Synthesis, spectroscopy and metallation of mixed carbaporphyrinoid systems?

Chemical Communications Pub Date: 2002-09-23 DOI: 10.1039/B206276N

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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