Construction of a Lanthanide Cage with a Hollow-Walled Cavity and Large Windows to Promote Nucleophilic Additions
Source abstract
Abstract
Metal–organic cages (MOCs) as artificial mimic enzymes can allow small organic molecules to freely move in and out of the cavity with confined space, which often can increase intermolecular collisions and accelerate those reactions that are difficult to occur. This kind of homogeneous catalyst possesses high catalytic activity and regioselectivity, attracting growing interest recently. However, the rational design of MOCs with large openings as well as rich active sites for efficient chemical conversions remains a great challenge. Herein, we report a decanuclear 3d-4f MOC, Zn 2 Yb 8, with a hollow-walled cavity and four large windows self-assembled cooperatively by bridging ligands, Zn-based metalloligands, and lanthanide Yb 3+ ions. The lantern-like Zn 2 Yb 8 not only exposes unblocked passageways for allowing more guest molecules to penetrate the cage smoothly but also provides rich Lewis centers within the cavity, which could promote nucleophilic additions to effectively boost Friedel–Crafts alkylation and the three-component Strecker reaction. With the Zn 2 Yb 8 catalyst, more than 13 bis(indolyl)methane derivatives could be synthesized easily in 53–98% through Friedel–Crafts alkylation, and the conversion of the Strecker reaction for aniline, benzaldehyde, and trimethylsilyl cyanide could achieve approximately 98% in 3 h. Furthermore, host–guest relationship investigations confirmed that the catalytic function of the Zn 2 Yb 8 cage could be mainly attributed to the synergy of the inherent confinement effect, multiple Lewis catalytic sites, and host–guest electrostatic interactions in the coordination cage. The construction of the discrete 3d-4f MOC with large windows and its catalytic applications in nucleophilic additions may represent a potential approach for developing enzyme-like supramolecular nanoreactors.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Supramolecular Chemistry and Complexes · Molecular Sensors and Ion Detection · Covalent Organic Framework Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
MOE Frontiers Science Center for Rare Isotopes, Key Laboratory of Nonferrous Metal Chemistry and Resources Utilization of Gansu Province, Engineering Research Center of Rare Earth Functional Materials, Ministry of Education, State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, China
Funding
Fundamental Research Funds for the Central Universities · National Natural Science Foundation of China
References (65)
Show source-provided references
1. 10.1021/acs.accounts.5b0051610.1021/acs.accounts.5b00516 ↗
2. 10.1038/nature0926510.1038/nature09265 ↗
3. 10.1021/acs.chemrev.8b0020110.1021/acs.chemrev.8b00201 ↗
4. 10.1002/anie.20171335110.1002/anie.201713351 ↗
5. 10.1038/s41565-020-0652-210.1038/s41565-020-0652-2 ↗
6. 10.1021/jacs.1c0149310.1021/jacs.1c01493 ↗
