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Gold@Polymer Nanostructures with Tunable Permeability Shells for Selective Catalysis

机译:具有可调节渗透性壳的金@聚合物纳米结构,用于选择性催化

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摘要

We have introduced a novel "outside-in" route to encapsulate Au NPs in mesoporous polymer shells. By simply adjusting the reaction time, Au@polymer nano-structures with controllable permeability shells were obtained. As the mesoporous shell allows the materials exchange between inner core and environment, secondary growth of the encapsulated Au NPs can be easily realized. This advantage makes the diameter of the Au core controllable. More importantly, the hydrophobic mesoporous shell endows the Au@polymer nanostruclure with selective catalytic activity. Only hydrophobic molecules can pass through the hydrophobic shell and be catalyzed by the encapsulated Au NP. We believe that this "outside-in" route may be of interest in encapsulating metal NEs in mesoporous polymer shells, and the selective catalytic activity of this type of Au@polymer nanostructure may prove to be useful in the field of selective catalysis.
机译:我们已经引入了一种新颖的“由内而外”的途径,将金纳米颗粒包裹在中孔聚合物壳中。通过简单地调节反应时间,获得具有可控渗透性壳的Au @聚合物纳米结构。由于中孔壳允许内核和环境之间的材料交换,因此可以容易地实现包封的Au NPs的二次生长。该优点使得Au芯的直径可控。更重要的是,疏水性介孔壳赋予Au @聚合物纳米结构以选择性催化活性。只有疏水分子才能通过疏水壳,并被包封的Au NP催化。我们认为,这种“由外而内”的途径可能是将金属NEs包封在介孔聚合物壳中的兴趣所在,这种类型的Au @聚合物纳米结构的选择性催化活性可能被证明在选择性催化领域很有用。

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