Separation of Xylene Isomers through Selective Inclusion: 1D → 2D, 1D → 3D, and 2D → 3D Assembled Coordination Polymers via β-Sheets

被引:21
|
作者
Nath, Karabi [1 ]
Biradha, Kumar [1 ]
机构
[1] Indian Inst Technol, Dept Chem, Kharagpur 721302, W Bengal, India
关键词
METAL-ORGANIC FRAMEWORKS; HYDROGEN-BONDS; HYDROCARBON SEPARATIONS; PHASE ADSORPTION; SMALL MOLECULES; AMIDE GROUPS; GAS-STORAGE; LIGAND; SORPTION; RECOGNITION;
D O I
10.1021/acs.cgd.6b01311
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The separation of xylene,isomers has been achieved through sequential and selective crystallization of coordination polymers of Cu(II) with flexible bis(pyridylcarboxamide) ligand (L). The order of preference for inclusion induced crystallization was Shown to be o-xylene > m-xylene > p-xylene. Although all three xylenes included CPs having distinct;differences in terms of their crystal structures, they all have exhibited a tendency to assemble-via beta-sheet hydrogen bonds to form 3D architectures containing channels. The preferential inclusion of isomers of xylenes was confirmed by single crystal X-ray, 1H NMR, and GC. The bulk purity of xylenes was also confirmed by XRPD patterns.
引用
收藏
页码:5606 / 5611
页数:6
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