| 要約: | Previous biomimetic studies clearly proved that equatorial ligands significantly influence the redox potential and thus the stability/reactivity of biologically important oxoiron intermediates; however, no such studies were performed on Fe<sup>III</sup>OIPh species. In this study, the influence of substituted pyridine co-ligands on the reactivity of iron(III)-iodosylbenzene adduct has been investigated in sulfoxidation and epoxidation reactions. Selective oxidation of thioanisole, <i>cis</i>-cyclooctene, and <i>cis</i>- and <i>trans</i>-stilbene in the presence of a catalytic amount of [Fe<sup>II</sup>(PBI)<sub>3</sub>](OTf)<sub>2</sub> with PhI(OAc)<sub>2</sub> provide products in good to excellent yields through an Fe<sup>III</sup>OIPh intermediate depending on the co-ligand (4R-Py) used. Several mechanistic studies were performed to gain more insight into the mechanism of oxygen atom transfer (OAT) reactions to support the reactive intermediate and investigate the effect of the equatorial co-ligands. Based on competitive experiments, including a linear free-energy relationship between the relative reaction rates (log<i>k</i><sub>rel</sub>) and the <i>σ</i><sub>p</sub> (4R-Py) parameters, strong evidence has been observed for the electrophilic character of the reactive species. The presence of the [(PBI)<sub>2</sub>(4R-Py)Fe<sup>III</sup>OIPh]<sup>3+</sup> intermediates and the effect of the co-ligands was also supported by UV-visible measurements, including the color change from red to green and the hypsochromic shifts in the presence of co-ligands. This is another indication that the title iron(III)-iodosylbenzene adduct is able to oxygenate sulfides and alkenes before it is transformed into the oxoiron form by cleavage of the O−I bond.
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