Novel Chiral Macrocycles Containing Two Electronically Interacting Arylene Chromophores

Novel chiral macrocycles consisting of two rigid oligoarylene rods and two chiral spiroindane clips have been synthesized by condensation of spiroindane diols and CF3‐activated α‐ω‐difluorooligoaryls. Since a broad variety of planar aromatic macrocycles is known, our non‐planar, chiral rings represent a new class of macrocyclic compounds. The first two examples, which contain quaterphenylene and diphenylbithiophene rods, are presented in this communication; for one of them a crystal structure is given. The chiroptical properties of the macrocycles can be interpreted as an interplay of the “intra‐rod” helicity of individual oligoarylene rods and the “inter‐rod” helicity between both chromophores of the macrocycle. The macrocycles can act as chiral dopands of commercially available, and novel, polymeric nematic liquid crystals (emissive polyfluorenes). The “intra‐rod” helicity of individual oligoarylene rods is the main feature in determining the resulting helical twisting power (HTP). The cholestric induction in mesogenic, emissive polyfluorenes is of special interest for a realization of electronic devices that have a circularly polarized electroluminescence. The results are also important for an understanding of larger ensembles of chiral rodlike molecules, especially their π–π interactions. An interplay of the “intra‐rod” and “inter‐rod” helicity can be used to describe the chiroptical properties of the novel chiral macrocycles synthesized by the condensation of spiroindane diols and CF3‐activated α,ω‐difluorooligoaryls. The macrocycles (an example is shown here) can act as chiral dopands of nematic LC phases. The results are also important for an understanding of larger ensembles of chiral rodlike molecules, especially their π–π interactions.