Two Copper(II) Metal-Organic Frameworks with Nanoporous Channels and Vacant Coordination Sites

被引:25
作者
Huang, Yumei [1 ]
Zhang, Bingguang [2 ,3 ]
Duan, Jingui [5 ]
Liu, Wenlong [4 ]
Zheng, Xiaofang [1 ]
Wen, Lili [1 ]
Ke, Xiaohuan [1 ]
Li, Dongfeng [1 ]
机构
[1] Cent China Normal Univ, Key Lab Pesticide & Chem Biol, Minist Educ, Coll Chem, Wuhan 430079, Peoples R China
[2] South Cent Univ Nationalities, Key Lab Catalysis & Mat Sci, State Ethn Affairs Commiss, Wuhan 430074, Peoples R China
[3] South Cent Univ Nationalities, Minist Educ, Wuhan 430074, Peoples R China
[4] Yangzhou Univ, Coll Chem & Chem Engn, Yangzhou 225002, Peoples R China
[5] Nanjing Univ Technol, State Key Lab Mat Oriented Chem Engn, Nanjing 210009, Peoples R China
关键词
HIGH-CAPACITY HYDROGEN; PORE-SIZE; ADSORPTION PROPERTIES; CARBON-DIOXIDE; STORAGE; CO2; CATENATION; TOPOLOGY; SORPTION; MOF;
D O I
10.1021/cg500175k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Two three-dimensional microporous compounds, Cu-6(BTTC)(4)(H2O)(6)center dot xS (1) and [(CH3)(2)NH2](3)-[(Cu4Cl)(3)(BTTC)(8)]center dot yS (2, H3BTTC = benzo-(1,2;3,4;5,6)-tris (thiophene-2'-carboxylic acid), S represents noncoordinated solvent molecules), have been solvothermally synthesized and characterized, both of which are based upon truncated octahedron subunits and contain uniform nanosized cavities but exhibit different topological frameworks. Complex 1 demonstrates high adsorption enthalpies for H-2 and CO2 gas molecules, stemming principally from the presence of the exposed metal Cu(II) sites on the pore surface. In particular, activated complex 1 shows high efficiency for the separation of energy-correlated molecules, including CO2 over N-2 and CH4 under ambient conditions.
引用
收藏
页码:2866 / 2872
页数:7
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