The effect of different interfaces and confinement on the structure of the ionic liquid 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide entrapped in cationic and anionic reverse micelles

The behavior of the ionic liquid (IL) 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (bmim]Tf(2)N]) entrapped in two reverse micelles (RMs) formed in an aromatic solvent as dispersant pseudophase: bmim]Tf(2)N]/benzyl-n-hexadecyldimethylammonium chloride (BHDC)/chlorobenzene and bmim]Tf(2)N]/sodium 1,4-bis-2-ethylhexylsulfosuccinate (AOT)/chlorobenzene, was investigated using dynamic light scattering (DLS), FT-IR and (1)H NMR spectroscopies. DLS results reveal the formation of RMs containing bmim]Tf(2)N] as a polar component since the droplet size values increase as the W(s) (W(s) = bmim]Tf(2)N]]/surfactant]) increases. Furthermore, it shows that the RMs consist of discrete spherical and non-interacting droplets of bmim]Tf(2)N] stabilized by the surfactants. Important differences in the structure of bmim]Tf(2)N] entrapped inside BHDC RMs, in comparison with the neat IL, are observed from the FT-IR and (1)H NMR measurements. The electrostatic interactions between anions and cations from bmim]Tf(2)N] and BHDC determine the solvent structure encapsulated inside the nano-droplets. It seems that the IL structure is disrupted due to the electrostatic interaction between the Tf(2)N](-) and the cationic BHDC polar head (BHD(+)) giving a high ion pair degree between BHD(+) and Tf(2)N](-) at a low IL content. On the other hand, for the AOT RMs there is no evidence of strong IL-surfactant interaction. The electrostatic interaction between the SO(3)(-) group and the Na(+) counterion in AOT seems to be stronger than the possible bmim](+)-SO(3)(-) interaction at the interface. Thus, the structure of bmim]Tf(2)N] encapsulated is not particularly disrupted by the anionic surfactant at all W(s) studied, in contrast to the BHDC RM results. Nevertheless, there is evidence of confinement in the AOT RMs because the bmim](+)-Tf(2)N](-) interaction is stronger than in bulk solution. Thus, the IL is more associated upon confinement. Our results reveal that the bmim]Tf(2)N] structure can be modified in a different manner inside RMs by varying the kind of surfactant used to create the RMs and the IL content (W(s)). These facts can be very important if these media are used as nanoreactors because unique microenvironments can be easily created by simply changing the RM components and W(s).