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J Fluoresc ; 28(3): 795-800, 2018 May.
Artigo em Inglês | MEDLINE | ID: mdl-29808394

RESUMO

As a structural analogue of pyridylthiazole, 2-(2-benzothiazoyl)-phenylethynylquinoline (QBT) was designed as a fluorescent probe for Hg(II) based on an intramolecular charge transfer (ICT) mechanism. The compound was synthesized in three steps starting from 6-bromo-2-methylquinoline, with moderate yield. Corresponding studies on the optical properties of QBT indicate that changes in the fluorescence ratio of QBT in response to Hg(II) could be quantified based on dual-emission changes. More specifically, the emission spectrum of QBT before and after interactions with Hg(II) exhibited a remarkable red shift of about 120 nm, which is rarely reported in ICT-based fluorescent sensors. Finally, QBT was applied in the two-channel imaging of Hg(II) in live HeLa cells.


Assuntos
Corantes Fluorescentes/química , Mercúrio/análise , Imagem Óptica , Sobrevivência Celular , Corantes Fluorescentes/síntese química , Células HeLa , Humanos , Estrutura Molecular , Teoria Quântica , Espectrometria de Fluorescência
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