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Synthesis and Photophysical Study of Tetraphenyl Substituted BODIPY Based Phenyl-Monoselenide Probe for Selective Detection of Superoxide
Journal of Fluorescence ( IF 2.7 ) Pub Date : 2022-11-26 , DOI: 10.1007/s10895-022-03096-w
Shrikrishna T Salunke 1, 2 , Divyesh S Shelar 1 , Sudesh T Manjare 1
Affiliation  

Selenium containing tetraphenyl substituted BODIPY probe was successfully synthesized from respective selenium aldehyde and tetraphenyl pyrrole using Knoevenagel-type condensation. The product was characterized using various spectroscopic techniques (1 H, 13 C, 77Se, 11B, and 19 F) and mass spectrometry. The probe was found to be selective and sensitive towards detection of superoxide over other ROS with a “turn-off” (quenched) fluorescence response. The detection limit of the probe was found to be 4.87 µM. The probe reacted with superoxide in less than a sec with a stoke shift of 35 nm.



中文翻译:

四苯基取代 BODIPY 基苯基单硒化物探针的合成及光物理研究,用于超氧化物的选择性检测

使用 Knoevenagel 型缩合从各自的硒醛和四苯基吡咯成功合成了含硒四苯基取代的 BODIPY 探针。使用各种光谱技术(1  H、13  C、77 Se、11 B 和19  F)和质谱法对产物进行表征。发现该探针比其他 ROS 具有“关闭”(淬灭)荧光响应,对检测超氧化物具有选择性和敏感性。发现探针的检测限为 4.87 µM。探针在不到 1 秒的时间内与超氧化物反应,冲程位移为 35 nm。

更新日期:2022-11-27
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