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Synthesis and characterization of ortho-phenylene ethynylene oligomers: A new scaffold for foldamer research.

机译:邻苯撑乙炔低聚物的合成和表征:用于折叠剂研究的新型支架。

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摘要

As a new frontier of foldamer research based on the synthesis and characterization of oligomers programmed to fold and self assemble into secondary structures continues to open, new scaffolds with a variety of dimensions are required. Presented here is the synthesis and characterization of a new ortho -Phenylene Ethynylene (o-PE) backbone scaffold. This scaffold has been synthesized using Sonogashira methods with a variety of building blocks containing pi-rich and pi-poor elements substituted with non polar and polar substituents. Solvent induced folding of these short oligomers into well defined helices was confirmed via 1D and 2D NMR methods. Utilizing the electron rich and electron poor phenylene building blocks, variations of these o-PE oligomers have been synthesized to determine the folded stability of pi-rich vs. pi-poor vs. pi-poor/rich systems. Variations in temperature offer a route, aside from solvent denaturation, to probe the stability of the folded structures. This is the first report of a highly detailed solution NMR characterization using 1-D and 2-D methods examining the folding of a PE backbone without hydrogen bonds, and the first for an oPE system in general.
机译:随着基于折叠和自组装成二级结构的低聚物的合成和表征的折叠剂研究的新领域继续开放,需要具有各种尺寸的新支架。本文介绍了一种新型的邻苯撑乙炔(o-PE)骨架骨架的合成与表征。该支架已使用Sonogashira方法合成,具有多种结构单元,这些结构单元包含被非极性和极性取代基取代的富含pi和pi贫元素。通过1D和2D NMR方法证实了溶剂诱导的这些短低聚物折叠成明确定义的螺旋。利用富电子和贫电子的亚苯基结构单元,已合成了这些o-PE低聚物的变化形式,以确定了富pi相对于pi贫vs贫pi /富系统的折叠稳定性。除了溶剂变性以外,温度的变化还提供了一种途径来探测折叠结构的稳定性。这是首次使用1-D和2-D方法对没有氢键的PE主链折叠进行详细的溶液NMR表征的报道,也是首次报道oPE系统。

著录项

  • 作者

    Jones, Ticora V.;

  • 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 2007
  • 页码 223 p.
  • 总页数 223
  • 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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