High CO2 uptake capacity and selectivity in a N-oxide-functionalized 3D Ni(II) microporous metal–organic framework

A 3D rigid porous Ni(II) Metal−Organic Framework has been synthesized, possessing 1D diamond channels decorated with N-Oxide “open donor sites” (ODSs) and carboxylic sites. The gas adsorption behavior of this framework exhibit high capacity and selectivity of CO2 over CH4. [Display omitted] •The pyr...

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Bibliographic Details
Published in:Polyhedron Vol. 193; p. 114839
Main Author: Zhang, Wen-Qian
Format: Journal Article
Language:English
Published: Elsevier Ltd 01-01-2021
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Summary:A 3D rigid porous Ni(II) Metal−Organic Framework has been synthesized, possessing 1D diamond channels decorated with N-Oxide “open donor sites” (ODSs) and carboxylic sites. The gas adsorption behavior of this framework exhibit high capacity and selectivity of CO2 over CH4. [Display omitted] •The pyridine-N-O ligand possess superior characteristics than pyridine-N ligand.•A 3D rigid N-O functional porous Ni(II) MOF possesses 1D diamond channels.•There exist abundant N-Oxide “open donor sites” and vacant carboxyl sites.•The gas adsorption behavior shows high capacity and selectivity for CO2 over CH4. A three-dimensional (3D) rigid Ni(II) microporous metal–organic framework (MOF), {[Ni(bpdado)(bpe)(H2O)2]·2DMF·2H2O}n (1), has been synthesized upon axially chiral N-Oxide-functionalized 2,2′-bipyridine-3,3′-dicarboxylate-1,1′-dioxide (H2bpdado) ligand with auxiliary rigid linear trans-1,2-bis (4-pyridyl)ethene (bpe) linker. Structural analysis reveals that there exist 1D diamond channels in the framework of 1, decorated with abundant N-Oxide “open donor sites” (ODSs) and vacant carboxyl sites on the pore surfaces. The modification of pyridine-N into the N-oxide group endows the N-oxide group with unique charge-separated plus electron-rich character, which may provide an enhanced affinity towards CO2 molecules. The gas adsorption property of 1' has been investigated by N2, CH4 and CO2, and it exhibits a high capacity and selectivity for CO2 over CH4.
ISSN:0277-5387
DOI:10.1016/j.poly.2020.114839