Octaiodoporphyrin

Interaction of 3,4-diiodopyrrole with 4-trifluoromethylbenzaldeyde under carefully optimized, Lindsey-type conditions at −10 °C has led to the synthesis of the first β-octaiodoporphyrin, H2[I8TpCF3PP]. The free ligand readily yielded Ni, Cu, and Zn complexes, which all proved amenable to single-crys...

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Veröffentlicht in:Inorganic chemistry 2015-12, Vol.54 (23), p.11493-11497
Hauptverfasser: Thomassen, Ivar K, Vazquez-Lima, Hugo, Gagnon, Kevin J, Ghosh, Abhik
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container_title Inorganic chemistry
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creator Thomassen, Ivar K
Vazquez-Lima, Hugo
Gagnon, Kevin J
Ghosh, Abhik
description Interaction of 3,4-diiodopyrrole with 4-trifluoromethylbenzaldeyde under carefully optimized, Lindsey-type conditions at −10 °C has led to the synthesis of the first β-octaiodoporphyrin, H2[I8TpCF3PP]. The free ligand readily yielded Ni, Cu, and Zn complexes, which all proved amenable to single-crystal X-ray structure analyses. The zinc complex Zn­[I8TpCF3PP] exhibits the most saddled porphyrin core for any simple porphyrin known to date and a dramatically red-shifted optical spectrum with a Soret maximum at 495 nm.
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subjects Ligands
Nickel
Polypropylenes
Porphyrins
Structural analysis
Synthesis
X-rays
Zinc
title Octaiodoporphyrin
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