Chemical Reconfiguration via [2 + 2] Cycloaddition: Directing Photobleaching Switching in a Copper Complex
Source abstract
Abstract
Multifunctional photoresponsive materials exert significant research significance in the field of smart devices and sensors. A new copper-based complex ( 1 ) was synthesized via a simple solvothermal method using photoactive 1,2-bis(4-pyridyl)ethylene, multidentate hydroxyethylidenediphosphonic acid, and Cu 2+ ions, and it undergoes rapid “single-crystal to single-crystal” transformation via photoinduced [2 + 2] cycloaddition. The structural and chemical reconfiguration triggers second-scale photobleaching (blue-green to pale blue). Moreover, a “one-time write and erase” information encryption system was constructed using a single sample. This work demonstrates a new view of [2 + 2] cycloaddition-driven photobleaching in anticounterfeiting and encryption application.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organometallic Complex Synthesis and Catalysis · Photochromic and Fluorescence Chemistry · Metal complexes synthesis and properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Chemistry and Chemical Engineering
Qingdao University
Funding
National Natural Science Foundation of China · State Key Laboratory of Fine Chemicals, Dalian University of Technology
References (57)
Show source-provided references
1. 10.1002/anie.20241926610.1002/anie.202419266 ↗
2. 10.1002/smll.20220729110.1002/smll.202207291 ↗
3. 10.1038/s41467-022-30425-110.1038/s41467-022-30425-1 ↗
4. 10.1002/agt2.7018810.1002/agt2.70188 ↗
5. 10.1002/adom.20250031710.1002/adom.202500317 ↗
6. 10.1016/j.cej.2025.16603510.1016/j.cej.2025.166035 ↗
7. 10.1016/j.mtphys.2024.10146510.1016/j.mtphys.2024.101465 ↗
8. 10.1038/s41467-024-48411-010.1038/s41467-024-48411-0 ↗
9. 10.1002/inf2.7004910.1002/inf2.70049 ↗
10. 10.1021/acsami.5c0206210.1021/acsami.5c02062 ↗
11. 10.1038/s41467-020-14986-710.1038/s41467-020-14986-7 ↗
12. 10.1021/acsnano.5c1017510.1021/acsnano.5c10175 ↗
13. 10.1002/adfm.20221290710.1002/adfm.202212907 ↗
14. 10.1021/acsami.5c0851410.1021/acsami.5c08514 ↗
15. 10.1016/j.ccr.2026.21780210.1016/j.ccr.2026.217802 ↗
16. 10.34133/research.041110.34133/research.0411 ↗
17. Li L.-X. · Chin. J. Struct. Chem. · 2022 · 41 · 2203077
18. 10.1038/s41467-024-53705-410.1038/s41467-024-53705-4 ↗
19. 10.1016/j.cjsc.2025.10062210.1016/j.cjsc.2025.100622 ↗
20. 10.1002/advs.20250908810.1002/advs.202509088 ↗
21. 10.1002/anie.20250310410.1002/anie.202503104 ↗
22. 10.1002/adfm.20242511510.1002/adfm.202425115 ↗
23. 10.1002/adma.20230640210.1002/adma.202306402 ↗
24. 10.1039/D3QI00040K10.1039/D3QI00040K ↗
25. 10.1002/agt2.58310.1002/agt2.583 ↗
26. 10.1016/j.cej.2024.14955110.1016/j.cej.2024.149551 ↗
27. 10.1016/j.cej.2023.14835510.1016/j.cej.2023.148355 ↗
28. 10.1016/j.matt.2025.10219710.1016/j.matt.2025.102197 ↗
29. 10.1038/s41467-025-57638-410.1038/s41467-025-57638-4 ↗
30. 10.1002/adfm.20242379310.1002/adfm.202423793 ↗
31. 10.1021/jacs.5c0446610.1021/jacs.5c04466 ↗
32. 10.1016/j.cej.2024.15271310.1016/j.cej.2024.152713 ↗
33. 10.1002/chem.20240260110.1002/chem.202402601 ↗
34. Hulák P. · Dalton Trans. · 2025 · 54 · 1014010.1039/D5DT01004G ↗
35. 10.31635/ccschem.025.20250553210.31635/ccschem.025.202505532 ↗
36. 10.1021/jacs.5c0696210.1021/jacs.5c06962 ↗
37. 10.1002/anie.20240947210.1002/anie.202409472 ↗
38. 10.1002/anie.20230604810.1002/anie.202306048 ↗
39. 10.1021/jacs.5c0266910.1021/jacs.5c02669 ↗
40. 10.1021/acsami.6b0831510.1021/acsami.6b08315 ↗
41. 10.1021/acsnano.7b0745010.1021/acsnano.7b07450 ↗
42. 10.1021/acsami.1c0256110.1021/acsami.1c02561 ↗
43. 10.1016/j.cej.2025.15931610.1016/j.cej.2025.159316 ↗
44. 10.1002/anie.20221705410.1002/anie.202217054 ↗
45. 10.1039/C8DT01535J10.1039/C8DT01535J ↗
46. 10.1007/s11426-024-2201-610.1007/s11426-024-2201-6 ↗
47. 10.1038/s41467-025-63958-210.1038/s41467-025-63958-2 ↗
48. 10.1021/acs.cgd.5c0032110.1021/acs.cgd.5c00321 ↗
49. 10.1021/jacs.9b1346110.1021/jacs.9b13461 ↗
50. 10.1021/acs.inorgchem.3c0314810.1021/acs.inorgchem.3c03148 ↗
51. 10.1021/jacs.3c0122510.1021/jacs.3c01225 ↗
52. 10.1016/j.cej.2024.15473410.1016/j.cej.2024.154734 ↗
53. 10.1351/pac19712704064710.1351/pac197127040647 ↗
54. Viana da Silva A. L. · CrystEngComm · 2017 · 19 · 3450
55. 10.1021/acsami.6b0655110.1021/acsami.6b06551 ↗
56. 10.1002/anie.20100561310.1002/anie.201005613 ↗
57. 10.1016/j.cis.2005.04.00310.1016/j.cis.2005.04.003 ↗