The nucleophilic reactivity of a representative series of anions has been measured in [hmim][ClO4] 3i, [hm2im][ClO4] 30i, and [hmim][PF6] 3l ILs in the reaction with n-alkyl methanesulfonates and compared with that found in common molecular solvents (MeOH, DMSO, PhCl). The reactivity is found to depend on both the imidazolium cationeanion interaction and the specific solvation by water present in the IL, the water playing the main effect, in particular with hydrophilic anions. Removal of the largest quantity of water remarkably increases the ion pair reactivity in the IL up to rate constant value k comparable with those obtained in DMSO and in low polarity media (PhCl).

Reactivity of anionic nucleophiles in ionic liquids and in molecular solvents / C. Betti, D. Landini, A. Maia. - In: TETRAHEDRON. - ISSN 0040-4020. - 64:8(2008), pp. 1689-1695. [10.1016/j.tet.2007.12.009]

Reactivity of anionic nucleophiles in ionic liquids and in molecular solvents

C. Betti
Primo
;
D. Landini
Secondo
;
2008

Abstract

The nucleophilic reactivity of a representative series of anions has been measured in [hmim][ClO4] 3i, [hm2im][ClO4] 30i, and [hmim][PF6] 3l ILs in the reaction with n-alkyl methanesulfonates and compared with that found in common molecular solvents (MeOH, DMSO, PhCl). The reactivity is found to depend on both the imidazolium cationeanion interaction and the specific solvation by water present in the IL, the water playing the main effect, in particular with hydrophilic anions. Removal of the largest quantity of water remarkably increases the ion pair reactivity in the IL up to rate constant value k comparable with those obtained in DMSO and in low polarity media (PhCl).
Ionic liquids ; nucleophilic substitutions ; anionic reactivity ; alkyl methanesulfonates
Settore CHIM/04 - Chimica Industriale
2008
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/55455
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