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Anion-π interactions have been systematically studied using tetraoxacalix2arene2triazine 1, an electron-deficient and cavity self-tunable macrocyclic host, as an electron-neutral molecular probe. As revealed by electrospray ionization mass spectrometry (ESI-MS), fluorescence titration and X-ray crystallography, tetraoxacalix2arene2triazine has been found to form 1:1 complexes with four typical polyatomic anions of different geometries and shapes in the gaseous phase, in solution, and in the solid state. The association constants for the formation of anion-π complexes in acetonitrile are in the range of 239 to 16950 M(-1), following the order of 1·NO(3)(-) > 1·BF(4)(-) > 1·PF(6)(-) > 1·SCN(-). X-ray molecular structures of the complexes showed that two opposing triazine rings of tetraoxacalix2arene2triazine act as a pair of tweezers to interact with the included anions through cooperative anion-π and lone-pair electron-π interactions. The generality of anion-π interactions and diverse anion-π interaction motifs can provide a new dimension in the study of molecular recognition and self-assembly. Moreover, this study potentiates the effect of anion-π interactions in chemical and biological systems, especially those involving anion and electron-deficient aromatic species.
Wang et al. (Mon,) studied this question.