首页> 外文期刊>Macromolecular chemistry and physics >A Facile Visible-Light-Induced Route to Functionalize Polymeric Substrates by Combining Controlled Radical Grafting Polymerization and Thiol?Yne Click Chemistry with Photoredox Catalyst Ir(ppy)_3
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A Facile Visible-Light-Induced Route to Functionalize Polymeric Substrates by Combining Controlled Radical Grafting Polymerization and Thiol?Yne Click Chemistry with Photoredox Catalyst Ir(ppy)_3

机译:通过将受控的自由基接枝聚合和硫氧hi点击化学与光氧化还原催化剂Ir(ppy)_3结合起来的一种简便的可见光诱导的途径,将聚合物基质功能化

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摘要

A novel strategy, based on surface-initiated grafting polymerization and post-polymerization thiol-yne click chemistry, with Ir(ppy)_3 as a sole photoredox catalyst, under visible light irradiation is developed. The “livingness” of the grafting polymerization is demonstrated by the linear increase of the graft yield with irradiation time and the block grafting polymerization. Then, acetenyl groups of poly(propargyl methacrylate) (PPMA) grafting chains are reacted with pentaerythritoltetra-(3-mercaptopropionate) via the thiol-yne click reaction. The successful introduction of reactive thiol groups onto the low-density polyethylene- graft -poly(propargyl methacrylate) (LDPE- g -PPMA) fi lms is demonstrated by Fourier transform IR (FTIR) and X-ray photoelectron spectra (XPS) spectroscopy, and the thiol-ene click reaction with N -(1-pyrenyl) maleimide.
机译:提出了一种基于表面引发的接枝聚合和后聚合硫醇-炔点击化学的新策略,该方法以Ir(ppy)_3作为唯一的光氧化还原催化剂。接枝聚合的“活性”通过辐照时间和嵌段接枝聚合随接枝产率的线性增加来证明。然后,使聚(甲基丙烯酸炔丙酯)(PPMA)接枝链的乙炔基与季戊四醇四-(3-巯基丙酸酯)通过硫醇-炔-点击反应进行反应。通过傅立叶变换红外光谱(FTIR)和X射线光电子能谱(XPS)证明了将反应性硫醇基团成功引入低密度聚乙烯-接枝-聚(甲基丙烯酸炔丙酯)(LDPE-g-PPMA)膜中, N-(1-吡啶基)马来酰亚胺的硫醇-烯点击反应。

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