Isolated Iron Single-Atomic Site-Catalyzed Chemoselective Transfer Hydrogenation of Nitroarenes to Arylamines
Source abstract
Abstract
Selective hydrogenation of nitroarenes to arylamines is a great challenge because of the complicated mechanism and competitive hydrogenation of reducible functional groups. Isolated single-atomic site catalysts, benefitting from their uniform and well-defined catalytic sites, are promising to achieve high activity and selectivity. Herein, we prepared an isolated iron single-atomic catalyst supported on ordered mesoporous nitrogen-doped carbon (Fe1/N–C). The as-prepared Fe1/N–C showed excellent activity and tolerance for functional groups in the transfer hydrogenation of nitroarenes over hydrazine hydrate. Density functional theory calculations revealed that the single atomically dispersed, partially positively charged Fe atoms and the lowered energy barrier collectively contribute to the superior hydrogenation performances for nitroarenes.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Nanomaterials for catalytic reactions · Asymmetric Hydrogenation and Catalysis · Ammonia Synthesis and Nitrogen Reduction
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Tsinghua University, Beijing 100084, P. R. China
College of Chemistry and Materials Science, Anhui Normal University, Wuhu 241000, P. R. China
Funding
Ministry of Science and Technology of the People's Republic of China · Natural Science Foundation of Beijing Municipality · National Natural Science Foundation of China
References (40)
Show source-provided references
1. 10.1093/nsr/nwv01410.1093/nsr/nwv014 ↗
2. 10.1016/j.apcatb.2018.01.05210.1016/j.apcatb.2018.01.052 ↗
3. 10.1021/ja076721g10.1021/ja076721g ↗
4. 10.1002/anie.20070082310.1002/anie.200700823 ↗
5. 10.1021/acs.jpcc.8b0536410.1021/acs.jpcc.8b05364 ↗
6. 10.1039/c5ra19869k10.1039/c5ra19869k ↗
7. 10.1038/nchem.109510.1038/nchem.1095 ↗
8. 10.1038/s41929-018-0028-210.1038/s41929-018-0028-2 ↗
9. 10.1002/anie.20150507310.1002/anie.201505073 ↗
10. 10.1021/jacs.7b0147110.1021/jacs.7b01471 ↗
11. 10.1002/anie.20170247310.1002/anie.201702473 ↗
12. 10.1002/anie.20180434910.1002/anie.201804349 ↗
13. 10.1021/jacs.8b0081410.1021/jacs.8b00814 ↗
14. 10.1016/j.joule.2018.11.00810.1016/j.joule.2018.11.008 ↗
15. 10.1038/s41467-018-03380-z10.1038/s41467-018-03380-z ↗
16. 10.1021/jacs.8b1357910.1021/jacs.8b13579 ↗
17. 10.1038/ncomms663410.1038/ncomms6634 ↗
18. 10.1038/s41565-019-0366-510.1038/s41565-019-0366-5 ↗
19. 10.1126/science.112838310.1126/science.1128383 ↗
20. 10.1126/science.124200510.1126/science.1242005 ↗
21. 10.1038/nchem.164510.1038/nchem.1645 ↗
22. 10.1007/s12274-015-0703-410.1007/s12274-015-0703-4 ↗
23. 10.1002/cctc.20170021810.1002/cctc.201700218 ↗
24. 10.1021/jacs.8b1130310.1021/jacs.8b11303 ↗
25. 10.1039/c7cc06530b10.1039/c7cc06530b ↗
26. 10.1021/ja206103810.1021/ja2061038 ↗
27. 10.1016/j.cattod.2017.09.00210.1016/j.cattod.2017.09.002 ↗
28. 10.1021/acscatal.5b0096910.1021/acscatal.5b00969 ↗
29. 10.1007/s12274-017-1631-210.1007/s12274-017-1631-2 ↗
30. 10.1021/acsami.7b1451310.1021/acsami.7b14513 ↗
31. 10.1016/j.apcata.2018.04.02410.1016/j.apcata.2018.04.024 ↗
32. 10.1007/s12274-016-1080-310.1007/s12274-016-1080-3 ↗
33. 10.1002/anie.20160079910.1002/anie.201600799 ↗
34. 10.1002/anie.20120579210.1002/anie.201205792 ↗
35. 10.1126/science.279.5350.54810.1126/science.279.5350.548 ↗
36. 10.1002/anie.20180546710.1002/anie.201805467 ↗
37. 10.1002/aenm.20180195610.1002/aenm.201801956 ↗
38. 10.1002/anie.20190210910.1002/anie.201902109 ↗
39. Haber F. Z. · Elektrochem. Angew. Phys. Chem. · 1898 · 22 · 506
40. 10.1039/b411603h10.1039/b411603h ↗