偶氮苯
分子开关
胶束
材料科学
介观物理学
化学物理
层状结构
分子自组装
两亲性
纳米技术
化学
自组装
分子
结晶学
有机化学
物理
聚合物
共聚物
水溶液
量子力学
作者
Yiyang Lin,Xinhao Cheng,Yan Qiao,Cailan Yu,Zhibo Li,Yun Yan,Jianbin Huang
出处
期刊:Soft Matter
[The Royal Society of Chemistry]
日期:2010-01-01
卷期号:6 (5): 902-902
被引量:127
摘要
The creation of photo-modulated multi-state and multi-scale molecular self-assemblies was realized by the ingenuous utilization of a binary-state molecular switch, sodium (4-phenylazo-phenoxy)-acetate (AzoNa). Depending on the irradiation time, the binary state of the azobenzene group (i.e. trans/cis isomerization) can be exploited to generate multi-state nanostructures (including wormlike micelle, vesicle, lamellar structure, small micelle) by the coupling of conventional surfactant CTAB. Meanwhile, the conformation transition of azobenzene at molecular scale (∼Å), stimulated by light input can be amplified to regulate molecular architectures at mesoscopic scale (from nanometer to micrometer), leading to significant changes in solution property at macroscopic scale (naked-eye visible scale). By exposing to UV or visible light, the multi-state and multi-scale molecular self-assemblies can be reversibly controlled. It is proposed that light-triggered structural changes in the dipole moment and geometry of azobenzene group, which impart a significant effect upon molecular packing of surfactant aggregates, were responsible for this peculiar phenomenon.
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