Size-Selective Molecular Flasks

被引:118
|
作者
Otte, Matthias [1 ]
机构
[1] Univ Utrecht, Debye Inst Nanomat Sci, Organ Chem & Catalysis, Univ Weg 99, NL-3584 CG Utrecht, Netherlands
来源
ACS CATALYSIS | 2016年 / 6卷 / 10期
关键词
size-selective catalysis; cavities; supramolecular chemistry; organic cages; confined space; METAL-ORGANIC FRAMEWORKS; DIELS-ALDER REACTION; H BOND ACTIVATION; SUPRAMOLECULAR HOST; ARYLENEETHYNYLENE CAGES; CATALYTIC KNOEVENAGEL; NONCOVALENT SYNTHESIS; COBALT-PORPHYRIN; ACID CATALYSIS; GUEST BINDING;
D O I
10.1021/acscatal.6b01776
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Molecular flasks are compounds that are able to mediate or catalyze chemical transformations inside their cavities. The development of such compounds is often inspired by nature. Enzymes, nature's catalysts, are able to convert a certain substrate with very high turnover number and selectivity. In addition to their very high chemo-, regio-, and stereoselectivity, enzymes are also able to distinguish their substrates on the basis of size, resulting in size selectivity. To date, many synthetic materials such as metal organic frameworks are used to accomplish size-selective transformations. However, also the number of molecular flasks known to mediate or catalyze size-selective transformations is increasing. In this perspective an overview on classic and the most recent examples of size-selective molecular flasks is given. In addition, an outlook on promising developments in cavity chemistry that may lead to the development of additional size selective molecular flasks is given.
引用
收藏
页码:6491 / 6510
页数:20
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