原子转移自由基聚合
高分子化学
纳米颗粒
苯乙烯
丙烯腈
聚合物
配体(生物化学)
聚合
共聚物
化学
纳米复合材料
化学工程
锌
嫁接
材料科学
有机化学
纳米技术
生物化学
受体
工程类
作者
Zongyu Wang,Clare Mahoney,Jiajun Yan,Lu Zhao,Rachel Ferebee,Danli Luo,Michael R. Bockstaller,Krzysztof Matyjaszewski
出处
期刊:Langmuir
[American Chemical Society]
日期:2016-11-30
卷期号:32 (49): 13207-13213
被引量:32
标识
DOI:10.1021/acs.langmuir.6b03827
摘要
Poly(styrene- co -acrylonitrile) (PSAN)-capped ZnO nanoparticles (NPs) were synthesized by a “ligand exchange” method. First, octylamine (OA)-capped ZnO NPs were prepared by reaction of OA and zinc 2-ethylhexanoate (Zn(EH) 2 ). Then PSAN polymer ligands were synthesized by activators regenerated by electron transfer (ARGET) atom transfer radical polymerization (ATRP) and were efficiently exchanged with OA ligands on the ZnO particle surface benefiting from the relatively low boiling point of OA (175 °C). The morphology, content of ZnO, and grafting density of the nanocomposite were well controlled by altering the ratio between OA and polymer ligands as well as the molecular weight of PSAN-NH 2 used in the exchange reaction. The resulting ZnO/polymer nanocomposites were stable in THF with narrow size distributions and varying grafting densities from 0.9 to 2.5 nm –2 . With excess amount of polymer ligands, individual dispersed ZnO NPs were observed. However, with a limited amount of ligands, NPs clusters were formed, as confirmed by TEM and DLS.
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