4.8 Article

Effects of connecting sequences of building blocks on reticular synthesis of covalent organic frameworks

期刊

NANO RESEARCH
卷 14, 期 2, 页码 381-386

出版社

TSINGHUA UNIV PRESS
DOI: 10.1007/s12274-020-2723-y

关键词

reticular chemistry; covalent organic framework; connecting sequence; building block

资金

  1. National Natural Science Foundation of China [21632004, 51578224]
  2. Strategic Priority Research Program of the Chinese Academy of Sciences [XDB20020000]
  3. Key Laboratory of Synthetic and Self-Assembly Chemistry for Organic Functional Molecules, Chinese Academy of Sciences [K2018-2]
  4. Hunan Provincial Innovation Foundation for Postgraduate [CX2016B119]

向作者/读者索取更多资源

The principle of reticular chemistry is widely used in designing crystalline porous materials like MOFs and COFs. Recent research has shown that the connecting sequence of building blocks plays a crucial role in determining the crystalline structures of COFs. The article establishes a model system to demonstrate the impact of different connecting sequences on COFs structures and verifies it through target synthesis.
The principle of reticular chemistry has been widely used to guide the design of crystalline porous materials such as metal organic frameworks (MOFs) and covalent organic frameworks (COFs). While in the early strategies only the symmetries of the building blocks were considered for reticular synthesis of COFs, recently a few researches on COFs with hierarchical porosities indicate that connecting sequence of building blocks also plays a crucial role in determining crystalline structures of COFs. However, this important phenomenon has not been systematically investigated yet. In this article, a model system has been established to demonstrate how different connecting sequences of two C-2V-symmetric building blocks lead to the formation of four two-dimensional (2D) COFs with distinct framework structures. To verify this concept, target synthesis was conducted to produce three COFs, whose structures were confirmed by powder X-ray diffraction and pore size distribution analysis.

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