Issue 20, 2002
From the journal:

Chemical Communications

Synthesis, spectroscopy and metallation of mixed carbaporphyrinoid systems†

Dachun Liua  and  Timothy D. Lash*a  

* Corresponding authors

a Department of Chemistry, Illinois State University, Normal, Illinois 61790-4160, U.S.A
E-mail: tdlash@ilstu.edu

Abstract

Modified tripyrranes incorporating furan and thiophene rings were found to condense with benzene, pyridine and indene dialdehydes to give a series of novel porphyrin analogues, including thia- and oxa-carbaporphyrins; the latter readily forms nickel(II) and palladium(II) organometallic complexes.

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Article information

DOI
https://doi.org/10.1039/B206276N
Article type
Communication
Submitted
27 Jun 2002
Accepted
30 Aug 2002
First published
23 Sep 2002

Chem. Commun., 2002, 2426-2427

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Synthesis, spectroscopy and metallation of mixed carbaporphyrinoid systems

D. Liu and T. D. Lash, Chem. Commun., 2002, 2426 DOI: 10.1039/B206276N

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