Gao Yuxia, Hao Jie, Wu Jindan, Zhang Xun, Hu Jun, Ju Yong
Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology, Ministry of Education, Department of Chemistry, Tsinghua University, Beijing 100084, China.
Nanoscale. 2015 Aug 28;7(32):13568-75. doi: 10.1039/c5nr03699b. Epub 2015 Jul 23.
A glycyrrhetate-containing amphiphile, MGP (1-[2-(methyl glycyrrhetate)-2-oxoethyl]pyridinium bromide), has been synthesized, and found to assemble into supramolecular helical nanofibers in chloroform/aromatic solvents, which are primarily driven by π-π stacking, van der Waals forces, and hydrophobic interactions. During the assembly process, MGP stacked into J-aggregates resulting in the sequestration of the hydrophilic pyridinium cation within the interior with the concomitant projection of its hydrophobic skeleton on the outside surface. Ultimately, this protrusion generated a staggered angle due to the steric hindrance between stacked molecules. This staggered angle further led to molecular misalignments and the formation of helical fibrils, which could twist with each other to fabricate larger helical fibers. Consequently, a gel was formed by intertwining these nanofibers into three-dimensional networks. Using this strategy, we found that other triterpenoid-tailored pyridinium amphiphiles are also potential scaffolds for supramolecular helical structures. This work provides a facile approach for the fabrication of supramolecular macroscopic chiral nanostructures that originate from natural products.
一种含甘草次酸的两亲物,即MGP(1-[2-(甲基甘草次酸)-2-氧代乙基]溴化吡啶鎓)已被合成,并发现其在氯仿/芳烃溶剂中组装成超分子螺旋纳米纤维,这主要由π-π堆积、范德华力和疏水相互作用驱动。在组装过程中,MGP堆积形成J-聚集体,导致亲水性吡啶鎓阳离子被隔离在内部,同时其疏水骨架在外表面突出。最终,由于堆积分子之间的空间位阻,这种突出产生了一个交错角。这个交错角进一步导致分子错位并形成螺旋原纤维,这些原纤维可以相互缠绕形成更大的螺旋纤维。因此,通过将这些纳米纤维缠绕成三维网络形成了凝胶。利用这种策略,我们发现其他经三萜类修饰的吡啶鎓两亲物也是超分子螺旋结构的潜在支架。这项工作为源自天然产物的超分子宏观手性纳米结构的制备提供了一种简便方法。