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单体官能团协同配位在催化插入聚合中的协同效应。

Synergetic Effect of Monomer Functional Group Coordination in Catalytic Insertion Polymerization.

机构信息

Chair of Chemical Materials Science, Department of Chemistry, University of Konstanz , 78464 Konstanz, Germany.

出版信息

J Am Chem Soc. 2017 May 24;139(20):6823-6826. doi: 10.1021/jacs.7b03087. Epub 2017 May 15.

Abstract

PhS- and PhNH-functionalized dienes are copolymerized efficiently with butadiene to stereoregular copolymers by [(mesitylene)Ni(allyl)][BAr] (Ni-1). Overall polymerization rates and comonomer incorporations depend strongly on the linker length between the diene moiety and functional group, in, e.g., PhS-(CH)C(═CH)-CH═CH (PhS-x-BD, x = 3-7), in particular for certain linker lengths high comonomer reactivity ratios stand out. This effect is related to a favorable binding of the comonomer to the active site comprising coordination of its functional group, which significantly enhances comonomer incorporation in the growing polymer chain.

摘要

PhS- 和 PhNH 功能化的二烯与丁二烯通过 [(mesitylene)Ni(allyl)][BAr](Ni-1)高效共聚形成立体规整共聚物。聚合速率和单体插入率强烈依赖于二烯部分和功能基团之间的连接链长度,例如 PhS-(CH)C(═CH)-CH═CH(PhS-x-BD,x = 3-7),特别是对于某些特定的连接链长度,单体的竞聚率非常高。这种效应与单体与包含其功能基团配位的活性位点的有利结合有关,这显著增强了单体在增长聚合物链中的插入。

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