journal article·2026-07-22

Crystal Structure of a Cobalt MOF Containing Cyclotriveratrylene and Its Application for Electrochemical Detection of Dopamine and Epinephrine

Ting-Ting Liu, Xin-Hui Ji, Shuaitong Zhang, Wen-Yuan Pei, Jian-Fang Ma

ACS Applied Materials & Interfaces· Volume 18· Issue 28
Publisher page

Abstract

Dopamine (DA) is a key neurotransmitter regulating nervous system function, while epinephrine (EP) is an important hormone reflecting pathological status. The accurate detection of these two molecules is of great clinical significance for the early diagnosis and therapeutic evaluation of related diseases. Metal–organic frameworks (MOFs) exhibit considerable potential in electrochemical sensing; however, pristine MOFs suffer from poor conductivity. In this work, the ligand H 6 L, a derivative of cyclotriveratrylene containing six carboxylic groups, was synthesized. A Co–L MOF was then constructed via a solvothermal method, and its crystal structure was determined and discussed. Then, Co–L was compounded with mesoporous carbon (MC) to give the composites for the modification of an electrode. Benefiting from the MC, the conductivity of the composite was significantly enhanced, and the electrochemical sensors containing the composite for the detection of DA and EP were constructed. Cyclic voltammetry (CV) was used to optimize of testing conditions, and differential pulse voltammetry (DPV) was used to detect the contents of analytes. For the detection of DA, the Co–L@MC(1:2)/GCE ( ES-I ) sensor displayed a linear range of 0.05–35 μM and a detection limit of 1.09 nM (GCE = glassy carbon electrode). For EP, the Co–L@MC(2:1)/GCE ( ES-II ) sensor possessed the linear range of 0.03–75 μM, and the detection limit was 1.55 nM. Meanwhile, both sensors exhibited good selectivity, repeatability, and stability, with all relative standard deviations (RSDs) below 5%.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Electrochemical sensors and biosensors · Conducting polymers and applications · Metal-Organic Frameworks: Synthesis and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Key Laboratory of Polyoxometalate and Reticular Material Chemistry of the Ministry of Education, Department of Chemistry

Northeast Normal University

Academic Affairs Office

Shijiazhuang University

Funding

National Natural Science Foundation of China

References (40)

Show source-provided references
1. 10.1016/j.tics.2025.09.00810.1016/j.tics.2025.09.008 ↗
2. 10.1038/s41593-025-01906-510.1038/s41593-025-01906-5 ↗
3. 10.1038/s41593-026-02227-x10.1038/s41593-026-02227-x ↗
4. 10.1016/j.microc.2025.11466110.1016/j.microc.2025.114661 ↗
5. 10.1016/j.colsurfb.2025.11488210.1016/j.colsurfb.2025.114882 ↗
6. 10.1016/j.microc.2024.11232710.1016/j.microc.2024.112327 ↗
7. 10.1016/j.apsusc.2025.16495610.1016/j.apsusc.2025.164956 ↗
8. 10.1111/all.7027710.1111/all.70277 ↗
9. 10.1016/j.trac.2026.11868710.1016/j.trac.2026.118687 ↗
10. 10.1016/j.sbsr.2025.10078610.1016/j.sbsr.2025.100786 ↗
11. 10.1016/j.jiec.2024.07.06310.1016/j.jiec.2024.07.063 ↗
12. 10.34133/research.126610.34133/research.1266 ↗
13. 10.1038/s12276-024-01223-010.1038/s12276-024-01223-0 ↗
14. 10.1038/s41378-025-00941-310.1038/s41378-025-00941-3 ↗
15. 10.1016/j.diamond.2025.11325710.1016/j.diamond.2025.113257 ↗
16. 10.1016/j.microc.2025.11631310.1016/j.microc.2025.116313 ↗
17. 10.1016/j.aca.2024.34348910.1016/j.aca.2024.343489 ↗
18. 10.1016/j.jallcom.2024.17778610.1016/j.jallcom.2024.177786 ↗
19. 10.1016/j.diamond.2025.11309310.1016/j.diamond.2025.113093 ↗
20. 10.1002/adfm.20252378210.1002/adfm.202523782 ↗
21. 10.1002/admt.20250210810.1002/admt.202502108 ↗
22. 10.1021/acs.analchem.5c0678810.1021/acs.analchem.5c06788 ↗
23. 10.1007/s00604-025-07069-110.1007/s00604-025-07069-1 ↗
24. 10.34133/cbsystems.056610.34133/cbsystems.0566 ↗
25. 10.1016/j.micromeso.2025.11372610.1016/j.micromeso.2025.113726 ↗
26. 10.1016/j.matchemphys.2025.13187710.1016/j.matchemphys.2025.131877 ↗
27. 10.1016/j.microc.2025.11350310.1016/j.microc.2025.113503 ↗
28. 10.1002/adma.7274710.1002/adma.72747 ↗
29. 10.1016/j.cej.2026.17314610.1016/j.cej.2026.173146 ↗
30. 10.1016/j.ijhydene.2024.01.02610.1016/j.ijhydene.2024.01.026 ↗
31. 10.1002/smtd.20240108210.1002/smtd.202401082 ↗
32. 10.1002/advs.20252436310.1002/advs.202524363 ↗
33. 10.1016/j.cej.2025.16911910.1016/j.cej.2025.169119 ↗
34. 10.1016/j.foodchem.2026.14834310.1016/j.foodchem.2026.148343 ↗
35. 10.1016/j.ijhydene.2026.15452210.1016/j.ijhydene.2026.154522 ↗
36. 10.1021/acs.inorgchem.5c0417110.1021/acs.inorgchem.5c04171 ↗
37. 10.1016/j.cej.2025.16197810.1016/j.cej.2025.161978 ↗
38. 10.1021/acs.inorgchem.5c0047710.1021/acs.inorgchem.5c00477 ↗
39. 10.1021/acsanm.5c0587310.1021/acsanm.5c05873 ↗
40. 10.26599/NR.2025.9490823510.26599/NR.2025.94908235 ↗