Monomer Emission Mechanism Research of Tetraphenylethene Derivative with Supramolecular Self-Assembly in Polymer Microspheres
Source abstract
Abstract
The monomer emission property of the tetraphenylethene (TPE) derivative is rarely reported, and its photoluminescence (PL) mechanism related to supramolecular self-assembly needs further in-depth research. Two long alkyl chain modified derivatives, the TPE derivative (TPE-C 10 ) and pyrene derivative (Pyrene-C 10 ), are designed and synthesized, which possess similar supramolecular assembly behavior but exhibit different PL properties. TPE-C 10 not only forms self-assembly morphologies with monomer emission but also emits aggregation-induced emission (AIE). Moreover, the polymer microspheres containing TPE-C 10 and Pyrene-C 10 are prepared, which can dissolve or swell in different organic solvents. The changed binding effect of polymer chains achieves the luminescence transformation of TPE-C 10 from AIE to monomer emission. This work hopefully can enrich luminescent materials based on the monomer emission of the TPE derivative and provide a new method for mechanism studies about supramolecular self-assembly and luminescence.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Luminescence and Fluorescent Materials · Molecular Sensors and Ion Detection · Polydiacetylene-based materials and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Biological & Chemical Engineering, Zhejiang University of Science and Technology, Hangzhou, Zhejiang 310023, P. R. China
College of Materials Science and Engineering, Zhejiang University of Technology, Hangzhou, Zhejiang 310014, P. R. China
Funding
Primary Research and Development Plan of Zhejiang Province · Zhejiang University of Science and Technology
References (29)
Show source-provided references
1. 10.1039/b105159h10.1039/b105159h ↗
2. 10.1021/acs.chemrev.5b0026310.1021/acs.chemrev.5b00263 ↗
3. 10.1002/adfm.20221189310.1002/adfm.202211893 ↗
4. 10.1002/adma.20190427310.1002/adma.201904273 ↗
5. 10.1002/adma.20220994010.1002/adma.202209940 ↗
6. 10.1039/D2CS00610C10.1039/D2CS00610C ↗
7. 10.1039/D3TB00219E10.1039/D3TB00219E ↗
8. Yan D. · Angew. Chem., Int. Ed. · 2022 · 61 · 20220261410.1002/anie.202202614 ↗
9. 10.1524/zpch.1954.1.5_6.27510.1524/zpch.1954.1.5_6.275 ↗
10. 10.1021/ac060412b10.1021/ac060412b ↗
11. Dong Y. · Appl. Phys. Lett. · 2007 · 91 · 1404
12. 10.1039/b904665h10.1039/b904665h ↗
13. 10.1021/acs.langmuir.8b0327510.1021/acs.langmuir.8b03275 ↗
14. 10.1021/acsami.0c2163010.1021/acsami.0c21630 ↗
15. 10.1039/C4RA15240A10.1039/C4RA15240A ↗
16. 10.1039/c1cc12431e10.1039/c1cc12431e ↗
17. 10.1021/jo500884z10.1021/jo500884z ↗
18. 10.1021/ol500638c10.1021/ol500638c ↗
19. 10.1021/acs.macromol.5b0241210.1021/acs.macromol.5b02412 ↗
20. 10.1039/C6CC07216J10.1039/C6CC07216J ↗
21. 10.1039/C4TC00788C10.1039/C4TC00788C ↗
22. 10.1039/c3tc32161d10.1039/c3tc32161d ↗
23. 10.1002/chem.20100338210.1002/chem.201003382 ↗
24. 10.1016/j.ccr.2022.21475310.1016/j.ccr.2022.214753 ↗
25. 10.1021/acs.langmuir.7b0387310.1021/acs.langmuir.7b03873 ↗
26. 10.1002/advs.20220484810.1002/advs.202204848 ↗
27. 10.1039/C6CC01706A10.1039/C6CC01706A ↗
28. 10.1038/srep4289810.1038/srep42898 ↗
29. 10.1016/j.jcis.2023.01.13310.1016/j.jcis.2023.01.133 ↗