A novel solid state photocatalyst for living radical polymerization under UV irradiation

被引:28
|
作者
Fu, Qiang [1 ]
McKenzie, Thomas G. [1 ]
Ren, Jing M. [1 ]
Tan, Shereen [1 ]
Nam, Eunhyung [1 ]
Qiao, Greg G. [1 ]
机构
[1] Univ Melbourne, Polymer Sci Grp, Dept Chem & Biomol Engn, Melbourne, Vic 3010, Australia
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
基金
澳大利亚研究理事会;
关键词
FRAGMENTATION CHAIN-TRANSFER; RAFT POLYMERIZATION; LIGHT; XANTHATE;
D O I
10.1038/srep20779
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
This study presents the development of a novel solid state photocatalyst for the photoinduced controlled radical polymerization of methacrylates under mild UV irradiation (lambda(max) approximate to 365 nm) in the absence of conventional photoinitiators, metal-catalysts or dye sensitizers. The photocatalyst design was based on our previous finding that organic amines can act in a synergistic photochemical reaction with thiocarbonylthio compounds to afford well controlled polymethacrylates under UV irradiation. Therefore, in the current contribution an amine-rich polymer was covalently grafted onto a solid substrate, thus creating a heterogeneous catalyst that would allow for facile removal, recovery and recyclability when employed for such photopolymerization reactions. Importantly, the polymethacrylates synthesized using the solid state photocatalyst (ssPC) show similarly excellent chemical and structural integrity as those catalysed by free amines. Moreover, the ssPC could be readily recovered and re-used, with multiple cycles of polymerization showing minimal effect on the integrity of the catalyst. Finally, the ssPC was employed in various photo-"click" reactions, permitting high yielding conjugations under photochemical control.
引用
收藏
页数:11
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