journal article·2024-10

Bi2O2CO3/g‐C3N4 Catalyst for Photocatalytic Coupling of Benzylamine under Mild Conditions

Yunan Teng, Zhonghao Tan, Yingzhe Zhao, Zhuizhui Su, Meiling Li, Zixuan Zhang, Jianling Zhang

ChemNanoMat· Volume 10· Issue 10
Publisher page

Abstract

Abstract The photocatalytic conversion of benzylamine into imine is promising for industrial production and environmental protection. To develop photocatalysts with desirable compositions and microstructures is key to achieve high activity and selectivity. Here we propose the immobilization of Bi2O2CO3 on g‐C3N4 for the photocatalytic conversion of benzylamine. The Bi2O2CO3/g‐C3N4 catalyst possesses improved light absorption capacity, electron transmission rate and reduced electron‐hole recombination than pure Bi2O2CO3. It can efficiently catalyze benzylamine coupling reaction under mild conditions, i. e., at room temperature, with air as oxidant and no additional oxidant involved. The maximum turnover frequency value of N‐benzylbenzaldimine reaches 1555.3 μmol g−1 h−1 under this condition. The Bi2O2CO3/g‐C3N4 catalyst has potential in other photocatalytic reactions.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Advanced Photocatalysis Techniques · Sulfur-Based Synthesis Techniques · Chemical Synthesis and Reactions

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

Affiliations

Beijing National Laboratory for Molecular Sciences CAS Key Laboratory of Colloid Interface and Chemical Thermodynamics CAS Research/Education Center for Excellence in Molecular Sciences Institute of Chemistry Chinese Academy of Sciences Beijing 100190 P. R. China

School of Chemical Sciences University of Chinese Academy of Sciences Beijing 100049 P. R. China

Funding

National Natural Science Foundation of China

References (52)

Show source-provided references
1.
2. 10.1002/anie.20180998410.1002/anie.201809984 ↗
3. 10.1016/j.cis.2023.10303210.1016/j.cis.2023.103032 ↗
4. 10.1002/anie.20230308610.1002/anie.202303086 ↗
5. 10.1016/j.cej.2023.14506610.1016/j.cej.2023.145066 ↗
6. 10.1016/j.joule.2021.12.01110.1016/j.joule.2021.12.011 ↗
7.
8. 10.1021/jacs.3c0820610.1021/jacs.3c08206 ↗
9. 10.1038/s41578-022-00422-310.1038/s41578-022-00422-3 ↗
10. 10.1039/D2DT01899C10.1039/D2DT01899C ↗
11. 10.1021/acscatal.3c0582610.1021/acscatal.3c05826 ↗
12. 10.1016/j.cclet.2024.10958010.1016/j.cclet.2024.109580 ↗
13.
14. 10.1002/ajoc.20130001210.1002/ajoc.201300012 ↗
15. 10.1002/anie.20171129110.1002/anie.201711291 ↗
16. 10.1016/j.mtchem.2023.10147510.1016/j.mtchem.2023.101475 ↗
17. 10.1002/ente.20220036210.1002/ente.202200362 ↗
18.
19. 10.1039/D0GC02040K10.1039/D0GC02040K ↗
20. 10.1016/j.jssc.2022.12308710.1016/j.jssc.2022.123087 ↗
21. 10.1039/D0SE00095G10.1039/D0SE00095G ↗
22. 10.1039/D1CY01233A10.1039/D1CY01233A ↗
23.
24. 10.31635/ccschem.022.20220206810.31635/ccschem.022.202202068 ↗
25. 10.1016/j.cej.2020.12440210.1016/j.cej.2020.124402 ↗
26. 10.1016/j.cclet.2020.08.01810.1016/j.cclet.2020.08.018 ↗
27.
28. 10.1016/j.jcis.2019.10.06010.1016/j.jcis.2019.10.060 ↗
29. 10.1016/j.jcat.2019.10.01810.1016/j.jcat.2019.10.018 ↗
30. 10.1016/j.jcis.2016.09.01810.1016/j.jcis.2016.09.018 ↗
31. 10.3390/nano1112339010.3390/nano11123390 ↗
32.
33. 10.1002/anie.20210189410.1002/anie.202101894 ↗
34. 10.1002/adfm.20220379410.1002/adfm.202203794 ↗
35. 10.1007/s11356-018-1418-310.1007/s11356-018-1418-3 ↗
36. 10.1016/j.colsurfa.2022.12875810.1016/j.colsurfa.2022.128758 ↗
37.
38. 10.1016/j.apsusc.2021.15019710.1016/j.apsusc.2021.150197 ↗
39. 10.1016/j.apsusc.2019.14356110.1016/j.apsusc.2019.143561 ↗
40.
41. 10.1039/D1CC00209K10.1039/D1CC00209K ↗
42. 10.1039/D3GC00337J10.1039/D3GC00337J ↗
43. 10.31635/ccschem.023.20230329810.31635/ccschem.023.202303298 ↗
44.
45. Lin L. · Angew. Chem. Int. Ed. · 2023 · 62 · 8
46. 10.1016/j.apcatb.2019.11854510.1016/j.apcatb.2019.118545 ↗
47. 10.1186/s11671-019-2965-310.1186/s11671-019-2965-3 ↗
48. 10.1021/jacs.7b0979210.1021/jacs.7b09792 ↗
49. 10.1002/aenm.20200400110.1002/aenm.202004001 ↗
50.
51. 10.1039/D2NR02585J10.1039/D2NR02585J ↗
52. 10.1021/jacs.3c0686010.1021/jacs.3c06860 ↗