Abstract
A facile method for the exocyclic π-extension of the carbaporphyrinoid embedding phenanthrene moiety – phenanthriporphyrin – has been described. The reaction between 5,6-dioxophenanthriporphyrin and a series of aliphatic and aromatic amines provided a family of carbaporphyrinoids incorporating azaacene components. The 1H NMR spectroscopic, electrochemical, and optical properties of azaaceneporphyrinoids strongly depend on the structure of the incorporated moiety. The π-system extension of the attached azaacene subunit reduces the macrocyclic antiaromatic character.