期刊
NEW JOURNAL OF CHEMISTRY
卷 41, 期 23, 页码 14334-14341出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7nj03296j
关键词
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资金
- National Science Foundation [CHE 1464886]
- Graduate School of WKU
- WKU Office of Research
High-valent porphyrin-iron-oxo intermediates are the central oxidizing species in heme-containing enzymes and synthetic oxidation catalysts. In this work, we investigated a new photochemical entry to porphyrin-iron(IV)-oxo derivatives in a variety of porphyrin ligands with different electronic and steric environments. In non-electron-deficient ligand systems, the visible light photolysis of porphyrin-iron(III) bromates gave porphyrin-iron(IV)-oxo radical cations (compound I analogues). In contrast, the photolysis of porphyrin-iron(III) bromates with electron-deficient and sterically encumbered ligands produced one-electron reduced iron(IV)-oxo porphyrins (compound II analogues). Formation of iron(III) mu-oxo dimers was also observed in the sterically unencumbered systems containing electron-deficient substituents. The photochemical generation of porphyrin-iron(IV)-oxo radical cations and iron(IV)-oxo porphyrins permits direct kinetic studies of their oxidations with organic reductants. As expected, more oxidized porphyriniron( IV)-oxo radical cations reacted 2-3 orders of magnitudes faster than the iron(IV)-oxo porphyrins, and the rate constants obtained in this work are in comparison to those of iron(IV)-oxo derivatives formed by chemical methods. A model including internal electron-transfer (ET) and comproportionation of the putative iron(V)-oxo species pathways is presented.
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