An investigation of ligand effects on the visible light-induced formation of porphyrin–iron(iv)-oxo intermediates. (31st October 2017)

• Record Type: Journal Article
• Authors: Kwong, Ka Wai; Patel, Dharmesh; Malone, Jonathan; Lee, Ngo Fung; Kash, Benjamin; Zhang, Rui
• Is Part Of: New journal of chemistry. Volume 41:Number 23(2017)
• Page Start: 14334
• Page End: 14341
• Publication Date: 2017-10-31
• Subjects: Chemistry -- Periodicals; Chimie -- Périodiques; 540
• DOI: 10.1039/c7nj03296j
• Languages: English
• ISSNs: 1144-0546

Abstract

Abstract : Depending on the structure of the porphyrin ligands, the visible light photolysis of porphyrin–iron(iii ) bromates produced iron(iv )-oxo radical cations or iron(iv )-oxo porphyrins, permitting direct kinetic studies of their oxidation reactions. Abstract : 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 ) μ-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 porphyrin–iron(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.