From Two, to Three, to Multi‐Color Switches: Developing AIEgen‐Based Mechanochromic Materials
Source abstract
Abstract
Abstract A multi‐color switching mechanochromic aggregation‐induced emission luminogen (AIEgen) whose fluorescence spectra nearly covers the whole visible region was obtained from attaching spiropyran (SP) moiety on tetraphenylethylene (TPE). The covalent attachment of SP to TPE is crucial. It enables the tuning of the fluorescence of SP‐TPE dyads from no color change, to two‐color switching, to three‐color switching under grinding, based on the amorphization of TPE moiety and isomerization of spiropyran moiety. Under quantifiable hydrostatic pressures, the multi‐color switch with wide spectral response region was obtained resulting from distinct pressure thresholds for supramolecular and chemical structural changes. The attached spiropyran helped to enhance the response of the mechanochromic AIEgens to show more fantastic and obvious responses. The multi‐color changes and obvious responses in a wider visible region and an enhancement of fluorescence intensity give this molecule great potential for applications in visual pressure sensors, pressure calibration, etc.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Luminescence and Fluorescent Materials · Photochromic and Fluorescence Chemistry · Polydiacetylene-based materials and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Beijing National Laboratory for Molecular Sciences Center for Soft Matter Science and Engineering Key Lab of Polymer Chemistry and Physics of Ministry of Education College of Chemistry Peking University Beijing 100871 China
Department of Chemistry and Physics Simmons College Boston MA 02115 USA
State Key Laboratory of Superhard Materials Jilin University Changchun 130012 China
Funding
National Natural Science Foundation of China · Department of S and T for Social Development
References (47)
Show source-provided references
1. 10.1002/adma.20140135610.1002/adma.201401356 ↗
2. 10.1039/b105159h10.1039/b105159h ↗
3.
4. 10.1039/c1cs15113d10.1039/c1cs15113d ↗
5. 10.1039/b904665h10.1039/b904665h ↗
6.
7. 10.1039/b921451h10.1039/b921451h ↗
8. 10.1002/adfm.20120263910.1002/adfm.201202639 ↗
9.
10. 10.1039/C1CC15681K10.1039/C1CC15681K ↗
11. 10.1002/adfm.20110203010.1002/adfm.201102030 ↗
12. 10.1021/mz400588710.1021/mz4005887 ↗
13.
14. 10.1002/chem.20090182310.1002/chem.200901823 ↗
15. 10.1002/adfm.20100257210.1002/adfm.201002572 ↗
16. 10.1021/acs.chemrev.5b0026310.1021/acs.chemrev.5b00263 ↗
17.
18. 10.1021/ol102872x10.1021/ol102872x ↗
19. 10.1002/asia.20110021110.1002/asia.201100211 ↗
20.
21. 10.1021/jz501371k10.1021/jz501371k ↗
22. 10.1002/adma.20120504310.1002/adma.201205043 ↗
23. 10.1021/cm501414b10.1021/cm501414b ↗
24. 10.1021/acs.jpclett.5b0109010.1021/acs.jpclett.5b01090 ↗
25. 10.1021/ja305645x10.1021/ja305645x ↗
26. 10.1002/anie.20160340910.1002/anie.201603409 ↗
27. 10.1002/ange.20160340910.1002/ange.201603409 ↗
28.
29. 10.1039/c3cc46153j10.1039/c3cc46153j ↗
30. 10.1039/c2gc36069a10.1039/c2gc36069a ↗
31.
32. 10.1038/nchem.16710.1038/nchem.167 ↗
33. 10.1039/C5SC03297K10.1039/C5SC03297K ↗
34. 10.1038/nchem.172010.1038/nchem.1720 ↗
35.
36. 10.1038/nature0797010.1038/nature07970 ↗
37. 10.1002/anie.20151017110.1002/anie.201510171 ↗
38. 10.1002/ange.20151017110.1002/ange.201510171 ↗
39. 10.1126/science.124849410.1126/science.1248494 ↗
40. 10.1021/ma502555d10.1021/ma502555d ↗
41.
42. 10.1039/C5CC01064K10.1039/C5CC01064K ↗
43. 10.1039/C6TC02578A10.1039/C6TC02578A ↗
44. 10.1002/anie.20120032010.1002/anie.201200320 ↗
45. 10.1002/ange.20120032010.1002/ange.201200320 ↗
46. 10.1039/C6RA21639K10.1039/C6RA21639K ↗
47. 10.1002/chem.20140542610.1002/chem.201405426 ↗