Enhanced catalytic decomposition of a phosphate triester by modularly accessible bimetallic porphyrin dyads and dimers

被引:37
作者
Totten, Ryan K. [1 ]
Ryan, Patrick [2 ]
Kang, Byungman [1 ]
Lee, Suk Joong [1 ]
Broadbelt, Linda J. [2 ]
Snurr, Randall Q. [2 ]
Hupp, Joseph T. [1 ]
Nguyen, SonBinh T. [1 ]
机构
[1] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[2] Northwestern Univ, Dept Chem & Biol Engn, Evanston, IL 60208 USA
关键词
MESO-ALKYNYL PORPHYRINS; OLEFIN METATHESIS; SUPRAMOLECULAR CHEMISTRY; METALLOPORPHYRIN HOSTS; NANOSTRUCTURES; ACCELERATION; HYDROLYSIS; ARRAYS;
D O I
10.1039/c2cc17568a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of metalloporphyrin dimers were modularly prepared and shown to catalyze the methanolysis of a phosphate triester, yielding rates that are large compared to the rate of the uncatalyzed reaction. Up to 1300-fold rate acceleration can be achieved via a combination of cavity-localized Lewis-acid activation and methoxide-induced methanolysis.
引用
收藏
页码:4178 / 4180
页数:3
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