluoromethylsulfonyl)imide (Tf2N) 1-butyl-3-methylimidazolium (BMIm), which acted as both a solvent and a template. The nanocomposite contained uniformly dispersed spherical silver nanoparticles with an average diameter of around 10 nm in polythiophene doped with Tf2N anions. The catalytic efficiency of the composite was assessed by reducing 4-nitrophenol to 4-aminophenol using sodium borohydride. This transformation converts environmentally harmful 4-nitrophenol into the less toxic 4-aminophenol, a crucial intermediate in pharmaceuticals, such as paracetamol. The composite displayed notable efficiency, achieving a 99.9% conversion rate within 10 min, and exhibited recyclability over multiple cycles. This study represents the first use of a polythiophene derivative and a silver nanoparticle composite as a heterogeneous catalyst, marking an advancement in catalysis and materials science.
引用
收藏
页码:3756 / 3766
页数:11
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