Issue 21, 2014

Base-promoted aryl–bromine bond cleavage with cobalt(ii) porphyrins via a halogen atom transfer mechanism

Abstract

Aryl–bromine bonds are successfully cleaved by cobalt(II) porphyrins in basic media to give Co(por)Ar (por = porphyrin) in good yields. Mechanistic studies suggested that the aryl–bromine bond is cleaved through a halogen atom transfer mechanism, which is different from the aryl–halogen bond cleavage mechanism with other group 9 metalloporphyrins.

Graphical abstract: Base-promoted aryl–bromine bond cleavage with cobalt(ii) porphyrins via a halogen atom transfer mechanism

Supplementary files

Article information

Article type
Paper
Submitted
16 Jan 2014
Accepted
03 Mar 2014
First published
04 Mar 2014

Dalton Trans., 2014,43, 7771-7779

Base-promoted aryl–bromine bond cleavage with cobalt(II) porphyrins via a halogen atom transfer mechanism

C. R. Liu, Y. Y. Qian and K. S. Chan, Dalton Trans., 2014, 43, 7771 DOI: 10.1039/C4DT00155A

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