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A generalizable method for the construction of MOF@polymer functional composites through surface-initiated atom transfer radical polymerization

机译:通过表面引发的原子转移自由基聚合构建MOF @聚合物功能复合材料的通用方法

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摘要

We report a generalizable approach to construct MOF@polymer functional composites through surface-initiated atom transfer radical polymerization (SI-ATRP). Unlike conventional SI-ATRP that requires covalent pre-anchoring of the initiating group on substrate surfaces, in our approach, a rationally designed random copolymer (RCP) macroinitiator first self-assembles on MOF surfaces through inter-chain hydrogen bond crosslinking. Subsequent polymerization in the presence of a crosslinking monomer covalently threads these polymer chains into a robust network, physically confining the MOF particle inside the polymer shell. We demonstrated the universality of this approach by growing various polymers on five MOFs of different metals (Zr, Zn, Co, Al, and Cr) with complete control over shell thickness, functionality and layer sequence while still retaining the inherent porosity of the MOFs. Moreover, the wettability of UiO-66 can be continuously tuned from superhydrophilic to superhydrophobic simply through judicious monomer(s) selection. We also demonstrated that a 7 nm polystyrene shell can effectively shield UiO-66 particles against 1 M H2SO4 and 1 M NaOH at elevated temperature, enabling their potential application in demanding chemical environments.
机译:我们报告了一种通过表面引发的原子转移自由基聚合(SI-ATRP)构建MOF @聚合物功能复合材料的通用方法。与传统的SI-ATRP需要在基材表面上共价预固定引发基团不同,在我们的方法中,合理设计的无规共聚物(RCP)大分子引发剂首先通过链间氢键交联在MOF表面上自组装。随后在交联单体存在下的聚合将这些聚合物链共价键合到一个牢固的网络中,从而将MOF颗粒物理地限制在聚合物壳内部。我们通过在五种不同金属(Zr,Zn,Co,Al和Cr)的MOF上生长各种聚合物,并完全控制壳的厚度,功能和层序,同时仍保留MOF的固有孔隙率,证明了这种方法的普遍性。此外,仅通过明智的单体选择,就可以将UiO-66的润湿性从超亲水性连续调节为超疏水性。我们还证明了7 nm的聚苯乙烯壳可以在高温下有效屏蔽UiO-66颗粒使其免受1 M H2SO4和1 M NaOH的侵蚀,从而使其有可能在苛刻的化学环境中使用。

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