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Synthesis of Terpyridine-Terminated Amphiphilic Block Copolymers and Their Self-Assembly into Metallo-Polymer Nanovesicles

机译:联吡啶终止的两亲嵌段共聚物的合成及其自组装成金属聚合物纳米囊泡。

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摘要

Polystyrene-b-polyethylene glycol (PS-b-PEG) amphiphilic block copolymers featuring a terminal tridentate N,N,N-ligand (terpyridine) were synthesized for the first time through an efficient route. In this approach, telechelic chain-end modified polystyrenes were produced via reversible addition-fragmentation chain-transfer (RAFT) polymerization by using terpyridine trithiocarbonate as the chain-transfer agent, after which the hydrophilic polyethylene glycol (PEG) block was incorporated into the hydrophobic polystyrene (PS) block in high yields via a thiol-ene process. Following metal-coordination with Mn2+, Fe2+, Ni2+, and Zn2+, the resulting metallo-polymers were self-assembled into spherical, vesicular nanostructures, as characterized by dynamic light scattering and transmission electron microscopy (TEM) imaging.
机译:通过有效途径首次合成了具有末端三齿N,N,N-配体(三吡啶)的聚苯乙烯-b-聚乙二醇(PS-b-PEG)两亲嵌段共聚物。在这种方法中,通过使用三硫代吡啶碳吡啶作为链转移剂,通过可逆的加成-断裂链转移(RAFT)聚合反应生产远螯链末端改性的聚苯乙烯,然后将亲水性聚乙二醇(PEG)嵌段引入疏水性聚苯乙烯(PS)通过硫醇-烯工艺以高收率嵌段。与Mn 2 + ,Fe 2 + ,Ni 2 + 和Zn 2 + 进行金属配位后,通过动态光散射和透射电子显微镜(TEM)成像,可以将所得的金属聚合物自组装成球形,囊状纳米结构。

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