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A Meisenheimer complex or Jackson–Meisenheimer complex in organic chemistry is a 1:1 reaction adduct between an arene carrying electron withdrawing groups and nucleophile. These complexes are found as reactive intermediates in nucleophilic aromatic substitution but stable and isolated Meisenheimer salts are also known. ==Background== The early development of this type of complex takes place around the turn of the 19th century. In 1886 Janovski observed an intense violet color when he mixed ''meta''-dinitrobenzene with an alcoholic solution of alkali. In 1895 Lobry de Bruyn investigated a red substance formed in the reaction of trinitrobenzene with potassium hydroxide in methanol. In 1900 Jackson and Gazzolo reacted trinitroanisole with sodium methoxide and proposed a quinoid structure for the reaction product. : In 1902 Jakob Meisenheimer observed that by acidifying their reaction product, the starting material was recovered. With three electron withdrawing groups, the negative charge in the complex is located at one of the nitro groups according to the quinoid model. When less electron poor arenes this charge is delocalized over the entire ring (structure to the right in ''scheme 1''). In one study a Meisenheimer arene (4,6-Dinitrobenzofuroxan) was allowed to react with a strongly electron-releasing arene (1,3,5-tris(N-pyrrolidinyl)benzene) forming a zwitterionic Meisenheimer–Wheland complex. The Wheland intermediate is its opposite number and the reactive intermediate in electrophilic aromatic substitution. : The structure of this complex was confirmed by NMR spectroscopy. 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「Meisenheimer complex」の詳細全文を読む スポンサード リンク
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