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Enhanced Electron Transfer Reactivity of a Nonheme Iron(IV)-Imido Complex as Compared to the Iron(IV)-Oxo Analogue

机译:与铁(IV)-氧代类似物相比,非血红素铁(IV)-亚氨基配合物的电子转移反应性增强

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摘要

Reactions of N,N-dimethylaniline (DMA) with nonheme iron(IV)-oxo and iron(IV)-tosylimido complexes occur via different mechanisms, such as an N-demethylation of DMA by a nonheme iron(IV)-oxo complex or an electron transfer dimerization of DMA by a nonheme iron(IV)-tosylimido complex. The change in the reaction mechanism results from the greatly enhanced electron transfer reactivity of the iron(IV)-tosylimido complex, such as the much more positive one-electron reduction potential and the smaller reorganization energy during electron transfer, as compared to the electron transfer properties of the corresponding iron(IV)-oxo complex.
机译:N,N-二甲基苯胺(DMA)与非血红素铁(IV)-氧代和铁(IV)-甲苯磺酰氨基配合物的反应是通过不同的机理发生的,例如通过非血红素铁(IV)-氧代配合物对DMA进行N-去甲基化或非血红素铁(IV)-甲苯磺酰亚胺配合物对DMA的电子转移二聚作用。反应机理的变化是由于铁(IV)-甲苯磺酰亚胺配合物的电子转移反应性大大提高,例如与电子转移相比,正电子的单电子还原电位高得多,电子转移过程中的重组能更小铁(IV)-氧配合物的性质

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