Stable Subporphyrin meso-Aminyl Radicals without Resonance Stabilization by a Neighboring Heteroatom.

Most aminyl radicals studied so far are resonance-stabilized by neighboring heteroatoms, and those without such stabilization are usually short-lived. We report herein that subporphyrin meso-2,4,6-trichlorophenylaminyl radicals and a bis(5-subporphyrinyl)aminyl radical are fairly stable under ambient conditions without such stabilization. The subporphyrin meso-2,4,6-trichlorophenylaminyl radical crystal structure displays a characteristically short Cmeso -N bond and a perpendicular arrangement of the meso-arylamino group. The stabilities of these radicals have been ascribed to extensive spin delocalization over the subporphyrin π-electronic network as well as steric protection around the aminyl radical center.