Tunable Chiroptical Switching via 2-Fold Chiral Conflict in Statistical Racemic Copolymer Assemblies

Chiral communication between mirror-imaged enantiomers is important for the development of homochirality in nature. However, polymers made from racemic mixtures usually show no chiroptical activity. Here, we present a new strategy to create global chirality in statistical racemic copolymers and to switch their chiroptical activity using a 2-fold chiral conflict. Chiroptically active assemblies consisting of racemic building units within two heterochiral segments were constructed via a stepwise statistical polymerization-induced chiral self-assembly (<i>stat</i>-PICSA) method. Furthermore, the stacking patterns and resulting chiroptical activity could be switched by changing the ratio of enantiomeric monomers. This switching exhibited distinct chiral conflict effects: "first come, first served" (FF)/"late-comer lives above" (LA) chiral conflict effects. We expect this 2-fold chiral conflict self-assembly strategy to offer a unique approach for developing chiroptical racemic polymer nanoassemblies and to deepen our understanding of how homochiral structures originate in nature.

Authors

Institutions

Publication Details

Journal
ACS Macro Letters
Published
2025-10-16
DOI
https://doi.org/10.1021/acsmacrolett.5c00604
Citations
1
Primary Topic
Molecular spectroscopy and chirality
Type
article
Field-Weighted Citation Impact
0.76
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Tunable Chiroptical Switching via 2-Fold Chiral Conflict in Statistical Racemic Copolymer Assemblies

Xiao Yuan, Zixiang He, Haotian Ma, Xiaoxiao Cheng et al.
1 citations
ACS Macro Letters
Molecular spectroscopy and chirality
0.76
article

Tunable Chiroptical Switching via 2-Fold Chiral Conflict in Statistical Racemic Copolymer Assemblies

Xiao Yuan, Zixiang He, Haotian Ma, Xiaoxiao Cheng, Wei Zhang
article en
1 citations

Abstract

Chiral communication between mirror-imaged enantiomers is important for the development of homochirality in nature. However, polymers made from racemic mixtures usually show no chiroptical activity. Here, we present a new strategy to create global chirality in statistical racemic copolymers and to switch their chiroptical activity using a 2-fold chiral conflict. Chiroptically active assemblies consisting of racemic building units within two heterochiral segments were constructed via a stepwise statistical polymerization-induced chiral self-assembly (<i>stat</i>-PICSA) method. Furthermore, the stacking patterns and resulting chiroptical activity could be switched by changing the ratio of enantiomeric monomers. This switching exhibited distinct chiral conflict effects: "first come, first served" (FF)/"late-comer lives above" (LA) chiral conflict effects. We expect this 2-fold chiral conflict self-assembly strategy to offer a unique approach for developing chiroptical racemic polymer nanoassemblies and to deepen our understanding of how homochiral structures originate in nature.

ACS Macro LettersVol. 14(11)
Kanazawa University (JP), Zhengzhou University (CN), Soochow University (CN), Life Science Institute (JP), Ingenierie des Materiaux polymeres (FR)
Openalex Percentile: Top 25%
Molecular spectroscopy and chirality
0.76
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.