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通过柱撑金属模板可调结构层实现金属有机骨架的等孔扩张:储氢和选择性 CO 捕获。

Isoreticular Expansion of Metal-Organic Frameworks via Pillaring of Metal Templated Tunable Building Layers: Hydrogen Storage and Selective CO Capture.

机构信息

Department of Chemistry, Indian Institute of Technology, Kharagpur, 721302, India.

Physical and Computational Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, 99352, USA.

出版信息

Chemistry. 2019 Nov 18;25(64):14500-14505. doi: 10.1002/chem.201902491. Epub 2019 Oct 21.

Abstract

The deliberate construction of isoreticular eea-metal-organic frameworks (MOFs) (Cu-eea-1, Cu-eea-2 and Cu-eea-3) and rtl-MOFs (Co-rtl-1 and Co-rtl-2) has been accomplished based on the ligand-to-axial pillaring of supermolecular building layers. The use of different metal ions resulted in two types of supermolecular building layers (SBLs): Kagome (kgm) and square lattices (sql) which further interconnect to form anticipated 3D-MOFs. The isoreticular expansion of (3,6)-connected Cu-MOFs has been achieved with desired eea-topology based on kgm building layers. In addition, two (3,6)-connected Co-rtl-MOFs were also successfully constructed based on sql building layers. The Cu-eea-MOFs were shown to act as hydrogen storage materials with appreciable amount of hydrogen uptake abilities. Moreover Cu-eea-MOFs have also exhibited remarkable CO capture ability at ambient condition compared to nitrogen and methane, due to the presence of amide functionalities.

摘要

基于超分子建筑层的轴向柱撑作用,成功构建了等孔 ee 金属有机骨架(MOFs)(Cu-eea-1、Cu-eea-2 和 Cu-eea-3)和 rtl-MOFs(Co-rtl-1 和 Co-rtl-2)。不同金属离子的使用产生了两种超分子建筑层(SBLs):Kagome(kgm)和正方形晶格(sql),它们进一步相互连接形成预期的 3D-MOFs。基于 kgm 建筑层,具有所需 eea 拓扑结构的(3,6)连接的 Cu-MOFs 实现了等孔扩展。此外,还基于 sql 建筑层成功构建了两个(3,6)连接的 Co-rtl-MOFs。Cu-eea-MOFs 被证明是储氢材料,具有相当数量的吸氢能力。此外,与氮和甲烷相比,由于存在酰胺官能团,Cu-eea-MOFs 在环境条件下也表现出显著的 CO 捕获能力。

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