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Stable Radical Cations of N,N′‐Diarylated Dihydrodiazapentacenes

A series of quinoidal N,N′‐diaryldiaza‐N,N′‐dihydropentacenes (Quino) was prepared in a two‐step reaction, starting from quinacridone. Oxidation of Quino furnishes stable radical cations, isoelectronic to the radical anions of the azaacenes, whereas the dicationic species are isoelectronic to neutra...

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Detalles Bibliográficos
Autores principales: Xie, Gaozhan, Brosius, Victor, Han, Jie, Rominger, Frank, Dreuw, Andreas, Freudenberg, Jan, Bunz, Uwe H. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6973034/
https://www.ncbi.nlm.nih.gov/pubmed/31538683
http://dx.doi.org/10.1002/chem.201904308

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