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Oxidoreductase catalyzed synthesis of conjugated polypyrrole and polypyrrole derivatives.

机译:氧化还原酶催化的共轭聚吡咯和聚吡咯衍生物的合成。

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摘要

Polypyrrole (PPy), a conjugated polymer, has been extensively investigated in recent years, due to its potential biocompatibility and promising electrical and optical properties. Recently, there has been tremendous interest in developing new and environmentally friendly procedures for the synthesis of conjugated polymers, such as polypyrrole. An enzymatic pathway to polyaniline, another conjugated polymer, was demonstrated nearly a decade ago; however a similar approach for the synthesis of polypyrrole has not been well established. Very recently, the use of redox mediators coupled with an oxidoreductase enzyme has shown promise in facilitating the enzymatic synthesis of polypyrrole. However a direct enzymatic route has not been developed to date.;With the objective of addressing the challenges involved in the direct enzymatic synthesis of polypyrrole and its derivatives, this thesis presents a generic methodology based on the use of the enzyme soybean peroxidase (SBP). Under appropriate conditions, the enzyme has been demonstrated to facilitate the oxidative polymerization of pyrrole and several of its derivative monomers in a mild, non-toxic, environmentally benign manner. This one pot synthesis is carried in a mild pH aqueous solution.;More importantly this research also explores the fundamental aspects pertaining to reaction conditions (temperature, reaction pH and time, dopant type) and reaction feasibility (reduction potential match) that can yield conjugated polymers with interesting electrical and optical properties. Appropriate control of the reaction conditions are shown to be important for the synthesis of a highly conductive polymer. A low synthesis temperature (2 °C) was shown to produce PPy that was more conductive and produced at a faster rate. Optimized reaction conditions produced PPy with a conductivity as high as 3 S/cm when doped with 10-camphor sulfonic acid. Additionally, the use of the SBP as a catalyst was observed to facilitate the synthesis of PPy which contains fewer structural defects than that prepared via traditional chemical and electrochemical polymerization techniques.;The role of redox potential in evaluating reaction feasibility and its influence on the initiation of polymerization has been investigated. Linear sweep voltametry was used to evaluate the reduction potentials of 10 pyrrole monomers containing a diverse array of substituents. It was observed that the enzyme SBP could oxidize or polymerize pyrrole monomers with reduction potentials equal to or less than 1.38 V (Ag/AgCl), with the exception of N-methylpyrrole. Pyrrole monomers with reduction potentials greater than 1.38 V could not be oxidized with SBP and hydrogen peroxide. SBP was shown to successfully catalyze the polymerization of 3-methylpyrrole and 3,4-diethylpyrrole to semi-conductive polymers.;This thesis also explores the enzyme catalyzed synthesis of fluorescent polypyrrole derivatives. The pyrrole derivative 4-(3-Pyrrolyl)butyric acid (3-BAP) was successfully polymerized using SBP as the catalyst. Under conditions previously optimized for the synthesis of PPy, poly(4-(3-Pyrrolyl)butyric acid) (P3-BAP) with an electrical conductivity as high as 10-2 S/cm was produced. When 3-BAP was polymerized in unbuffered deionized water, for the first time a fluorescent conjugated polypyrrole was produced enzymatically. Solutions of P(3-BAP) were observed to have a stable fluorescence that was effectively quenched by presence of metal ions in solution. Stern-Volmer constants for fluorescence quenching of P(3-BAP) were observed to be as high as 125,000 for metal ions such as cobalt(II). Scatchard plots suggest that P(3-BAP) exhibits cooperative binding with a wide variety of metals(II) salts.;Using polypyrrole and its derivatives this thesis seeks to extend the current understanding of the fundamental aspects involved in the oxidoreductase catalyzed synthesis of conjugated polymers. The electrically conducting and fluorescent polypyrrole derivatives synthesized and studied in this thesis provide new opportunities for exploring their possible use in applications, such as antistatic coating and sensors.
机译:聚吡咯(PPy)是一种共轭聚合物,由于其潜在的生物相容性以及有希望的电学和光学性能,近年来已受到广泛研究。最近,对开发用于合成共轭聚合物如聚吡咯的新的和环境友好的方法引起了极大的兴趣。大约十年前,已经证明了另一种共轭聚合物聚苯胺的酶促途径。然而,还没有很好的合成聚吡咯的类似方法。最近,氧化还原介体与氧化还原酶结合使用已显示出促进聚吡咯的酶促合成的希望。然而,迄今为止尚未开发出直接的酶促途径。为了解决聚吡咯及其衍生物的直接酶促合成所面临的挑战,本文提出了基于大豆过氧化物酶(SBP)的通用方法学。 。在适当的条件下,已证明该酶以温和,无毒,对环境无害的方式促进吡咯及其几种衍生物单体的氧化聚合。一锅法合成是在温和的pH水溶液中进行的;更重要的是,该研究还探讨了与反应条件(温度,反应pH和时间,掺杂剂类型)和反应可行性(还原电势匹配)有关的基本方面,可以产生共轭具有有趣的电学和光学特性的聚合物。已显示对反应条件的适当控制对于高导电聚合物的合成很重要。较低的合成温度(2°C)显示产生的PPy更具导电性,并且产生速度更快。优化的反应条件可以使掺杂10樟脑磺酸的PPy的电导率高达3 S / cm。此外,观察到使用SBP作为催化剂可促进PPy的合成,其中PPy的结构缺陷少于通过传统化学和电化学聚合技术制备的PPy .;氧化还原电势在评估反应可行性及其对引发的影响中的作用已经研究了聚合反应。线性扫描伏安法用于评估10种含有多种取代基的吡咯单体的还原电位。观察到,除N-甲基吡咯外,酶SBP可以氧化或聚合还原电位等于或小于1.38 V(Ag / AgCl)的吡咯单体。还原电位大于1.38 V的吡咯单体无法被SBP和过氧化氢氧化。结果表明,SBP能够成功催化3-甲基吡咯和3,4-二乙基吡咯聚合成半导体聚合物。本文还探索了酶催化合成荧光聚吡咯衍生物的方法。使用SBP作为催化剂成功地聚合了吡咯衍生物4-(3-吡咯基)丁酸(3-BAP)。在先前为PPy合成优化的条件下,生产了电导率高达10-2 S / cm的聚(4-(3-吡咯基)丁酸)(P3-BAP)。当3-BAP在未缓冲的去离子水中聚合时,第一次通过酶促方法产生了荧光共轭聚吡咯。观察到P(3-BAP)溶液具有稳定的荧光,该荧光可通过溶液中金属离子的存在而有效地猝灭。对于金属离子(例如钴(II)),用于P(3-BAP)荧光猝灭的Stern-Volmer常数高达125,000。斯卡查德图表明,P(3-BAP)与多种金属盐(II)表现出协同结合。;本论文试图利用聚吡咯及其衍生物来扩展对氧化还原酶催化共轭合成的基本理解。聚合物。本文合成和研究的导电和荧光聚吡咯衍生物为探索其在抗静电涂料和传感器等应用中的可能用途提供了新的机会。

著录项

  • 作者

    Bouldin, Ryan Michael.;

  • 作者单位

    University of Massachusetts Lowell.;

  • 授予单位 University of Massachusetts Lowell.;
  • 学科 Chemistry Biochemistry.;Chemistry Polymer.;Engineering Chemical.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 130 p.
  • 总页数 130
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:44:41

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