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The nature of associates of 1,4-dinitrobenzene dianion with 1-butyl-3-methylimidazolium and 1-butyl-2,3-dimethylimidazolium cations
Authors:Syroeshkin  M. A.  Mendkovich  A. S.  Mikhal’chenko  L. V.  Gul’tyai  V. P.
Affiliation:1.N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation
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Abstract:Association of 1,4-dinitrobenzene (1,4-DNB) dianion (DA) with 1-butyl-3-methylimidazolium (bmim+) and 1-butyl-2,3-dimethylimidazolium (bdmim+) cations, whose salts are widely used as ionic liquids, was studied by cyclic voltammetry. In 0.1 M solution of Bu4NClO4 in DMF, associates with the number of coordinated cations up to four in the case of bmim+ and two in the case of bdmim+ are formed. The partial stability constant values for the associates of bmim+ are 40, 20, 5, and 3.2 L mol−1, of bdmim+ − 24 and 1.9 L mol−1. The higher number of coordinated bmim+ cations is attributed to the formation of, along with ion pairs, hydrogen bonds between 1,4-DNB DA and bmim+ due to the labile hydrogen atom at position 2 of the imidazole ring, in contrast to bdmim+, which is involved only into the ion-pair interactions.
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