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A Ratiometric Fluorescent Sensor for Cd(2+) Based on Internal Charge Transfer

This work reports on a novel fluorescent sensor 1 for Cd(2+) ion based on the fluorophore of tetramethyl substituted bis(difluoroboron)-1,2-bis[(1H-pyrrol-2-yl)methylene]hydrazine (Me(4)BOPHY), which is modified with an electron donor moiety of N,N-bis(pyridin-2-ylmethyl)benzenamine. Sensor 1 has ab...

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Detalles Bibliográficos
Autores principales: Cheng, Dandan, Liu, Xingliang, Xie, Yadian, Lv, Haitang, Wang, Zhaoqian, Yang, Hongzhi, Han, Aixia, Yang, Xiaomei, Zang, Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5713183/
https://www.ncbi.nlm.nih.gov/pubmed/29099088
http://dx.doi.org/10.3390/s17112517
Descripción
Sumario:This work reports on a novel fluorescent sensor 1 for Cd(2+) ion based on the fluorophore of tetramethyl substituted bis(difluoroboron)-1,2-bis[(1H-pyrrol-2-yl)methylene]hydrazine (Me(4)BOPHY), which is modified with an electron donor moiety of N,N-bis(pyridin-2-ylmethyl)benzenamine. Sensor 1 has absorption and emission in visible region, at 550 nm and 675 nm, respectively. The long wavelength spectral response makes it easier to fabricate the fluorescence detector. The sensor mechanism is based on the tunable internal charge transfer (ICT) transition of molecule 1. Binding of Cd(2+) ion quenches the ICT transition, but turns on the π − π transition of the fluorophore, thus enabling ratiometric fluorescence sensing. The limit of detection (LOD) was projected down to 0.77 ppb, which is far below the safety value (3 ppb) set for drinking water by World Health Organization. The sensor also demonstrates a high selectivity towards Cd(2+) in comparison to other interferent metal ions.