...
首页> 外文期刊>Journal of Colloid and Interface Science >Ordering transitions in micrometer-thick films of nematic liquid crystals driven by self-assembly of ganglioside GM_1
【24h】

Ordering transitions in micrometer-thick films of nematic liquid crystals driven by self-assembly of ganglioside GM_1

机译:由神经节苷脂GM_1的自组装驱动的向列液晶的微米厚膜的有序转变

获取原文
获取原文并翻译 | 示例

摘要

We report an investigation of the self-assembly of the monosialoganglioside (GM_1) at interfaces formed between aqueous solutions of 10 μM GM_1 (at 25 °C) and micrometer-thick films of the nematic liquid crystal (LC) 4′-pentyl-4-cyanobiphenyl (5CB). We observe the process of spontaneous transfer of GM_1 onto the interfaces to be accompanied by continuous ordering transitions within the micrometer-thick films of the LC. At saturation coverage, the GM_1 orders the LC in an orientation that is perpendicular to the interface, an orientation that is similar to that caused by phospholipids such as dilauroylphosphatidylcholine (DLPC). This result suggests an interaction between the LC and GM_1 that is dominated by the hydrophobic tails of the GM_1. Relative to DLPC, however, we observe the dynamics of the LC ordering transition driven by GM_1 to be slow (2 h for DLPC versus 100 h for GM_1). To provide insight into the origins of the slow dynamics of the GM_1-induced ordering transition in the LC, we performed two additional measurements. First, we quantified the time-dependent adsorption of GM_1 at the LC interface by using fluorescently-labeled GM_1. Second, we used the Langmuir-Schaefer method to transfer preorganized monolayers of GM_1 from an air-water interface to the aqueous-LC interface. Results obtained from these two experiments are consistent with a physical picture in which the final stages of spontaneous adsorption/ordering of GM_1 at the aqueous-LC interface dictate the dynamics of the LC ordering transition. This rate limiting process underlying the ordering transition was substantially accelerated by heating the system above the phase transition temperature of GM_1(26 °C), suggesting that the phase state of the GM_1 micellar aggregates in bulk solution strongly influences the kinetics of the final stages of ordering/adsorption of GM_1 at the LC interface. Overall, these results and others presented in this manuscript reveal that it is possible to decorate interfaces of a nematic LC with GM_1, and that the assembly of GM_1 at these interfaces impacts the dynamic and equilibrium ordering of the LC.
机译:我们报告了对口唾液酸神经节苷脂(GM_1)在10μMGM_1(在25°C)的水溶液和向列液晶(LC)4'-pentyl-4的微米厚度薄膜之间形成的界面处自组装的研究-氰基联苯(5CB)。我们观察到GM_1自发转移到界面上的过程,伴随着LC微米级薄膜内的连续有序过渡。在饱和范围内,GM_1将LC定向在垂直于界面的方向上,该方向类似于由磷脂(例如二月桂酰磷脂酰胆碱(DLPC))引起的方向。该结果表明LC和GM_1之间的相互作用主要由GM_1的疏水性尾部控制。但是,相对于DLPC,我们观察到由GM_1驱动的LC有序过渡的动力学很慢(DLPC为2 h,而GM_1为100 h)。为了提供对LC中GM_1诱导的有序过渡的缓慢动力学的起源的了解,我们进行了两次额外的测量。首先,我们通过使用荧光标记的GM_1定量分析了LC_1界面上GM_1的时间依赖性吸附。其次,我们使用Langmuir-Schaefer方法将GM_1的预组织单层从空气-水界面转移到LC水溶液界面。从这两个实验获得的结果与物理图相吻合,其中在水-LC界面上GM_1的自发吸附/有序的最终阶段决定了LC有序跃迁的动力学。通过将系统加热到GM_1(26°C)的相变温度以上,可以大大加速有序转变的速率限制过程,这表明整体溶液中GM_1胶束聚集体的相态强烈地影响了最后阶段的动力学。 LC接口上GM_1的排序/吸附。总体而言,这些结果以及本手稿中的其他结果表明,可以用GM_1装饰向列型LC的界面,并且GM_1在这些界面上的组装会影响LC的动态和平衡顺序。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号