From helix to macrocycle: anion-driven conformation control of π-conjugated acyclic oligopyrroles.

Anion-responsive pyrrole-based linear receptor oligomers were newly synthesized and their anion-driven dynamic conformation changes were investigated. Phenylene-bridged dimers and a tetramer of dipyrrolyldiketone boron complexes as π-conjugated acyclic anion receptors formed anion-driven helical structures in the solid and solution states. In fact, single-crystal X-ray analyses of the receptor-anion complexes exhibited various helical structures, such as [1+1]- and [1+2]-type single helices and a [2+2]-type double helix according to the lengths of oligomers and the existence of terminal aryl substituents. Anion-binding modes and behaviors of the oligomers in solution state were also examined by (1)H NMR and UV/Vis spectra along with ESI-TOF MS. Differences in the binding modes were observed in the solid and solution states. The oligomers showed augmented anion-binding constants and anion-tunable electronic and optical properties in comparison with the monomer receptor. A negative cooperative effect in the tetramer was observed in the second anion binding of the [1+2]-type single helix due to electrostatic repulsion between two anions captured in the helix. Further, an anion-template coupling reaction from the linear dimer provided a receptor macrocycle, which was obtained as a Cl(-) complex with distinct electronic and optical properties. The macrocycle exhibited extremely high anion-binding constants (>10(10) m(-1) in CH(2)Cl(2)) through multiple hydrogen bonding.