journal article·2022-04-13

Multistimuli-Responsive Squaraine Dyad Exhibiting Concentration-Controlled Vapochromic Luminescence

Shuaijun Yang, Shaoxin Zhou, Hui Li, Yong Nie, Huiyan Xu, Wei Liu, Jinling Miao, Yexin Li, Ge Gao, Jingsong You, Xuchuan Jiang

ACS Applied Materials & Interfaces· Volume 14· Issue 14
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Abstract

Stimuli-responsive organic materials with controllable luminescence are of enormous importance because of their potential applications in sensing, data security, and display devices. In this study, a multistimuli-responsive squaraine dyad (SQ-d) composed of two rigid squaraine moieties and a flexible ethylene linker was rationally designed and synthesized. SQ-d exhibits polymorphic luminescence, which can be reversibly switched by various external stimuli, including solvent vapor exposure, heat, and shear force. Unexpectedly, the weakly luminescent phase (O1) of SQ-d exhibits concentration-controlled vapochromic behavior. Film O1 can convert to a highly green-emissive phase (G1) under a low concentration of CHCl3 vapor and convert to a highly yellow-emissive phase (Y) under a high concentration of CHCl3 vapor; these originate from two distinct crystallization-induced emission enhancement processes. To the best of our knowledge, this is the first investigation of the effect of vapor concentration on the phase transitions of organic vapochromic luminophores. By analyzing the single-crystal structures and photophysical properties of SQ-d, we concluded that the green and yellow emissions probably originated from a zigzag stacking mode and an H-type π–π stacking mode, respectively. Finally, two prototypes based on SQ-d for applications in information encryption and vapor sensing were successfully demonstrated.
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Research context

OpenAlex topics: Luminescence and Fluorescent Materials · Polydiacetylene-based materials and applications · Synthesis and Properties of Aromatic Compounds

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

Affiliations

Institute for Smart Materials & Engineering, University of Jinan, No. 336 Nanxinzhuang West Road, 250022 Jinan, P.R. China

School of Chemistry and Chemical Engineering, University of Jinan, No. 336 Nanxinzhuang West Road, 250022 Jinan, P.R. China

Key Laboratory of Green Chemistry and Technology of Ministry of Education, College of Chemistry, Sichuan University, Chengdu, Sichuan 610064, P.R. China

Funding

University of Jinan · National Natural Science Foundation of China · Shandong Shenna Smart Advanced Materials Co., Ltd.

References (50)

Show source-provided references
1. 10.1021/acs.jpclett.5b0109010.1021/acs.jpclett.5b01090 ↗
2. 10.1002/adma.20150258910.1002/adma.201502589 ↗
3. 10.1016/j.cclet.2018.08.01110.1016/j.cclet.2018.08.011 ↗
4. 10.1039/C8QM00062J10.1039/C8QM00062J ↗
5. 10.1039/c3tc32414a10.1039/c3tc32414a ↗
6. 10.1039/C3MH00023K10.1039/C3MH00023K ↗
7. 10.1002/chem.20180564110.1002/chem.201805641 ↗
8. 10.1039/C7QM00201G10.1039/C7QM00201G ↗
9. 10.1021/cr300396p10.1021/cr300396p ↗
10. 10.1039/C9CS00098D10.1039/C9CS00098D ↗
11. 10.1039/c2jm30394a10.1039/c2jm30394a ↗
12. 10.1021/acsomega.9b0227710.1021/acsomega.9b02277 ↗
13. 10.1021/acsami.8b2122110.1021/acsami.8b21221 ↗
14. 10.1039/D0NH00186D10.1039/D0NH00186D ↗
15. 10.1002/chem.20110164210.1002/chem.201101642 ↗
16. 10.1021/jacs.0c0805910.1021/jacs.0c08059 ↗
17. 10.1002/adma.20150244210.1002/adma.201502442 ↗
18. 10.3390/sym1211190310.3390/sym12111903 ↗
19. 10.1021/jacs.9b0505410.1021/jacs.9b05054 ↗
20. 10.1039/D0TC03645E10.1039/D0TC03645E ↗
21. 10.1021/acs.cgd.9b0159610.1021/acs.cgd.9b01596 ↗
22. 10.1021/jacs.0c0748210.1021/jacs.0c07482 ↗
23. 10.1021/acsami.1c0393710.1021/acsami.1c03937 ↗
24. 10.1002/adfm.20190189510.1002/adfm.201901895 ↗
25. 10.1021/jacs.7b1245510.1021/jacs.7b12455 ↗
26. 10.1039/B707734C10.1039/B707734C ↗
27. 10.1016/j.dyepig.2019.10764510.1016/j.dyepig.2019.107645 ↗
28. 10.1021/acs.bioconjchem.9b0048210.1021/acs.bioconjchem.9b00482 ↗
29. 10.1021/ja304082h10.1021/ja304082h ↗
30. 10.1002/anie.20191443710.1002/anie.201914437 ↗
31. 10.1002/chem.20180151810.1002/chem.201801518 ↗
32. 10.1002/adom.20180154910.1002/adom.201801549 ↗
33. 10.1002/chem.20180439310.1002/chem.201804393 ↗
34. 10.1021/jacs.0c1215310.1021/jacs.0c12153 ↗
35. Anslyn, E. V.; Dougherty, D. A. Modern Physical Organic Chemistry; University Science Books: Sausalito, 2006; Chapter 1, pp 26–51.
36. 10.1021/ie50448a02210.1021/ie50448a022 ↗
37. 10.1021/acs.chemrev.5b0026310.1021/acs.chemrev.5b00263 ↗
38. 10.1142/S225123731340010810.1142/S2251237313400108 ↗
39. 10.1021/ic901198210.1021/ic9011982 ↗
40. 10.1021/jz400985t10.1021/jz400985t ↗
41. 10.1002/adom.20200225110.1002/adom.202002251 ↗
42. 10.1021/acs.jpcc.7b0806010.1021/acs.jpcc.7b08060 ↗
43. 10.1039/D0TC01032D10.1039/D0TC01032D ↗
44. 10.1002/adom.20120006410.1002/adom.201200064 ↗
45. 10.1039/C4TC01763C10.1039/C4TC01763C ↗
46. 10.1002/adom.20190074910.1002/adom.201900749 ↗
47. 10.1002/anie.20120466010.1002/anie.201204660 ↗
48. The wavenumber of C-H stretching of CHCl3 (3020 cm–1) in Fourier transform infrared was obtained from NIST Chemistry WebBook, NIST Standard Reference Database Number 69, http://webbook.nist.gov/chemistry/ (accessed Oct 2021).
49. 10.1002/1521-3773(20020104)41:1<48::AID-ANIE48>3.0.CO;2-U10.1002/1521-3773(20020104)41:1<48::AID-ANIE48>3.0.CO;2-U ↗
50. 10.1021/ac402070z10.1021/ac402070z ↗