Photoorganocatalyzed Divergent Reversible-Deactivation Radical Polymerization towards Linear and Branched Fluoropolymers

被引:56
|
作者
Zhao, Yucheng [1 ]
Ma, Mingyu [1 ]
Lin, Xinrong [2 ]
Chen, Mao [1 ]
机构
[1] Fudan Univ, Dept Macromol Sci, State Key Lab Mol Engn Polymers, Shanghai 200433, Peoples R China
[2] Yunnan Univ, Key Lab Med Chem Nat Resource, Minist Educ, Sch Chem Sci & Technol, Kunming 650091, Yunnan, Peoples R China
关键词
fluorine; photocatalysis; polymerization; synthetic methods; topology; HYPERBRANCHED POLYMERS; ELECTROLYTES; MONOMERS;
D O I
10.1002/anie.202009475
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Topology influences the properties and applications of polymers. Consequently, considerable efforts have been made to control topological structures. In this work, we have developed a photoorganocatalyzed divergent synthetic approach based on reversible-deactivation radical polymerization (RDRP) that enables the preparation of both linear and branched fluoropolymers of low dispersity (<SIC>), a tunable degree of branching and high chain-end fidelity by exposure to LED light irradiation under metal-free conditions. This method promotes the generation of complicated structures (e.g., necklace-like and mop-like fluoropolymers) via chain-extension photo-RDRP, and provides a novel and versatile platform to access fluoropolymer electrolytes with high Li-ion transference number and good ionic conductivity, which should create improved opportunities for advanced material engineering.
引用
收藏
页码:21470 / 21474
页数:5
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