Cheung Leong-Hung, Kajitani Takashi, Leung Franco King-Chi
State Key Laboratory of Chemical Biology and Drug Discovery, Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Hong Kong, China.
Open Facility Development Office, Open Facility Center, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226-8503, Japan.
J Colloid Interface Sci. 2022 Dec 15;628(Pt A):984-993. doi: 10.1016/j.jcis.2022.08.034. Epub 2022 Aug 8.
Designing responsive, adaptive, and dynamic supramolecular systems in water, the incorporation of photoresponsive units in amphiphilic molecular structures enables functional responses in a non-invasive way by using light. However, in aqueous media, vast majority of reported synthetic photoresponsive molecular amphiphiles are commonly driven by high energy and bio-damaging UV-light for supramolecular transformation at multiple length-scale. Herein, we present newly designed visible-light controlled supramolecular assembly of donor-acceptor Stenhouse adducts amphiphiles (DA) with excellent stability and solubility in aqueous media. The excellent photoswitchability in organic media and photoresponsiveness in aqueous media driven by visible-light are found, as confirmed with UV-vis absorption and NMR spectroscopies. Supramolecular assembly at multiple length-scale of DAs is investigated with electron microscopies and X-ray diffraction to show large aspect-ratio of nanostructures assembled into macroscopic soft scaffolds. Upon visible-light irradiation, the large geometrical transformation of DAs enables supramolecular transformations, and subsequently destabilizes the macroscopic soft scaffold to release fluorophores from the scaffolds. These results provide the feasibility in developing the next generation of visible-light controlled macroscopic soft functional scaffold from supramolecular assembly across multiple length-scale without and offer ample opportunity to design future soft robotic materials and functional biomaterials.
在水中设计响应性、适应性和动态超分子体系时,在两亲分子结构中引入光响应单元能够通过光以非侵入性方式实现功能响应。然而,在水性介质中,绝大多数已报道的合成光响应分子两亲物通常由高能且对生物有损伤的紫外光驱动,以实现多长度尺度下的超分子转变。在此,我们展示了新设计的供体-受体施滕豪斯加合物两亲物(DA)的可见光控制超分子组装体,其在水性介质中具有出色的稳定性和溶解性。通过紫外-可见吸收光谱和核磁共振光谱证实,发现其在有机介质中具有出色的光开关性,在水性介质中由可见光驱动具有光响应性。利用电子显微镜和X射线衍射研究了DA在多长度尺度下的超分子组装,结果表明组装成宏观软支架的纳米结构具有较大的纵横比。在可见光照射下,DA的大几何转变实现了超分子转变,随后使宏观软支架不稳定,从而从支架中释放荧光团。这些结果为从多长度尺度的超分子组装开发下一代可见光控制的宏观软功能支架提供了可行性,并为设计未来的软机器人材料和功能生物材料提供了充足的机会。