Photochemical synthesis of carbazole-fused Blatter radicals: effective spin injection to the carbazole system

Photocyclization of N-substituted carbazole derivatives of benzo[<i>e</i>][1,2,4]triazine gave two carbazole-fused Blatter radicals with a novel heterocyclic skeleton. No photocyclization was observed for the analogous dibenzocarbazole, indole, benzimidazole, and phenoxazine precursors, which was rationalized with DFT computational methods. The two carbazole-derived radicals were characterized by spectroscopic (UV-vis, EPR) and electrochemical methods, while one of them was analyzed structurally (XRD) and magnetically (SQUID). The latter analysis revealed ferromagnetic interactions in the solid state with 2<i>J</i>/<i>k</i> _B = 16.6 K. Properties of these first examples of a new class of stable radicals were analyzed with DFT methods, which confirmed significant impact of the <i>peri</i>-nitrogen atom on electronic properties and additional 15% spin delocalization.