Please use this identifier to cite or link to this item:
http://hdl.handle.net/10397/110870
| Title: | Supramolecular assemblies of amphiphilic donor–acceptor Stenhouse adducts as macroscopic soft scaffolds | Authors: | Hung, KL Cheung, LH Ren, Y Chau, MH Lam, YY Kajitani, T Leung, FKC |
Issue Date: | 2024 | Source: | Beilstein journal of organic chemistry, 2024, v. 20, p. 1590-1603 | Abstract: | In the design of photoharvesting and photoresponsive supramolecular systems in aqueous medium, the fabrication of amphiphilic photoswitches enables a noninvasive functional response through photoirradiation. Although most aqueous supramolecular assemblies are driven by high-energy and biodamaging UV light, we have previously reported a design of amphiphilic donor–acceptor Stenhouse adducts (DASAs) controlled by white light. Herein, we present a series of DASA amphiphiles (DAs) with minor structural modifications on the alkyl linker chain length connecting the DASA motif with the hydrophilic moiety. The excellent photoswitchability in organic medium and the photoresponsiveness in aqueous medium, driven by visible light, were investigated by UV–vis absorption spectroscopy. The assembled supramolecular nanostructures were confirmed by electron microscopy, while the supramolecular packing was revealed by X-ray diffraction analysis. Upon visible-light irradiation, significant transformations of the DA geometry enabled transformations of the supramolecular assemblies on a microscopic scale, subsequently disassembling macroscopic soft scaffolds of DAs. The current work shows promising use for the fabrication of visible-light-controlled macroscopic scaffolds, offering the next generation of biomedical materials with visible-light-controlled microenvironments and future soft-robotic systems. | Keywords: | Donor–acceptor Stenhouse adduct Photoresponsive molecular amphiphile Supramolecular transformation Visible light |
Publisher: | Beilstein - Institut zur Foerderung der Chemischen Wissenschaften | Journal: | Beilstein journal of organic chemistry | ISSN: | 2195-951X | EISSN: | 1860-5397 | DOI: | 10.3762/bjoc.20.142 | Rights: | © 2024 Hung et al.; licensee Beilstein-Institut. This is an open access article licensed under the terms of the Beilstein-Institut Open Access License Agreement (https://www.beilstein-journals.org/bjoc/terms), which is identical to the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0). The reuse of material under this license requires that the author(s), source and license are credited. Third-party material in this article could be subject to other licenses (typically indicated in the credit line), and in this case, users are required to obtain permission from the license holder to reuse the material. The definitive version of this article is the electronic one which can be found at: https://doi.org/10.3762/bjoc.20.142 The following publication Hung, K.-L.; Cheung, L.-H.; Ren, Y.; Chau, M.-H.; Lam, Y.-Y.; Kajitani, T.; Leung, F. K.-C. Beilstein J. Org. Chem. 2024, 20, 1590–1603 is available at https://doi.org/10.3762/bjoc.20.142. |
| Appears in Collections: | Journal/Magazine Article |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| 1860-5397-20-142.pdf | 10.18 MB | Adobe PDF | View/Open |
Page views
17
Citations as of Apr 14, 2025
Downloads
4
Citations as of Apr 14, 2025
SCOPUSTM
Citations
3
Citations as of Dec 5, 2025
Google ScholarTM
Check
Altmetric
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.



