Helicity control of a polyaromatic coordination capsule through stereoselective CH-π interactions.

Although square-planar ML units are essential building blocks for coordination cages and capsules, the non-covalent control of the chirality and helicity of the resultant nanostructures is quite difficult. Here we report the helicity control of an ML polyaromatic capsule, formed from metal ions with square-planar coordination geometry and bent bispyridine ligands, through stereoselective CH-π interactions with monosaccharide derivatives. Thanks to host-guest CH-π multi-interactions, one molecule of various permethylated monosaccharides is quantitatively bound by the capsule in water ( up to >10 M). In the polyaromatic cavity, among them, the selective binding of a β-glucose derivative (>80 : 20 ratio) is demonstrated from a mixture of the α/β-glucoses, through the -selective recognition of the anomeric (C1) group. A similar stereoselective binding is accomplished from an α/β-galactose mixture. Interestingly, single equatorial/axial configurations on the bound monosaccharides can regulate the helical conformation of the capsule in water, confirmed by CD, NMR, and theoretical analyses. An intense capsule-based Cotton effect is exclusively observed upon encapsulation of the permethylated α-glucose (>20-fold enhancement as compared to the β-glucose derivative), the induction of a single-handed host helicity to a large extent. Inverse capsule helicity is induced by the binding of a β-galactose derivative under the same conditions.