偶氮苯
聚合物
两亲性
小泡
吸光度
材料科学
光化学
聚乙二醇
胶束
辐照
高分子化学
松香
化学工程
化学
共聚物
有机化学
色谱法
水溶液
复合材料
核物理学
工程类
物理
生物化学
膜
树脂酸
作者
Wanbing Li,Haibo Zhang,Zhaolan Zhai,Xujuan Huang,Shibin Shang,Zhanqian Song
标识
DOI:10.1021/acs.jafc.2c04389
摘要
Designing stimulus-responsive amphiphilic polymers with a fast photoresponsive self-assembly behavior remains a challenge. Two series of rosin-terminated and azobenzene-terminated amphiphilic polymers (PAMn and PMAn) with fast and reversible photoresponsive properties were prepared using rosin-based azobenzene groups and polyethylene glycol, respectively. Under 5-10 s of UV irradiation, the polymers showed trans-to-cis isomerization and reached a photosteady state. For the PAMn polymer, the absorbance of the absorption peak at 325 nm recovered to more than 95% of the initial value under visible light for 5-10 s, whereas that of the PMAn polymer recovered completely. Notably, the PAMn and PMAn polymers initially self-assembled to vesicles or spherical micelles, and various morphological changes were achieved by manipulating UV irradiation time, with the initial morphology again recovered under dark conditions or visible-light irradiation. Remarkably, vesicles of the PAM34 and PMA34 polymers presented an intermediate open-vesicle state before being completely deformed under UV irradiation because of the existence of a π-π interaction. Finally, the ability of PAM34 and PMA34 polymer vesicles to perform the controlled release and reversible loading of a fluorescent probe was evaluated.
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