Photo‐Activated In Situ Supramolecular Reversible Self‐Assembly Based on Amphiphilic Calix[4]arene for Information Encryption
Source abstract
Abstract
Abstract Photoacid sulfonato‐merocyanine (MEH) serving as a photoisomer is added in mixed solution of amphiphilic calix[4]arene (SC4A8) and tetra‐(4‐pyridylphenyl) ethylene (TPE‐4Py), which not only activates the in situ supramolecular self‐assembly or disassembly, but also regulates two kinds of fluorescence emission. Benefiting from that MEH releases protons and becomes a ring‐closed isomer spiropyran (SP) under 420 nm irradiation, TPE‐4Py is protonated and then assembled with SC4A8 to form a supramolecular assembly with yellow fluorescence at 540 nm via electrostatic interactions. In the dark, SP changes to ring‐opened MEH, realizing a spontaneous disassembly accompanied by fluorescence emission at 495 nm, and thus, a photo‐activated reversible in situ supramolecular system is obtained successfully. Furthermore, Rhodamine B (RhB) acting as an energy acceptor is doped in the ternary supramolecular assembly, enabling the efficient energy transfer by the light irradiation. The formed tunable multicolor supramolecular assemblies have been successfully applied to the information encryption by 3D color codes.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Photochromic and Fluorescence Chemistry · Luminescence and Fluorescent Materials · Supramolecular Self-Assembly in Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Chemistry State Key Laboratory of Elemento‐Organic Chemistry Nankai University Tianjin 300071 P. R. China
Funding
National Natural Science Foundation of China · Fundamental Research Funds for the Central Universities
References (37)
Show source-provided references
1. 10.1002/adma.20200807110.1002/adma.202008071 ↗
2. 10.1021/acs.accounts.1c0006110.1021/acs.accounts.1c00061 ↗
3. 10.1002/adma.20220126210.1002/adma.202201262 ↗
4. 10.1021/jacs.0c0550610.1021/jacs.0c05506 ↗
5. 10.1038/s41467-021-27233-410.1038/s41467-021-27233-4 ↗
6. 10.1016/j.cclet.2020.12.05310.1016/j.cclet.2020.12.053 ↗
7. 10.1002/advs.20180039710.1002/advs.201800397 ↗
8. 10.1016/j.cclet.2021.02.06510.1016/j.cclet.2021.02.065 ↗
9. 10.1002/adma.20120152110.1002/adma.201201521 ↗
10. 10.1002/advs.20190152910.1002/advs.201901529 ↗
11. 10.1039/D0CS00547A10.1039/D0CS00547A ↗
12. 10.1002/anie.20220846010.1002/anie.202208460 ↗
13. 10.1021/jacs.1c0592310.1021/jacs.1c05923 ↗
14. 10.1021/acs.chemrev.8b0026010.1021/acs.chemrev.8b00260 ↗
15. 10.1002/advs.20200080310.1002/advs.202000803 ↗
16. 10.1002/adma.20200326310.1002/adma.202003263 ↗
17. Zhang Y. M. · Adv. Mater. · 2020 · 32
18. 10.1002/adom.20210216910.1002/adom.202102169 ↗
19. Li Z. · Angew. Chem., Int. Ed. · 2022 · 61
20. 10.1021/accountsmr.1c0004210.1021/accountsmr.1c00042 ↗
21. 10.1021/ja107341f10.1021/ja107341f ↗
22. 10.1002/adfm.20210836510.1002/adfm.202108365 ↗
23. 10.1038/s41467-021-21677-410.1038/s41467-021-21677-4 ↗
24. 10.1021/jacs.1c0637710.1021/jacs.1c06377 ↗
25. 10.1002/smll.20220173710.1002/smll.202201737 ↗
26. 10.1039/C9CC06545H10.1039/C9CC06545H ↗
27. 10.1002/smll.20220436010.1002/smll.202204360 ↗
28. Liu Z. X. · J. Mater. Chem. · 2021 · 9 · 1958
29. 10.1002/adma.20200648310.1002/adma.202006483 ↗
30. 10.1038/s41467-021-25299-810.1038/s41467-021-25299-8 ↗
31. 10.1038/s41467-022-30969-210.1038/s41467-022-30969-2 ↗
32. 10.1021/ja005699n10.1021/ja005699n ↗
33. 10.1039/C7CC03280C10.1039/C7CC03280C ↗
34. 10.1002/adfm.20170553210.1002/adfm.201705532 ↗
35. 10.1002/adma.20190649310.1002/adma.201906493 ↗
36. Lin Z. · J. Mater. Chem. · 2019 · 7
37. 10.1038/s41467-022-31978-x10.1038/s41467-022-31978-x ↗