Structural Engineering of Red Luminogens to Realize High Emission Efficiency through ACQ‐to‐AIE Transformation

Abstract Deep red/near‐infrared (NIR, >650 nm) emissive organic luminophores with aggregation‐induced emission (AIE) behaviours have emerged as promising candidates for applications in optoelectronic devices and biological fields. However, the molecular design philosophy for AIE luminogens (AIEgens) with narrow band gaps are rarely explored. Herein, we rationally designed two red organic luminophores, FITPA and FIMPA, by considering the enlargement of transition dipole moment in the charge‐transfer state and the transformation from aggregation‐caused quenching (ACQ) to AIE. The transition dipole moments were effectively enhanced with a “V‐shaped” molecular configuration. Meanwhile, the ACQ‐to‐AIE transformation from FITPA to FIMPA was induced by a methoxy‐substitution strategy. The experimental and theoretical results demonstrated that the ACQ‐to‐AIE transformation originated from a crystallization‐induced emission (CIE) effect because of additional weak interactions in the aggregate state introduced by methoxy groups. Owing to the enhanced transition dipole moment and AIE behaviour, FIMPA presented intense luminescence covering the red‐to‐NIR region, with a photoluminescence quantum yield (PLQY) of up to 38 % in solid state. The promising cell‐imaging performance further verified the great potential of FIMPA in biological applications. These results provide a guideline for the development of red and NIR AIEgens through comprehensive consideration of both the effect of molecular structure and molecular interactions in aggregate states.