Synthesis of Contorted Polycyclic Aromatic Compounds via Alkyne Benzannulation on Zigzag‐Edged Dibenzochrysene Derivatives

Organic dyes are interesting building blocks for the preparation of organic semiconductors as they possess synthetic handles that can be used to functionalize them and, consequently, change their electronic properties. However, reactions to extend their π‐conjugated framework through ring annulation have only been scarcely tested. Herein, we report the use of alkyne benzannulation on 2,8‐dibromo‐dibenzo[def,mno]chrysene (vat orange 3) and 2,9‐dibromo‐dibenzo[b,def]chrysene (vat orange 1) to extend the conjugation and reduce their bandgap. Unexpectedly, the ring closure reaction takes place at the most sterically hindered positions (peri to the substituent) to yield contorted polycyclic compounds. More surprisingly, both TIPS‐acetylene‐functionalized derivatives underwent a tandem dearomative spirocyclization to form bent polycyclic compounds. Absorption spectroscopy reveals that ring annulation on both 2,9‐dibromo‐dibenzo[b,def]chrysene and 2,8‐dibromo‐dibenzo[def,mno]chrysene resulted in a decrease of 0.38 and 0.12 eV in bandgap values, respectively, despite inducing a contorted conformation. Herein, we report the use of alkyne benzannulation on zigzag‐edged dibenzochrysene derivatives to extend the conjugation and reduce their bandgap. Unexpectedly, the ring closure reaction takes place at the most sterically hindered positions (peri to the substituent) to yield contorted polycyclic compounds. Moreover, both TIPS‐acetylene‐functionalized dibenzochrysene derivatives underwent a tandem dearomative spirocyclization to form bent polycyclic compounds.