

FOLLOWUS
State Key Laboratory of Molecular Engineering of Polymers, Department of Macromolecular Science, Fudan University, Shanghai 200438, China
panxc@fudan.edu.cn
Received:29 March 2021,
Revised:2021-4-19,
Accepted:20 April 2021,
Online First:22 July 2021,
Published:18 July 2021
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Li, N.; Pan, X. C. Controlled radical polymerization: from oxygen inhibition and tolerance to oxygen initiation. Chinese J. Polym. Sci. 2021, 39, 1084–1092
Ning Li, Xiang-Cheng Pan. Controlled Radical Polymerization: from Oxygen Inhibition and Tolerance to Oxygen Initiation[J]. Chinese Journal of Polymer Science, 2021, 39(9): 1084-1092.
Li, N.; Pan, X. C. Controlled radical polymerization: from oxygen inhibition and tolerance to oxygen initiation. Chinese J. Polym. Sci. 2021, 39, 1084–1092 DOI: 10.1007/s10118-021-2597-9.
Ning Li, Xiang-Cheng Pan. Controlled Radical Polymerization: from Oxygen Inhibition and Tolerance to Oxygen Initiation[J]. Chinese Journal of Polymer Science, 2021, 39(9): 1084-1092. DOI: 10.1007/s10118-021-2597-9.
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.
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