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Adaptive polymeric nanomaterials utilizing reversible covalent and hydrogen bonding.

机译:利用可逆共价键和氢键的自适应聚合物纳米材料。

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摘要

Adaptive materials based on stimuli responsive and reversible bonding moieties are a rapidly developing area of materials research. Advances in supramolecular chemistry are now being adapted to novel molecular architectures including supramolecular polymers to allow small, reversible changes in molecular and nanoscale structure to affect large changes in macroscale properties. Meanwhile, dynamic covalent chemistry provides a complementary approach that will also play a role in the development of smart adaptive materials. In this thesis, we present several advances to the field of adaptive materials and also provide relevant insight to the areas of polymer nanocomposites and polymer nanoparticles. First, we have utilized the innate molecular recognition and binding capabilities of the quadruple hydrogen bonding group ureidopyrimidinone (UPy) to prepare supramolecular polymer nanocomposites based on supramolecular poly(caprolactone) which show improved mechanical properties, but also an increase in particle aggregation with nanoparticle UPy functionalization. We also present further insight into the relative effects of filler-filler, filler-matrix, and matrix-matrix interactions using a UPy side-chain functional poly(butyl acrylate). These nanocomposites have markedly different behavior depending on the amount of UPy sidechain functionality. Meanwhile, our investigations of reversible photo-response showed that coumarin functionality in polymer nanoparticles not only facilitates light mediated aggregation/dissociation behavior, but also provides a substantial overall reduction in particle size and improvement in nanoparticle stability for particles prepared by Flash NanoPrecipitation. Finally, we have combined these stimuli responsive motifs as a starting point for the development of multiresponsive adaptive materials. The synthesis of a library of multifunctional materials has provided a strong base for future research in this area, although our initial investigations were ultimately unsuccessful due to photodegradation of the UPy moiety in chloroform solution. This thesis has provided the Priestley lab with a solid base for the further investigation of the diverse applications and unsolved science of stimuli responsive adaptive materials.
机译:基于刺激响应和可逆结合部分的自适应材料是材料研究的快速发展领域。超分子化学的进展现已适应包括超分子聚合物在内的新型分子结构,以允许分子和纳米级结构的微小可逆变化,从而影响宏观性质的大变化。同时,动态共价化学提供了一种补充方法,该方法也将在智能自适应材料的开发中发挥作用。在本文中,我们介绍了自适应材料领域的一些进展,并提供了有关聚合物纳米复合材料和聚合物纳米颗粒领域的相关见解。首先,我们利用四重氢键团脲基嘧啶酮(UPy)的先天分子识别和结合能力,制备了基于超分子聚己内酯的超分子聚合物纳米复合材料,该复合材料显示出改善的机械性能,但随着纳米颗粒UPy的出现,颗粒聚集增加功能化。我们还介绍了使用UPy侧链功能聚丙烯酸丁酯对填料-填料,填料-基体和基体-基体相互作用的相对影响的进一步了解。这些纳米复合材料具有明显不同的行为,具体取决于UPy侧链功能的数量。同时,我们对可逆光响应的研究表明,聚合物纳米颗粒中的香豆素官能度不仅促进了光介导的聚集/解离行为,而且还为通过Flash NanoPrecipitation制备的颗粒提供了总体上的粒径减小和纳米颗粒稳定性的大幅提高。最后,我们结合了这些刺激响应性图案作为开发多响应性自适应材料的起点。多功能材料库的合成为该领域的未来研究提供了坚实的基础,尽管我们的初步研究最终由于氯仿溶液中UPy部分的光降解而最终未能成功。本论文为普里斯特利实验室的进一步研究奠定了坚实的基础,进一步研究了刺激响应性自适应材料的各种应用和尚未解决的科学问题。

著录项

  • 作者

    Neikirk, Colin.;

  • 作者单位

    Princeton University.;

  • 授予单位 Princeton University.;
  • 学科 Nanotechnology.;Polymer chemistry.
  • 学位 Ph.D.
  • 年度 2015
  • 页码 156 p.
  • 总页数 156
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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