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氨基酸/冠醚杂化材料:电荷如何影响液晶自组装。

Amino acid/crown ether hybrid materials: how charge affects liquid crystalline self-assembly.

机构信息

Institut für Organische Chemie, Universität Stuttgart, Pfaffenwaldring 55, 70569 Stuttgart, Germany.

出版信息

Soft Matter. 2017 Nov 22;13(45):8379-8391. doi: 10.1039/c7sm01484h.

Abstract

To probe the influence of electrostatic interactions on the mesomorphic self-assembly and phase behaviour of hybrid liquid crystals a series of crown ether/tyrosine hybrid systems was prepared by Steglich esterification of alkyl N-(tert-butoxycarbonyl)-l-tyrosinates with 4-carboxybenzo[15]crown-5 and 4-carboxybenzo[18]crown-6. The obtained derivatives allowed further manipulations at the NH functional group and complexation of the crown ether unit with NaI to give neutral or charged hybrid materials. All compounds were investigated by differential scanning calorimetry (DSC), polarizing optical microscopy (POM) and X-ray diffraction (XRD) measurements. Neither the variation of the N-protecting group, introduction of charge at the N-terminus nor anion exchange (Cl vs. I) resulted in mesomorphism. In contrast, N-Boc-protected and unprotected hybrids formed rectangular columnar (Col) mesophases with phase widths up to 35 K. NaI complexation switched these neutral thermotropic derivatives into ionic liquid crystals (ILCs) and induced a change of mesophase type from Col to smectic A (SmA). A comparison of experimentally obtained layer distances and theoretically calculated molecular lengths indicated bilayer SmA formation with interdigitated alkyl chains. Packing models for both mesophase types are proposed and discussed with respect to stabilizing interactions.

摘要

为了探究静电相互作用对混合液晶的介晶自组装和相行为的影响,通过烷基 N-(叔丁氧羰基)-l-酪氨酸与 4-羧基苯并[15]冠-5 和 4-羧基苯并[18]冠-6 的 Steglich 酯化反应,制备了一系列冠醚/酪氨酸混合体系。所得衍生物允许进一步在 NH 官能团上进行操作,并使冠醚单元与 NaI 络合,得到中性或带电的混合材料。所有化合物均通过差示扫描量热法(DSC)、偏光显微镜(POM)和 X 射线衍射(XRD)测量进行了研究。N-保护基的变化、N-末端引入电荷或阴离子交换(Cl 对 I)都不会导致介晶形成。相比之下,N-Boc 保护的和未保护的混合物形成了矩形柱状(Col)介晶相,相宽可达 35 K。NaI 络合将这些中性热致衍生化合物转化为离子液晶(ILC),并导致介晶相类型从 Col 转变为向列 A(SmA)。实验获得的层间距与理论计算的分子长度的比较表明形成了具有交错烷基链的双层 SmA。提出了两种介晶相的堆积模型,并就稳定相互作用进行了讨论。

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