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In chemistry, redistribution usually refers to the exchange of anionic ligands bonded to metal and metalloid centers. The conversion does not involve redox, in contrast to disproportionation reactions. Redistribution reactions are usefully conducted at higher temperatures; upon cooling the mixture, the product mixture is kinetically frozen and the individual products can be separated. In cases where redistribution is rapid at mild temperatures, the reaction is less useful synthetically but still important mechanistically. ==Examples== Useful redistribution reactions are found in organoaluminium-, organoboron-, and organosilicon chemistry.〔Greenwood, N. N.; & Earnshaw, A. (1997). Chemistry of the Elements (2nd Edn.), Oxford:Butterworth-Heinemann. ISBN 0-7506-3365-4.〕〔Many mixed organo-chloro derivatives of many metalloids are produced in this manner. In one example, 〕 : BCl3 + 2 B(C2H5)3 → 3 BCl(C2H5)2 In another example, tetramethylsilane is an undesirable product of the industrially important direct process, but it can be converted (recycled) into more useful products by redistribution with silicon tetrachloride: : SiMe4 + SiCl4 → 2 SiMe2Cl2 In organotin chemistry, the mixed alkyl tin chlorides are produced by redistribution, a reaction called the Kocheshkov comproportionation:〔G. G. Graf "Tin, Tin Alloys, and Tin Compounds" in Ullmann's Encyclopedia of Industrial Chemistry, 2005 Wiley-VCH, Weinheim 〕 : 3 SnBu4 + SnCl4 → 4 SnBu3Cl Many metal halides undergo redistribution reactions, usually to afford nearly statistical mixtures of products. For example, titanium tetrachloride and titanium tetrabromide redistribute their halide ligands, one of many reactions in this conversion is shown: : TiCl4 + TiBr4 → 2 TiBr2Cl2 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「Redistribution (chemistry)」の詳細全文を読む スポンサード リンク
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