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Effective Mercury Sorption by Thiol-Laced Metal-Organic Frameworks: in Strong Acid and the Vapor Phase

机译:硫醇系金属有机骨架对汞的有效吸附:在强酸和气相中

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摘要

Free-standing, accessible thiol (-SH) functions have been installed in robust, porous coordination networks to provide wide-ranging reactivities and properties in the solid state. The frameworks were assembled by reacting ZrCl_4 or A1C1_3 with 2,5-dimercapto-1,4-benzenedicarboxylic acid (H_2DMBD), which features the hard carboxyl and soft thiol functions. The resultant Zr-DMBD and Al-DMBD frameworks exhibit the UiO-66 and CAU-1 topologies, respectively, with the carboxyl bonded to the hard Zr(Ⅳ) or Al(Ⅲ) center and the thiol groups decorating the pores. The thiol-laced Zr-DMBD crystals lower the Hg(Ⅱ) concentration in water below 0.01 ppm and effectively take up Hg from the vapor phase. The Zr-DMBD solid also features a nearly white photoluminescence that is distinctly quenched after Hg uptake. The carboxyl/thiol combination thus illustrates the wider applicability of the hard-and-soft strategy for functional frameworks.
机译:独立的,易接近的硫醇(-SH)功能已安装在坚固的多孔配位网络中,以提供广泛的固态反应性和性能。通过使ZrCl_4或AlCl3_3与具有硬羧基和软硫醇功能的2,5-二巯基-1,4-苯二甲酸(H_2DMBD)反应来组装骨架。生成的Zr-DMBD和Al-DMBD骨架分别表现出UiO-66和CAU-1拓扑结构,羧基键合到硬Zr(Ⅳ)或Al(Ⅲ)中心,硫醇基修饰孔。硫醇包覆的Zr-DMBD晶体将水中的Hg(Ⅱ)浓度降低到0.01 ppm以下,并有效地从气相吸收Hg。 Zr-DMBD固体还具有近白色的光致发光特性,在吸收Hg后会明显淬灭。因此,羧基/硫醇的结合说明了功能框架的硬策略和软策略的更广泛的适用性。

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  • 来源
    《Journal of the American Chemical Society》 |2013年第21期|7795-7798|共4页
  • 作者单位

    Department of Biology and Chemistry, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong, China;

    Institut fuer Anorganische Chemie, Christian-Albrechts Universitat, Max-Eyth-Str. 2, 24118 Kiel, Germany;

    Department of Biology and Chemistry, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong, China;

    Department of Biology and Chemistry, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong, China;

    Department of Biology and Chemistry, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong, China;

    Department of Colloid Chemistry, Max Planck Institute of Colloids and Interfaces, Research Campus Golm, 14476 Golm, Germany;

    Institut fuer Anorganische Chemie, Christian-Albrechts Universitat, Max-Eyth-Str. 2, 24118 Kiel, Germany;

    Department of Biology and Chemistry, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong, China;

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