In-situ Fourier transform infrared spectroelectrochemical studies of the oxidation of some tetraphenylporphyrin complexes
- 1 July 1988
- journal article
- research article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 66 (7) , 1589-1595
- https://doi.org/10.1139/v88-257
Abstract
In-situ FTIR spectroelectrochemistry has been applied to determine difference spectra in the region 1800 to 1000 cm−1 associated with the oxidation of TPPH2, TPPMg, TPPCu, TPPZn, TPPCo, TPPMnCl, and TPPFeCl. In all cases, formation of the π-cation radical results in two characteristic absorbance decreases near 1600 and 1485 cm−1, and five characteristic absorbance increases near 1415, 1350, 1285, 1225, and 1005 cm−1. Formation of the π-dication was observed for TPPZn, TPPMg, and TPPCo, and gave rise to a new absorbance increase near 1600 cm−1, and a shift to higher frequency of bands in the 1200 to 1400 cm−1 region. Perchlorate coordination to oxidized TPPZn, TPPMg, and TPPCo gives rise to bands near 1140 and 1030 cm−1.This publication has 2 references indexed in Scilit:
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- High-valent iron porphyrins: synthesis, x-ray structures, .pi.-cation radical formulation, and notable magnetic properties of chloro(meso-tetraphenylporphinato)iron(III) hexachloroantimonate and bis(perchlorato)(meso-tetraphenylporphinato)iron(III)Journal of the American Chemical Society, 1986