Related Experiment Video
Updated: Jan 15, 2026

High-Contrast and Fast Photorheological Switching of a Twist-Bend Nematic Liquid Crystal
Published on: October 31, 2019
Tunable Chiroptical Switching via 2-Fold Chiral Conflict in Statistical Racemic Copolymer Assemblies
Zixiang He1,2, Xingyue Yuan2, Haotian Ma2
1College of Chemistry, Zhengzhou University, Zhengzhou 450001, China.
Researchers created chiral racemic copolymers with switchable chiroptical activity using a novel 2-fold chiral conflict self-assembly strategy. This method mimics natural homochirality development and offers new possibilities for chiral polymer nanoassemblies.
Area of Science:
- Polymer Chemistry
- Supramolecular Chemistry
- Chirality Studies
Background:
- Chiral communication is vital for homochirality in nature.
- Polymers from racemic mixtures typically lack chiroptical activity.
Purpose of the Study:
- To develop a method for creating global chirality in statistical racemic copolymers.
- To enable switching of chiroptical activity in these polymers.
Main Methods:
- Utilized a stepwise statistical polymerization-induced chiral self-assembly (stat-PICSA) method.
- Constructed chiroptically active assemblies from racemic building units within heterochiral segments.
Main Results:
- Achieved global chirality in statistical racemic copolymers.
- Demonstrated switchable chiroptical activity by altering monomer ratios.
- Observed distinct chiral conflict effects: "first come, first served" (FF) and "late-comer lives above" (LA).
Conclusions:
- The 2-fold chiral conflict self-assembly strategy provides a unique approach for chiral racemic polymer nanoassemblies.
- This strategy deepens the understanding of homochiral structure origins in nature.
More Related Videos
Related Concept Videos
Racemic Mixtures and the Resolution of Enantiomers
Properties of Enantiomers and Optical Activity
Stereoisomerism of Cyclic Compounds
Prochirality
Molecules with Multiple Chiral Centers
SN1 Reaction: Stereochemistry
In the first step of an SN1 reaction, the bond between the electrophilic carbon and the leaving group ionizes to generate the carbocation intermediate. The second step of the mechanism is the nucleophilic attack.
In the formed carbocation, the positively charged carbon is sp2 hybridized with a trigonal planar geometry. As all the three substituents lie on the same plane, a plane of symmetry for the...

