Crystal structure of a methimazole-based ionic liquid.

The structure of 1-methyl-2-(prop-2-en-1-ylsulfan-yl)-1H-imidazol-3-ium bromide, C7H11N2S(+)·Br(-), has monoclinic (P21/c) symmetry. In the crystal, the components are linked by N-H⋯Br and C-H⋯Br hydrogen bonds. The crystal structure of the title compound undeniably proves that methimazole reacts through the thione tautomer, rather than the thiol tautomer in this system.

Crystal structure of tri-phenyl(vinyl)-phospho-nium tetra-phenyl-borate.

The title ionic salt, C21H20P(+)·C24H20B(-), crystallized with two independent vinyl-tri-phenyl-phospho-nium cations and two independent tetra-phenyl-borate anions per asymmetric unit. These four independent moieties contain nearly perfect tetra-hedral symmetry about their respective central C atoms. In the crystal, there are no π-stacking or other inter-molecular inter-actions present.

On the formation of a protic ionic liquid in nature.

The practical utility of ionic liquids (ILs) makes the absence (heretofore) of reported examples from nature quite puzzling, given the facility with which nature produces many other types of exotic but utilitarian substances. In that vein, we report here the identification and characterization of a naturally occurring protic IL. It can be formed during confrontations between the ants S. invicta and N. fulva. After being sprayed with alkaloid-based S. invicta venom, N. fulva detoxifies by grooming with its own venom, formic acid. The mixture is a viscous liquid manifestly different from either of the constituents. Further, we find that the change results as a consequence of formic acid protonation of the N centers of the S. invicta venom alkaloids. The resulting mixed-cation ammonium formate milieu has properties consistent with its classification as a protic IL.