Structural and Morphological Engineering of Benzothiadiazole-Based Covalent Organic Frameworks for Visible Light-Driven Oxidative Coupling of Amines
Source abstract
Abstract
Covalent organic frameworks (COFs) are appealing platforms for photocatalysts because of their structural diversity and adjustable optical band gaps. The construction of efficient COFs for heterogeneous photocatalysis of organic transformations is highly desirable. Herein, we constructed a photoactive COF containing benzothiadiazole and triazine (BTDA-TAPT), for which the morphology and crystallinity might be easily tuned by slight synthetic variation. To unveil the relationship of photocatalytic properties between the structure and morphology, analogous COFs were synthesized by precisely tailoring building blocks. Systematic investigations indicated that tuning the structure and morphology might greatly impact photoelectric properties. The BTDA-TAPT featuring ordered alignment and perfect crystalline nature was more beneficial for promoting charge transfer and separation, which exhibited superior photocatalytic activity for visible light-driven oxidative coupling of amines. Outcomes from this study reveal the intrinsic synergy effects between the structure and morphology of COFs for photocatalysis.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Covalent Organic Framework Applications · Advanced Photocatalysis Techniques · Metal-Organic Frameworks: Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Chemical Biology of Hebei Province, College of Chemistry and Environmental Science, Hebei University, Baoding, Hebei 071002, P. R. China
Department of Chemical Engineering, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada
Funding
Natural Science Foundation of Hebei Province · National Natural Science Foundation of China · Key Laboratory of Photochemical Conversion and Optoelectronic Materials
References (66)
Show source-provided references
1. 10.1093/nsr/nwx03910.1093/nsr/nwx039 ↗
2. 10.1039/c3cs60188a10.1039/c3cs60188a ↗
3. 10.1021/acscatal.0c0359710.1021/acscatal.0c03597 ↗
4. 10.1039/c8cc04048f10.1039/c8cc04048f ↗
5. 10.1021/acscatal.8b0309310.1021/acscatal.8b03093 ↗
6. 10.1021/acs.chemrev.8b0040010.1021/acs.chemrev.8b00400 ↗
7. 10.1039/c6gc01582d10.1039/c6gc01582d ↗
8. 10.1039/c9cs00377k10.1039/c9cs00377k ↗
9. 10.1016/j.apcatb.2019.11802710.1016/j.apcatb.2019.118027 ↗
10. 10.1021/jacs.8b1242810.1021/jacs.8b12428 ↗
11. 10.1002/anie.20151054210.1002/anie.201510542 ↗
12. 10.1021/acscatal.0c0348010.1021/acscatal.0c03480 ↗
13. 10.1021/acscatal.8b0040710.1021/acscatal.8b00407 ↗
14. 10.1038/s41557-018-0141-510.1038/s41557-018-0141-5 ↗
15. 10.1126/science.aal158510.1126/science.aal1585 ↗
16. 10.1021/acs.chemrev.9b0055010.1021/acs.chemrev.9b00550 ↗
17. 10.1002/advs.20180141010.1002/advs.201801410 ↗
18. 10.1039/d0cs00278j10.1039/d0cs00278j ↗
19. 10.1016/j.chempr.2019.04.01510.1016/j.chempr.2019.04.015 ↗
20. 10.1021/acscatal.9b0195110.1021/acscatal.9b01951 ↗
21. 10.1021/acssuschemeng.9b0474910.1021/acssuschemeng.9b04749 ↗
22. 10.1021/jacs.0c0341810.1021/jacs.0c03418 ↗
23. 10.1002/anie.20200692510.1002/anie.202006925 ↗
24. 10.1016/j.apcatb.2018.08.00410.1016/j.apcatb.2018.08.004 ↗
25. 10.1021/jacs.9b0950210.1021/jacs.9b09502 ↗
26. 10.1021/jacs.9b0299710.1021/jacs.9b02997 ↗
27. 10.1039/d0sc01747g10.1039/d0sc01747g ↗
28. 10.1016/j.apcatb.2020.11909610.1016/j.apcatb.2020.119096 ↗
29. 10.1021/jacs.8b0057110.1021/jacs.8b00571 ↗
30. 10.1002/anie.20200072310.1002/anie.202000723 ↗
31. 10.1021/acs.macromol.9b0160010.1021/acs.macromol.9b01600 ↗
32. 10.1021/jacs.0c0660510.1021/jacs.0c06605 ↗
33. 10.1021/acscatal.0c0124210.1021/acscatal.0c01242 ↗
34. 10.1002/anie.20190254310.1002/anie.201902543 ↗
35. 10.1021/jacs.0c0102610.1021/jacs.0c01026 ↗
36. 10.1021/acscatal.8b0062310.1021/acscatal.8b00623 ↗
37. 10.1021/acscatal.7b0171910.1021/acscatal.7b01719 ↗
38. 10.1016/j.apcatb.2018.12.06510.1016/j.apcatb.2018.12.065 ↗
39. 10.1016/j.apcatb.2018.08.00510.1016/j.apcatb.2018.08.005 ↗
40. 10.1016/j.matt.2019.10.02610.1016/j.matt.2019.10.026 ↗
41. 10.1021/acscatal.0c0029010.1021/acscatal.0c00290 ↗
42. 10.1016/j.apcatb.2019.11791510.1016/j.apcatb.2019.117915 ↗
43. 10.1002/adfm.20190478110.1002/adfm.201904781 ↗
44. 10.1039/c8ta10046b10.1039/c8ta10046b ↗
45. 10.1038/ncomms950810.1038/ncomms9508 ↗
46. 10.1039/d0cc05222a10.1039/d0cc05222a ↗
47. 10.1039/c5cc02147b10.1039/c5cc02147b ↗
48. 10.1039/c9cc03623g10.1039/c9cc03623g ↗
49. 10.1039/c8nr06691d10.1039/c8nr06691d ↗
50. 10.1016/j.snb.2016.07.17610.1016/j.snb.2016.07.176 ↗
51. 10.1002/anie.20190004610.1002/anie.201900046 ↗
52. 10.1039/c9ta00339h10.1039/c9ta00339h ↗
53. 10.1039/d0nr02950e10.1039/d0nr02950e ↗
54. 10.1016/j.apcatb.2019.11813110.1016/j.apcatb.2019.118131 ↗
55. 10.1039/c8gc03295e10.1039/c8gc03295e ↗
56. 10.1016/j.apcatb.2017.09.05910.1016/j.apcatb.2017.09.059 ↗
57. 10.1002/solr.20190044010.1002/solr.201900440 ↗
58. 10.1021/acscatal.5b0147910.1021/acscatal.5b01479 ↗
59. 10.1016/j.apcatb.2019.02.03710.1016/j.apcatb.2019.02.037 ↗
60. 10.1021/acssuschemeng.9b0296910.1021/acssuschemeng.9b02969 ↗
61. 10.1016/j.apcatb.2017.10.00210.1016/j.apcatb.2017.10.002 ↗
62. 10.1016/j.apcatb.2018.03.09810.1016/j.apcatb.2018.03.098 ↗
63. 10.1021/acs.jpcc.0c0695010.1021/acs.jpcc.0c06950 ↗
64. 10.1016/j.apcatb.2020.11896410.1016/j.apcatb.2020.118964 ↗
65. 10.1021/acscatal.9b0240810.1021/acscatal.9b02408 ↗
66. 10.1002/anie.20180032010.1002/anie.201800320 ↗