π-Electron Systems That Form Planar and Interlocked Anion Complexes and Their Ion-Pairing Assemblies.

Abstract

Interactions between designed charged species are important for the ordered arrangements of π-electron systems in assembled structures. As precursors of π-electron anion units, new arylethynyl-substituted dipyrrolyldiketone boron complexes, which showed anion-responsive behavior, were synthesized. They formed a variety of receptor-anion complexes ([1+1] and [2+1] types) in solution, and the stabilities of these complexes were discussed in terms of their thermodynamic parameters. Solid-state ion-pairing assemblies of [1+1]- and [2+1]-type complexes with countercations were also revealed by single-crystal X-ray analysis. In particular, a totally charge-segregated assembly was constructed based on negatively and positively charged layers fabricated from [2+1]-type receptor-anion complexes and tetrabutylammonium cations, respectively. Furthermore, the [1+1]-type anion complex of the receptor possessing long alkyl chains exhibited mesophases based on columnar assembled structures with contributions from charge-by-charge and charge-segregated arrangements, which exhibited charge-carrier transporting properties.