An Amino-Decorated Self-Catenated Metal-Organic Framework for Efficient Capture and Conversion of CO2

被引:8
|
作者
Zhou, Ting [1 ]
Liu, Shuang [1 ]
Alexandrov, Eugeny, V [2 ]
Guo, Huadong [1 ]
Gao, Pan [1 ]
Mi, Shengyong [1 ]
Su, Qijin [1 ]
Guo, Xianmin [1 ]
Hu, Ting [3 ,4 ]
机构
[1] Changchun Normal Univ, Dept Chem, Changchun 130032, Peoples R China
[2] Samara Univ, Samara Ctr Theoret Mat Sci, Samara 443011, Russia
[3] Chinese Acad Sci, Fujian Inst Res Struct Matter, CAS Key Lab Design & Assembly Funct Nanostruct, Fujian Prov Key Lab Nanomat, Fuzhou 350002, Fujian, Peoples R China
[4] Chinese Acad Sci, Xiamen Inst Rare Earth Mat, Haixi Inst, Xiamen Key Lab Rare Earth Photoelect Funct Mat, Xiamen 361021, Peoples R China
基金
俄罗斯基础研究基金会; 中国国家自然科学基金;
关键词
SELECTIVE ADSORPTION; CARBON-DIOXIDE; CYCLOADDITION; MOF; EPOXIDES; SEPARATION; CATALYST;
D O I
10.1021/acs.cgd.1c00564
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Efficient capture and conversion of CO2 are important in energy utilization and environmental protection. A new porous metal-organic framework [Zn4O(NH2-bpdc)(3)(bpe)(0.5)(H2O)]center dot 10DMF [NH2-H(2)bpdc = 2-amino-biphenyl-4,4'-dicarboxylic acid, bpe = 1,2-bi(4-pyridyl)ethylene] has been synthesized based on an amino-tagged organic linker and tetranuclear {Zn4O} SBU. This compound exhibits an unusual self-catenated underlying net of topological type hxg-d-7-R-3c. The framework shows excellent thermal stability for the high connectivity and consists of abundant exposed metal sites and coordination-free amino groups, which make it an efficient heterogeneous catalyst for the cycloaddition of CO2 with epoxides under mild conditions.
引用
收藏
页码:5724 / 5730
页数:7
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