X-ray Crystallography in Open-Framework Materials

被引:70
作者
Bloch, Witold M. [1 ]
Champness, Neil R. [2 ]
Doonan, Christian J. [1 ]
机构
[1] Univ Adelaide, Sch Phys Sci, Ctr Adv Nanomat, Adelaide, SA 5005, Australia
[2] Univ Nottingham, Sch Chem, Nottingham NG7 2RD, England
基金
英国工程与自然科学研究理事会;
关键词
coordination polymers; crystallization matrix; metal-organic frameworks; structure elucidation; X-ray crystallography; METAL-ORGANIC FRAMEWORK; POST-SYNTHETIC METALATION; COORDINATION NETWORKS; SNAPSHOT; MOLECULES; CHEMISTRY; ISOMERISM;
D O I
10.1002/anie.201501545
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Open-framework materials, such as metal-organic frameworks (MOFs) and coordination polymers have been widely investigated for their gas adsorption and separation properties. However, recent studies have demonstrated that their highly crystalline structures can be used to periodically organize guest molecules and non-structural metal compounds either within their pore voids or by anchoring to their framework architecture. Accordingly, the open framework can act as a matrix for isolating and elucidating the structures of these moieties by X-ray diffraction. This concept has broad scope for development as an analytical tool where obtaining single crystals of a target molecule presents a significant challenge and it additionally offers potential for obtaining insights into chemically reactive species that can be stabilized within the pore network. However, the technique does have limitations and as yet a general experimental method has not been realized. Herein we focus on recent examples in which framework materials have been utilized as a scaffold for ordering molecules for analysis by diffraction methods and canvass areas for future exploration.
引用
收藏
页码:12860 / 12867
页数:8
相关论文
共 53 条
[1]   Ligand design for functional metal-organic frameworks [J].
Almeida Paz, Filipe A. ;
Klinowski, Jacek ;
Vilela, Sergio M. F. ;
Tome, Joao P. C. ;
Cavaleiro, Jose A. S. ;
Rocha, Joao .
CHEMICAL SOCIETY REVIEWS, 2012, 41 (03) :1088-1110
[2]   Confined Nanospaces in Metallocages: Guest Molecules, Weakly Encapsulated Anions, and Catalyst Sequestration [J].
Amouri, Hani ;
Desmarets, Christophe ;
Moussa, Jamal .
CHEMICAL REVIEWS, 2012, 112 (04) :2015-2041
[3]   A Five-Coordinate Heme Dioxygen Adduct Isolated within a Metal-Organic Framework [J].
Anderson, John S. ;
Gallagher, Audrey T. ;
Mason, Jarad A. ;
Harris, T. David .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2014, 136 (47) :16489-16492
[4]  
[Anonymous], 2013, ANGEW CHEM
[5]  
Batten S.R., 1998, ANGEW CHEM, V110, P1558, DOI DOI 10.1002/(SICI)1521-3757(19980605)110:11<1558::AID-ANGE1558>3.0.CO
[6]  
2-7
[7]  
Batten S. R., 2008, COORDINATION POLYM D
[8]  
Batten SR, 1998, ANGEW CHEM INT EDIT, V37, P1460, DOI 10.1002/(SICI)1521-3773(19980619)37:11<1460::AID-ANIE1460>3.0.CO
[9]  
2-Z
[10]   Characterization of the Key Intermediates of Carbene-Catalyzed Umpolung by NMR Spectroscopy and X-Ray Diffraction: Breslow Intermediates, Homoenolates, and Azolium Enolates [J].
Berkessel, Albrecht ;
Yatham, Veera Reddy ;
Elfert, Silvia ;
Neudoerfl, Joerg-M .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2013, 52 (42) :11158-11162