Late first-row transition-metal complexes of texaphyrin

Abstract

The preparation of first-row transition-metal complexes of texaphyrin, a porphyrin-like, monoanionic penta-aza macrocyclic ligand, is reported. Specifically, the synthesis of organic-soluble Mn(II) (1), Co(II) (2), Ni(II) (3), Zn(II) (4), and Fe(III) (5) texaphyrin derivatives and their water-soluble counterparts (6-10) from appropriate metal-free, nonaromatic macrocyclic precursors is described. It was found that metal cations of sufficient reduction potential could act to oxidize the nonaromatic macrocyclic precursor in the course of metal insertion. Complexes were characterized by X-ray diffraction analysis, electrochemistry, flash photolysis, and EPR spectroscopy. The structural and electronic properties of these "expanded porphyrin" complexes are compared with those of analogous porphyrins. Notably, the texaphyrin ligand is found to support the complexation of cations in a lower valence and a higher spin state than do porphyrins. Interactions between the coordinated cation and the ligand π system appear to contribute to the overall bonding. Texaphyrin complexes of Mn(II), Co(II), and Fe(III) in particular may possess sufficient aqueous stability to permit their use in pharmaceutical applications.

Document Type

Article

DOI

https://doi.org/10.1021/ja012747a

Publication Date

7-17-2002

Journal Title

Journal of the American Chemical Society

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