Centre for Advanced Macromolecular Design, School of Chemical Engineering, The University of New South Wales, Sydney NSW 2052, Australia.
J Am Chem Soc. 2011 Jul 27;133(29):11128-31. doi: 10.1021/ja205080u. Epub 2011 Jun 30.
We report a new approach for the facile synthesis of high-order multiblock copolymers comprising very short blocks. The approach entails sequential addition of different monomers via an iterative single electron transfer-living radical polymerization technique, allowing nearly perfect control of the copolymer microstructure. It is possible to synthesize high-order multiblock copolymers with unprecedented control, i.e., A-B-C-D-E-etc., without any need for purification between iterative 24 h block formation steps. To illustrate this concept, we report the synthesis of model P(MA-b-MA...) homopolymer and P(MA-b-nBuA-b-EA-b-2EHA-b-EA-b-nBuA) copolymer in extremely high yield. Finally, the halide end-group can be modified via "click chemistry", including thiol-bromide click chemistry, sodium methanethiosulfonate nucleophilic substitution, and atom transfer radical nitroxide coupling reaction, to yield functional, structurally complex macromolecules.
我们报告了一种新的方法,可用于通过迭代单电子转移-活性自由基聚合技术轻松合成包含非常短链段的高阶多嵌段共聚物。该方法允许近乎完美地控制共聚物的微观结构,通过连续添加不同的单体。几乎可以在无需在迭代的 24 小时链段形成步骤之间进行纯化的情况下,以空前的控制合成高阶多嵌段共聚物,例如 A-B-C-D-E-等。为了说明这一概念,我们报告了模型 P(MA-b-MA...)均聚物和 P(MA-b-nBuA-b-EA-b-2EHA-b-EA-b-nBuA)共聚物的高产率合成。最后,卤化物端基可以通过“点击化学”进行修饰,包括巯基-溴点击化学、甲硫代硫酸钠的亲核取代反应和原子转移自由基氮氧自由基偶联反应,以得到功能化的、结构复杂的大分子。