光化学
系统间交叉
荧光
卤化
光热治疗
量子产额
光动力疗法
材料科学
光敏剂
荧光寿命成像显微镜
猝灭(荧光)
纳米颗粒
光生物学
分子内力
消散
化学
体内
活性氧
产量(工程)
作者
Hanming Dai,Jinjun Shao,Dan Lei,Kang Xu,Tian Zhang,Anqing Mei,Peng Chen,Yuxin Guo,Xiaochen Dong
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-10-01
卷期号:19 (40): 35842-35852
被引量:7
标识
DOI:10.1021/acsnano.5c12563
摘要
Dominant nonradiative decay pathways in second-near-infrared (NIR-II) small-molecule fluorescent dyes critically impair both radiative emission and intersystem crossing (ISC) efficiencies, limiting their utility in fluorescence imaging (FLI) and phototherapy. Herein, we report a donor bromination strategy to suppress nonradiative decay in a boron difluoride (BF2) formazanate dye BDFTBr for NIR-II FLI-guided tumor photothermal and photodynamic therapy. Compared with the unbrominated analogue BDFTH, BDFTBr with donor bromination maintains a stereoscopic conformation and suppresses intramolecular vibrations, reducing vibrationally induced nonradiative heat dissipation and enhancing the fluorescence quantum yield by ∼3.75-fold. Additionally, donor bromination narrows the singlet–triplet energy gap (ΔES-T) and facilitates ISC, leading to the improved generation of multiple reactive oxygen species, even under the hypoxic tumor microenvironment. In vitro and in vivo studies confirm that BDFTBr nanoparticles enable efficient NIR-II FLI-guided tumor ablation with minimal systemic toxicity. This work provides a generalizable strategy for suppressing nonradiative decay in NIR-II small-molecule fluorescent dyes, advancing their potential in multimodal cancer phototheranostics.
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