磷光
兴奋剂
光化学
激发态
量子产额
荧光
材料科学
荧光团
发光
紧身衣
发色团
近红外光谱
分析化学(期刊)
化学
光电子学
光学
有机化学
物理
核物理学
作者
Shinji Iwakiri,Ryohei Hasegawa,Yuji Kubo
标识
DOI:10.1002/cptc.202200073
摘要
Abstract Near‐infrared (NIR) luminescent materials have received considerable attention owing to their intriguing applications in fields such as high‐resolution biological imaging and information technology. In this context, room‐temperature phosphorescence (RTP) materials with emission bands in the NIR region are rare. Metal‐free arylselanyl‐BODIPY triplet photosensitizers were doped into a benzophenone ( BP ) matrix. When excited at 350 nm, RTP emission was observed in the NIR region with λ em values of 750–816 nm, and the phosphorescence quantum yield was up to 0.48 %. The detection of an extremely large Stokes shift (≥400 nm) was responsible for the triplet‐triplet energy transfer from BP to the BODIPY guest. Furthermore, the RTP properties were tuned by derivatization of the selenium‐containing BODIPY guests. NIR‐RTP properties were also detected upon excitation at 470 nm with a persistent lifetime of up to 17.5 ms. Notably, in addition to NIR RTP emission, thermally activated delayed fluorescence was detected at 620 nm when 10 ms delayed spectra were measured for the MeOSeBOD ‐doped system. Considering the synthetic versatility of the BODIPY chromophore, this work opens up a new strategy for developing small molecule‐based NIR RTP systems.
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