Dynamic porous metal-organic frameworks: synthesis, structure and sorption property

被引:36
作者
Hou, Chao [1 ]
Liu, Qing [1 ]
Okamura, Taka-aki [2 ]
Wang, Peng [1 ]
Sun, Wei-Yin [1 ]
机构
[1] Nanjing Univ, Nanjing Natl Lab Microstruct, Sch Chem & Chem Engn, Coordinat Chem Inst,State Key Lab Coordinat Chem, Nanjing 210093, Jiangsu, Peoples R China
[2] Osaka Univ, Grad Sch Sci, Dept Macromol Sci, Toyonaka, Osaka 5600043, Japan
基金
中国国家自然科学基金;
关键词
SELECTIVE CO2 CAPTURE; LAYER COORDINATION POLYMER; CARBON-DIOXIDE; ADSORPTION; SEPARATION; WATER; GAS; NETWORKS; SURFACE; LIGAND;
D O I
10.1039/c2ce26533h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Three new porous metal-organic frameworks {[Co(L)(PIN)]center dot dioxane center dot H2O}(n) (1), {[Co(L)(DPE)]center dot 0.5DPE}(n) (2) and {[Co(L)(BPE)]center dot 4H(2)O}(n) (3) with the same 2-fold interpenetrating hms topology based on 5-(pyridin-4-yl)isophthalate (L2-) and different pillar ligands of N-(4-pyridyl) isonicotinamide (PIN), 1,2-di(4-pyridyl) ethylene (DPE) and 1,2-bis(4-pyridyl) ethane (BPE) have been prepared and characterized by IR, thermogravimetric analysis, single crystal and powder X-ray diffractions. Interestingly, 1 possesses a flexible framework upon desolvation and H2O/MeOH/EtOH vapor adsorption, and the desolvated sample exhibits a stepwise uptake of CO2 (195 K), H2O (298 K) and MeOH (298 K). More importantly, the desolvated 1 shows high enthalpy of CO2 adsorption and high selectivity for CO2 over N-2 as well as H2O/MeOH over EtOH at 298 K.
引用
收藏
页码:8569 / 8576
页数:8
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