Design and Electrochemical Chiral Sensing of the Robust Sandwich Chiral Composite d-His-ZIF-8@Au@ZIF-8
Source abstract
Abstract
In the pursuit of chiral materials with significant chiral recognition effects and stability, various strategies have been explored, among which the integration of metal nanoparticles and chiral metal-organic frameworks (CMOFs) is highly promising. However, metal nanoparticles (MNPs)/CMOFs show high chiral properties but inferior stabilities due to the MNPs being easily detached from the outside layer under certain conditions. Sandwich MOFs@MNPs@CMOF chiral materials can overcome this dilemma because the sandwich structure can maximize the regulation of the chiral interface activity, while the controlled outer layer can stop the MNPs from falling off in the procedure of chiral recognition. Here, a novel sandwich chiral material (d-His-ZIF-8@Au@ZIF-8) was synthesized by a ligand-assisted strategy with a well-defined sandwich morphology and chiral recognition capabilities. The electrochemical chiral recognition showed that d-His-ZIF-8@Au@ZIF-8 was the most efficient for the enantiomer of phenylalanine (Phe). This experiment presents a novel perspective for the fabrication of a chiral electrochemical sensing platform based on a solid sandwich chiral nanocomposite.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Molecular Sensors and Ion Detection · Supramolecular Self-Assembly in Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Petrochemical Technology, Lanzhou University of Technology, 730050 Lanzhou, PR China
Funding
Innovation and Entrepreneurship Talent Project of Lanzhou · National Natural Science Foundation of China · Lanzhou University of Technology · Natural Science Foundation of Gansu Province · Key Research Program of Gansu Province
References (36)
Show source-provided references
1. 10.1021/acs.accounts.0c0060410.1021/acs.accounts.0c00604 ↗
2. 10.1038/s41377-022-00913-610.1038/s41377-022-00913-6 ↗
3. 10.1021/acs.accounts.9b0061210.1021/acs.accounts.9b00612 ↗
4. 10.1016/j.bios.2017.03.06910.1016/j.bios.2017.03.069 ↗
5. 10.1007/s00604-019-3682-410.1007/s00604-019-3682-4 ↗
6. 10.1021/acsami.6b0762010.1021/acsami.6b07620 ↗
7. 10.1016/j.snb.2017.08.07710.1016/j.snb.2017.08.077 ↗
8. 10.1021/acs.analchem.9b0037810.1021/acs.analchem.9b00378 ↗
9. 10.1016/j.trac.2019.11566210.1016/j.trac.2019.115662 ↗
10. 10.1002/adma.20160489810.1002/adma.201604898 ↗
11. 10.1021/acsami.1c0923810.1021/acsami.1c09238 ↗
12. 10.1021/acs.chemrev.1c0074010.1021/acs.chemrev.1c00740 ↗
13. 10.1021/acsami.9b1818310.1021/acsami.9b18183 ↗
14. 10.1021/acs.analchem.1c0032210.1021/acs.analchem.1c00322 ↗
15. 10.1039/d0ay01831g10.1039/d0ay01831g ↗
16. 10.1039/d0cs01236j10.1039/d0cs01236j ↗
17. 10.1039/c6cs00051g10.1039/c6cs00051g ↗
18. 10.1021/acssuschemeng.8b0604010.1021/acssuschemeng.8b06040 ↗
19. 10.1021/acs.langmuir.1c0242310.1021/acs.langmuir.1c02423 ↗
20. 10.1016/j.jelechem.2022.11628310.1016/j.jelechem.2022.116283 ↗
21. 10.1038/ncomms1442910.1038/ncomms14429 ↗
22. 10.1016/j.jelechem.2021.11581710.1016/j.jelechem.2021.115817 ↗
23. 10.1002/ange.20180128910.1002/ange.201801289 ↗
24. 10.1038/nature1976310.1038/nature19763 ↗
25. 10.1039/c5ta00998g10.1039/c5ta00998g ↗
26. 10.1002/ange.20131117710.1002/ange.201311177 ↗
27. 10.1021/jacs.0c0037810.1021/jacs.0c00378 ↗
28. 10.1002/ange.20181092510.1002/ange.201810925 ↗
29. 10.1016/j.aca.2019.10.06510.1016/j.aca.2019.10.065 ↗
30. 10.1021/cm102529c10.1021/cm102529c ↗
31. 10.1038/s41467-020-19327-210.1038/s41467-020-19327-2 ↗
32. 10.1016/j.bioelechem.2019.03.00610.1016/j.bioelechem.2019.03.006 ↗
33. 10.1016/j.electacta.2019.07.04010.1016/j.electacta.2019.07.040 ↗
34. 10.1038/s41467-019-13090-910.1038/s41467-019-13090-9 ↗
35. 10.1016/s0140-6736(10)60961-010.1016/s0140-6736(10)60961-0 ↗
36. 10.1038/s41572-021-00267-010.1038/s41572-021-00267-0 ↗