Template-controlled reactivity in the organic solid state by principles of coordination-driven self-assembly

被引:66
|
作者
Bucar, Dejan-Kresimir
Papaefstathiou, Giannis S.
Hamilton, Tamara D.
Chu, Qianli L.
Georgiev, Ivan G.
MacGillivray, Leonard R. [1 ]
机构
[1] Univ Iowa, Dept Chem, Iowa City, IA 52242 USA
[2] Natl & Kapodistrian Univ Athens, Dept Chem, Inorgan Chem Lab, Zografos 15771, Greece
关键词
self-assembly; dimerization; solid-state reactivity; hydrogen bonds;
D O I
10.1002/ejic.200700442
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
In this microreview, we show how principles of coordination-driven self -assembly can be used to direct chemical reactivity in the organic solid state. We also show how products obtained from the templated solid-state reactions can be used as organic building units of metal-organic frameworks and coordination capsules. Self-assembled structures based on dinuclear Zn-II and Ag-I complexes are used to direct stereocontrolled [2+2] photodimerizations of vinylpyridines in the solid state in up to quantitative yield. The products are used as bi- and polytopic ligands of self-assembled coordination capsules and metal-organic frameworks. We also describe emerging metal-based approaches to conduct mechanochemical reactions in organic solids. In addition to the field of supramolecular coordination chemistry, these observations impact the field of green chemistry.
引用
收藏
页码:4559 / 4568
页数:10
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