首页> 外文学位 >Design and synthesis of organic chiroptical switches: Part I. Improvement of the chiroptical liquid crystal switch by modifying the structure of [3.2.1]bicyclooctanone. Part II. Design and synthesis of photoresponsive polyisocyanates.
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Design and synthesis of organic chiroptical switches: Part I. Improvement of the chiroptical liquid crystal switch by modifying the structure of [3.2.1]bicyclooctanone. Part II. Design and synthesis of photoresponsive polyisocyanates.

机译:有机手性开关的设计和合成:第一部分,通过修改[3.2.1]双环辛酮的结构来改进手性液晶开关。第二部分设计和合成光响应性多异氰酸酯。

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摘要

By increasing the structural similarity between the trigger and the applied liquid crystal, it was found that the twisting power of [3.2.1]bicycloketone derivative 4 has been improved up to 7.5 times higher than that of [3.2.1]bicyclooctan-3-one 2 in the applied liquid crystal PCH1115. This improvement leads to the development of chiroptical liquid crystal switch with greater potential for the application.;By incorporating the bicycloketone chromophore into the helical polyisocyanate backbone, a model system has been created, subject to quantitative interpretation with statistical physical ideas, in which chiral information inherent in circularly polarized light can be used to control the helical characteristics of a polymer. For this purpose, the racemic bicycloketone chromophore was pended through different linkage patterns to the helical polyisocyanate backbone with dynamically interconverting equal populations of left and right handed helical backbone conformations. Irradiation with circularly polarized light in the chromophore of the chiral pendant gave rise to easily measurable circular dichroism signals of the helical amide backbone of the polyisocyanate, which changed sign with change in the sense of the circularly polarized light. This demonstrated that the minute enantiomeric excess produced by the irradiation was capable of being transferred to the polyisocyanate backbone, leading to one handed helical sense of the polymer chain becoming predominant over the other. The results, expressed as the optical activity as a function of the degree of polymerization, could be analyzed using an approximate solution of a one-dimensional quenched random field Ising model. The experimental data were perfectly fit to the theory, allowing determination of the chiral-bias-magnitude controlled crossover between "statistical and thermal randomness".
机译:通过增加触发物和所施加的液晶之间的结构相似性,发现[3.2.1]双环酮衍生物4的扭曲力提高了至[3.2.1]双环辛烷-3-的7.5倍。在所施加的液晶PCH1115中为1。这种改进导致了具有更大应用潜力的手性液晶开关的发展。通过将双环酮生色团引入螺旋多异氰酸酯骨架中,创建了一个模型系统,该模型系统经过统计物理思想的定量解释,其中手性信息圆偏振光所固有的固有特性可用于控制聚合物的螺旋特性。为此,外消旋双环酮发色团通过不同的连接方式连接到螺旋多异氰酸酯骨架上,该骨架动态地相互转换相等数量的左手和右手螺旋骨架构象。在手性侧链的生色团中用圆偏振光照射会产生易于测量的多异氰酸酯螺旋酰胺主链的圆二色性信号,该信号随圆偏振光方向的变化而改变符号。这证明了由辐射产生的微小对映体过量能够转移到多异氰酸酯主链上,从而导致聚合物链的一方面的螺旋感变得优先于另一种。可以使用一维淬灭随机场伊辛模型的近似解来分析表示为光学活性随聚合度变化的结果。实验数据完全符合该理论,从而可以确定“统计和热随机性”之间的手性-偏置-幅度控制交叉。

著录项

  • 作者

    Li, Jie.;

  • 作者单位

    Georgia Institute of Technology.;

  • 授予单位 Georgia Institute of Technology.;
  • 学科 Chemistry Organic.;Physics Optics.;Engineering Electronics and Electrical.;Chemistry Polymer.
  • 学位 Ph.D.
  • 年度 1999
  • 页码 191 p.
  • 总页数 191
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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