聚合
链式转移
聚合物
可逆加成-断裂链转移聚合
材料科学
光催化
水溶液
木筏
单体
自由基聚合
高分子化学
化学工程
光化学
化学
有机化学
催化作用
工程类
复合材料
作者
Jiyuan Sun,Shusu Ren,Haitao Zhao,Shunhu Zhang,Xiang Xu,Lifen Zhang,Zhenping Cheng
出处
期刊:ACS Macro Letters
[American Chemical Society]
日期:2023-01-19
卷期号:12 (2): 165-171
被引量:20
标识
DOI:10.1021/acsmacrolett.2c00708
摘要
In order to give an answer for the challenges of long wavelength-photocontrolled radical polymerization in aqueous solutions and to address the shortcomings of conventional near-infrared (NIR) photocatalysts (PCs) that are difficult to subject to post-treatment, we designed and synthesized a series of β-tetra-substituted water-soluble zinc phthalocyanines (β-TS-Zns) as the NIR PCs for reversible addition-fragmentation chain transfer (RAFT) polymerization successfully under irradiation with NIR (λmax = 730 nm) light at room temperature. Importantly, the NIR PCs can also be designed as polymerizable monomers and covalently loaded on the polymer chains, which are endowed with permanent NIR photocatalysis of the resultant polymers. Moreover, the polymerization can not only be carried out in water but also in phosphate buffer saline (PBS) solution, yielding polymers with controlled molar mass and narrow dispersities (Đ = 1.03-1.25). Therefore, this NIR-photocontrolled aqueous RAFT polymerization system may provide a charming strategy for possible applications in tissue engineering biomaterial in situ benefiting from the high penetration ability of NIR light.
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