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Mechanistic aspects of vanadium catalysed oxidations with peroxides

机译:钒催化过氧化物氧化的机理

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摘要

The enhancement of the reactivity of peroxides, particularly hydrogen peroxide and alkylhydroperoxides, in the presence of vanadium catalysis is a very well known process. The catalytic effect is determined by the formation of an intermediate whose nature depends on the peroxides used and on its interaction with the metal precursor, high-valent peroxo vanadium species being usually the reactive oxidants. During the last decades the mechanistic details for several types of oxidation reactions have been elucidated. Interestingly, in a number of cases theoretical calculations offered support to the proposed reaction pathways. In general, V(V) peroxo species behave as electrophilic oxygen transfer reagents thus reacting preferentially with the more nucleophilic functional group present in the molecule. In several instance the chemoselectivity observed in such processes is very high when not absolute. As far as vanadium peroxides are concerned, a radical oxidative reactivity toward alkanes and aromatics has been also observed; also for this latter chemistry, diverse research groups studied in detail the mechanism. On the other hand, no clear-cut evidence of nucleophilic reactivity of vanadium peroxo complexes has been obtained. Here we collect a selection of recent achievements concerning the reaction mechanisms in the vanadium catalysed oxidation and bromination reactions with peroxides.
机译:在钒催化下提高过氧化物,特别是过氧化氢和烷基氢过氧化物的反应性是众所周知的方法。催化效果取决于中间体的形成,该中间体的性质取决于所用的过氧化物及其与金属前体的相互作用,高价过氧钒通常是反应性氧化剂。在过去的几十年中,已经阐明了几种类型的氧化反应的机理细节。有趣的是,在许多情况下,理论计算为提出的反应途径提供了支持。通常,V(V)过氧物质起亲电子氧转移试剂的作用,因此优先与分子中存在的更多亲核官能团反应。在一些情况下,在这种方法中观察到的化学选择性很高,即使不是绝对的。就过氧化钒而言,还观察到了对烷烃和芳烃的自由基氧化反应性。同样对于后一种化学,各种各样的研究小组详细研究了其机理。另一方面,尚未获得钒过氧配合物的亲核反应性的明确证据。在这里,我们收集了有关钒在过氧化物催化的氧化和溴化反应中反应机理的最新研究成果的精选。

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