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All-Carbon-Linked Continuous Three-Dimensional Porous Aromatic Framework Films with Nanometer-Precise Controllable Thickness

机译:具有纳米精确可控制厚度的全碳键连续三维多孔芳香骨架膜

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摘要

Inherently porous materials that are chemically and structurally robust are challenging to construct. Conventionally, dynamic chemistry is thought to be needed for the formation of uniform porous organic frameworks, but dynamic bonds can limit the stability of these materials. For this reason, all-carbon-linked frameworks are expected to exhibit higher stability performance than more traditional porous frameworks. However, the limited reversibility of carbon-carbon bond-forming reactions has restricted the exploration of these materials. In particular, the challenges associated with producing uniform thin films of all-carbon-linked frameworks has inhibited the study of these materials in applications where well-defined films are required. Here, we synthesize continuous and homogeneous films of two different all-carbon-linked three-dimensional porous aromatic frameworks with nanometer-precision thickness (PAF-1 and BCMP-2). This was accomplished by kinetically promoting surface reactivity while suppressing homogeneous nucleation. Through connection of the PAF film to a gold substrate via a self-assembled monolayer and use of flow conditions to continually introduce monomers, smooth and continuous PAF films can be grown with controlled thickness. This strategy allows traditional transition metal mediated carbon-carbon cross-coupling reactions to form porous, organic thin films. We expect that the chemical principles uncovered in this study will enable the synthesis of a variety of chemically and structurally diverse carbon-carbon-linked frameworks as high-quality films, which are inaccessible by conventional methods.
机译:具有化学和结构坚固性的固有多孔材料难以制造。通常,动态化学被认为是形成均匀的多孔有机骨架所必需的,但是动态键会限制这些材料的稳定性。因此,与传统的多孔骨架相比,全碳连接骨架有望表现出更高的稳定性能。但是,碳-碳键形成反应的可逆性有限,限制了对这些材料的探索。尤其是,与生产全碳连接框架的均匀薄膜相关的挑战已阻碍了在需要清晰膜的应用中对这些材料的研究。在这里,我们合成了具有纳米精度厚度的两种不同的全碳连接的三维多孔芳香族骨架(PAF-1和BCMP-2)的连续且均匀的膜。这是通过动力学促进表面反应性同时抑制均相成核来实现的。通过将PAF膜通过自组装单层连接到金基底上,并使用流动条件连续引入单体,可以在受控的厚度下生长光滑连续的PAF膜。该策略允许传统的过渡金属介导的碳-碳交叉偶联反应形成多孔的有机薄膜。我们希望本研究中发现的化学原理将能够合成各种化学和结构多样的碳-碳连接的骨架,如传统方法无法获得的高质量薄膜。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2020年第14期|6548-6553|共6页
  • 作者单位

    Department of Chemistry and Molecular Biology University of Gothenburg 412 96 Goeteborg Sweden;

    Department of Chemistry and Molecular Biology University of Gothenburg 412 96 Goeteborg Sweden;

    Division of Energy and Environmental Measurement National Institute of Metrology China NIM Beijing 100013 P.R. China;

    Department of Chemistry Northwestern University Evanston Illinois 60208 United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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  • 入库时间 2022-08-18 05:28:38

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