Nucleophilicity in ionic liquids. 2. Cation effects on halide nucleophilicity in a series of bis(trifluoromethylsulfonyl)imide ionic liquids

被引:202
|
作者
Lancaster, NL [1 ]
Salter, PA [1 ]
Welton, T [1 ]
Young, GB [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Chem, London SW7 2AY, England
来源
JOURNAL OF ORGANIC CHEMISTRY | 2002年 / 67卷 / 25期
关键词
D O I
10.1021/jo026113d
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
In this work, the nucleophilicities of chloride, bromide, and iodide have been determined in the ionic liquids [bmiml [N(Tf)(2)], [bM(2)iM] [N(Tf)(2)], and [bmpyl [N(Tf)21 (where bmim = 1-butyl-3-methylimidazolium, bM2iM = 1-butyl-2,3-dimethylimidazolium, bmpy = 1-butyl-1-methylpyrrolidinium, and N(Tf)(2) = bis(trifluoromethylsulfonyl)imide). It was found that in the [bmim](+) ionic liquid, chloride was the least nucleophilic halide, but that changing the cation of the ionic liquid affected the relative nucleophilicities of the halides. The activation parameters DeltaH(double dagger), DeltaS(double dagger), and DeltaG(double dagger) have been estimated for the reaction of chloride in each ionic liquid, and compared to a similar reaction in dichloromethane, where these parameters were found for reaction by both the free ion and the ion pair.
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收藏
页码:8855 / 8861
页数:7
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