截断2D框架材料到单个孔:合成方法和机会

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Phuong H. Le, Leo B. Zasada, Dianne J. Xiao
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引用次数: 0

摘要

在这篇文章中,我们总结了我们最近在截断共轭二维框架材料到单个孔或单个宏循环方面的工作。共轭二维结构已成为金属有机骨架(mof)和共价有机骨架(COFs)中耦合半导体性和多孔性的最具综合适应性的基序之一。然而,尽管它们很流行,2D架构仍有一些局限性。特别是,层间的强π -π堆积会限制可加工性和内部活性位点的可及性。我们发现,简单的大循环保留了2D框架结构和功能的关键方面,包括孔隙率和面外导电性,同时提供了改进的可加工性、表面可调节性和质量输运性。在本文中,我们首先描述我们的综合方法和一般设计注意事项。具体来说,我们展示了在二维mof和COFs合成中常见的三异位配体的双异位类似物如何用于实现在形式和功能上类似于半导体框架片段的各种共轭大环库。外围侧链的长度、芳香族核心的大小和中间体的溶解度都是有利于选择性形成大环而不是不需要的线性聚合物和低聚物的关键变量。接下来,我们强调了大循环提供的独特优势,包括改进的可加工性、原子精确的表面可调性和更大的活性位点可及性。特别是,外周侧链的特性极大地影响了溶解度和胶体稳定性,以及晶体的大小和形态。我们进一步展示了溶液可加工性和纳米尺度的大环如何简化电子器件的制造和提高电化学性能。最后,我们以前瞻性的讨论结束,讨论了大环如何在共轭分子和扩展框架之间提供独特的桥梁,从而实现新的应用领域和基础科学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Truncating 2D Framework Materials Down to a Single Pore: Synthetic Approaches and Opportunities

Truncating 2D Framework Materials Down to a Single Pore: Synthetic Approaches and Opportunities
In this Accounts article, we summarize our recent work on truncating conjugated two-dimensional framework materials down to a single pore, or a single macrocycle. Conjugated 2D architectures have emerged as one of the most synthetically adaptable motifs for coupling semiconductivity and porosity in metal–organic frameworks (MOFs) and covalent organic frameworks (COFs). However, despite their prevalence, 2D architectures have several limitations. In particular, the strong interlayer π–π stacking can limit both processability and the accessibility of internal active sites. We have found that simple macrocycles preserve key aspects of 2D framework structure and function, including porosity and out-of-plane electrical conductivity, while providing improved processability, surface tunability, and mass transport properties. In this article, we first describe our synthetic approach and general design considerations. Specifically, we show how ditopic analogues of the tritopic ligands commonly found in the synthesis of 2D MOFs and COFs can be used to achieve a diverse library of conjugated macrocycles that resemble fragments of semiconducting frameworks in both form and function. The length of the peripheral side chains, the size of the aromatic core, and the solubility of intermediates are all key variables in favoring selective macrocycle formation over undesired linear polymers and oligomers. Next, we highlight the unique advantages that macrocycles provide, including improved processability, atomically precise surface tunability, and greater active site accessibility. In particular, the identity of the peripheral side chains dramatically impacts both solubility and colloidal stability as well as crystal size and morphology. We further show how the solution processability and nanoscale dimensions of macrocycles can simplify electronic device fabrication and improve electrochemical performance. Finally, we end with a forward-looking discussion on how macrocycles offer a unique bridge between conjugated molecules and extended frameworks, enabling new application areas and fundamental science.
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来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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