7. 10.1039/C5CS00096C10.1039/C5CS00096C ↗
8. 10.1016/j.ccr.2019.02.01110.1016/j.ccr.2019.02.011 ↗
9. 10.1039/C9CS00091G10.1039/C9CS00091G ↗
10. 10.1021/cr500081p10.1021/cr500081p ↗
11. 10.1021/acs.chemrev.9b0083910.1021/acs.chemrev.9b00839 ↗
12. 10.1039/C1CS15169J10.1039/C1CS15169J ↗
13. 10.1002/anie.20231569110.1002/anie.202315691 ↗
14. 10.1038/nchem.59710.1038/nchem.597 ↗
15. 10.1021/jacs.3c0108410.1021/jacs.3c01084 ↗
16. 10.1039/C5CS00861A10.1039/C5CS00861A ↗
17. 10.1021/cr300282410.1021/cr3002824 ↗
18. 10.1039/C3CS60371G10.1039/C3CS60371G ↗
19. 10.1021/jacs.5b1319010.1021/jacs.5b13190 ↗
20. 10.1021/jacs.7b0670910.1021/jacs.7b06709 ↗
21. 10.1016/j.ccr.2017.10.03110.1016/j.ccr.2017.10.031 ↗
22. 10.1021/jacs.3c0949110.1021/jacs.3c09491 ↗
23. 10.1002/anie.20231948810.1002/anie.202319488 ↗
24. 10.1021/jacs.4c0187310.1021/jacs.4c01873 ↗
25. 10.1002/ange.20220473210.1002/ange.202204732 ↗
26. 10.1038/s44160-023-00276-910.1038/s44160-023-00276-9 ↗
27. 10.1039/D1CS01143J10.1039/D1CS01143J ↗
28. 10.1016/j.chempr.2021.06.00310.1016/j.chempr.2021.06.003 ↗
29. 10.1021/jacs.3c0086610.1021/jacs.3c00866 ↗
30. 10.1021/jacs.3c1073410.1021/jacs.3c10734 ↗
31. 10.1021/jacs.4c0025710.1021/jacs.4c00257 ↗
32. 10.1021/jacs.2c0418210.1021/jacs.2c04182 ↗
33. 10.1021/jacs.7b1133410.1021/jacs.7b11334 ↗
34. 10.1021/jacs.8b0039410.1021/jacs.8b00394 ↗
35. 10.1021/acsnano.2c1085610.1021/acsnano.2c10856 ↗
36. 10.1021/cr400122610.1021/cr4001226 ↗
37. 10.1016/j.ccr.2020.21365610.1016/j.ccr.2020.213656 ↗
38. 10.1021/jacs.9b1127310.1021/jacs.9b11273 ↗
39. 10.1038/s41467-018-06872-010.1038/s41467-018-06872-0 ↗
40. 10.1021/jacs.3c1019110.1021/jacs.3c10191 ↗
41. 10.1021/jacs.4c0295610.1021/jacs.4c02956 ↗
42. 10.1021/acs.chemrev.1c0060210.1021/acs.chemrev.1c00602 ↗
43. 10.1021/jacs.2c0076010.1021/jacs.2c00760 ↗
44. 10.1021/acs.inorgchem.8b0307710.1021/acs.inorgchem.8b03077 ↗
45. 10.1021/acs.inorgchem.1c0372910.1021/acs.inorgchem.1c03729 ↗
46. 10.1039/C8GC02645A10.1039/C8GC02645A ↗
47. 10.1021/jacs.7b0276410.1021/jacs.7b02764 ↗
48. 10.1021/ja204474v10.1021/ja204474v ↗
49. 10.1021/jacs.1c0116810.1021/jacs.1c01168 ↗
50. 10.1002/anie.20201724410.1002/anie.202017244 ↗
51. 10.1002/anie.20070420610.1002/anie.200704206 ↗
52. 10.1021/jacs.3c0129910.1021/jacs.3c01299 ↗
53. 10.1021/jacs.0c0999110.1021/jacs.0c09991 ↗
54. 10.1021/acs.inorgchem.3c0058710.1021/acs.inorgchem.3c00587 ↗
55. 10.1016/j.bioorg.2016.07.01110.1016/j.bioorg.2016.07.011 ↗
56. 10.1021/cr050580o10.1021/cr050580o ↗
57. 10.1039/D0CS00292E10.1039/D0CS00292E ↗
58. 10.1021/jacs.1c0356110.1021/jacs.1c03561 ↗
59. 10.1002/ange.20201151910.1002/ange.202011519 ↗
60. 10.1002/anie.20221085710.1002/anie.202210857 ↗
61. 10.1021/ja017252010.1021/ja0172520 ↗
62. 10.1016/j.molstruc.2021.13128310.1016/j.molstruc.2021.131283 ↗
63. 10.1016/j.foodchem.2017.09.09210.1016/j.foodchem.2017.09.092 ↗
64. 10.1002/jcc.2288510.1002/jcc.22885 ↗
65. 10.1002/jcc.2681210.1002/jcc.26812 ↗