Abstract
A negatively charged π-electronic system was prepared by the complexation of a dipyrrolyldiketone BF2 complex as an anion receptor with a trialkyl-substituted azobenzene carboxylate. The bulk-state properties and photo-responsive behaviors of the azobenzene carboxylate in the ion-pairing form were controlled by complexation with the receptor molecule. The formation of receptor–carboxylate complexes was found to modulate the sizes, shapes, and electronic states of the anionic π-electronic systems, exhibiting the potential to form a variety of ion-pairing assemblies.
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