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隐形银客体在一个使AgSb纳米点环化并沉积的框架中促进有序排列。

Invisible Silver Guests Boost Order in a Framework That Cyclizes and Deposits AgSb Nanodots.

作者信息

Cheng Shengxian, Xin Yinger, Hu Jieying, Feng Weijin, Ahn Dohyun, Zeller Matthias, He Jun, Xu Zhengtao

机构信息

Department of Chemistry, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong, China.

School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou, 510006, China.

出版信息

Inorg Chem. 2021 Apr 19;60(8):5757-5763. doi: 10.1021/acs.inorgchem.1c00012. Epub 2021 Mar 31.

DOI:10.1021/acs.inorgchem.1c00012
PMID:33787239
Abstract

The infusion of metal guests into (i.e., metalating) the porous medium of metal-organic frameworks (MOFs) is a topical approach to wide-ranging functionalization purposes. We report the notable interactions of AgSbF guests with the designer MOF host Zr [ZrO(OH)()(HO)]. (1) The heavy-atom guests of AgSbF induce order in the MOF host to allow the movable alkyne side arm to be fully located by X-ray diffraction, but they themselves curiously remain highly disordered and absent in the strucutral model. The enhanced order of the framework can be generally ascribed to interaction of the silver guests with the host alkyne and thioether functions, while the invisible heavy-atom guest represents a new phenomenon in the metalation of open framework materials. (2) The AgSbF guests also participate in the thermocyclization of the vicinal alkyne units of the linker (at 450 °C) and form the rare nanoparticle of AgSb supported on the concomitantly formed nanographene network. The resulted composite exhibits high electrical conductivity (1.0 S/cm) as well as useful, mitigated catalytic activity for selectively converting nitroarenes into the industrially important azo compounds, i.e., without overshooting to form the amine side products. The heterogeneous/cyclable catalysis entails only the cheap reducing reagents of NaBH, ethanol, and water, with yields being generally close to 90%.

摘要

将金属客体注入(即金属化)金属有机框架(MOF)的多孔介质中是一种用于广泛功能化目的的热门方法。我们报道了AgSbF客体与定制MOF主体Zr[ZrO(OH)()(HO)]之间的显著相互作用。(1)AgSbF的重原子客体在MOF主体中诱导有序,使得可移动的炔烃侧臂能够通过X射线衍射完全定位,但它们自身却奇怪地保持高度无序,并且在结构模型中不存在。框架有序性的增强通常可归因于银客体与主体炔烃和硫醚官能团的相互作用,而不可见的重原子客体代表了开放框架材料金属化中的一种新现象。(2)AgSbF客体还参与了连接体中邻位炔烃单元在450℃下的热环化反应,并形成了负载在同时形成的纳米石墨烯网络上的罕见AgSb纳米颗粒。所得复合材料表现出高电导率(1.0 S/cm)以及有用的、减轻的催化活性,可将硝基芳烃选择性地转化为工业上重要的偶氮化合物,即不会过度生成胺类副产物。这种多相/可循环催化仅需要NaBH、乙醇和水等廉价的还原剂,产率通常接近90%。

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