journal article·2025-10

Construction of Hollow Structured Covalent Organic Framework with Chiral Internal Catalytic Sites for Asymmetric Hydrogenation

Jian‐Cheng Wang, Hua Qiao, Zhi Chen, Ting Sun, Zi‐Ran Liu, Cong‐Xue Liu, Xin‐Ran Zhang, Jin‐Qiu Li, Yu‐Bin Dong

Small· Volume 21· Issue 43
Publisher page

Abstract

Abstract The functionality of covalent organic frameworks (COFs) is usually highly related to their morphologies. Among various morphologies, the hollow‐structured COFs have recently attracted intense attention due to their unique properties. Herein, the synthesis of hollow structured COFs are first reported with the chiral internal sites via combining the chiral templating method with the acid etching approach. After Rh(III)‐metalation by postsynthetic modification, the generated hollow spherical CCOFs can be powerful chiral nanoreactors to highly promote the asymmetric hydrogenation of acetophenones in aqueous phase under mild conditions. The hollow structured heterosurface CCOFs may open a new way for their application in asymmetric catalysis.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Covalent Organic Framework Applications · Metal-Organic Frameworks: Synthesis and Applications · Advanced Photocatalysis Techniques

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

Affiliations

College of Chemistry, Chemical Engineering and Materials Science, Collaborative Innovation Center of Functionalized Probes for Chemical Imaging in Universities of Shandong, Key Laboratory of Molecular and Nano Probes Ministry of Education, Shandong Normal University Jinan 250014 P. R. China

School of Advanced Materials Peking University, Shenzhen Graduate School Shenzhen 518055 P. R. China

Funding

National Natural Science Foundation of China

References (45)

Show source-provided references
1. 10.1126/science.112041110.1126/science.1120411 ↗
2. 10.1126/science.aal158510.1126/science.aal1585 ↗
3. 10.1039/C9CS00827F10.1039/C9CS00827F ↗
4. 10.1039/D0CS00278J10.1039/D0CS00278J ↗
5. Wang G.‐B. · Chem. Rev. · 2022 · 472
6. 10.1039/D0TA00556H10.1039/D0TA00556H ↗
7. 10.1039/D1CS00600B10.1039/D1CS00600B ↗
8. 10.1039/D0CS00017E10.1039/D0CS00017E ↗
9. 10.1039/D0NA00537A10.1039/D0NA00537A ↗
10. 10.1039/D1CS00804H10.1039/D1CS00804H ↗
11. 10.1039/C9CS00299E10.1039/C9CS00299E ↗
12. 10.1021/jacs.7b0409610.1021/jacs.7b04096 ↗
13. 10.1021/acsnano.9b0646710.1021/acsnano.9b06467 ↗
14. 10.1021/jacs.9b0918910.1021/jacs.9b09189 ↗
15. 10.1039/C9SC00289H10.1039/C9SC00289H ↗
16. 10.1021/jacs.7b0264810.1021/jacs.7b02648 ↗
17. 10.1021/jacs.9b1078810.1021/jacs.9b10788 ↗
18. 10.1002/adfm.20210650710.1002/adfm.202106507 ↗
19. 10.1021/acs.chemrev.5b0073110.1021/acs.chemrev.5b00731 ↗
20. 10.1021/acs.chemrev.6b0037410.1021/acs.chemrev.6b00374 ↗
21. 10.1038/s41570-020-0161-810.1038/s41570-020-0161-8 ↗
22. 10.1038/ncomms778610.1038/ncomms7786 ↗
23. 10.1021/jacs.0c0028510.1021/jacs.0c00285 ↗
24. 10.1038/s41467-020-18844-410.1038/s41467-020-18844-4 ↗
25. 10.1039/D1CC02646A10.1039/D1CC02646A ↗
26. 10.1039/C5CC04130A10.1039/C5CC04130A ↗
27. 10.1002/adfm.20190478110.1002/adfm.201904781 ↗
28. 10.1021/jacs.2c0208910.1021/jacs.2c02089 ↗
29. 10.1016/j.memsci.2018.08.04310.1016/j.memsci.2018.08.043 ↗
30. 10.1039/C8CC02381F10.1039/C8CC02381F ↗
31. 10.1002/anie.20230183110.1002/anie.202301831 ↗
32. 10.1002/chem.20200100610.1002/chem.202001006 ↗
33. 10.1039/D1CS00983D10.1039/D1CS00983D ↗
34. 10.1021/acs.inorgchem.0c0378310.1021/acs.inorgchem.0c03783 ↗
35. Li F. · Angew. Chem., Int. Ed. · 2022 · 61
36. 10.1021/ja805222x10.1021/ja805222x ↗
37. 10.1038/nchem.235210.1038/nchem.2352 ↗
38. 10.1021/acs.iecr.1c0415610.1021/acs.iecr.1c04156 ↗
39. 10.1021/ja00255a01810.1021/ja00255a018 ↗
40. 10.1021/jp804413a10.1021/jp804413a ↗
41. 10.1021/jacs.2c1126410.1021/jacs.2c11264 ↗
42. 10.1021/acsaem.0c0229310.1021/acsaem.0c02293 ↗
43. 10.1021/acs.energyfuels.2c0045410.1021/acs.energyfuels.2c00454 ↗
44. Vries J. G. · 2007
45. Caprio V. · 2009