journal article·2017-06

Optically Switchable Luminescent Hydrogel by Synergistically Intercalating Photochromic Molecular Rotor into Inorganic Clay

Guoxing Liu, Ying‐Ming Zhang, Xiufang Xu, Lu Zhang, Yu Liu

Advanced Optical Materials· Volume 5· Issue 11
Publisher page

Abstract

Photomodulated luminescent hydrogels are of great potential for construction of functional soft materials. Herein a simple yet effective approach, by synergistically intercalating the dithienylethene‐bridged bispyridinium dye into the inorganic clay of Laponite, is proposed to immobilize the dye's molecular conformation and then to activate the hydrogel's fluorescence emission. The incorporation with dithienylethene unit can not only increase the π‐conjugation of organic dye but also endow the obtained supramolecular hydrogel with desirable photoswitchable capability. It can be envisioned that this organic–inorganic hybrid hydrogel featuring reversible luminescence switching behavior, high water content, good transparency, and mouldability may offer a practical strategy to create more advanced intelligent materials.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Luminescence and Fluorescent Materials · Photochromic and Fluorescence Chemistry · Supramolecular Self-Assembly in Materials

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

Affiliations

Department of Chemistry State Key Laboratory of Elemento‐Organic Chemistry Collaborative Innovation Center of Chemical Science and Engineering (Tianjin) Nankai University Tianjin 300071 P. R. China

Funding

National Natural Science Foundation of China

References (43)

Show source-provided references
1. 10.1039/c3cs60031a10.1039/c3cs60031a ↗
2. 10.1021/ja109692z10.1021/ja109692z ↗
3. 10.1002/anie.20150620510.1002/anie.201506205 ↗
4. 10.1021/jacs.5b1235710.1021/jacs.5b12357 ↗
5. 10.1002/anie.20120579110.1002/anie.201205791 ↗
6. 10.1002/adfm.20090181210.1002/adfm.200901812 ↗
7. 10.1039/C4CS00341A10.1039/C4CS00341A ↗
8. 10.1002/adma.20150155810.1002/adma.201501558 ↗
9. 10.1021/acs.chemrev.5b0030310.1021/acs.chemrev.5b00303 ↗
10. 10.1002/adma.20150109910.1002/adma.201501099 ↗
11. 10.1038/nmat454410.1038/nmat4544 ↗
12. 10.1039/C4CS00392F10.1039/C4CS00392F ↗
13. 10.1039/C4CS00372A10.1039/C4CS00372A ↗
14. 10.1002/adma.20150435510.1002/adma.201504355 ↗
15. 10.1039/C4CS00532E10.1039/C4CS00532E ↗
16. 10.1021/cr200359p10.1021/cr200359p ↗
17. 10.1021/acs.chemrev.5b0009110.1021/acs.chemrev.5b00091 ↗
18. 10.1039/c3cs60060b10.1039/c3cs60060b ↗
19. 10.1039/C5CC02709H10.1039/C5CC02709H ↗
20. 10.1021/jacs.6b0392410.1021/jacs.6b03924 ↗
21. 10.1021/acs.chemrev.5b0026310.1021/acs.chemrev.5b00263 ↗
22. 10.1021/ja037936310.1021/ja0379363 ↗
23. 10.1021/ja209572m10.1021/ja209572m ↗
24. 10.1021/cr500249p10.1021/cr500249p ↗
25. 10.1021/cr500634210.1021/cr5006342 ↗
26. 10.1039/C6CC02996E10.1039/C6CC02996E ↗
27. 10.1021/jacs.5b1152510.1021/jacs.5b11525 ↗
28. 10.1002/anie.20160965610.1002/anie.201609656 ↗
29. 10.1021/acs.jpcb.6b0264610.1021/acs.jpcb.6b02646 ↗
30. 10.1039/C3OB41757C10.1039/C3OB41757C ↗
31. 10.1038/nchem.261210.1038/nchem.2612 ↗
32. 10.1038/nature0869310.1038/nature08693 ↗
33. 10.1002/adma.20080091410.1002/adma.200800914 ↗
34. 10.1021/acs.macromol.6b0245910.1021/acs.macromol.6b02459 ↗
35. 10.1002/adfm.20160437910.1002/adfm.201604379 ↗
36. 10.1039/C4CC08721F10.1039/C4CC08721F ↗
37. 10.1002/anie.20130195610.1002/anie.201301956 ↗
38. 10.1002/adma.20150110210.1002/adma.201501102 ↗
39. 10.1002/anie.20120323610.1002/anie.201203236 ↗
40. 10.1002/ange.20120323610.1002/ange.201203236 ↗
41. 10.1021/nn800375e10.1021/nn800375e ↗
42. 10.1021/ar300053p10.1021/ar300053p ↗
43. 10.1021/jo981199p10.1021/jo981199p ↗