An alteration of a metalloporphyrin coordination core, exemplified by 21-heteroporphyrins and 2-aza-21-carbaporphyrin (N-confused porphyrin, inverted porphyrin), provides a route of choice to stabilize unusual oxidation states and coordination geometries, affording a stabilization of such rare species as organometallic high-spin nickel(II) or copper(II) derivatives. This review focuses on reactivity and electronic structure of peculiar organometallic compounds trapped due to the appropriate choice of the suitable macrocyclic platform. (c) 2005 Elsevier B.V. All rights reserved.
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Univ Tecn Federico Santa Maria, Dept QuIrn, Av Santa Maria 6400, Santiago 7660251, ChileUniv Tecn Federico Santa Maria, Dept QuIrn, Av Santa Maria 6400, Santiago 7660251, Chile
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Univ Roma Tor Vergata, Dipartimento Sci & Tecnol Chim, I-00133 Rome, ItalyUniv Roma Tor Vergata, Dipartimento Sci & Tecnol Chim, I-00133 Rome, Italy
Vecchi, Andrea
Galloni, Pierluca
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Univ Roma Tor Vergata, Dipartimento Sci & Tecnol Chim, I-00133 Rome, ItalyUniv Roma Tor Vergata, Dipartimento Sci & Tecnol Chim, I-00133 Rome, Italy
Galloni, Pierluca
Floris, Barbara
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Univ Roma Tor Vergata, Dipartimento Sci & Tecnol Chim, I-00133 Rome, ItalyUniv Roma Tor Vergata, Dipartimento Sci & Tecnol Chim, I-00133 Rome, Italy
Floris, Barbara
Nemykin, Victor N.
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Univ Minnesota, Dept Chem & Biochem, Duluth, MN 55812 USAUniv Roma Tor Vergata, Dipartimento Sci & Tecnol Chim, I-00133 Rome, Italy