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Selective Catalytic Oxidation of C-H Bonds with Molecular Oxygen

机译:用分子氧的选择性催化氧化C-H键

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摘要

Although catalytic reductions, cross-couplings, metathesis, and oxidation of C=C double bonds are well established, the corresponding catalytic hydroxylations of C-H bonds in alkanes, arenes, or benzylic (allylic) positions, particularly with O-2, the cheapest, "greenest", and most abundant oxidant, are severely lacking. Certainly, some promising examples in homogenous and heterogenous catalysis exist, as well as enzymes that can perform catalytic aerobic oxidations on various substrates, but these have never achieved an industrial-scale, owing to a low space-time-yield and poor stability. This review illustrates recent advances in aerobic oxidation catalysis by discussing selected examples, and aims to stimulate further exciting work in this area. Theoretical work on catalyst precursors, resting states, and elementary steps, as well as model reactions complemented by spectroscopic studies provide detailed insight into the molecular mechanisms of oxidation catalyses and pave the way for preparative applications. However, O-2 also poses a safety hazard, especially when used for large scale reactions, therefore sophisticated methodologies have been developed to minimize these risks and to allow convenient transfer onto industrial scale.
机译:虽然C = C双键的催化还原,交叉偶联,复分解和氧化是很好的,但是烷烃,芳香或苄基(烯丙基)位置的相应CH键的相应催化羟基,特别是与O-2,最便宜的, “最逼近”,最丰富的氧化剂,严重缺乏。当然,存在均匀和异源性催化的一些有希望的实例,以及可以在各种基材上进行催化有氧氧化的酶,但由于节省时间 - 产量和稳定性差,这些从未实现了工业规模。该综述说明了通过讨论所选实施例,旨在通过讨论所选择的实施例,并旨在刺激该区域的进一步激动化的工作。催化剂前体,休息状态和基本步骤的理论上,以及光谱研究辅以模型反应,提供了对氧化催化剂的分子机制并铺平制备应用方法的详细洞察。然而,O-2也构成了安全危害,特别是当用于大规模反应时,因此开发了复杂的方法以最大限度地减少这些风险,并使方便地转移到工业规模上。

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