Flexibility in Metal-Organic Frameworks: A fundamental understanding

被引:177
|
作者
Elsaidi, Sameh K. [1 ,2 ]
Mohamed, Mona H. [1 ]
Banerjee, Debasis [2 ]
Thallapally, Praveen K. [2 ]
机构
[1] Alexandria Univ, Fac Sci, Chem Dept, POB 426, Alexandria 21321, Egypt
[2] Pacific Northwest Natl Lab, Phys & Computat Sci Directorate, Richland, WA 99352 USA
关键词
Metal-Organic Framework; Porous Coordination Polymers; Flexibility; Soft crystals; Breathing; Gate opening; Gas adsorption; ANISOTROPIC THERMAL-EXPANSION; POROUS COORDINATION POLYMERS; PRESSURE METHANE ADSORPTION; CARBON-DIOXIDE CAPTURE; BUILDING-BLOCKS SBBS; GAS-ADSORPTION; SURFACE-AREA; PORE-SIZE; BOND REARRANGEMENT; CRYSTAL-SIZE;
D O I
10.1016/j.ccr.2017.11.022
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Expansion and contraction of structurally flexible Metal-Organic Frameworks (MOFs) or Porous Coordination Polymers (PCPs) have been extensively studied from different structural and application perspectives including crystal engineering, structural characterization, and gas adsorption-separation applications. The flexibility of the MOFs or PCPs depends on a number of factors including the nature of secondary building units (SBUs), organic linkers, pore geometry and/or solvent molecules. The flexibility can lead to unique properties, especially in gas-adsorption-separation related applications that is not observed in rigid frameworks. In this review, we offer a brief summary regarding a fundamental understanding of framework expansion-contraction in flexible porous MOFs in terms of their design and structure tunability by covering representative examples in the literature. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:125 / 152
页数:28
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