首页> 外文期刊>Journal of the American Chemical Society >KHARASCH AND METALLOPORPHYRIN CATALYSIS IN THE FUNCTIONALIZATION OF ALKANES, ALKENES, AND ALKYLBENZENES BY T-BUOOH - FREE RADICAL MECHANISMS, SOLVENT EFFECT, AND RELATIONSHIP WITH THE GIF REACTION
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KHARASCH AND METALLOPORPHYRIN CATALYSIS IN THE FUNCTIONALIZATION OF ALKANES, ALKENES, AND ALKYLBENZENES BY T-BUOOH - FREE RADICAL MECHANISMS, SOLVENT EFFECT, AND RELATIONSHIP WITH THE GIF REACTION

机译:T-BUOOH在碱,烯烃和烷基苯官能化中的KARASCH和金属卟啉催化作用-自由基机理,溶剂作用以及与GIF反应的关系

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摘要

New results for the oxidation of alkanes, alkenes, and alkylbenzenes by t-BuOOH according to the Kharasch reaction and Mn(III)- and Fe(III)-porphyrin catalysis are reported. Chemical and kinetic evidence show the role of t-BuO(.) and t-BuOO(.) radicals in these oxidations and the strict relationship with the Gif reaction, for which recently a free-radical mechanism has been emphasized in contrast with the Barton interpretation. A key step appears to be the hydrogen abstraction from t-BuOOH by t-BuO(.), very fast in nonbasic solvents, but inhibited by solvents which form hydrogen bonds with t-BuOOH. As a consequence, the generally accepted Kochi mechanism of the Kharasch reaction must be modified, and the similar mechanistic features of the three types of catalysis (Kharasch, metalloporphyrins, and Gif) are discussed. [References: 32]
机译:据报道,根据Kharasch反应以及Mn(III)-和Fe(III)-卟啉催化,t-BuOOH氧化烷烃,烯烃和烷基苯的新结果。化学和动力学证据表明t-BuO(。)和t-BuOO(。)自由基在这些氧化中的作用以及与Gif反应的严格关系,最近与Barton相比,人们强调了自由基机理解释。关键的步骤似乎是t-BuO(。)从t-BuOOH夺氢,在非碱性溶剂中非常快,但受与t-BuOOH形成氢键的溶剂抑制。因此,必须修改普遍接受的Kharasch反应的高知机理,并讨论三种催化类型(Kharasch,金属卟啉和Gif)的相似机理。 [参考:32]

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