N-Heterocyclic carbenes:: Effective organic catalysts for living polymerization

被引:128
作者
Dove, Andrew P.
Pratt, Russell C.
Lohmeijer, Bas G. G.
Culkin, Darcy A.
Hagberg, Eric C.
Nyce, Gregory W.
Waymouth, Robert M. [1 ]
Hedrick, James L.
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[2] IBM Almaden Res Ctr, San Jose, CA 95120 USA
基金
美国国家卫生研究院;
关键词
carbene; ring-opening polymerization; lactide;
D O I
10.1016/j.polymer.2006.02.037
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
An organocatalytic approach to living and condensation polymerization using N-heterocyclic carbenes as nucleophilic catalysts is detailed. The N-heterocyclic carbene catalyst platform is extremely versatile with the nature of the substituents having a pronounced effect upon catalyst stability and activity towards different substrates. Rapid screening of libraries of catalysts provided a basic understanding of catalyst structure (sterics, electronics, etc.) as it influences the polymerization rate, control, substrate and range of molecular weights. ROP from an immiscible ionic liquid (precatalyst reservoir) and a THF solution of monomer and initiator is presented as a simplified method of carbene formation. In situ activation of the ionic liquid generated a nucleophilic N-heterocyclic carbene, which migrates to the organic phase effecting ROP. Other simplified methods of generating carbene thermally from carbene adducts are also presented as polymerization catalysts. (c) 2006 Published by Elsevier Ltd.
引用
收藏
页码:4018 / 4025
页数:8
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