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逐步自组装制备嵌段共聚物 PMOCs。

Block Co-PolyMOCs by Stepwise Self-Assembly.

机构信息

Department of Chemistry, Massachusetts Institute of Technology , 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.

John A. Paulson School of Engineering and Applied Sciences, Harvard University , Cambridge, Massachusetts 02138, United States.

出版信息

J Am Chem Soc. 2016 Aug 24;138(33):10708-15. doi: 10.1021/jacs.6b06712. Epub 2016 Aug 16.

Abstract

We report a stepwise assembly strategy for the integration of metal-organic cages (MOCs) into block copolymers (BCPs). This approach creates "block co-polyMOC" (BCPMOC) materials whose microscopic structures and mechanical properties are readily tunable by adjusting the size and geometry of the MOCs and the composition of the BCPs. In the first assembly step, BCPs functionalized with a pyridyl ligand on the chain end form star-shaped polymers triggered by metal-coordination-induced MOC assembly. The type of MOC junction employed precisely determines the number of arms for the star polymer. In the second step, microphase separation of the BCP is induced, physically cross-linking the star polymers and producing the desired BCPMOC networks in the bulk or gel state. We demonstrate that large spherical M12L24 MOCs, small paddlewheel M2L4 MOCs, or a mixture of both can be incorporated into BCPMOCs to provide materials with tailored branch functionality, phase separation, microdomain spacing, and mechanical properties. Given the synthetic and functional diversity of MOCs and BCPs, our method should enable access to BCPMOCs for a wide range of applications.

摘要

我们报告了一种逐步组装策略,用于将金属有机笼(MOC)整合到嵌段共聚物(BCP)中。这种方法创建了“嵌段共聚多金属氧酸盐”(BCPMOC)材料,其微观结构和机械性能可以通过调整 MOC 的大小和几何形状以及 BCP 的组成来轻松调节。在第一步组装中,链末端带有吡啶配体的 BCP 形成由金属配位诱导的 MOC 组装引发的星形聚合物。所采用的 MOC 连接类型精确地确定了星形聚合物的臂数。在第二步中,诱导 BCP 的微相分离,物理交联星形聚合物,并在本体或凝胶状态下产生所需的 BCPMOC 网络。我们证明可以将大的球形 M12L24 MOC、小的桨轮 M2L4 MOC 或两者的混合物掺入 BCPMOC 中,以提供具有定制支化功能、相分离、微区间距和机械性能的材料。鉴于 MOC 和 BCP 的合成和功能多样性,我们的方法应该能够为广泛的应用提供 BCPMOC。

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