L. Ðorđević, C. Valentini, N. Demitri, C. Mézière, M. Allain, M. Sallé, A. Folli, D. Murphy, S. M.-Valero, E. Coronado, D. Bonifazi.
Angew. Chem. Int. Ed., 2020, 59, 4106.
Herein we report an efficient synthesis to prepare O-doped nanographenes, which derive from the longitudinally and latitudinally p-extension of pyrene. The derivatives are highly fluorescent and feature low-oxidation potentials. Exploiting electrooxidation, crystals of cationic mixed valence (MV) complexes were grown in which the organic salts organize into face-to-face pp stacks, a favorable solid-state arrangement for organic electronics. Variable-temperature EPR measurements and relaxation studies suggest a strong electron delocalization along the
longitudinal axis of the columnar p-stacking architectures. Electric measurements of single crystals of the MV salts exhibited a semiconducting behavior with a remarkable high conductivity at room temperature. These findings further support the idea for which the
p-extension of polycyclic aromatic hydrocarbons featuring precise heteroatom doping topologies, is an attractive approach to enable
nanographenes with a broad spectrum of semiconducting properties and high charge mobilities.