A thiophene-based dicyanovinyl as an anion chemosensor

In recent years, push-pull dicyanovinyl derivatives have been reported for several optical applications, including as fluorescent probes for cyanide ion detection. In presence of cyanide ions, this type of compound exhibits an ICT mechanism associated with the addition of the cyanide ion to the β-po...

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Bibliographic Details
Main Author: Castro, João P. (author)
Other Authors: Raposo, M. Manuela M. (author), Costa, Susana P. G. (author)
Format: conferencePaper
Language:eng
Published: 2022
Subjects:
Online Access:https://hdl.handle.net/1822/80286
Country:Portugal
Oai:oai:repositorium.sdum.uminho.pt:1822/80286
Description
Summary:In recent years, push-pull dicyanovinyl derivatives have been reported for several optical applications, including as fluorescent probes for cyanide ion detection. In presence of cyanide ions, this type of compound exhibits an ICT mechanism associated with the addition of the cyanide ion to the β-position of the dicyanovinyl group, due to the strong electron-withdrawing effect of the cyano groups. These structural changes caused by the addition reaction are accompanied by changes in the probe’s absorption and emission. In this work, we report a thiophene-based dicyanovinyl derivative and its prospective application as an anion chemosensor. The photophysical characterization was carried out in acetonitrile and aqueous acetonitrile solutions. Preliminary sensing assays in the presence of various anions of biological, medicinal and environmental relevance were conducted and the interaction with CN- was further explored through spectrophotometric titrations.