Metal-Organic Framework Nodes Support Single-Site Magnesium-Alkyl Catalysts for Hydroboration and Hydroarnination Reactions

被引:221
|
作者
Manna, Kuntal [1 ]
Ji, Pengfei [1 ]
Greene, Francis X. [1 ]
Lin, Wenbin [1 ]
机构
[1] Univ Chicago, Dept Chem, 929 East 57th St, Chicago, IL 60637 USA
基金
美国国家科学基金会;
关键词
RING-OPENING POLYMERIZATION; INTRAMOLECULAR HYDROAMINATION; COBALT CATALYSTS; HYDROGEN STORAGE; HIGHLY EFFICIENT; CALCIUM; TRANSFORMATIONS; ACTIVATION; COMPLEXES; ALKENES;
D O I
10.1021/jacs.6b03689
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Here we present the first example of a single-site main group catalyst stabilized by a metal-organic framework (MOF) for organic transformations. The straightforward metalation of the secondary building units of a Zr-MOF with Me2Mg affords a highly active and reusable solid catalyst for hydroboration of carbonyls and imines and for hydroamination of aminopentenes. Impressively, the Mg-functionalized MOF displayed very high turnover numbers of up to 8.4 x 10(4) for ketone hydroboration and could be reused more than 10 times. MOFs can thus be used to develop novel main group solid catalysts for sustainable chemical synthesis.
引用
收藏
页码:7488 / 7491
页数:4
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