An Uncommon Carboxyl-Decorated Metal-Organic Framework with Selective Gas Adsorption and Catalytic Conversion of CO2

被引:118
|
作者
Li, Yong-Zhi [1 ]
Wang, Hai-Hua [1 ]
Yang, Hong-Yun [1 ]
Hou, Lei [1 ]
Wang, Yao-Yu [1 ]
Zhu, Zhonghua [2 ]
机构
[1] Northwest Univ, Coll Chem & Mat Sci, Shaanxi Key Lab Physicoinorgan Chem, Key Lab Synthet & Nat Funct Mol Chem,Minist Educ, Xian 710069, Shaanxi, Peoples R China
[2] Univ Queensland, Sch Chem Engn, Brisbane, Qld 4072, Australia
基金
澳大利亚研究理事会;
关键词
CO2 capture and conversion; crystal engineering; crystal structures; metal-organic frameworks; microporous materials; DIOXIDE CAPTURE; CYCLIC CARBONATES; SINGLE-CRYSTAL; POROUS MOF; SORPTION; CYCLOADDITION; TRANSFORMATION; SEPARATION; UNITS; HYDROCARBONS;
D O I
10.1002/chem.201704027
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new three-dimensional (3D) framework, [Ni(btzip)(H(2)btzip)]center dot 2DMF center dot 2H(2)O (1) (H(2)btzip= 4,6-bis(triazol-1-yl)isophthalic acid) as an acidic heterogeneous catalyst was constructed by the reaction of nickel wire and a triazolyl-carboxyl linker. Framework 1 possesses intersected 2D channels decorated by free COOH groups and uncoordinated triazolyl N atoms, leading to not only high CO2 and C2H6 adsorption capacity but also significant selective capture for CO2 and C2H6 over CH4 and CO in 273-333 K. Moreover, 1 reveals chemical stability toward water. Grand Canonical Monte Carlo simulations confirmed the multiple CO2-and C2H6-philic sites. As a result of the presence of accessible Bronsted acidic COOH groups in the channels, the activated framework demonstrates highly efficient catalytic activity in the cycloaddition reaction of CO2 with propylene oxide/4-chloro-methyl-1,3-dioxolan-2-one/3-butoxy-1,2-epoxypropane into cyclic carbonates.
引用
收藏
页码:865 / 871
页数:7
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