Issue 36, 2014

Switchable regioselectivity in the PIFA–BF3·Et2O mediated oxidative coupling of meso-brominated Ni(ii) porphyrin

Abstract

A simple and efficient method has been developed for the switchable synthesis of directly linked meso-brominated Ni(II) porphyrin dimers through PIFA–BF3·Et2O mediated oxidative coupling. The respective syntheses of mesomeso or meso–β singly, doubly, and triply linked porphyrin dimers can be easily realized with the same reagent system.

Graphical abstract: Switchable regioselectivity in the PIFA–BF3·Et2O mediated oxidative coupling of meso-brominated Ni(ii) porphyrin

Supplementary files

Article information

Article type
Communication
Submitted
18 Jul 2014
Accepted
23 Jul 2014
First published
29 Jul 2014

Org. Biomol. Chem., 2014,12, 6990-6993

Author version available

Switchable regioselectivity in the PIFA–BF3·Et2O mediated oxidative coupling of meso-brominated Ni(II) porphyrin

C. Feng, Y. Zhu, Y. Zang, Y. Tong and J. Zheng, Org. Biomol. Chem., 2014, 12, 6990 DOI: 10.1039/C4OB01517G

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