Ball-Milled Co–N–C Nanocomposite for Benzylic C–H Bond Oxidation: a Facile, Practical, and Recyclable Catalyst under Neat Conditions and Atmospheric Pressure Oxygen
Source abstract
Abstract
A novel Co–N–C nanocomposite catalyst was prepared using a mechanical ball-milling method from melamine and Co(NO3)2, and no high-temperature calcination procedures were required. The superior nanocomposite catalyst shows excellent catalytic activity in the selective liquid-phase oxidation of benzylic C–H bonds with atmospheric pressure oxygen as an oxidant under solvent-free conditions. With 0.5 mol % of the Co–N–C nanocomposite catalyst, up to a 95% conversion and 98% selectivity are achieved in the oxidation of ethylbenzene to acetophenone. Furthermore, the catalyst shows good recyclability and can be simply recovered by filtration and reused several times without a significant loss in catalytic activity.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Oxidative Organic Chemistry Reactions · Catalytic C–H Functionalization Methods · Catalysis and Oxidation Reactions
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Applied Chemistry, College of Material Science and Technology, Nanjing University of Aeronautics & Astronautics, Nanjing, Jiangsu 210016, P. R. China
Department of Chemistry, School of Pharmacy, Nanjing Medical University, Nanjing, Jiangsu 211166, P. R. China
Funding
National Natural Science Foundation of China · Priority Academic Program Development of Jiangsu Higher Education Institutions
References (43)
Show source-provided references
1. 10.1002/cctc.20120026610.1002/cctc.201200266 ↗
2. 10.1021/cr300527g10.1021/cr300527g ↗
3. 10.1039/c3gc41459k10.1039/c3gc41459k ↗
4. 10.1039/c3gc42135j10.1039/c3gc42135j ↗
5. 10.1039/C4CC03728F10.1039/C4CC03728F ↗
6. 10.1002/anie.20140958010.1002/anie.201409580 ↗
7. 10.1002/anie.20170251110.1002/anie.201702511 ↗
8. 10.1039/C4RA09269D10.1039/C4RA09269D ↗
9. 10.1021/acscatal.6b0261410.1021/acscatal.6b02614 ↗
10. 10.1002/anie.20100169910.1002/anie.201001699 ↗
11. 10.1021/ja109856y10.1021/ja109856y ↗
12. 10.1021/jacs.6b1071010.1021/jacs.6b10710 ↗
13. 10.1021/acscatal.7b0133710.1021/acscatal.7b01337 ↗
14. 10.1016/j.tetlet.2015.01.17710.1016/j.tetlet.2015.01.177 ↗
15. 10.1002/adsc.20160013810.1002/adsc.201600138 ↗
16. 10.1039/C7GC03120C10.1039/C7GC03120C ↗
17. 10.1021/ja200997a10.1021/ja200997a ↗
18. 10.1021/cs300413x10.1021/cs300413x ↗
19. 10.1002/anie.20120791810.1002/anie.201207918 ↗
20. 10.1038/ncomms258610.1038/ncomms2586 ↗
21. 10.1039/C7GC00469A10.1039/C7GC00469A ↗
22. 10.1021/jacs.7b0513010.1021/jacs.7b05130 ↗
23. 10.1039/C6RA18288G10.1039/C6RA18288G ↗
24. 10.1021/ja407552k10.1021/ja407552k ↗
25. 10.1021/jacs.5b0202710.1021/jacs.5b02027 ↗
26. 10.1038/srep2614610.1038/srep26146 ↗
27. 10.1002/anie.20120653410.1002/anie.201206534 ↗
28. 10.1021/acs.langmuir.7b0033110.1021/acs.langmuir.7b00331 ↗
29. 10.1088/2053-1583/2/4/04400110.1088/2053-1583/2/4/044001 ↗
30. 10.1002/celc.20170047910.1002/celc.201700479 ↗
31. 10.1038/srep3337510.1038/srep33375 ↗
32. 10.1021/cm010106910.1021/cm0101069 ↗
33. 10.1016/j.apsusc.2010.10.05110.1016/j.apsusc.2010.10.051 ↗
34. 10.1039/c4ra03290j10.1039/c4ra03290j ↗
35. 10.1039/C4NR04357J10.1039/C4NR04357J ↗
36. 10.1021/ja309164310.1021/ja3091643 ↗
37. 10.1039/c1jm10819k10.1039/c1jm10819k ↗
38. 10.1039/c1jm11192b10.1039/c1jm11192b ↗
39. 10.1039/C1CS15171A10.1039/C1CS15171A ↗
40. 10.1016/0040-4039(95)01431-G10.1016/0040-4039(95)01431-G ↗
41. 10.1021/jo00118a00210.1021/jo00118a002 ↗
42. 10.1021/jo951970l10.1021/jo951970l ↗
43. 10.1002/adsc.20040411010.1002/adsc.200404110 ↗