战术性
化学
聚丙烯
聚合
链式转移
高分子化学
链条(单位)
高分子科学
化学工程
聚合物
自由基聚合
有机化学
物理
天文
工程类
作者
Zong-Lun Yu,Xingwang Han,Peizhi Li,Yanan Zhao,Xun Zhang,Xiu‐Li Sun,Yanshan Gao,You‐Yun Zhou,Yong Tang
摘要
While synthesizing circular polymers with telechelic polyolefin building blocks recently emerged as a promising strategy for addressing conventional polyethylenes' sustainability challenges, the lack of telechelic iPP (tPP) with sufficient difunctional purity for polycondensation has been limiting the development of circular polypropylenes with iPP-like structures and properties. Here we described a combined approach of coordinative chain transfer polymerization and transition-metal-catalyzed quenching reaction with various acyl chlorides, affording tPPs with a high difunctional ratio (up to ∼99%) and broad end functional group scope. The steric effect of polymeryl-Zn species and the role of Pd catalyst were revealed by DFT. This method also solved the low difunctional ratio challenge for telechelic polyethylenes. Ester-linked iPPs with iPP-like structure and thermomechanical properties and PE/iPP multiblock copolymers were synthesized by the resulting tPPs.
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