聚集诱导发射
深铬移
材料科学
硫化氢
半色移
荧光
猝灭(荧光)
纳米技术
有机发光二极管
光化学
组合化学
化学
硫黄
物理
图层(电子)
量子力学
冶金
作者
Ming Chen,Rui Chen,Yang Shi,Jianguo Wang,Yanhua Cheng,Ying Li,Xuedong Gao,Yun Yan,Jing Zhi Sun,Anjun Qin,Ryan T. K. Kwok,Jacky W. Y. Lam,Ben Zhong Tang
标识
DOI:10.1002/adfm.201704689
摘要
Abstract Development of new aggregation‐induced emission (AIE) luminogens has been a hot research topic because they thoroughly solve the notorious aggregation‐caused quenching effect confronted in conventional fluorogens and their promising applications in, for example, organic light‐emitting diodes, chemo‐ and biosensors and bioimaging. Many AIE luminogens (AIEgens) have been prepared but most of them are silole, tetraphenylethene, distyrylanthracene, and their derivatives. In this work, based on the skeleton of tetraphenylpyrazine (TPP), a new AIEgen, named TPP‐PDCV, is generated by functionalizing TPP with malonitrile group. TPP‐PDCV can serve as a sensitive ratiometric fluorescent probe for detecting hydrogen sulfide with high speciality and low detection limit of down to 0.5 × 10 −6 m . The mechanism for such detection is fully investigated and deciphered. Unlike most reported mechanochromic AIEgens, which undergo turn‐off or ‐on emission or emission bathochromic shift in the presence of external stimuli, TPP‐PDCV exhibits an abnormal and reversible mechanochromism with hypsochromic effect. These indicate that TPP‐PDCV possesses a huge potential for high‐tech applications through rational modification of TPP core.
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