Stimuli-Responsive π-Conjugated Polymers Showing Solid-State Emission Based on Boron-Fused Azomethine Complexes with NNO-Tridentate Ligands
Source abstract
Abstract
We report stimuli-responsive luminescent π-conjugated polymers involving the boron-fused azomethine (BAm) structure with the NNO-tridentate ligands and demonstrate their application to film-type sensors. The acid-responsive properties of the polymers are provided by the free lone-pair electrons of the nitrogen atom on the BAm unit. The polymer films showed red shifts in emission wavelengths under acid vapor, and the responses were reversible and corresponded to deprotonation. Furthermore, owing to environmental sensitivity in the film state, unique luminescent color changes were observed. The bilayer films of the BAm polymer coated by poly( n -butyl methacrylate) exhibited vapochromic luminescence with gradual blue shifts (orange → yellow → green) by vapor annealing with chloroform depending on the exposure time. We demonstrated that these changes were applicable for evaluating solvent-vapor permeability of target membranes. This study shows that nitrogen substitution into existing organic compounds is effective for creating stimuli-responsive materials.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Luminescence and Fluorescent Materials · Molecular Sensors and Ion Detection · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Polymer Chemistry, Graduate School of Engineering, Kyoto University, Katsura, Nishikyo-ku, Kyoto 615-8510, Japan
Funding
Japan Society for the Promotion of Science · Research Foundation for the Electrotechnology of Chubu
References (36)
Show source-provided references
1. 10.1021/ma100581510.1021/ma1005815 ↗
2. 10.1021/cr980101410.1021/cr9801014 ↗
3. 10.1039/c7dt04324d10.1039/c7dt04324d ↗
4. 10.1021/jacs.8b1318910.1021/jacs.8b13189 ↗
5. 10.1016/j.snb.2018.05.06210.1016/j.snb.2018.05.062 ↗
6. 10.1016/j.dyepig.2017.06.00610.1016/j.dyepig.2017.06.006 ↗
7. 10.1002/adma.20200807110.1002/adma.202008071 ↗
8. 10.1002/adfm.20211327410.1002/adfm.202113274 ↗
9. 10.1021/jacs.7b0034210.1021/jacs.7b00342 ↗
10. 10.1016/j.cclet.2021.05.05310.1016/j.cclet.2021.05.053 ↗
11. 10.1016/j.snb.2020.12832310.1016/j.snb.2020.128323 ↗
12. 10.1039/c5py00055f10.1039/c5py00055f ↗
13. 10.1002/anie.20130572810.1002/anie.201305728 ↗
14. 10.1002/tcr.20200015610.1002/tcr.202000156 ↗
15. 10.1021/acs.macromol.9b0025910.1021/acs.macromol.9b00259 ↗
16. 10.1039/d1py00213a10.1039/d1py00213a ↗
17. 10.1246/bcsj.2015008110.1246/bcsj.20150081 ↗
18. 10.1021/ja015957w10.1021/ja015957w ↗
19. 10.1039/d2cs00139j10.1039/d2cs00139j ↗
20. 10.1246/bcsj.2021023510.1246/bcsj.20210235 ↗
21. 10.1021/acs.orglett.1c0177610.1021/acs.orglett.1c01776 ↗
22. 10.1002/chem.20140294610.1002/chem.201402946 ↗
23. 10.1016/j.jphotochemrev.2019.03.00110.1016/j.jphotochemrev.2019.03.001 ↗
24. 10.1002/pola.2736610.1002/pola.27366 ↗
25. 10.1021/ja510985v10.1021/ja510985v ↗
26. 10.1002/pol.2021032910.1002/pol.20210329 ↗
27. 10.1246/cl.20075610.1246/cl.200756 ↗
28. 10.1002/anie.20180301310.1002/anie.201803013 ↗
29. 10.1021/acs.chemmater.6b0085010.1021/acs.chemmater.6b00850 ↗
30. 10.1021/ma500082e10.1021/ma500082e ↗
31. 10.1021/ja00479a07710.1021/ja00479a077 ↗
32. 10.1246/cl.1977.30110.1246/cl.1977.301 ↗
33. 10.1002/chem.20170230910.1002/chem.201702309 ↗
34. 10.1021/acsami.9b1565110.1021/acsami.9b15651 ↗
35. 10.1021/acs.jpcc.8b0176710.1021/acs.jpcc.8b01767 ↗
36. 10.1016/j.polymer.2020.12275310.1016/j.polymer.2020.122753 ↗