Post-Synthetic Ligand Exchange by Mechanochemistry: Toward Green, Efficient, and Large-Scale Preparation of Functional Metal–Organic Frameworks
Source abstract
Abstract
Green, facile, and large-scale preparation of functionalized metal–organic frameworks (MOFs) remains a challenge. Herein, we report a rapid synthesis of functionalized MOFs by the integration of post-synthetic ligand exchange (PSLE) and mechanochemistry. This mechano-PSLE approach can circumvent the hurdles of PSLE such as long reaction time, excessive solvent, and even failure of PSLE caused by redissolution and recrystallization under solvothermal conditions. More importantly, the gram-scale MOF functionalized with the chiral group can be obtained facilely and greenly. It exhibited excellent asymmetric catalytic performance (81% conversion and 92.1% ee) for α-alkylation of aldehydes irradiated by a xenon lamp, providing a basis for industrial batch production of functionalized MOFs.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Crystallography and molecular interactions · Machine Learning in Materials Science
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Jiangxi Province for Environment and Energy Catalysis, School of Chemistry and Chemical Engineering, Nanchang University, Nanchang 330031, P. R. China
Funding
National Natural Science Foundation of China · Government of Jiangxi Province · Nanchang City
References (44)
Show source-provided references
1. 10.1021/cr200324t10.1021/cr200324t ↗
2. 10.1002/adma.20160613410.1002/adma.201606134 ↗
3. 10.1021/ja710973k10.1021/ja710973k ↗
4. 10.1021/cr200327210.1021/cr2003272 ↗
5. 10.1021/cr200190s10.1021/cr200190s ↗
6. 10.1021/cr200217c10.1021/cr200217c ↗
7. 10.1021/acs.iecr.7b0420610.1021/acs.iecr.7b04206 ↗
8. 10.1038/s41467-019-10218-910.1038/s41467-019-10218-9 ↗
9. 10.1016/j.ccr.2017.11.01510.1016/j.ccr.2017.11.015 ↗
10. 10.1002/anie.20130692310.1002/anie.201306923 ↗
11. 10.1021/jacs.7b0834910.1021/jacs.7b08349 ↗
12. 10.1039/c1sc00394a10.1039/c1sc00394a ↗
13. 10.1039/c7cc06522a10.1039/c7cc06522a ↗
14. 10.1021/acsami.9b1996410.1021/acsami.9b19964 ↗
15. 10.1021/cm303624p10.1021/cm303624p ↗
16. 10.1021/acs.chemmater.8b0473410.1021/acs.chemmater.8b04734 ↗
17. 10.1021/acs.inorgchem.9b0194710.1021/acs.inorgchem.9b01947 ↗
18. 10.1021/ic400048g10.1021/ic400048g ↗
19. 10.1021/acs.chemmater.6b0274910.1021/acs.chemmater.6b02749 ↗
20. 10.1021/acsami.9b0074010.1021/acsami.9b00740 ↗
21. 10.1021/jp505062810.1021/jp5050628 ↗
22. 10.1039/d0ta02975k10.1039/d0ta02975k ↗
23. 10.1002/anie.20090658310.1002/anie.200906583 ↗
24. 10.1039/c7cs00109f10.1039/c7cs00109f ↗
25. 10.1002/adsc.20070025210.1002/adsc.200700252 ↗
26. 10.1039/c7ta04829g10.1039/c7ta04829g ↗
27. 10.1021/acscentsci.1c0074310.1021/acscentsci.1c00743 ↗
28. 10.1016/j.cej.2022.14009310.1016/j.cej.2022.140093 ↗
29. 10.1002/anie.20211288010.1002/anie.202112880 ↗
30. 10.1039/c5cc08972g10.1039/c5cc08972g ↗
31. 10.1039/d0sc00333f10.1039/d0sc00333f ↗
32. 10.1016/j.cej.2022.13536410.1016/j.cej.2022.135364 ↗
33. 10.1016/j.mattod.2021.01.00810.1016/j.mattod.2021.01.008 ↗
34. 10.3390/cryst1101001510.3390/cryst11010015 ↗
35. 10.1021/acs.inorgchem.2c0126110.1021/acs.inorgchem.2c01261 ↗
36. 10.1021/acs.inorgchem.8b0104410.1021/acs.inorgchem.8b01044 ↗
37. 10.1016/j.apsusc.2022.15389910.1016/j.apsusc.2022.153899 ↗
38. 10.1021/jacs.1c0880910.1021/jacs.1c08809 ↗
39. 10.1038/s42004-021-00613-z10.1038/s42004-021-00613-z ↗
40. 10.1126/sciadv.170116210.1126/sciadv.1701162 ↗
41. 10.1126/science.114269610.1126/science.1142696 ↗
42. 10.1021/acscatal.5b0157310.1021/acscatal.5b01573 ↗
43. 10.1039/c2gc35118h10.1039/c2gc35118h ↗
44. 10.1002/anie.20150378910.1002/anie.201503789 ↗