Optically Active Helical Poly(phenyl isocyanide)s Bearing Achiral Benzanilide Pendants: from Controlled Synthesis to Enantioseparation Application

Jing Wang; Shuai Wang; Hai-Xu Tong; Na Liu; Zong-Quan Wu

doi:10.1007/s10118-026-3775-6

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Optically Active Helical Poly(phenyl isocyanide)s Bearing Achiral Benzanilide Pendants: from Controlled Synthesis to Enantioseparation Application

RESEARCH ARTICLE | Updated：2026-08-03

- Optically Active Helical Poly(phenyl isocyanide)s Bearing Achiral Benzanilide Pendants: from Controlled Synthesis to Enantioseparation Application
- Optically Active Helical Poly(phenyl isocyanide)s Bearing Achiral Benzanilide Pendants: from Controlled Synthesis to Enantioseparation Application
- Chinese Journal of Polymer Science 2026年44卷页码：1-10
- Affiliations：
  
  a.The School of Pharmaceutical Sciences, Jilin University, Changchun 130021, China
  b.State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun 130012, China
- Author bio：
  
  liuna606@jlu.edu.cn (N.L.)
  zqwu@jlu.edu.cn (Z.Q.W.)
- Funds：
  
  This work was financially supported by the National Natural Science Foundation of China (Nos. 52573008, 22571117 and 52273006), Major Research Plan of the National Natural Science Foundation of China (Nos. 92256201 and 92356302), and the Science and Technology Development Plan of Jilin Province (No. 20240101181JC).;The authors declare no interest conflict.Electronic supplementary information (ESI) is available free of charge in the online version of this article at http://doi.org/10.1007/s10118-026-3775-6.The data supporting the findings of this study are available from the corresponding author upon reasonable request.
- DOI：10.1007/s10118-026-3775-6
  中图分类号：
- 收稿：2026-05-28，
  
  录用：2026-06-08，
  
  网络首发：2026-08-03，
  
  纸质出版：2026-09-05
- Accepted：
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Wang, J.; Wang, S.; Tong, H. X.; Liu, N.; Wu, Z. Q. Optically active helical poly(phenyl isocyanide)s bearing achiral benzanilide pendants: from controlled synthesis to enantioseparation application. Chinese J. Polym. Sci. https://doi.org/10.1007/s10118-026-3775-6

Jing Wang, Shuai Wang, Hai-Xu Tong, et al. Optically Active Helical Poly(phenyl isocyanide)s Bearing Achiral Benzanilide Pendants: from Controlled Synthesis to Enantioseparation Application[J/OL]. Chinese Journal of Polymer Science, 2026, 441-10.
Wang, J.; Wang, S.; Tong, H. X.; Liu, N.; Wu, Z. Q. Optically active helical poly(phenyl isocyanide)s bearing achiral benzanilide pendants: from controlled synthesis to enantioseparation application. Chinese J. Polym. Sci. https://doi.org/10.1007/s10118-026-3775-6 DOI：

Jing Wang, Shuai Wang, Hai-Xu Tong, et al. Optically Active Helical Poly(phenyl isocyanide)s Bearing Achiral Benzanilide Pendants: from Controlled Synthesis to Enantioseparation Application[J/OL]. Chinese Journal of Polymer Science, 2026, 441-10. DOI： 10.1007/s10118-026-3775-6.

摘要

Abstract

The helical structures found in biological systems

such as DNA

have inspired significant research interest in artificial helical polymers

owing to their strong potential for applications including chiral recognition and resolution

asymmetric catalysis

and other related areas. However

the preparation of single-handed helices from achiral starting materials

as well as the exploration of their chiral resolution behavior

continues to represent a considerable challenge. In this work

we present the rational design and synthesis of optically active helical poly(phenyl isocyanide)s through helix-sense selective polymerization (HSSP) of achiral phenyl isocyanide monomers

catalyzed by enantiopure Pd(II) complexes bearing

- or

-configured ligands (Pd(I

I)/L

or L

). The polymerization exhibits living and controlled characteristics

allowing for the precise modulation of molecular weights (

) with exceptionally narrow distributions (

). The resulting polymers exhibit intense optical activity and demonstrate outstanding performance in chiral recognition. Specifically

these chiral materials are utilized as a chiral stationary phase (CSP)

which can separate various racemates including

-methylbenzylamine

cobaltic acetylacetonate

and 2-hydroxy-2-phenylacetophenone. Additionally

when applied as a chiral crystallization agent

the polymer enabled the resolution of racemic

-Alanine

via

enantioselective crystallization

yielding an enantiomeric excess (

) as high as 81%.

关键词

Keywords

references

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