journal article·2026-07-14

Thiophene Decoration Modulated Excimer Emission of Arylamine-Fluorene Luminophore for Visual and Ultrasensitive Physiological Temperature Sensing

Hao Zhang, Rui Wang, Can Tang, Chengkai Xu, Shuting Zhai, Weijun Zhao, Yongzhen Wu

Chemistry of Materials· Volume 38· Issue 13
Publisher page

Abstract

Organic single-luminophore systems featuring regulated monomer–excimer emission constitute an attractive framework for adaptive photonic materials. Here, we report two thiophene-decorated fluorene derivatives, TDDF and MTDDF, designed to modulate molecular packing and excimer formation through heteroarene-involved interactions. Compared with the nonthiophene analogue DDF, thiophene incorporation decreases optical bandgaps, enhances thermal robustness, and promotes close intermolecular association, leading to pronounced excimer emission in aggregated states. Single-crystal analyses reveal that methyl substitution in MTDDF increases intermolecular spacing, enabling a finely tunable balance between monomeric and excimeric states. When dispersed in a fatty-acid phase-change matrix, MTDDF exhibits a distinct, reversible thermally modulated luminescence transition across the physiological temperature range, producing a continuous color shift from yellow-green to blue. This thermally driven packing reorganization enables highly sensitive ratiometric temperature readout, delivering a maximum sensitivity of 44% °C –1 near 37 °C, among the highest reported for organic luminescent thermometers. This work demonstrates thiophene decoration as an effective approach for stabilizing excimer states and provide a versatile design strategy for advanced thermoresponsive luminophores and stimuli-adaptive photonic materials.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Luminescence and Fluorescent Materials · Organic Electronics and Photovoltaics · Perovskite Materials and Applications

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

Affiliations

State Key Laboratory of Advanced Separation Membrane Materials, State Key Laboratory of Green Chemical Synthesis and Conversion, Zhejiang Province Key Laboratory of Biofuel, College of Chemical Engineering

Zhejiang University of Technology

Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Shanghai Key Laboratory of Functional Materials Chemistry, Feringa Nobel Prize Scientist Joint Research Center, Frontiers Science Center for Materiobiology and Dynamic Chemistry, Institute of Fine Chemicals, School of Chemistry and Molecular Engineering

East China University of Science and Technology

Funding

National Natural Science Foundation of China (NSFC)

References (44)

Show source-provided references
1. 10.1038/nature2475510.1038/nature24755 ↗
2. 10.1038/s41467-018-05298-y10.1038/s41467-018-05298-y ↗
3. 10.1002/adfm.20240363510.1002/adfm.202403635 ↗
4. 10.1039/D0MH01316A10.1039/D0MH01316A ↗
5. 10.1002/adfm.20241540010.1002/adfm.202415400 ↗
6. 10.1038/s41467-017-00362-510.1038/s41467-017-00362-5 ↗
7. 10.1002/anie.20241581510.1002/anie.202415815 ↗
8. 10.1002/anie.20181166010.1002/anie.201811660 ↗
9. 10.1002/anie.20140529310.1002/anie.201405293 ↗
10. 10.1002/anie.20231664710.1002/anie.202316647 ↗
11. 10.1002/adfm.20240251010.1002/adfm.202402510 ↗
12. 10.1002/anie.20140015510.1002/anie.201400155 ↗
13. 10.1002/agt2.41010.1002/agt2.410 ↗
14. 10.31635/ccschem.021.20210087110.31635/ccschem.021.202100871 ↗
15. 10.1002/anie.20170386210.1002/anie.201703862 ↗
16. 10.1039/C5TC03289J10.1039/C5TC03289J ↗
17. 10.1039/D4SC08001G10.1039/D4SC08001G ↗
18. 10.1038/s41467-024-51792-x10.1038/s41467-024-51792-x ↗
19. 10.1039/C8TC03035A10.1039/C8TC03035A ↗
20. 10.1039/C6CC01993E10.1039/C6CC01993E ↗
21. 10.1021/jp402330n10.1021/jp402330n ↗
22. 10.1021/jz501953a10.1021/jz501953a ↗
23. 10.1351/pac20067812234110.1351/pac200678122341 ↗
24. 10.1039/C8QM00411K10.1039/C8QM00411K ↗
25. 10.1016/j.dyepig.2022.11045010.1016/j.dyepig.2022.110450 ↗
26. 10.1002/anie.20221565210.1002/anie.202215652 ↗
27. 10.1016/j.cclet.2020.10.01510.1016/j.cclet.2020.10.015 ↗
28. 10.1021/jacs.1c0459710.1021/jacs.1c04597 ↗
29. 10.1039/C9CC00614A10.1039/C9CC00614A ↗
30. 10.1021/jacs.5c0117310.1021/jacs.5c01173 ↗
31. 10.1039/D3CC04441F10.1039/D3CC04441F ↗
32. 10.1016/j.scib.2024.08.03710.1016/j.scib.2024.08.037 ↗
33. 10.1002/anie.20231938010.1002/anie.202319380 ↗
34. 10.1039/D5SC02314A10.1039/D5SC02314A ↗
35. 10.1021/acsami.9b0165610.1021/acsami.9b01656 ↗
36. 10.1039/D2TC02436E10.1039/D2TC02436E ↗
37. 10.1039/D1TC05354J10.1039/D1TC05354J ↗
38. 10.1039/C8SC00731D10.1039/C8SC00731D ↗
39. 10.1016/j.jphotochem.2019.02.01510.1016/j.jphotochem.2019.02.015 ↗
40. 10.1021/jp111685510.1021/jp1116855 ↗
41. 10.1021/cr078381n10.1021/cr078381n ↗
42. 10.1002/chem.20250081010.1002/chem.202500810 ↗
43. 10.1002/mame.20230032910.1002/mame.202300329 ↗
44. 10.1016/j.dyepig.2016.02.02310.1016/j.dyepig.2016.02.023 ↗