分子内力
荧光
光化学
化学
吲哚试验
量子产额
吸收(声学)
猝灭(荧光)
电子转移
硫化氢
共轭体系
分子
立体化学
材料科学
硫黄
有机化学
聚合物
物理
量子力学
复合材料
作者
Shuai Zhao,Yonggan Xue,Lijuan Hu,Fang Sun,Jun Nie,Yincheng Chang
标识
DOI:10.1002/slct.202300554
摘要
Abstract A NIR‐II fluorescent probe (Et‐1080) for H 2 S detection was fabricated based on the intramolecular charge transfer blocking mechanism. The enhanced electron density of the indole donor further drove the Et‐1080′s absorption and emission to the NIR‐II region with a high molar absorption coefficient and acceptable fluorescence quantum yield. The C=N double bond of electron‐deficient indole can react with H 2 S rapidly via a nucleophilic addition mechanism, resulting in the destruction of conjugated structure and fluorescence quenching of the Et‐1080 molecule. The probe showed high selectivity and sensitivity to H 2 S, which could realize the rapid detection of H 2 S in NIR‐II band and showed great potential in the further disease diagnosis associated with H 2 S.
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