Abstract

AbstractOrganic photosensitizers (PSs) with aggregation‐induced emission (AIE) characteristics have shown several advantages in photodynamic therapy (PDT). However, how to design PSs with the required optical and biological properties is a formidable challenge. In this work, a series of AIE active pyridine‐ and pyridinium‐functionalized carbazole with different substituents are designed and synthesized. Compared to other analogs, BK‐Pys‐BP containing benzophenone moiety on the pyridinium unit produces reactive oxygen species (ROS) efficiently in the presence of light due to its large spin‐orbit coupling constant to promote efficient intersystem crossing. Based on its structure, three molecules with enhanced donor–acceptor strength and conjugation are further investigated to realize emission covering the whole visible region. The cationic nature and excellent ROS generation ability of benzophenone‐containing AIE photosensitizers allows for specific imaging of mitochondria, killing cancer cells, and as a singlet oxygen donor to catalyze the formation of endoperoxides. Thus, the present work presents an effective strategy for creating AIE photosensitizers with efficient ROS generation for wide biological applications.

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