Anomalous deep-red luminescence of perylene black analogues with strong p-p interactions

Perylene bisimide (PBI) dyes are known as red, maroon and black pigments, whose colors depend on the close p-p stacking arrangement. However, contrary to the luminescent monomers, deep-red and black PBI pigments are commonly non- or only weakly fluorescent due to (multiple) quenching pathways. Here, we introduce N-alkoxybenzyl substituted PBIs that contain close p stacking arrangement (exhibiting d(n-n) approximate to 3.5 A, and longitudinal and transversal displacements of 3.1 angstrom and 1.3 angstrom); however, they afford deep-red emitters with solid-state fluorescence quantum yields (phi(F)) of up to 60%. Systematic photophysical and computational studies in solution and in the solid state reveal a sensitive interconversion of the PBI-centred locally excited state and a charge transfer state, which depends on the dihedral angle (theta) between the benzyl and alkoxy groups. This effectively controls the emission process, and enables high FF by circumventing the common quenching pathways commonly observed for perylene black analogues.