Structure, characterization, and catalytic properties of open-metal sites in metal organic frameworks

被引:122
作者
Hall, Jacklyn N. [1 ]
Bollini, Praveen [1 ]
机构
[1] Univ Houston, Dept Chem & Biomol Engn, 4722 Calhoun Rd, Houston, TX 77004 USA
关键词
COORDINATIVELY UNSATURATED SITES; CHROMIUM TEREPHTHALATE MIL-101; GIANT PORES; MICROWAVE SYNTHESIS; LEWIS-ACID; HETEROGENEOUS CATALYSTS; SELECTIVE DIMERIZATION; FRIEDLANDER REACTION; PROTON CONDUCTION; HYDROGEN STORAGE;
D O I
10.1039/c8re00228b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Metal organic framework materials (MOFs) offer a unique opportunity for investigating active sites that have either previously not been studied from a catalytic standpoint or have only been evaluated as homogeneous catalysts. One of the common themes in MOF research is a metal site endowed with labile ligands that can be eliminated to create a coordinatively unsaturated site, referred to as an open-metal site. Despite the ubiquitous nature of these sites, relationships between their atomic-level structure and catalytic properties are just beginning to emerge. This review summarizes the structure, characterization, and catalytic properties of three prototypical MOFs with open-metal sites (MIL-100/101, Cu-BTC, and UiO-66), with the goal of better identifying open questions in the MOF catalysis literature. Structure-catalytic property relationships for these three MOFs are discussed, with an emphasis on the effect of metal oxidation state, site proximity, defect density, and ligand functionalization on catalytic rates and selectivities.
引用
收藏
页码:207 / 222
页数:16
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