journal article·2024-11-26

Enhanced C(sp3)–H Selective Oxidation Using Efficient Polyoxometalate-Based Metal–Organic Framework Photocatalysts Synergized with Ir Metalloligands and Polyoxometalates

Jing Wang, Luoning Li, Yanan Liu, Zelong Yuan, Pengtao Ma, Jingping Wang, Jingyang Niu

Chemistry of Materials· Volume 36· Issue 22
Publisher page

Abstract

Achieving efficient selective visible light-induced oxidation of benzyl C(sp 3 )–H to more valuable double-bonded compounds holds significant promise for organic synthesis. In this work, we fabricated an example of Ir metalloligand-modified POMOF crystalline material, CI-SiW, which is noteworthy as the first example of POM immobilized in a metalloligand-modified MOF via coordination bonding. Under the excitation of visible light (10 W, λ = 410 nm), CI-SiW can catalyze the efficient oxidation of benzyl C(sp 3 )–H of isochromane with a turnover number and turnover frequency of 954 and 1740 h –1, respectively. Excitingly, CI-SiW displays the best TOF compared with previous photocatalysts under the same conditions, realizing the maximum yield with the minimum amount of photocatalyst. Furthermore, CI-SiW had good cyclic and structural stability, and a 90.4% yield was still obtained after three reaction cycles.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Polyoxometalates: Synthesis and Applications · Metal-Organic Frameworks: Synthesis and Applications · Chemical Synthesis and Reactions

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

Affiliations

Henan Key Laboratory of Polyoxometalate Chemistry, College of Chemistry and Molecular Sciences, Henan University, Kaifeng, Henan 475004, P. R. China

Puyang Institute of Technology, Henan University, Puyang, Henan 457000, P. R. China

Funding

National Natural Science Foundation of China

References (64)

Show source-provided references
1. 10.1039/D2GC02755K10.1039/D2GC02755K ↗
2. 10.1021/acsanm.1c0116910.1021/acsanm.1c01169 ↗
3. 10.1021/acssuschemeng.1c0669110.1021/acssuschemeng.1c06691 ↗
4. 10.1039/D2GC04223A10.1039/D2GC04223A ↗
5. 10.1002/ange.20191503410.1002/ange.201915034 ↗
6. 10.1002/ange.20191060210.1002/ange.201910602 ↗
7. 10.1016/j.cclet.2021.12.02310.1016/j.cclet.2021.12.023 ↗
8. 10.1016/j.apsusc.2021.14973210.1016/j.apsusc.2021.149732 ↗
9. 10.1002/ajoc.20220003010.1002/ajoc.202200030 ↗
10. 10.1039/C9GC02270H10.1039/C9GC02270H ↗
11. 10.1039/C9GC02870F10.1039/C9GC02870F ↗
12. 10.1039/D3RA00332A10.1039/D3RA00332A ↗
13. 10.1002/anie.20110808010.1002/anie.201108080 ↗
14. 10.1002/adsc.20220107610.1002/adsc.202201076 ↗
15. 10.1039/C5CC06015J10.1039/C5CC06015J ↗
16. 10.1016/j.jcis.2023.11.16410.1016/j.jcis.2023.11.164 ↗
17. 10.1002/anie.20120275010.1002/anie.201202750 ↗
18. 10.1016/j.ccr.2018.02.01010.1016/j.ccr.2018.02.010 ↗
19. 10.1016/j.ccr.2019.04.00810.1016/j.ccr.2019.04.008 ↗
20. 10.1002/chem.20230340110.1002/chem.202303401 ↗
21. 10.1038/s41557-020-0436-110.1038/s41557-020-0436-1 ↗
22. 10.1126/science.abb468810.1126/science.abb4688 ↗
23. 10.1016/j.jcat.2020.10.01310.1016/j.jcat.2020.10.013 ↗
24. 10.1021/acs.chemmater.3c0012010.1021/acs.chemmater.3c00120 ↗
25. 10.1016/j.apcatb.2018.08.01210.1016/j.apcatb.2018.08.012 ↗
26. 10.1039/c1jm10166h10.1039/c1jm10166h ↗
27. 10.1021/ja056639q10.1021/ja056639q ↗
28. 10.1038/nchem.68110.1038/nchem.681 ↗
29. 10.1021/acs.inorgchem.3c0390110.1021/acs.inorgchem.3c03901 ↗
30. 10.1021/acscatal.3c0584410.1021/acscatal.3c05844 ↗
31. 10.1021/acs.accounts.6b0021410.1021/acs.accounts.6b00214 ↗
32. 10.1002/anie.20181430810.1002/anie.201814308 ↗
33. 10.1021/jacs.3c0491210.1021/jacs.3c04912 ↗
34. 10.1002/anie.20180074910.1002/anie.201800749 ↗
35. 10.1039/C8SC02965B10.1039/C8SC02965B ↗
36. 10.1021/ja510269510.1021/ja5102695 ↗
37. 10.1016/j.ccr.2023.21550610.1016/j.ccr.2023.215506 ↗
38. 10.1016/j.jece.2023.11056810.1016/j.jece.2023.110568 ↗
39. 10.1039/D1TA02792A10.1039/D1TA02792A ↗
40. 10.1002/anie.20180607710.1002/anie.201806077 ↗
41. 10.1039/C5TA03322E10.1039/C5TA03322E ↗
42. 10.1002/aenm.20180158710.1002/aenm.201801587 ↗
43. 10.1021/acs.jpcc.2c0733310.1021/acs.jpcc.2c07333 ↗
44. 10.1021/acsami.2c0565410.1021/acsami.2c05654 ↗
45. 10.1002/anie.20180686210.1002/anie.201806862 ↗
46. 10.1016/j.jcat.2022.10.02410.1016/j.jcat.2022.10.024 ↗
47. 10.1039/D1NR01447A10.1039/D1NR01447A ↗
48. 10.1021/acsami.2c0565410.1021/acsami.2c05654 ↗
49. 10.1016/j.fuel.2023.12964710.1016/j.fuel.2023.129647 ↗
50. 10.1039/C4SC00940A10.1039/C4SC00940A ↗
51. 10.1002/anie.20240539610.1002/anie.202405396 ↗
52. 10.1021/acscatal.7b0171910.1021/acscatal.7b01719 ↗
53. 10.1038/s41557-018-0172-y10.1038/s41557-018-0172-y ↗
54. 10.1016/j.jcis.2023.09.06010.1016/j.jcis.2023.09.060 ↗
55. 10.1021/acscatal.1c0523310.1021/acscatal.1c05233 ↗
56. 10.1016/j.cej.2022.13615710.1016/j.cej.2022.136157 ↗
57. 10.1016/j.apcatb.2022.12213410.1016/j.apcatb.2022.122134 ↗
58. 10.1002/cphc.20150031310.1002/cphc.201500313 ↗
59. 10.1016/j.apsusc.2021.15195310.1016/j.apsusc.2021.151953 ↗
60. 10.1021/jacs.2c0643210.1021/jacs.2c06432 ↗
61. 10.1016/j.apcatb.2014.08.04510.1016/j.apcatb.2014.08.045 ↗
62. 10.1039/D2GC01381A10.1039/D2GC01381A ↗
63. 10.3390/mi1211130710.3390/mi12111307 ↗
64. 10.1002/ajoc.20160042610.1002/ajoc.201600426 ↗