Achieving enhanced ML or RTP performance: alkyl substituent effect on the fine-tuning of molecular packing

Mechanoluminescence (ML) and room temperature phosphorescence (RTP) have generally been considered to be highly related to the molecular packing in the solid state; accordingly, the regulation of packing through molecular design is particularly important. Unlike most previous research, flexible alkyl substituents instead of aromatic substituents were utilized to fine-tune the molecular packing in this work. Really, just simply modifying different alkyl substituents on the aromatic core, the PIth-C derivatives exhibited regular changes in molecular packing accompanied by tunable ML/RTP properties. Among them, PIth-C3 and PIth-C4 displayed largely enhanced ML intensities, while PIth-C5 and PIth-C6 had much better RTP performance. The enhancement of ML and RTP could be ascribed to the effective suppression of nonradiation under different conditions, through distinct crystal packing modes and strong intermolecular interactions. This alkyl substituent effect reveals an effective strategy for the molecular design of ML and RTP luminogens, with deep understanding of the structure-packing-property relationship.

Automated summary

In this study, flexible alkyl substituents were used to fine-tune molecular packing, resulting in regular changes in molecular packing of PIth-C derivatives. The alkyl substituent effect revealed an effective strategy for the molecular design of ML and RTP luminogens.