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翻訳と辞書　辞書検索 [ 開発暫定版 ] スポンサード リンク Autoxidation ： ウィキペディア英語版 Autoxidation Autoxidation is any oxidation that occurs in open air or in presence of oxygen (and sometimes UV radiation) and forms peroxides and hydroperoxides. A classic example of autoxidation is that of simple ethers like diethyl ether, whose peroxides can be dangerously explosive. It can be considered to be a slow, flameless combustion of materials by reaction with oxygen. Autoxidation is important because it is a useful reaction for converting compounds to oxygenated derivatives, and also because it occurs in situations where it is not desired (as in the destructive cracking of the rubber in automobile tires or in rancidification). Although virtually all types of organic materials can undergo air oxidation, certain types are particularly prone to autoxidation, including unsaturated compounds that have allylic or benzylic hydrogen atoms; these materials are converted to hydroperoxides by autoxidation. ==Mechanism== Autoxidation is a free radical chain process. Such reactions can be divided into three stages: chain initiation, propagation, and termination. In the initiation process, some event causes free radicals to be formed. For example, free radicals can be produced purposefully by the decomposition of a radical initiator, such as benzoyl peroxide. In some cases, initiation occurs by a process that is not well understood but is thought to be the spontaneous reaction of oxygen with a material with a readily abstractable hydrogen. Destructive autoxidation processes also are initiated by pollutants such as those in smog. Once free radicals are formed, they react in a chain to convert the material to a hydroperoxide. The chain is ended by termination reactions in which free radicals collide and combine their odd electrons to form a new bond. Chain initiation :$\backslash mathrm\; +\; OH\; +\; RH\; \backslash \; \backslash longrightarrow\; \backslash quad\}$ :$\backslash mathrm\; \backslash \; R\; +\; ROH\; \backslash quad\}$ Chain propagation〔I.V. Berezin, E.T. Denisov, ''The Oxidation of Cyclohexane'', Pergamon Press, New York, 1996.〕 :$\backslash mathrm\; \backslash \; ROO$ :$\backslash mathrm\; \backslash \; ROOH\; +$ Chain termination :$\backslash mathrm\; \backslash \; 2\; RO\; \backslash \; ROH\; +\; QO\; +\; O\_2\}$ Source of alcohol and ketone〔I. Hermans, T.L. Nguyen, P.A. Jacobs, J. Peeters, ''ChemPhysChem'' 2005, ''6'', 637-645.〕 :$\backslash mathrm\; \backslash \; ROOH\; +\; Q\; \backslash \; ROOH\; +\; QO\; +\; ^OH\; \}$ :$\backslash mathrm\; \backslash \; ROOH\; +\; QO\; +\; H\_2O\; +\; R^\; \backslash \; \backslash longrightarrow$ 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「Autoxidation」の詳細全文を読む スポンサード リンク 翻訳と辞書 : 翻訳のためのインターネットリソース Copyright(C) kotoba.ne.jp 1997-2016. All Rights Reserved.