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Introduction of Functionalized Mesopores to Metal-Organic Frameworks via Metal-Ligand-Fragment Coassembly

机译:通过金属配体-片段共组装将功能化介孔引入金属有机骨架

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摘要

Introduction of functionalized mesopores into microporous metal-organic frameworks (MOFs) can endow them with suitable properties for applications in gas storage, separation, catalysis, and drug delivery. However, common methods for functionalization (including pre- and post-synthetic modifications) of the internal surface of a MOF reduce the pore size of the MOF because the additional functional groups fill up the pores. We present a metal-ligand-fragment coassembly strategy for the introduction of (meso)pores functionalized with various substituent groups on the ligand fragments. Astonishingly, this new functionalization strategy increases the pore volume of a MOF instead of reducing it. Since the ligand fragments are often readily available or easily prepared, the new procedure for synthesis of the modified MOFs becomes much easier and more applicable than existing approaches. Remarkably, mesopores can be generated conveniently and controllably by the coassembly of a ligand and its fragment containing the desired functional groups. The fragment/ligand ratio has been optimized to preserve the parent structure and to promote maximum mesopore introduction, which has led to a systematic evaluation of the effectiveness of a series of functional groups for the adsorption of guest molecules.
机译:将功能化的中孔引入微孔金属有机骨架(MOF)可使它们具有适合在气体存储,分离,催化和药物输送中应用的特性。但是,用于MOF内表面的功能化(包括合成前和合成后修饰)的常用方法会降低MOF的孔径,因为附加的官能团会填满孔。我们提出了一种金属-配体-片段共组装策略,用于引入在配体片段上被各种取代基官能化的(介)孔。令人惊讶的是,这种新的功能化策略增加了MOF的孔体积,而不是减小了它。由于配体片段通常容易获得或易于制备,因此与现有方法相比,用于合成修饰的MOF的新方法变得更加容易和适用。值得注意的是,中孔可以通过配体及其包含所需官能团的片段的共组装而方便且可控地产生。已优化片段/配体比率,以保留母体结构并促进最大程度的中孔引入,从而导致系统评估了一系列官能团对客体分子吸附的有效性。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2012年第49期|20110-20116|共7页
  • 作者单位

    Department of Chemistry, Texas A&M University, P.O. Box 30012, College Station, Texas 77842-3012, United States;

    Department of Chemistry, Texas A&M University, P.O. Box 30012, College Station, Texas 77842-3012, United States;

    Department of Chemistry, Texas A&M University, P.O. Box 30012, College Station, Texas 77842-3012, United States;

    Department of Chemistry, Texas A&M University, P.O. Box 30012, College Station, Texas 77842-3012, United States;

    Department of Chemistry, Texas A&M University, P.O. Box 30012, College Station, Texas 77842-3012, 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
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  • 入库时间 2022-08-18 03:13:40

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