Revealing the Hydrolysis Mechanism of a Hg2+-Reactive Fluorescein Probe: Novel Insights on Thionocarbonated Dyes
Author(s) -
Audrey PicardLafond,
Dominic Larivière,
Denis Boudreau
Publication year - 2019
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.9b03333
Subject(s) - mercury (programming language) , hydrolysis , metal ions in aqueous solution , fluorescein , chemistry , fluorescence , chloride , pollutant , mechanism (biology) , metal , combinatorial chemistry , molecule , environmental chemistry , photochemistry , nanotechnology , computer science , organic chemistry , materials science , optics , philosophy , physics , epistemology , programming language
As one of the most toxic metal pollutants, mercury is the subject of extensive research to improve current detection strategies, notably to develop sensitive, selective, fast, and affordable Hg 2+ -responsive fluorescent probes. Comprehending the sensing mechanism of these molecules is a crucial step in their design and optimization of their performance. Herein, a new fluorescein-based thionocarbonate-appended Hg 2+ -sensitive probe was synthesized to study the hydrolysis reactions involved in the sensing process. Autohydrolysis was revealed as a significant component of the signal generation mechanism, occurring concurrently with Hg 2+ -catalyzed hydrolysis. This knowledge was used to investigate the effects of key experimental conditions (pH, temperature, chloride ions) on sensing efficiency. Overall, the chemical and physical properties of this new thionocarbonated dye and the insights into its sensing mechanism will be instrumental in designing reliable and effective portable sensing strategies for mercury and other heavy metals.
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