Enhanced Red Persistent Room-Temperature Phosphorescence Induced by Orthogonal Structure Disruption during Electronic Relaxation

autofluorescence. However, efficient long-wavelength RTP is difficult. Here, enhanced red RTP based on a unique mechanism was observed from deuterated dibenzo[g.p]chrysenes substituted with a phenoxazine. The yield was 16%, with an average lifetime of 1.8 s. An orthogonal dihedral angle between the dibenzo[g.p]chrysene and the phenoxazine in the lowest excited singlet state allowed a forbidden fluorescence to increase triplet generation. When the dihedral angle changed, disengagement of the forbidden fluorescence from the excited singlet state occurred, and the lowest triplet excited state had a facilitated phosphorescence rate without increasing its nonradiative transition rate. The facilitated phosphorescence rate as well as the large triplet yield led to the enhanced red RTP.