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Controlled free-radical polymerization at high pressures: Synthesis and properties of poly(alpha-substituted acrylates).

机译:高压下的受控自由基聚合:聚(α-取代的丙烯酸酯)的合成和性能。

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摘要

The free-radical polymerization of a series of α-substituted acrylic acid derivatives has been achieved by using hydrostatic pressure as a kinetic and thermodynamic driving force. It is shown that conducting polymerization in a range of pressures between 1 and 9 kbar dramatically improves the polymerizabilities of the investigated acrylates, opening the way to the synthesis of high-molecular weight polymers in short reaction times. The polymerizabilities of α-alkylacrylates at ambient pressure, obtained by extrapolation from high-pressure kinetic data, correlate well with Meyer's steric parameters for the relevant α-alkyl group. While the polymerization of α-alkylacrylates with linear alkyl groups proceeded via a vinyl double-bond addition in a traditional way, methyl α-isobutylacrylate polymerized though alternating steps of addition and 1,5-hydrogen transfer from the penultimate unit to provide an isomeric α-branched polymer structure.; Structure-property relationships for the synthesized poly(α-substituted acrylates) have been investigated. Increasing the size of the α-alkyl group decreases thermodynamic stability of the poly(α-alkylacrylates), and facilitates their thermal and photo-degradation. Conformational transitions of poly(α-alkylacrylic acid)s in aqueous solutions are shown to be highly dependent on the size of the α-alkyl group. The transition pH can be fine-tuned by adjusting the total hydrophobic content of the polymer via copolymerization of α-alkylacrylic acid with different alkyl substituents.; A high-pressure reversible addition-fragmentation chain transfer (HP-RAFT) protocol for controlled/living free-radical polymerization has been developed. It is demonstrated that this HP-RAFT technique can be used to livingly polymerize sterically hindered monomers, such as methyl ethacrylate, to provide polymers with low polydispersities, controlled molecular weights and end-groups. A methodology for the synthesis of well-defined poly(ethacrylic acid) has been developed.; The controlled polymerization of polystyrene-methacrylate macromonomers has been achieved by HP-RAFT, providing densely branched comb-like polymers with controlled molecular weight characteristics. The synthesis of linear-comb diblock copolymers is also achievable by this technique.; The HP-RAFT polymerization of traditional monomers, such as methyl methacrylate (MMA), has been investigated. It is demonstrated that the methodology allows for the synthesis of ultra-high molecular weight polymers with low polydispersities. The technique was used to obtain well-defined PMMAs with molecular weights of more than one million.
机译:通过使用静水压力作为动动力和热动力驱动力,已经实现了一系列α-取代丙烯酸衍生物的自由基聚合。结果表明,在1kbar至9kbar的压力范围内进行聚合可显着提高所研究的丙烯酸酯的可聚合性,从而为在短反应时间内合成高分子量聚合物开辟了道路。通过从高压动力学数据外推获得的在环境压力下α-烷基丙烯酸酯的可聚合性与相关α-烷基基团的迈耶空间参数密切相关。虽然具有直链烷基的α-丙烯酸烷基酯的聚合以传统方式通过乙烯基双键加成进行,但是αα-异丁丙烯酸甲酯通过交替的加成步骤和从倒数第二个单元转移1,5-氢来聚合,从而提供异构体α -支链聚合物结构。已经研究了合成的聚(α-取代的丙烯酸酯)的结构-性质关系。增加α-烷基的尺寸会降低聚(α-烷基丙烯酸酯)的热力学稳定性,并促进其热降解和光降解。聚(α-烷基丙烯酸)在水溶液中的构象转变显示出高度依赖于α-烷基的大小。过渡pH可以通过α-烷基丙烯酸与不同烷​​基取代基的共聚来调节聚合物的总疏水含量来进行微调。已经开发了用于可控/活性自由基聚合的高压可逆加成-断裂链转移(HP-RAFT)方案。已经证明,该HP-RAFT技术可以用于使位阻单体,例如乙基丙烯酸甲酯活跃地聚合,以提供具有低多分散性,可控制的分子量和端基的聚合物。已经开发出合成明确的聚(乙基丙烯酸)的方法。聚苯乙烯-甲基丙烯酸酯大分子单体的可控聚合已通过HP-RAFT实现,可提供具有可控分子量特性的致密支链梳状聚合物。线性梳状二嵌段共聚物的合成也可以通过该技术实现。已经研究了传统单体(例如甲基丙烯酸甲酯(MMA))的HP-RAFT聚合。结果表明,该方法可以合成具有低多分散性的超高分子量聚合物。该技术用于获得分子量超过一百万的定义明确的PMMA。

著录项

  • 作者

    Rzayev, Javid.;

  • 作者单位

    University of Massachusetts Amherst.;

  • 授予单位 University of Massachusetts Amherst.;
  • 学科 Chemistry Polymer.
  • 学位 Ph.D.
  • 年度 2004
  • 页码 p.243
  • 总页数 183
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 高分子化学(高聚物);
  • 关键词

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