journal article·2025-12

Dual‐Mechanism Synergy in Chiral Conjugated Microporous Polymer Membranes for Enhanced Enantioselective Permeability

Yu Zang, Shuang Xia, Zixiang He, Chengming Yang, Minyi Fan, Jianjun Wang, Jiao Liu, Liang Xu, Xiaoqiang Xue, Wei Zhang

Small· Volume 21· Issue 50
Publisher page

Abstract

Abstract Chiral membrane separation, an emerging enantiomer separation technology featuring low‐energy consumption, high efficiency, and environmental sustainability, faces a significant challenge in simultaneously enhancing enantioselectivity and permeability. Herein, chiral conjugated microporous polymer composite membranes ( CCMP‐SiO 2 ) via surface‐initiated Sonogashira‐Hagihara coupling reaction, enabling exceptional chiral resolution properties is developed. The membrane exhibits excellent chemical stability and thermostability, achieving the highest enantiomer permeability (3.3 × 10 −8 m 2 h −1 ) among the chiral membranes with enantioselectivity exceeding 99% ee (99.7% ee in this study) for the separation of D , L ‐phenylalanine ( D , L ‐Phe) racemic mixture. The 3D conjugated frameworks of chiral conjugated microporous polymer ( CCMP) provide both mechanical stability and porous transport channels, collectively enhancing permeability. In addition, strategic incorporation of amide and aromatic functionalities into chiral recognition sites, synergistically enhances enantioselectivity and permeability through stereoselective recognition and non‐stereoselective interactions. Density functional theory (DFT) and non‐covalent interaction (NCI) analysis reveal dual‐mechanism synergy for enhanced enantioselective permeability of CCMP‐SiO 2 membranes. Notably, the membrane demonstrates retarded transport behavior, enabling precise enantiomer separation. This work establishes a dual‐objective synergistic strategy for concurrent optimization of enantioselectivity and permeability, providing a generalizable platform for rational design of chiral membranes.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Covalent Organic Framework Applications · Analytical Chemistry and Chromatography · Metal-Organic Frameworks: Synthesis and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Engineering Research Center for Hemp and Product in Cold Region of Ministry of Education, College of Chemistry and Chemical Engineering Qiqihar University Wenhua Street 42 Qiqihar Heilongjiang 161006 China

College of Materials Science and Engineering Qiqihar University Wenhua Street 42 Qiqihar Heilongjiang 161006 China

College of Chemistry Zhengzhou University Zhengzhou 450001 China

Jiangsu Engineering Laboratory of Novel Functional Polymeric Materials College of Chemistry, Chemical Engineering and Materials Science Soochow University No. 199, Renai Road, Suzhou Industrial Park Suzhou 215123 China

Industrial College of Carbon Fiber and New Materials, School of Chemical Engineering and Materials Changzhou Institute of Technology No. 666, Liaohe Road Changzhou 213000 China

Funding

National Natural Science Foundation of China · Natural Science Foundation of Anhui Province

References (38)

Show source-provided references
1. 10.1016/j.cej.2020.12824710.1016/j.cej.2020.128247 ↗
2. 10.1021/acsami.0c0089810.1021/acsami.0c00898 ↗
3. 10.1002/anie.20242026910.1002/anie.202420269 ↗
4. 10.1002/anie.20210235010.1002/anie.202102350 ↗
5. 10.1016/0376-7388(92)80011-810.1016/0376-7388(92)80011-8 ↗
6. 10.1016/S0376-7388(00)00647-510.1016/S0376-7388(00)00647-5 ↗
7. 10.1002/anie.20220401210.1002/anie.202204012 ↗
8. 10.1002/anie.20221213910.1002/anie.202212139 ↗
9. 10.1016/j.seppur.2022.12064210.1016/j.seppur.2022.120642 ↗
10. 10.1021/acs.chemrev.9b0039910.1021/acs.chemrev.9b00399 ↗
11. 10.1016/j.ccr.2019.21309310.1016/j.ccr.2019.213093 ↗
12. 10.1002/anie.20240387810.1002/anie.202403878 ↗
13. 10.1039/C8CS00376A10.1039/C8CS00376A ↗
14. 10.1021/acssuschemeng.8b0576410.1021/acssuschemeng.8b05764 ↗
15. 10.1002/anie.20241317110.1002/anie.202413171 ↗
16. 10.1021/acs.analchem.4c0371610.1021/acs.analchem.4c03716 ↗
17. 10.1002/adfm.20190073510.1002/adfm.201900735 ↗
18. 10.1002/anie.20241991610.1002/anie.202419916 ↗
19. 10.1038/s41557-018-0093-910.1038/s41557-018-0093-9 ↗
20. 10.1002/anie.20241708810.1002/anie.202417088 ↗
21. 10.1021/acsami.9b1414410.1021/acsami.9b14144 ↗
22. 10.1002/cctc.20150037410.1002/cctc.201500374 ↗
23. 10.1039/C5CY00038F10.1039/C5CY00038F ↗
24. 10.1002/anie.20070159510.1002/anie.200701595 ↗
25. 10.1002/anie.20190353410.1002/anie.201903534 ↗
26. 10.1039/C7PY01127J10.1039/C7PY01127J ↗
27. 10.1016/j.seppur.2021.11852910.1016/j.seppur.2021.118529 ↗
28. 10.1021/acsami.0c0089810.1021/acsami.0c00898 ↗
29. 10.1039/b713350b10.1039/b713350b ↗
30. 10.1016/j.memsci.2022.12119810.1016/j.memsci.2022.121198 ↗
31. 10.1016/j.colsurfa.2021.12646410.1016/j.colsurfa.2021.126464 ↗
32. 10.1016/j.seppur.2022.12188010.1016/j.seppur.2022.121880 ↗
33. 10.1016/j.memsci.2024.12366010.1016/j.memsci.2024.123660 ↗
34. 10.1021/acsapm.9b0111110.1021/acsapm.9b01111 ↗
35. 10.1021/ma101999k10.1021/ma101999k ↗
36. 10.1016/j.memsci.2011.11.00210.1016/j.memsci.2011.11.002 ↗
37. 10.1016/j.chempr.2021.01.00310.1016/j.chempr.2021.01.003 ↗
38. 10.1021/ja100936w10.1021/ja100936w ↗