Synthesis and self-assembly of a dual-responsive monocleavable ABCD star quaterpolymer
作者：Huanhuan Liu, Jian Zhang, Wenxue Dai, Youliang Zhao*
關(guān)鍵字：star polymer, self-assembly
論文來源：期刊
具體來源：Polym. Chem., 2017, 8, 6865-6878
發(fā)表時(shí)間：2017年
ABCD star quaterpolymers acquired by precision synthesis may provide us with insights into self-assembly due to their fused architectures of di?erent arm segments and a central core. Considering the crucial role of external stimuli in smart materials, the aims of this study are the facile synthesis of a pH/redox-responsive 4-arm miktoarm star and the study of its stimuli-dependent aggregation behaviors. A click reaction between azide/bromine-functionalized poly(ethylene glycol)-block-polystyrene (PEG-b-PSt) and alkyne/ disul?de-functionalized poly(ε-caprolactone)-block-poly(tert-butyl acrylate) (PCL-b-PtBA) and subsequent selective hydrolysis were used to synthesize the target star with bromomethyl and disul?de functionalities in the core and a poly(acrylic acid) (PAA) segment. The PEG-PSt-PCL-PAA star can self-assemble into nanocapsules with hollow caves; the sizes and morphologies of these assemblies are dependent on pH and reductive stimuli due to stimuli-tunable destabilization and reassembly. By virtue of polyion and hydrogen bonding complexation using a partly quaternized copolymer, the nanocapsules can be further converted into versatile coaggregates such as compound vesicles and micelles, multicompartment vesicles, and hyperbranched micelles. Our research a?ords a robust method to synthesize corefunctionalized stimuli-labile multicomponent miktoarm stars; these stimuli-responsive nanocapsules hold great promise in smart biomedical and interfacial materials.