To have an evaluation of the basic strength of aliphatic amines in ionic liquid solution, the stability constants relevant to the formation of amine/p-nitrophenol ion pairs were determined in different ionic liquids at 298 K. In particular, aliphatic (pyrrolidinium) and aromatic (imidazolium) ionic liquids were used. Imidazolium ions, bmim+ and bm2im+, having different hydrogen bond donor abilities were taken into account. Anions were chosen ([BF4 -], [PF6 -], and [NTf2 -]; where NTf 2 = bis(trifluoromethansulfonyl)imide) showing different shape, size, and coordination ability. Several primary, secondary (cyclic or not), and tertiary amines were used to study the effect of amine structure on the ion pair stability. The comparison between data collected in this work and those previously obtained in ordinary molecular solvents evidence that ionic liquids are solvent media able to exalt the amine basicity. Furthermore, the experimental trends obtained in different ionic liquids can only be rationalized considering the whole of parameters affecting their tridimensional structure.
|Numero di pagine||7|
|Rivista||Journal of Organic Chemistry|
|Stato di pubblicazione||Published - 2009|
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