Stereospecific synthesis of chiral P-containing polyaromatics based on 7-membered P-rings

We present the stereospecific synthesis of helicenoid-based phosphepines (7-membered P-rings) as well as chiral P-containing polycyclic aromatic hydrocarbons. In these systems, an axial to central chirality transfer takes place from the BINAP moiety to the P-atom. The impact of the molecular design on the structure, the (chir)optical (including circularly polarized luminescence) and redox properties are investigated. Stereospecific synthesis and (chir)optical and redox properties of helicenoid-based phosphepine as well as chiral P-containing polycyclic aromatic hydrocarbons are presented.