Related Experiment Video
Updated: Feb 21, 2026

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
Published on: February 7, 2017
Self-Assembled Polydiacetylene Vesicle and Helix with Chiral Interface for Visualized Enantioselective Recognition of
Shuai Li1,2, Li Zhang1, Jian Jiang3
1Beijing National Laboratory for Molecular Science (BNLMS), CAS Key Laboratory of Colloid, Interface and Chemical Thermodynamics, Institute of Chemistry, Chinese Academy of Sciences , Beijing 100190, China.
Abstract:
An l-glutamic acid terminated amphiphilic diacetylene was designed and found to self-assemble into vesicles in water and supramolecular gel with helical structures in mixed methanol/water solvent. Both the vesicles and the helices underwent topochemical photopolymerization under UV irradiation and changed to a blue color. During the self-assembly and photopolymerization, the chirality of localized l-glutamic acid was successfully transferred to polydiacetylene (PDA), which resulted in obvious CD signals in the PDA blue phase. Interestingly, the CD signals for PDA vesicles and helices were opposite due to the different packing modes in the PDA skeleton. However, although these two assembly systems own opposite supramolecular chirality, both of them showed the same enantioselective recognition of sulfinamide enantiomers, in which the assemblies with S-enantiomer turned red while the other remained blue in the presence of the R-enantiomer. It is suggested that the chiral interface composed of l-glutamic acid played an important role in the enantioselective recognition. This work revealed the function of molecular and supramolecular chirality in the supramolecular self-assembly system.
Related Concept Videos
Chirality at Nitrogen, Phosphorus, and Sulfur
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...
Prochirality
Preparation and Reactions of Sulfides

