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通过立体选择性后合成溴化作用实现金属有机骨架的单晶到单晶机械收缩。

Single-Crystal to Single-Crystal Mechanical Contraction of Metal-Organic Frameworks through Stereoselective Postsynthetic Bromination.

机构信息

WestChem School of Chemistry, University of Glasgow, University Avenue, Glasgow G12 8QQ, U.K.

出版信息

J Am Chem Soc. 2015 Aug 5;137(30):9527-30. doi: 10.1021/jacs.5b05434. Epub 2015 Jul 21.

Abstract

The properties of metal-organic frameworks (MOFs) can be tuned by postsynthetic modification (PSM) to introduce specific functionalities after their synthesis. Typically, PSM is carried out on pendant functional groups or through metal/ligand exchange, preserving the structure of the MOF. We report herein the bromination of integral alkyne units in a pair of Zr(4+) and Hf(4+) MOFs, which proceeds stereoselectively in a single-crystal to single-crystal manner. The chemical and mechanical changes in the MOFs are extensively characterized, including the crystal structures of the postsynthetically brominated materials, which show a mechanical contraction of up to 3.7% in volume. The combination of stability and chemical reactivity in these MOFs leads to the possibility of tuning mechanical properties by chemical transformation while also opening up new routes to internal pore functionalization.

摘要

金属-有机骨架(MOFs)的性质可以通过后合成修饰(PSM)进行调节,在合成后引入特定的功能。通常,PSM 是在悬垂官能团上进行的,或者通过金属/配体交换进行,从而保留 MOF 的结构。本文报道了一对 Zr(4+)和 Hf(4+) MOFs 中整炔基单元的溴化反应,该反应以单晶到单晶的方式进行立体选择性。对 MOFs 的化学和机械变化进行了广泛的表征,包括后合成溴化材料的晶体结构,其体积收缩高达 3.7%。这些 MOFs 中稳定性和化学反应性的结合使得通过化学转化来调节机械性能成为可能,同时也为内部孔功能化开辟了新途径。

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