Issue 5, 2011

Fullerene-templated synthesis of a cyclic porphyrin trimer using olefin metathesis

Abstract

An olefination approach to the construction of covalently linked cyclic metalloporphyrin trimers is presented using fullerenes such as C60 or C70 as a template. Yields of the trimer approach 60%. In the absence of a template, the major product is the cyclic dimer (50% yield) with only a small amount of trimer (<10%) formed, indicating this is a template-directed approach.

Graphical abstract: Fullerene-templated synthesis of a cyclic porphyrin trimer using olefin metathesis

Supplementary files

Article information

Article type
Communication
Submitted
18 Oct 2010
Accepted
29 Nov 2010
First published
23 Dec 2010

Chem. Commun., 2011,47, 1494-1496

Fullerene-templated synthesis of a cyclic porphyrin trimer using olefin metathesis

A. R. Mulholland, C. P. Woodward and S. J. Langford, Chem. Commun., 2011, 47, 1494 DOI: 10.1039/C0CC04474A

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