Interconvertible Living Radical and Cationic Polymerization through Reversible Activation of Dormant Species with Dual Activity

被引:84
作者
Aoshima, Hiroshi [1 ]
Uchiyama, Mineto [1 ]
Satoh, Kotaro [1 ]
Kamigaito, Masami [1 ]
机构
[1] Nagoya Univ, Grad Sch Engn, Dept Appl Chem, Chikusa Ku, Nagoya, Aichi 4648603, Japan
基金
日本学术振兴会;
关键词
block copolymers; copolymerization; dual activity; thioesters; DIRECT MECHANISTIC TRANSFORMATION; BLOCK-COPOLYMERS; METHYL-METHACRYLATE; P-METHOXYSTYRENE; COMBINATION; STYRENE; ETHER;
D O I
10.1002/anie.201406590
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The polymerization of vinyl monomers generally requires the selection of an appropriate single intermediate, whereas in copolymerization, the selection of the comonomer is limited by the intermediate. Herein, we propose interconvertible dual active species that can connect comonomers through different mechanisms to produce specific comonomer sequences in a single polymer chain. More specifically, two different stimuli, that is, a radical initiator and a Lewis acid, are used to activate the common dormant C-SC(S)Z group into radical and cationic species, thereby inducing interconvertible radical and cationic copolymerization of acrylate and vinyl ether to produce a copolymer chain that consists of radically and cationically polymerized segments. The dual reversible activation provides control over molecular weights and multiblock copolymers with tunable segment lengths.
引用
收藏
页码:10932 / 10936
页数:5
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