Design and Construction of an Artificial Light‐Harvesting System Based on Polyacrylic Acid and a Cyanostilbene Derivative
Source abstract
Abstract
Abstract The development of materials with tunable fluorescence properties is critical for advancing applications in sensing, imaging, and information encryption. In this study, we synthesized a cyanostilbene derivative (CSA) that combines the benefits of aggregation‐induced emission (AIE) and self‐assembly in water. CSA, featuring a cyanostilbene core and hydrophilic carboxylate groups, exhibits weak fluorescence in solution but forms highly fluorescent nanoaggregates (CSA‐PAA) upon self‐assembly with polyacrylic acid (PAA). By integrating rhodamine 6G (Rh6G) as an energy acceptor, we constructed a light‐harvesting system (CSA‐PAA‐Rh6G) with high Förster resonance energy transfer (FRET) efficiency and tunable emission from green to yellow. This work presents a facile approach for the development of aqueous light‐harvesting systems and shows promise for future applications in tunable luminescent materials.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Photochromic and Fluorescence Chemistry · Polydiacetylene-based materials and applications · Analytical Chemistry and Sensors
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Chemical and Printing-Dyeing Engineering Henan University of Engineering Zhengzhou 450006 China
School of Petrochemical Engineering Changzhou University Changzhou 213164 China
Beijing Sino Advanced Chemical Materials Institution Co. Ltd. Beijing 100723 China
References (56)
Show source-provided references
1.
2. 10.1126/science.aav910410.1126/science.aav9104 ↗
3. 10.1038/nature1802010.1038/nature18020 ↗
4. 10.1021/cr500705710.1021/cr5007057 ↗
5. 10.1038/nchem.114510.1038/nchem.1145 ↗
6.
7. 10.1016/j.cclet.2023.10882910.1016/j.cclet.2023.108829 ↗
8. 10.1039/D1CC06011B10.1039/D1CC06011B ↗
9. 10.1016/j.cclet.2018.05.03410.1016/j.cclet.2018.05.034 ↗
10. 10.1039/C7TA11274B10.1039/C7TA11274B ↗
11. 10.1002/chem.20140339310.1002/chem.201403393 ↗
12. 10.1016/j.jcis.2023.08.18410.1016/j.jcis.2023.08.184 ↗
13.
14. 10.1002/anie.20240113610.1002/anie.202401136 ↗
15. 10.1016/j.cogsc.2023.10082310.1016/j.cogsc.2023.100823 ↗
16. 10.1039/D2NA00934J10.1039/D2NA00934J ↗
17. 10.1016/j.chphma.2022.05.00210.1016/j.chphma.2022.05.002 ↗
18.
19. 10.1039/D0TA03169K10.1039/D0TA03169K ↗
20. 10.1002/anie.20180017510.1002/anie.201800175 ↗
21.
22. 10.1021/acs.chemrev.5b0035210.1021/acs.chemrev.5b00352 ↗
23. 10.1021/ja100936w10.1021/ja100936w ↗
24. 10.1126/science.851158210.1126/science.8511582 ↗
25.
26. 10.1002/anie.20200752510.1002/anie.202007525 ↗
27. 10.1039/c1cs15113d10.1039/c1cs15113d ↗
28.
29. 10.1038/s42004-024-01175-610.1038/s42004-024-01175-6 ↗
30. 10.1039/C9CS00318E10.1039/C9CS00318E ↗
31.
32. 10.1039/D4CC03693J10.1039/D4CC03693J ↗
33. 10.1021/acs.chemrev.1c0105010.1021/acs.chemrev.1c01050 ↗
34. 10.1002/agt2.110.1002/agt2.1 ↗
35. 10.1002/adom.20200026510.1002/adom.202000265 ↗
36. 10.1021/acs.accounts.8b0062010.1021/acs.accounts.8b00620 ↗
37.
38. 10.1016/j.cclet.2023.10861810.1016/j.cclet.2023.108618 ↗
39. 10.1038/s41467-024-45252-910.1038/s41467-024-45252-9 ↗
40. 10.1039/D4YA00252K10.1039/D4YA00252K ↗
41. 10.1039/D3TA03498D10.1039/D3TA03498D ↗
42. 10.1002/anie.20230582710.1002/anie.202305827 ↗
43. 10.1016/j.cclet.2023.10861710.1016/j.cclet.2023.108617 ↗
44. 10.1002/adfm.20221288610.1002/adfm.202212886 ↗
45. 10.1002/adfm.20170514110.1002/adfm.201705141 ↗
46. 10.1039/D3SC00375B10.1039/D3SC00375B ↗
47. 10.1002/anie.20181264210.1002/anie.201812642 ↗
48.
49. 10.1016/j.cclet.2022.10808110.1016/j.cclet.2022.108081 ↗
50. 10.1039/D2TA04124C10.1039/D2TA04124C ↗
51. 10.1039/D1CC06647A10.1039/D1CC06647A ↗
52.
53. 10.1002/chem.20240142610.1002/chem.202401426 ↗
54. 10.1039/D4CC00616J10.1039/D4CC00616J ↗
55. 10.1002/anie.20191265410.1002/anie.201912654 ↗
56. 10.1039/C3CC48618D10.1039/C3CC48618D ↗