Rotational Dynamics of Linkers in Metal-Organic Frameworks

被引:86
|
作者
Gonzalez-Nelson, Adrian [1 ,2 ]
Coudert, Francois-Xavier [3 ]
van der Veen, Monique A. [1 ]
机构
[1] Delft Univ Technol, Catalysis Engn, Dept Chem Engn, NL-2629 Delft, Netherlands
[2] DPI, POB 902, NL-5600 AX Eindhoven, Netherlands
[3] PSL Univ, Chim ParisTech, CNRS, Inst Rech Chim Paris, F-75005 Paris, France
来源
NANOMATERIALS | 2019年 / 9卷 / 03期
基金
欧洲研究理事会;
关键词
metal-organic frameworks; linker dynamics; rotation; gate-opening effect; H-2; NMR; computational chemistry; NEGATIVE THERMAL-EXPANSION; SOLID-STATE; MOLECULAR-DYNAMICS; DEUTERIUM NMR; TEREPHTHALATE PHENYLENES; RING DYNAMICS; CO2; UPTAKE; FLEXIBILITY; ADSORPTION; ZIF-8;
D O I
10.3390/nano9030330
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Among the numerous fascinating properties of metal-organic frameworks (MOFs), their rotational dynamics is perhaps one of the most intriguing, with clear consequences for adsorption and separation of molecules, as well as for optical and mechanical properties. A closer look at the rotational mobility in MOF linkers reveals that it is not only a considerably widespread phenomenon, but also a fairly diverse one. Still, the impact of these dynamics is often understated. In this review, we address the various mechanisms of linker rotation reported in the growing collection of literature, followed by a highlight of the methods currently used in their study, and we conclude with the impacts that such dynamics have on existing and future applications.
引用
收藏
页数:36
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