化学
取代基
吸附
选择性
多孔性
配体(生物化学)
化学工程
多孔介质
气体分离
组合化学
纳米技术
有机化学
催化作用
膜
材料科学
生物化学
受体
工程类
作者
Lianglan Yue,Xinxin Wang,Chao Lv,Ting Zhang,Bing Li,De‐Li Chen,Yabing He
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2022-12-12
卷期号:61 (51): 21076-21086
被引量:5
标识
DOI:10.1021/acs.inorgchem.2c03657
摘要
Construction of porous solid materials applied to the adsorptive removal of CO2 from C2 hydrocarbons is highly demanded thanks to the important role C2 hydrocarbons play in the chemical industry but quite challenging owing to the similar physical parameters between C2 hydrocarbons and CO2. In particular, the development of synthetic strategies to simultaneously enhance the uptake capacity and adsorption selectivity is very difficult due to the trade-off effect frequently existing between both of them. In this work, a combination of the dicopper paddlewheel unit and 4-pyridylisophthalate derivatives bearing different substituents afforded an isoreticular family of coordination framework compounds as a platform. Their adsorption properties toward C2 hydrocarbons and CO2 were systematically investigated, and subsequent IAST and density functional theory calculations combined with column breakthrough experiments verified their promising potential for C2/CO2 separations. Furthermore, the substituent engineering endowed the resulting compounds with simultaneous enhancement of uptake capacity and adsorption selectivity and thus better C2/CO2 separation performance compared to their parent compound. The substituent introduction not only mitigated the framework distortion via fixing the ligand conformation for establishment of better permanent porosity required for gas adsorption but also polarized the framework surface for host-guest interaction improvement, thus resulting in enhanced separation performance.
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