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具有环内极性基团的形状持久性大环化合物:合成、液晶性及二维组装

Shape-persistent macrocycles with intraannular polar groups: synthesis, liquid crystallinity, and 2D organization.

作者信息

Fischer Matthias, Lieser Günter, Rapp Almut, Schnell Ingo, Mamdouh Wael, De Feyter Steven, De Schryver Frans C, Höger Sigurd

机构信息

Max Planck Institute for Polymer Research, Ackermannweg 10, D-55128 Mainz, Germany.

出版信息

J Am Chem Soc. 2004 Jan 14;126(1):214-22. doi: 10.1021/ja038484x.

Abstract

The synthesis of macrocycles with intraannular polar ester groups and extraannular oligo-alkyl groups is described. The compounds exhibit stable liquid crystalline phases showing fan-shaped textures under the polarizing microscope, typical for a columnar order of the molecules. X-ray powder diffraction data of the LC phase indicate that the unit cell contains two symmetry-related units, a feature pointing most probably to a restricted rotation of the macrocycles within a stack. The X-ray data were further supported by solid-state NMR experiments, showing that the rigid core of the compounds does not rotate with kHz or higher frequencies within the column in the LC phase. Apart from the organization of the molecules in the LC phase, the 2D organization of the macrocycles at the solvent-highly oriented pyrolytic graphite (HOPG) interface was investigated and showed that these compounds are capable of nanofunctionalizing the HOPG surface in the multinanometer regime.

摘要

本文描述了具有环内极性酯基和环外低聚烷基的大环化合物的合成。这些化合物呈现出稳定的液晶相,在偏光显微镜下显示出扇形纹理,这是分子柱状排列的典型特征。液晶相的X射线粉末衍射数据表明,晶胞包含两个对称相关的单元,这一特征很可能表明大环化合物在堆积中存在受限旋转。固态核磁共振实验进一步支持了X射线数据,结果表明,在液晶相中,化合物的刚性核心在柱内不会以千赫兹或更高频率旋转。除了液晶相中分子的排列外,还研究了大环化合物在溶剂高度取向热解石墨(HOPG)界面的二维排列,结果表明这些化合物能够在多纳米尺度上对HOPG表面进行纳米功能化。

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