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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.
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