Modulation of pore shape and adsorption selectivity by ligand functionalization in a series of "rob"-like flexible metal-organic frameworks

被引:14
作者
Cepeda, Javier [1 ]
Perez-Mendoza, Manuel [2 ]
Calahorro, Antonio J. [2 ]
Casati, Nicola [3 ]
Manuel Seco, Jose [1 ]
Aragones-Anglada, Marta [4 ]
Moghadam, Peyman Z. [4 ]
Fairen-Jimenez, David [4 ]
Rodriguez-Dieguez, Antonio [2 ]
机构
[1] Univ Basque Country, Fac Quim, Dept Quim Aplicada, San Sebastian 20018, Spain
[2] Univ Granada, Dept Quim Inorgan, E-18071 Granada, Spain
[3] Paul Scherrer Inst, CH-5232 Villigen, Switzerland
[4] Univ Cambridge, Dept Chem Engn & Biotechnol, AAML, Cambridge, England
基金
欧洲研究理事会;
关键词
CARBON-DIOXIDE; HYDROGEN STORAGE; CRYSTAL-STRUCTURES; POROUS MATERIALS; CO2; ADSORPTION; SURFACE-AREAS; GAS MOLECULES; SORPTION; MOFS; SIMULATION;
D O I
10.1039/c8ta04316g
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report the synthesis of a new family of four new isoreticular metal-organic frameworks (MOFs) based on Cu-Cu paddle-wheel building units. The four MOFs contain 1D microchannels modulated by chemical functionalisation of a dicarboxylate ligand or the use of different bis-4,4'-pyridyl-like connectors behaving as ancillary linkers. A deep analysis of their CO2, H-2 and CH4 adsorption properties, combining both experimental and grand canonical Monte Carlo isotherms as well as in situ synchrotron X-ray diffraction, shows variable adsorption behaviour towards the studied gases, with some materials acting as molecular sieves with virtually infinite selectivity.
引用
收藏
页码:17409 / 17416
页数:8
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