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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 (PAM n and PMA n ) 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 PAM n 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 PMA n polymer recovered completely. Notably, the PAM n and PMA n 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 PAM 34 and PMA 34 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 PAM 34 and PMA 34 polymer vesicles to perform the controlled release and reversible loading of a fluorescent probe was evaluated.
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Li et al. (2022) studied this question.
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