Metalation of a Thiocatechol-Functionalized Zr(IV)-Based Metal-Organic Framework for Selective C-H Functionalization

被引:218
作者
Fei, Honghan [1 ]
Cohen, Seth M. [1 ]
机构
[1] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
基金
美国国家科学基金会;
关键词
POSTSYNTHETIC MODIFICATION; ROBUST; ACTIVATION; COMPLEXES; CHEMISTRY; CATALYST; INCREASE; EXCHANGE; UIO-66; ROUTE;
D O I
10.1021/ja5126885
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The incorporation of 2,3-dimercaptoterephthalate (thiocatecholate, tcat) into a highly robust UiO-type metal-organic framework (MOF) has been achieved via postsynthetic exchange (PSE). The anionic, electron-donating thiocatecholato motif provides an excellent platform to obtain site-isolated and coordinatively unsaturated soft metal sites in a robust MOF architecture. Metalation of the thiocatechol group with palladium affords unprecedented Pd-mono(thiocatecholato) moieties within these MOFs. Importantly, Pd-metalated MOFs are efficient, heterogeneous, and recyclable catalysts for regioselective functionalization of sp(2) C-H bond. This material is a rare example of chelation-assisted C-H functionalization performed by a MOF catalyst.
引用
收藏
页码:2191 / 2194
页数:4
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