链式转移
木筏
可逆加成-断裂链转移聚合
聚合
黄药
聚合物
材料科学
活性聚合
高分子化学
自由基聚合
复合材料
作者
Stephanie Allison‐Logan,Fatemeh Karimi,Yongkang Sun,Thomas G. McKenzie,Mitchell D. Nothling,Gary Bryant,Greg G. Qiao
出处
期刊:ACS Macro Letters
[American Chemical Society]
日期:2019-09-20
卷期号:8 (10): 1291-1295
被引量:62
标识
DOI:10.1021/acsmacrolett.9b00643
摘要
Star polymers are highly functional materials that display unique properties in comparison to linear polymers, making them valuable in a wide range of applications. Currently, ultra-high molecular weight (UHMW) star polymers synthesized using controlled radical polymerization are prone to termination reactions that have undesirable effects, such as star-star coupling. Herein, we report the synthesis of the largest star polymers to date using controlled radical techniques via xanthate-mediated photo-reversible addition-fragmentation chain transfer (RAFT) polymerization using a core-first approach. Polymerization from xanthate-functionalized cores was highly living, enabling the synthesis of well-defined star polymers with molecular weights in excess of 20 MDa.
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