Nanoluminophores Composed of 1,1′-Ferrocenedicarboxylic Acid and Tetrakis-(4-carboxyphenyl) Porphyrin for Electrochemiluminescence Sensing
Source abstract
Abstract
Development of nanoluminophores with high efficiency, good stability, and excellent electronic transfer ability is one of the key challenges in electrochemiluminescence (ECL). Here, a porphyrin-based nanomaterial named Fc-TCPP was synthesized by self-assembly of 1,1′-ferrocenedicarboxylic acid (Fc(COOH)2) and tetrakis-(4-carboxyphenyl) porphyrin (TCPP) under infrared heating light. By tuning the ratio of the precursors, the morphology of Fc-TCPP can be regulated from primitive nanospheres to thorn-ball flowers decorated with branches and particles, and the possible formation mechanism was proposed. Nano-boron carbide (B4C) with carbon defect sites further boosts the ECL performance of Fc-TCPP, and thereby, an ECL biosensor for AFP was constructed innovatively. This study provides a simple and effective strategy for the preparation of ECL nanoluminophores taking the advantages of ferrocene and TCPP, opening a new horizon to design porphyrin-based nanomaterials with various structures and expanding their application in biosensing and disease diagnosis.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced biosensing and bioanalysis techniques · Electrochemical sensors and biosensors · Electrochemical Analysis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Chemical Biology & Traditional Chinese Medicine Research (Ministry of Education, China), College of Chemistry and Chemical Engineering, Hunan Normal University, Changsha410081, P. R. China
Funding
Hunan Provincial Science and Technology Department · Education Department of Hunan Province · National Natural Science Foundation of China · Hunan Province
References (48)
Show source-provided references
1. 10.1016/j.bios.2019.11153010.1016/j.bios.2019.111530 ↗
2. 10.1021/acs.analchem.9b0342510.1021/acs.analchem.9b03425 ↗
3. 10.1021/acs.accounts.6b0044110.1021/acs.accounts.6b00441 ↗
4. 10.1002/anie.20191344510.1002/anie.201913445 ↗
5. 10.1039/C5CS00086F10.1039/C5CS00086F ↗
6. 10.1021/jacs.1c0667310.1021/jacs.1c06673 ↗
7. 10.1021/acs.analchem.8b0502710.1021/acs.analchem.8b05027 ↗
8. 10.1002/anie.20160095510.1002/anie.201600955 ↗
9. 10.1002/adma.20190612910.1002/adma.201906129 ↗
10. 10.1021/acs.accounts.8b0030210.1021/acs.accounts.8b00302 ↗
11. 10.1039/C9CP01278H10.1039/C9CP01278H ↗
12. 10.1021/acs.analchem.0c0020810.1021/acs.analchem.0c00208 ↗
13. 10.1007/s00216-019-01821-210.1007/s00216-019-01821-2 ↗
14. 10.1021/acsami.9b1924610.1021/acsami.9b19246 ↗
15. 10.1002/anie.20060248210.1002/anie.200602482 ↗
16. 10.1002/anie.20170200610.1002/anie.201702006 ↗
17. 10.1002/anie.20160914710.1002/anie.201609147 ↗
18. 10.1002/anie.20140613510.1002/anie.201406135 ↗
19. 10.1021/acsomega.9b0378810.1021/acsomega.9b03788 ↗
20. 10.1021/acs.analchem.9b0544410.1021/acs.analchem.9b05444 ↗
21. 10.1007/s10008-022-05136-810.1007/s10008-022-05136-8 ↗
22. 10.1007/s00604-021-04833-x10.1007/s00604-021-04833-x ↗
23. 10.1021/acs.analchem.1c0450110.1021/acs.analchem.1c04501 ↗
24. 10.1021/acs.analchem.5b0116810.1021/acs.analchem.5b01168 ↗
25. 10.1016/j.electacta.2018.04.01910.1016/j.electacta.2018.04.019 ↗
26. 10.1021/acs.chemrev.9b0043710.1021/acs.chemrev.9b00437 ↗
27. 10.1021/acs.analchem.1c0430610.1021/acs.analchem.1c04306 ↗
28. 10.1021/acs.analchem.1c0447510.1021/acs.analchem.1c04475 ↗
29. 10.1016/j.bios.2011.10.03610.1016/j.bios.2011.10.036 ↗
30. 10.1021/acs.analchem.2c0047510.1021/acs.analchem.2c00475 ↗
31. 10.1021/acs.analchem.7b0439710.1021/acs.analchem.7b04397 ↗
32. 10.1039/D1AN00410G10.1039/D1AN00410G ↗
33. 10.1021/acs.analchem.7b0270110.1021/acs.analchem.7b02701 ↗
34. 10.1038/nprot.2006.3810.1038/nprot.2006.38 ↗
35. 10.1016/j.bios.2014.08.02410.1016/j.bios.2014.08.024 ↗
36. 10.1002/adfm.20150476510.1002/adfm.201504765 ↗
37. 10.1038/s41467-020-18969-610.1038/s41467-020-18969-6 ↗
38. 10.1021/jacs.6b0075710.1021/jacs.6b00757 ↗
39. 10.1002/adfm.20160649710.1002/adfm.201606497 ↗
40. 10.1016/j.cplett.2015.05.03110.1016/j.cplett.2015.05.031 ↗
41. 10.1007/s10854-019-01736-910.1007/s10854-019-01736-9 ↗
42. 10.1021/ja070943x10.1021/ja070943x ↗
43. 10.1002/anie.20201021610.1002/anie.202010216 ↗
44. 10.1002/anie.20200745110.1002/anie.202007451 ↗
45. 10.1002/smll.20210656710.1002/smll.202106567 ↗
46. 10.1039/B613962K10.1039/B613962K ↗
47. 10.1016/j.carbon.2012.05.00810.1016/j.carbon.2012.05.008 ↗
48. 10.1016/j.bios.2021.11349210.1016/j.bios.2021.113492 ↗