Goldstein S, Meyerstein D, Czapski G
Department of Physical Chemistry, Hebrew University of Jerusalem, Israel.
Free Radic Biol Med. 1993 Oct;15(4):435-45. doi: 10.1016/0891-5849(93)90043-t.
Numerous transition metal ions and their complexes in their lower oxidation states (LmMn+) were found to have the oxidative features of the Fenton reagent, and, therefore, the mixtures of these metal compounds with H2O2 were named "Fenton-like" reagents. Using the Marcus theory and the experimental data in the literature, it is shown that in most cases the reaction of these metal complexes with H2O2 is unlikely to occur via an outer-sphere electron-transfer mechanism. It is suggested that the first step in this process is the formation of a transient complex LmM-H2O2n+, which may decompose to an .OH radical or a higher oxidation state of the metal, LmM(n + 2)+, or it may yield an organic free radical in the presence of organic substrates. Thus, the question whether free .OH radicals are being formed or not via the Fenton reaction depends on the relative rates of the decomposition reactions of the metal-peroxide complex and that of its reaction with organic substrates. Contradictory conclusions described from the study of different systems might only indicate that these relative rates are different in these systems.
许多处于较低氧化态的过渡金属离子及其配合物(LmMn+)被发现具有芬顿试剂的氧化特性,因此,这些金属化合物与H2O2的混合物被称为“类芬顿”试剂。利用马库斯理论和文献中的实验数据表明,在大多数情况下,这些金属配合物与H2O2的反应不太可能通过外层电子转移机制发生。有人提出,该过程的第一步是形成瞬态配合物LmM-H2O2n+,它可能分解为·OH自由基或金属的更高氧化态LmM(n + 2)+,或者在有机底物存在下产生有机自由基。因此,是否通过芬顿反应形成游离·OH自由基的问题取决于金属过氧化物配合物的分解反应及其与有机底物反应的相对速率。从不同体系的研究中得出的相互矛盾的结论可能仅表明这些相对速率在这些体系中有所不同。