| Literature DB >> 29808394 |
Jian-Ying Bai1,2, Yu-Zhong Xie1,3, Chang-Jiang Wang4, Shu-Qing Fang4, Lin-Nan Cao1, Ling-Li Wang1, Jing-Yi Jin5,6.
Abstract
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.Entities:
Keywords: Fluorescence; ICT; Imaging; Mercury ion; Pyridylthiazole; Ratiometric sensor
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Year: 2018 PMID: 29808394 DOI: 10.1007/s10895-018-2241-4
Source DB: PubMed Journal: J Fluoresc ISSN: 1053-0509 Impact factor: 2.217