Photoresponsive Supramolecular Assemblies Based on a C3‐Symmetric Benzene‐1,3,5‐tricarboxamide‐Anchored Diarylethene
Source abstract
Abstract
A functional C3-symmetric benzene-1,3,5-tricarboxamide-anchored diarylethene molecule (C3-BTE) is synthesized, which evolves into ordered superstructures with tunable morphology properties both in different solvents and via alternative light stimuli. The formation of rod-like assemblies from C3-BTE is reported and the self-assembly property of C3-BTE can be realized through alternative light stimuli in nonpolar solvents such as toluene. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Supramolecular Chemistry and Complexes · Luminescence and Fluorescent Materials · Supramolecular Self-Assembly in Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory for Advanced Materials and Institute of Fine Chemicals East China University of Science and Technology Shanghai 200237 China
Division of Theoretical Chemistry and Biology School of Biotechnology KTH Royal Institute of Technology SE‐10691 Stockholm Sweden
Funding
National Natural Science Foundation of China
References (47)
Show source-provided references
1. 10.1126/science.120596210.1126/science.1205962 ↗
2. 10.1002/anie.19901304110.1002/anie.199013041 ↗
3. 10.1021/ar500033n10.1021/ar500033n ↗
4. 10.1021/cr500531510.1021/cr5005315 ↗
5. 10.1002/anie.20140740210.1002/anie.201407402 ↗
6. 10.1002/anie.20100669310.1002/anie.201006693 ↗
7. 10.1002/anie.20100699910.1002/anie.201006999 ↗
8. 10.1002/anie.20120306310.1002/anie.201203063 ↗
9. 10.1002/adma.20110322010.1002/adma.201103220 ↗
10. 10.1039/c0cc01551b10.1039/c0cc01551b ↗
11. 10.1039/C4CC08533G10.1039/C4CC08533G ↗
12. 10.1039/C4PY00894D10.1039/C4PY00894D ↗
13. 10.1038/ncomms723410.1038/ncomms7234 ↗
14. 10.1039/c2cs35156k10.1039/c2cs35156k ↗
15. 10.1246/cl.2000.29210.1246/cl.2000.292 ↗
16. 10.1039/c3cc46297h10.1039/c3cc46297h ↗
17. 10.1039/c3cc48491b10.1039/c3cc48491b ↗
18. 10.1021/ja401695210.1021/ja4016952 ↗
19. 10.1021/ja509350310.1021/ja5093503 ↗
20. 10.1002/anie.20140722310.1002/anie.201407223 ↗
21. 10.1021/la400159m10.1021/la400159m ↗
22. 10.1021/ja909103810.1021/ja9091038 ↗
23. 10.1021/la200419v10.1021/la200419v ↗
24. 10.1002/anie.20131077310.1002/anie.201310773 ↗
25. 10.1002/adma.20070245510.1002/adma.200702455 ↗
26. 10.1021/ja105356w10.1021/ja105356w ↗
27. 10.1002/adfm.20090205910.1002/adfm.200902059 ↗
28. 10.1002/adma.20120152110.1002/adma.201201521 ↗
29. 10.1039/c2cc34054b10.1039/c2cc34054b ↗
30. 10.1002/anie.20130467010.1002/anie.201304670 ↗
31. 10.1039/c1cc11385b10.1039/c1cc11385b ↗
32. 10.1039/c4cc02672a10.1039/c4cc02672a ↗
33. 10.1002/chem.20130028210.1002/chem.201300282 ↗
34. 10.1021/ja077476410.1021/ja0774764 ↗
35. 10.1039/b303028h10.1039/b303028h ↗
36. 10.1039/C2TC00742H10.1039/C2TC00742H ↗
37. 10.1021/la803436h10.1021/la803436h ↗
38. 10.1039/c1cs15113d10.1039/c1cs15113d ↗
39. 10.1021/la803572710.1021/la8035727 ↗
40. 10.1039/C4CC08602C10.1039/C4CC08602C ↗
41. 10.1038/nmat242710.1038/nmat2427 ↗
42. 10.1063/1.46491310.1063/1.464913 ↗
43. 10.1063/1.167752710.1063/1.1677527 ↗
44. 10.1002/jcc.2175910.1002/jcc.21759 ↗
45. 10.1021/j100142a00410.1021/j100142a004 ↗
46. 10.1002/jcc.2003510.1002/jcc.20035 ↗
47. 10.1021/ct700301q10.1021/ct700301q ↗