链烷
炔烃
点击化学
化学
高分子化学
聚合
单体
乙二醇
聚合物
有机化学
分子
催化作用
作者
Jinsa Li,Rui Hu,Ziqing Hu,Shaoyu Xu,Ao Yu,Xiaofan Ji
出处
期刊:Macromolecules
[American Chemical Society]
日期:2024-04-10
卷期号:57 (8): 3824-3830
被引量:5
标识
DOI:10.1021/acs.macromol.4c00431
摘要
Due to the combination of flexibility and mobility, polycatenanes have the potential in constructing various functional materials. To date, most of the previous works have reported poly[2]catenanes with a degree of polymerization (DP) of around 20. However, it remains a significant challenge to synthesize poly[2]catenanes with a higher DP value. Hydroxyl–yne click polymerization, bearing the merits of obtaining polymers with high DP values, short reaction time, and mild condition, is promising to be employed in preparing poly[2]catenanes with high DP values. Herein, a strategy using hydroxyl–yne click chemistry to fabricate poly[2]catenanes was proposed. With two hydroxyl groups on both the rings, [2]catenane monomer M1 was prepared. Meanwhile, hexaethylene glycol was alkyne functionalized as M2. With bicyclo[2.2.2]-1,4-diazaoctane (DABCO) catalyzing, M1 and M2 reacted via a hydroxyl–yne click reaction at room temperature. The DP of resultant poly[2]catenane reached up to 36. In addition, tetraphenylethylene (TPE) was modified with propiolic acid to obtain M3. Then, poly([2]catenane-alt-TPE) with aggregation-induced emission (AIE) properties was obtained via the polymerization between M1 and M3 as well.
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