Amino-Yne Click Polymerized β-Ketoenamine-Based Covalent Organic Frameworks for Enhanced Photocatalytic Performance
Source abstract
Abstract
Constructing β-ketoenamine-linked covalent organic frameworks (COFs) for photocatalysis is highly attractive but remains challenging due to limited reaction types and monomer availability. Herein, we highlight the critical role of amino-yne click polymerization in overcoming these challenges and enabling the successful synthesis of a novel β-ketoenamine-linked COF, named En-COF-P. This new approach not only simplifies the synthesis process but also significantly expands the types of chemical linkages available for COF construction. The resulting En-COF-P exhibits an enhanced visible light absorption range, facilitating improved charge generation and separation. These properties translate into remarkable photocatalytic performance, particularly in the blue-light-driven selective oxidation of organic sulfides, where En-COF-P achieves up to 99% conversion and 99% selectivity. Remarkably, En-COF-P’s photocatalytic efficiency is eight times higher than that of traditional imine-linked COFs. This work underscores the potential of click polymerization in COF synthesis and advances a new strategy for the design of highly efficient photocatalysts.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Covalent Organic Framework Applications · Advanced Photocatalysis Techniques · Caching and Content Delivery
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Materials Processing and Die & Mold Technology, School of Materials Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074, China
Funding
Natural Science Foundation of Hubei Province · National Natural Science Foundation of China
References (58)
Show source-provided references
1. 10.1126/science.abd640610.1126/science.abd6406 ↗
2. 10.1039/D3CS00287J10.1039/D3CS00287J ↗
3. 10.1002/anie.20240488610.1002/anie.202404886 ↗
4. 10.1021/jacs.0c0647410.1021/jacs.0c06474 ↗
5. 10.1021/jacs.4c0604910.1021/jacs.4c06049 ↗
6. 10.1016/j.ccr.2024.21587310.1016/j.ccr.2024.215873 ↗
7. 10.34133/research.045810.34133/research.0458 ↗
8. 10.1039/D3CS00908D10.1039/D3CS00908D ↗
9. 10.31635/ccschem.023.20230340410.31635/ccschem.023.202303404 ↗
10. 10.1021/jacs.3c0747110.1021/jacs.3c07471 ↗
11. 10.1002/anie.20240576310.1002/anie.202405763 ↗
12. 10.1002/anie.20220493810.1002/anie.202204938 ↗
13. 10.1021/jacs.3c1153910.1021/jacs.3c11539 ↗
14. 10.1002/adfm.20241107710.1002/adfm.202411077 ↗
15. 10.1038/s41467-024-50951-410.1038/s41467-024-50951-4 ↗
16. 10.1002/adfm.20231291210.1002/adfm.202312912 ↗
17. 10.1021/acs.accounts.5b0036910.1021/acs.accounts.5b00369 ↗
18. 10.1126/science.adk868010.1126/science.adk8680 ↗
19. 10.1021/acs.accounts.4c0006110.1021/acs.accounts.4c00061 ↗
20. 10.1002/anie.20231687310.1002/anie.202316873 ↗
21. 10.1126/science.112041110.1126/science.1120411 ↗
22. 10.1021/ja509293610.1021/ja5092936 ↗
23. 10.1021/ja204728y10.1021/ja204728y ↗
24. 10.1039/C6PY00561F10.1039/C6PY00561F ↗
25. 10.1038/ncomms550310.1038/ncomms5503 ↗
26. 10.1021/jacs.0c0096910.1021/jacs.0c00969 ↗
27. 10.1039/D0CS01027H10.1039/D0CS01027H ↗
28. 10.1038/s41570-022-00437-y10.1038/s41570-022-00437-y ↗
29. 10.1021/jacs.2c1244010.1021/jacs.2c12440 ↗
30. 10.1038/s41467-024-45457-y10.1038/s41467-024-45457-y ↗
31. 10.1021/acscatal.3c0385710.1021/acscatal.3c03857 ↗
32. 10.1002/smll.20230713810.1002/smll.202307138 ↗
33. 10.1038/s41467-023-40169-110.1038/s41467-023-40169-1 ↗
34. 10.1002/anie.20230613510.1002/anie.202306135 ↗
35. 10.31635/ccschem.023.20230331910.31635/ccschem.023.202303319 ↗
36. 10.1002/adfm.20231331410.1002/adfm.202313314 ↗
37. 10.1021/ja308278w10.1021/ja308278w ↗
38. 10.1021/jacs.7b1125510.1021/jacs.7b11255 ↗
39. 10.1021/jacs.0c0005410.1021/jacs.0c00054 ↗
40. 10.1021/jacs.6b1200510.1021/jacs.6b12005 ↗
41. 10.1039/C9SC03725J10.1039/C9SC03725J ↗
42. 10.1021/ma062859s10.1021/ma062859s ↗
43. 10.1016/j.apcatb.2020.11975010.1016/j.apcatb.2020.119750 ↗
44. 10.1021/jacs.3c1258810.1021/jacs.3c12588 ↗
45. 10.1002/anie.20240503010.1002/anie.202405030 ↗
46. 10.1002/agt2.35010.1002/agt2.350 ↗
47. 10.1002/pol.2023038310.1002/pol.20230383 ↗
48. 10.1021/ja809625610.1021/ja8096256 ↗
49. 10.1038/s44160-022-00224-z10.1038/s44160-022-00224-z ↗
50. 10.1021/jacs.6b0123310.1021/jacs.6b01233 ↗
51. 10.1021/acs.chemmater.2c0135810.1021/acs.chemmater.2c01358 ↗
52. 10.1002/adma.20210500210.1002/adma.202105002 ↗
53. 10.1002/anie.20230487510.1002/anie.202304875 ↗
54. 10.1016/j.apcatb.2022.12163010.1016/j.apcatb.2022.121630 ↗
55. 10.1039/D3TA07691A10.1039/D3TA07691A ↗
56. 10.1002/anie.20220148210.1002/anie.202201482 ↗
57. 10.1038/s41467-022-32449-z10.1038/s41467-022-32449-z ↗
58. 10.1002/anie.20240880210.1002/anie.202408802 ↗