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An N-linked disalicylaldehyde together with its caesium ion and dichloromethane sensing performances: 'dual key & lock' LMCT-enhanced fluorescence strategy.
Zhang, Kun; Chen, Ting-Ting; Shen, Yin-Jing; Yang, Zhuo-Ran; Huang, Yan; Zhang, Shishen; Xue, Jiadan; Li, Benxia.
Afiliación
  • Zhang K; Department of Chemistry, Zhejiang Sci-Tech University, Xiasha Higher Education District, Hangzhou 310018, P. R. China. zhangkun@zstu.edu.cn.
Analyst ; 145(17): 5826-5835, 2020 Aug 24.
Article en En | MEDLINE | ID: mdl-32648860
The development of inexpensive, selective and rapid-response chemosensors for detecting Cs+ in waste water is highly desirable in the nuclear power industry. Here we demonstrate an efficient Cs+ optical sensor based on the N-linked disalicylaldehyde H2Qj with excited state intramolecular proton transfer (ESIPT), and it will transform into the ligand-to-metal charge transfer (LMCT) process in the presence of Cs+, resulting in dramatically enhanced fluorescence together with a distinct change of color from light-green to green-yellow. Simultaneously, it is found that CH2Cl2 can serve as the quencher of LMCT-enhanced fluorescence, thus enabling selective CH2Cl2 detection in a turn-off fluorescence approach. Further detailed studies reveal that both Cs+ and CH2Cl2 sensing processes are rapid within 60 seconds. The corresponding limit of detection (LOD) values for sensing Cs+ and CH2Cl2 are as low as 0.37 mM and 0.37%. Moreover, it was also verified that Cs+ sensing is applicable in the range of pH = 7-11 and the reversibility of sensor H2Qj can be easily achieved by modulating pH values, and H2Qj is also assessed for its Cs+ sensing performces in real water samples. This H2Qj-Cs sensing system must provide a valuable reference for further Cs+ sensors.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Analyst Año: 2020 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Analyst Año: 2020 Tipo del documento: Article Pais de publicación: Reino Unido