Solvent-Induced Topological Diversity of Two Zn(II) Metal-Organic Frameworks and High Sensitivity in Recyclable Detection of Nitrobenzene

被引:121
作者
Chen, Di-Ming
Ma, Xiao-Zhou
Shi, Wei [1 ]
Cheng, Peng
机构
[1] Nankai Univ, Dept Chem, Key Lab Adv Energy Mat Chem MOE, Tianjin 300071, Peoples R China
关键词
COORDINATION POLYMERS; CRYSTAL-STRUCTURES; SINGLE-CRYSTAL; LUMINESCENCE; LIGAND; INTERPENETRATION; TRANSFORMATION; FLUORESCENCE; CD(II); LAYER;
D O I
10.1021/acs.cgd.5b00614
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The solvent-induced topological diversity and different framework stabilities were studied in two Zn(II) metalorganic frameworks (MOFs), {[Zn(L)]center dot DMA}(n) (1) and {[Zn(L)]center dot MeOH center dot 0.5NMP}(n) (2) (H2L = 5-(4H-1,2,4-triazol-4-yl)isophthalic acid). Despite the fact that both of these MOFs are (3,6)-connected networks based on the same coordination environment of Zn(II) ions and the same coordination mode of the ligands, they adopt distinct nets with apo and rtl topologies, respectively, which originate from the template effects of the solvents and the conformational flexibility of the ligand. The two Zn(II) MOFs show remarkably different framework stability upon guest exchange due to their different topological structures. The luminescent properties of MOF 1 with different solvents have been studied in detail, which shows high sensitivity in the detection of nitrobenzene (NB). In addition, MOF 1 can be reused by simply washing with fresh solvent.
引用
收藏
页码:3999 / 4004
页数:6
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