Controlled Radical Polymerization: from Oxygen Inhibition and Tolerance to Oxygen Initiation

被引:43
|
作者
Li, Ning [1 ]
Pan, Xiang-Cheng [1 ]
机构
[1] Fudan Univ, Dept Macromol Sci, State Key Lab Mol Engn Polymers, Shanghai 200438, Peoples R China
基金
中国国家自然科学基金;
关键词
Oxygen; Radical polymerization; Controlled; Alkylborane; RAFT; WELL-DEFINED POLYMERS; AGET ATRP; LIVING POLYMERIZATION; ELECTRON-TRANSFER; IRON CATALYST; RAFT; LIGHT; METHACRYLATE; CHEMISTRY;
D O I
10.1007/s10118-021-2597-9
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Molecular oxygen is a radical scavenger in both conventional and controlled radical polymerization (CRP), resulting in many time-consuming methods for physically removing oxygen before the polymerization. Different approaches have been developed to have oxygen tolerance by chemically consuming or converting molecular oxygen into non-initiating species to address this issue. Recently, we propose another approach called oxygen initiation that directly transforms molecular oxygen into the initiating carbon radical in CRP. This feature article summarizes our recent developments in this direction. Oxygen-initiated reversible addition-fragmentation transfer (RAFT) polymerization has been successfully conducted using oxygen and trialkylborane as co-initiators under the ambient conditions and atmosphere without any prior degassed procedures. This gas-triggered initiation provides the opportunity for spatiotemporal control of the polymerization by molecular oxygen or air. Rationally synthesized alkylborane compounds could derive the predesigned structure of the initiating alkyl radical to minimize the side reactions and free polymer chains, achieving the synthesis of ultra-high molecular weight polymers. The challenges and perspectives are also discussed in the end.
引用
收藏
页码:1084 / 1092
页数:9
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