journal article·2025-06-27

Silver Nanoparticles Embedded in COFs as Reusable Photocatalyst for Oxidative Coupling of Benzylic Amine and Carboxylation of Benzyl Alcohol Derivatives

Susmitha Kumar, Pekham Chakrabortty, Bipasha Banerjee, Bidhan Kumbhakar, Nasir Ali Siddiqui, Swarbhanu Ghosh, Sk. Manirul Islam

ACS Applied Nano Materials· Volume 8· Issue 25
Publisher page

Abstract

In the present study, we have synthesized a benzothiadiazole derivative-based 2D donor–acceptor BtCOF, which we then customized by incorporating AgNPs over the COF, denoted as Ag/BtCOF. The AgNP-embedded BtCOF catalyst was characterized by various techniques like IR, XRD, SEM, TEM, XPS, UV–vis, photoluminescence (PL), electrochemical impedance spectroscopy (EIS), transient photocurrent response (TPR), and time resolved fluorescence (TRF) analysis. The activity of the catalyst was studied for the visible-light-assisted oxidative coupling of benzylic amines and the photocatalytic carboxylation of benzyl alcohol derivatives. Herein, the COF served as a support for the metal particles as well as provided a synergistic impact that improved the yield of the product formed during the catalytic process. The incorporation of AgNPs significantly enhances charge separation and promotes efficient electron transfer, while the intrinsic narrow band gap of BtCOF facilitates superior light absorption and increases the photocatalytic productivity. This strategic modification enhanced photophysical properties and has led to extraordinary photocatalytic activity in photocatalytic oxidization of benzylamine derivatives (conversion and selectivity ≥90%) in 4 h and carboxylation of C(sp 3 )-O bonds of benzyl alcohols (conversion ≥78% and selectivity ≥92%) in 24 h. Furthermore, the catalyst demonstrated excellent recyclability over several cycles without losing its catalytic activity.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Carbon dioxide utilization in catalysis · Covalent Organic Framework Applications · CO2 Reduction Techniques and Catalysts

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

Affiliations

Department of Chemistry

University of Kalyani

Department of Chemical and Biological Sciences

S.N. Bose National Centre for Basic Sciences

Department of Pharmacognosy, College of Pharmacy

King Saud University

McGill University

Funding

University Grants Commission · Department of Atomic Energy, Government of India · Board of Research in Nuclear Sciences · King Saud University

References (53)

Show source-provided references
1. 10.1002/anie.20170976610.1002/anie.201709766 ↗
2. 10.1038/s41586-020-2278-910.1038/s41586-020-2278-9 ↗
3. 10.1021/acsami.9b0987910.1021/acsami.9b09879 ↗
4. 10.1021/acsapm.3c0231110.1021/acsapm.3c02311 ↗
5. 10.1039/D3CY01575K10.1039/D3CY01575K ↗
6. 10.1039/D4CY00402G10.1039/D4CY00402G ↗
7. 10.1021/acscatal.0c0124210.1021/acscatal.0c01242 ↗
8. 10.1021/acscatal.1c0492110.1021/acscatal.1c04921 ↗
9. 10.1021/acs.iecr.4c0129010.1021/acs.iecr.4c01290 ↗
10. 10.1016/j.catcom.2023.10662810.1016/j.catcom.2023.106628 ↗
11. 10.1016/j.gresc.2024.08.00510.1016/j.gresc.2024.08.005 ↗
12. 10.1016/j.jcou.2022.10225010.1016/j.jcou.2022.102250 ↗
13. 10.1021/acsaem.4c0036010.1021/acsaem.4c00360 ↗
14. 10.1021/acs.iecr.4c0276510.1021/acs.iecr.4c02765 ↗
15. 10.1002/aesr.20220012910.1002/aesr.202200129 ↗
16. 10.1016/j.jcou.2022.10223610.1016/j.jcou.2022.102236 ↗
17. 10.1039/D0TA00556H10.1039/D0TA00556H ↗
18. 10.1007/s12274-024-6544-210.1007/s12274-024-6544-2 ↗
19. 10.1039/D1QM00462J10.1039/D1QM00462J ↗
20. 10.1021/jacs.7b1125510.1021/jacs.7b11255 ↗
21. 10.1002/cctc.20190146110.1002/cctc.201901461 ↗
22. 10.1021/acscatal.1c0492110.1021/acscatal.1c04921 ↗
23. 10.1002/anie.20230486110.1002/anie.202304861 ↗
24. 10.1021/acsanm.3c0265710.1021/acsanm.3c02657 ↗
25. 10.1021/acsanm.4c0183610.1021/acsanm.4c01836 ↗
26. 10.1021/acscatal.4c0239110.1021/acscatal.4c02391 ↗
27. 10.1021/acssuschemeng.9b0670410.1021/acssuschemeng.9b06704 ↗
28. 10.1021/jacs.7b0748910.1021/jacs.7b07489 ↗
29. 10.1002/ejoc.20120116110.1002/ejoc.201201161 ↗
30. 10.1002/anie.20200692510.1002/anie.202006925 ↗
31. 10.1002/anie.20201440810.1002/anie.202014408 ↗
32. 10.1021/jacs.0c0263310.1021/jacs.0c02633 ↗
33. 10.1021/acsami.1c0488010.1021/acsami.1c04880 ↗
34. 10.1002/cctc.20230153910.1002/cctc.202301539 ↗
35. 10.1039/D4NJ00400K10.1039/D4NJ00400K ↗
36. 10.1039/D2NJ05794H10.1039/D2NJ05794H ↗
37. 10.3390/catal1312146710.3390/catal13121467 ↗
38. 10.1039/C8DT04458A10.1039/C8DT04458A ↗
39. 10.1016/j.polymer.2022.12548310.1016/j.polymer.2022.125483 ↗
40. 10.1039/D3TA07750K10.1039/D3TA07750K ↗
41. 10.1016/j.jre.2025.02.00310.1016/j.jre.2025.02.003 ↗
42. 10.1002/anie.20190004610.1002/anie.201900046 ↗
43. 10.1016/j.inoche.2020.10836710.1016/j.inoche.2020.108367 ↗
44. 10.1007/s00216-024-05460-010.1007/s00216-024-05460-0 ↗
45. Peng X. · J. Mol. Struct. · 1328 · 2025 · 141395
46. 10.1039/D3CP01455J10.1039/D3CP01455J ↗
47. 10.1021/acsami.1c0895110.1021/acsami.1c08951 ↗
48. 10.1021/acssuschemeng.4c0352910.1021/acssuschemeng.4c03529 ↗
49. 10.1016/j.jechem.2022.02.03810.1016/j.jechem.2022.02.038 ↗
50. 10.1021/jacs.3c1272410.1021/jacs.3c12724 ↗
51. 10.1002/aesr.20230011410.1002/aesr.202300114 ↗
52. 10.1021/acscatal.5c0116310.1021/acscatal.5c01163 ↗
53. 10.1021/acs.inorgchem.2c0159410.1021/acs.inorgchem.2c01594 ↗