作者: S.V. Zaitseva , E.Yu. Tyulyaeva , S.A. Zdanovich , O.I. Koifman
DOI: 10.1016/J.MOLLIQ.2019.111023
关键词: Reaction rate 、 Oxidizing agent 、 Organic peroxide 、 Reactivity (chemistry) 、 Photochemistry 、 Reactive intermediate 、 Catalysis 、 Reaction mechanism 、 Dication 、 Chemistry
摘要: Abstract The oxidative decomposition of β‑carotene mediated by μ-carbido diiron octapropyltetraazaporphyrin ([FeOPrTAP]2C)–tBuOOH system was investigated in benzene. Interaction between tBuOOH and the binuclear complex resulted generation powerful high-oxidized species those are capable oxidizing employed substrate within limits several minutes. explanation for such reactivity behavior involves existence a mixture reactive intermediates reaction medium: more stable singly oxidized at macrocyclic ligand π-cation radical as well much dication that is contributing to rate. introduction imidazole into coordination sphere initial accelerates destruction because high-oxidizing species, which applied organic peroxide resulting dioxygen release. Catalytic all observed active supported recycling under carotene adding. quantitative characteristics studied systems were obtained possible mechanisms proposed.