Nanocage containing metal-organic framework constructed from a newly designed low symmetry tetra-pyrazole ligand

被引:2
作者
Zhang, Yong-Zheng
He, Tao
Lv, Xiu-Liang
Wang, Bin
Xie, Lin-Hua
Liu, Xiao-Min [1 ]
Li, Jian-Rong [1 ]
机构
[1] Beijing Univ Technol, Coll Environm & Energy Engn, Beijing Key Lab Green Catalysis & Separat, Beijing, Peoples R China
基金
中国博士后科学基金;
关键词
Tetra-pyrazole; metal-organic framework; single-crystal structure; nanocage; CO2; adsorption; COORDINATION POLYMERS; GAS-ADSORPTION; BIOMEDICINE; CAPTURE;
D O I
10.1080/00958972.2016.1229865
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
1368-Tetra(1H-pyrazol-4-yl)-9H-carbazole (H4CTP), a tetra-pyrazole ligand with C-s symmetry, has been synthesized based on a carbazole core. A solvothermal reaction of this ligand with NiCl2 center dot 6H(2)O gave a three-dimensional (3-D) metal-organic framework (MOF), [Ni(H4CTP)Cl-2]center dot nS (BUT-41), which crystallized in the cubic space group Pm-3 in spite of H4CPT with a central carbazole core and four peripheral pyrazole rings has low symmetry. The framework of BUT-41 can be regarded as a four-connected 3-D net with the rhr topology when both the organic ligand and the metal center are considered as four-connected nodes. Nanocages with internal diameter of 2 nm are present in the framework of BUT-41, which are formed by interconnecting 12H(4)CTP ligands and 20 Ni(II) ions. Each nanocage connects with six adjacent cages through sharing hexagonal windows with diameter over 7 angstrom, resulting in 3-D intersecting channels of the MOF. Although the tetra-pyrazole ligand is not deprotonated after coordination with the metal ions, powder X-ray diffraction and N-2 adsorption experiments reveal that the framework of BUT-41 is rigid and permanently porous with the Brunauer-Emmett-Teller surface area up to 1551 m(2) g(-1). Furthermore, gas adsorption experiments show that this MOF selectively adsorbs CO2 over N-2 and CH4. [GRAPHICS] .
引用
收藏
页码:3242 / 3249
页数:8
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