journal article·2024-11

Achieve Full‐Color Emission in Multiple States through Reversible B←N Bond Formation and Multiple Configuration Transitions of a Single Fluorophore

Yitong Sun, Xueqi Cai, Wenjie He, Xinyu Ji, Liyan Zheng, Yonggang Shi, Qiue Cao

Advanced Optical Materials· Volume 12· Issue 31
Publisher page

Abstract

Abstract Multifunctional molecular switches have attracted much attention because of their unique stimulus response behavior and advanced applications. However, precise regulation of the structure for property enrichment is still a great challenge. Herein, the first case of a single‐molecule switch BN‐S with multiple structurally tunable and full‐color fluorescent properties is reported. Interestingly, BN‐S exhibits a butterfly‐like “metamorphosis” crystal growth process accompanied by full‐color fluorescence emission (including white light, CIE = 0.33, 0.33; 456 nm → 610 nm). It is shown that this is related to the reversible B←N bonding and the tunability of the spatial structure of the BN‐S. Thus, BN‐S exhibits superior multicolor tunability in different states (solid, liquid, and film), and its applications in white‐light optical light emitting diodes (OLEDs) and multicolor fluorescent inks also show great promise. This will provide a new strategy for designing and synthesizing the development of multifunctional molecular switching materials and enriching the variety of organoboron luminescent materials.
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Research context

OpenAlex topics: Luminescence and Fluorescent Materials · Molecular Sensors and Ion Detection · Supramolecular Self-Assembly in Materials

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

Affiliations

School of Chemical Science and Technology Yunnan University Kunming Yunnan 650091 China

Funding

National Natural Science Foundation of China · Yunnan University

References (39)

Show source-provided references
1. Sugden A. M. · Science · 2002 · 298 · 497
2. 10.1021/acs.jpclett.2c0273810.1021/acs.jpclett.2c02738 ↗
3. 10.1002/ange.20190289010.1002/ange.201902890 ↗
4. 10.1002/anie.20150119310.1002/anie.201501193 ↗
5. 10.1002/anie.20191555610.1002/anie.201915556 ↗
6. 10.1039/D1MH00696G10.1039/D1MH00696G ↗
7. 10.1002/anie.20231536210.1002/anie.202315362 ↗
8. 10.1002/adfm.20231413010.1002/adfm.202314130 ↗
9. 10.1021/acs.orglett.0c0061810.1021/acs.orglett.0c00618 ↗
10. 10.1021/jacs.1c1110010.1021/jacs.1c11100 ↗
11. 10.1021/jacs.4c0156810.1021/jacs.4c01568 ↗
12. 10.1021/ja209602z10.1021/ja209602z ↗
13. 10.1002/anie.20190056310.1002/anie.201900563 ↗
14. 10.1021/acs.orglett.1c0198310.1021/acs.orglett.1c01983 ↗
15. 10.1002/ange.20200190410.1002/ange.202001904 ↗
16. 10.1002/anie.20220061210.1002/anie.202200612 ↗
17. 10.1002/anie.20230309310.1002/anie.202303093 ↗
18. 10.1039/C9MH01041F10.1039/C9MH01041F ↗
19. 10.1002/anie.20240515810.1002/anie.202405158 ↗
20. 10.1039/C7SC03617E10.1039/C7SC03617E ↗
21. 10.1021/acs.orglett.9b0083110.1021/acs.orglett.9b00831 ↗
22. 10.1039/C9CS00153K10.1039/C9CS00153K ↗
23. 10.1021/acs.orglett.2c0234410.1021/acs.orglett.2c02344 ↗
24. 10.1002/anie.20231908910.1002/anie.202319089 ↗
25. 10.1002/anie.20211229010.1002/anie.202112290 ↗
26. 10.1021/acs.orglett.0c0177710.1021/acs.orglett.0c01777 ↗
27. 10.1002/adom.20210041110.1002/adom.202100411 ↗
28. 10.1039/D2TC01999J10.1039/D2TC01999J ↗
29. 10.1002/anie.20230372510.1002/anie.202303725 ↗
30. 10.1002/adfm.20210131210.1002/adfm.202101312 ↗
31. Jianxun L. · Adv. Opt. Mater. · 2023 · 12
32. 10.1021/jacs.3c0030610.1021/jacs.3c00306 ↗
33. 10.1002/adom.20230314210.1002/adom.202303142 ↗
34. 10.1002/asia.20180179110.1002/asia.201801791 ↗
35. 10.1021/acs.inorgchem.8b0357910.1021/acs.inorgchem.8b03579 ↗
36. 10.1039/D1CC04228A10.1039/D1CC04228A ↗
37. 10.1021/acs.orglett.9b0189210.1021/acs.orglett.9b01892 ↗
38. 10.1021/cr940745l10.1021/cr940745l ↗
39. 10.1021/acs.analchem.2c0504510.1021/acs.analchem.2c05045 ↗