Biao Xia, Hartmut Komber, Sven M. Elbert, Michael Mastalerz and Junzhi Liu
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引用次数: 0
Abstract
The precise construction of three-dimensional (3D) carbon networks consisting solely of sp2 hybridized atoms has long been pursued in carbon nanoscience. Herein, we report the bottom-up synthesis of a covalently interlocked macrocycle ([2]CIM) featuring a molecular core of 31 benzene units. X-ray crystallography unambiguously confirmed the covalently interlocked structure of [2]CIM, revealing a rigid 3D architecture with inherent porosity. Its conformational rigidity and solid-state packing enable it to be a promising molecular porous material, exhibiting a specific surface area (SABET) of 507 m2 g−1. Gas absorption studies demonstrated the preferential adsorption of ethane (C2H6) over ethene (C2H4) by the phenyl-based covalently interlocked macrocycle. [2]CIM exhibits a unique gas separation performance among discrete phenyl-based porous macrocycles.
期刊介绍:
Materials Chemistry Frontiers focuses on the synthesis and chemistry of exciting new materials, and the development of improved fabrication techniques. Characterisation and fundamental studies that are of broad appeal are also welcome.
This is the ideal home for studies of a significant nature that further the development of organic, inorganic, composite and nano-materials.