journal article·2023-05

An Ultra‐Sensitive Fluorescent Probe Based on Hybridized Local and Charge‐Transfer Materials for Quantitative Detection of Propanol Isomers

Changjiang Zhou, Haichao Liu, Jianai Chen, Shitong Zhang, Yujie Dong, Bing Yang, Weijun Li

Advanced Optical Materials· Volume 11· Issue 10
Publisher page

Abstract

Abstract Isopropanol has been widely applied in various fields as an important chemical solvent, which is produced by direct hydration of propylene accompanied with the byproduct of n‐propanol. Herein, an ultra‐sensitive fluorescent probe of TPA‐9AC, based on a non‐equivalent hybridized local and charge‐transfer (HLCT) material, is designed and synthesized to quantitatively detect the percentage of n‐propanol in propanol isomers. Owing to the stronger electron acceptor ability of n‐propanol, the excited state of probe transfers from highly emissive HLCT state to non‐emissive charge‐transfer state, resulting in the substantial fluorescence quenching. The low limit of detection (LOD) is achieved as sensitive as 0.02% v/v of n‐propanol in isopropanol. This contribution demonstrates a new approach to distinguish propanol isomers and an effective strategy for designing real‐time fluorescent sensors with high performances.
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Research context

OpenAlex topics: Molecular Sensors and Ion Detection · Luminescence and Fluorescent Materials · Analytical Chemistry and Sensors

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

Affiliations

College of Chemical Engineering Zhejiang University of Technology Hangzhou 310014 P. R. China

State Key Laboratory of Supramolecular Structure and Materials Institute of Theoretical Chemistry College of Chemistry Jilin University Changchun 130012 P. R. China

Funding

National Natural Science Foundation of China · Natural Science Foundation of Zhejiang Province · National Key Research and Development Program of China

References (55)

Show source-provided references
1. 10.1016/j.fluid.2017.11.01010.1016/j.fluid.2017.11.010 ↗
2. 10.1021/acsomega.8b0103910.1021/acsomega.8b01039 ↗
3. 10.1016/j.jct.2011.05.02610.1016/j.jct.2011.05.026 ↗
4. 10.1016/j.tet.2005.06.00810.1016/j.tet.2005.06.008 ↗
5. 10.1016/j.tca.2005.01.05210.1016/j.tca.2005.01.052 ↗
6. 10.1002/cplu.20190003610.1002/cplu.201900036 ↗
7. 10.1021/acssuschemeng.7b0385410.1021/acssuschemeng.7b03854 ↗
8. 10.1016/j.jngse.2017.05.01610.1016/j.jngse.2017.05.016 ↗
9. 10.1021/acssuschemeng.8b0160610.1021/acssuschemeng.8b01606 ↗
10. 10.1016/j.jct.2019.03.01810.1016/j.jct.2019.03.018 ↗
11. 10.3184/174751911X1320682404053610.3184/174751911X13206824040536 ↗
12. 10.1021/ac00192a02210.1021/ac00192a022 ↗
13. 10.1021/acs.analchem.5b0075910.1021/acs.analchem.5b00759 ↗
14. 10.1021/ja01365a05310.1021/ja01365a053 ↗
15. 10.1021/acs.analchem.5b0220210.1021/acs.analchem.5b02202 ↗
16. 10.1109/JSEN.2021.311995110.1109/JSEN.2021.3119951 ↗
17. 10.1039/D1TA10589B10.1039/D1TA10589B ↗
18. 10.1016/j.jallcom.2016.07.24810.1016/j.jallcom.2016.07.248 ↗
19. 10.1039/D0EN00449A10.1039/D0EN00449A ↗
20. 10.1016/j.snb.2017.12.02910.1016/j.snb.2017.12.029 ↗
21. 10.1016/j.talanta.2020.12143410.1016/j.talanta.2020.121434 ↗
22. 10.1039/D0TC05496H10.1039/D0TC05496H ↗
23. 10.1039/C8CS00185E10.1039/C8CS00185E ↗
24. 10.31635/ccschem.020.20200043310.31635/ccschem.020.202000433 ↗
25. 10.31635/ccschem.021.20200073110.31635/ccschem.021.202000731 ↗
26. 10.1016/j.snb.2018.11.06110.1016/j.snb.2018.11.061 ↗
27. 10.1038/s41377-022-00873-x10.1038/s41377-022-00873-x ↗
28. 10.1038/lsa.2016.13610.1038/lsa.2016.136 ↗
29. 10.1038/s41377-019-0188-010.1038/s41377-019-0188-0 ↗
30. 10.1039/D2MH00566B10.1039/D2MH00566B ↗
31. 10.1002/chem.20220011310.1002/chem.202200113 ↗
32. 10.1039/D1TC04920H10.1039/D1TC04920H ↗
33. 10.1002/adfm.20120011610.1002/adfm.201200116 ↗
34. 10.1002/adom.20140015410.1002/adom.201400154 ↗
35. 10.1002/adom.20130046710.1002/adom.201300467 ↗
36. 10.1016/j.cej.2022.13591110.1016/j.cej.2022.135911 ↗
37. 10.1002/adma.20180738810.1002/adma.201807388 ↗
38. 10.1002/anie.20130848610.1002/anie.201308486 ↗
39. 10.1002/adfm.20160227610.1002/adfm.201602276 ↗
40. 10.1016/j.orgel.2019.10541410.1016/j.orgel.2019.105414 ↗
41. 10.31635/ccschem.020.20200039210.31635/ccschem.020.202000392 ↗
42. 10.1002/adfm.20220114310.1002/adfm.202201143 ↗
43. 10.1016/j.mtchem.2022.10078510.1016/j.mtchem.2022.100785 ↗
44. 10.1002/adfm.20140426010.1002/adfm.201404260 ↗
45. 10.1021/acs.jpcc.8b0708310.1021/acs.jpcc.8b07083 ↗
46. 10.1016/j.dyepig.2022.11048810.1016/j.dyepig.2022.110488 ↗
47. 10.3389/fchem.2019.0014110.3389/fchem.2019.00141 ↗
48. 10.1021/acs.analchem.9b0208510.1021/acs.analchem.9b02085 ↗
49. 10.1016/j.jinorgbio.2014.11.00410.1016/j.jinorgbio.2014.11.004 ↗
50. 10.1063/1.155847110.1063/1.1558471 ↗
51. 10.1016/j.snb.2016.02.11210.1016/j.snb.2016.02.112 ↗
52. 10.1021/cr940745l10.1021/cr940745l ↗
53. 10.1016/j.molliq.2019.11096210.1016/j.molliq.2019.110962 ↗
54. 10.1002/chem.20130436410.1002/chem.201304364 ↗
55. 10.1016/j.dyepig.2017.07.05610.1016/j.dyepig.2017.07.056 ↗