A Thiophene-Based Dicyanovinyl as an Anion Chemosensor

ECSOC-25 Pub Date : 2021-11-14 DOI:10.3390/ecsoc-25-11769
J. P. Castro, M. Raposo, S. Costa
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引用次数: 1

Abstract

: In recent years, push–pull dicyanovinyl derivatives have been reported for several optical applications, including as fluorescent probes for cyanide ion detection. In the 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.
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噻吩基双氰乙烯基作为阴离子化学传感器
近年来,推挽式二氰乙烯基衍生物已被报道用于几种光学应用,包括作为氰化物离子检测的荧光探针。在氰化物离子存在的情况下,由于氰化物基团具有很强的吸电子作用,这类化合物表现出与氰化物离子加成到双氰乙烯基的β位置相关的ICT机制。这些由加成反应引起的结构变化伴随着探针吸收和发射的变化。在这项工作中,我们报道了一种基于噻吩的双氰乙烯基衍生物及其作为阴离子化学传感器的前景应用。在乙腈和乙腈水溶液中进行了光物理表征。在生物、医学和环境相关的各种阴离子存在下进行了初步的传感试验,并通过分光光度滴定法进一步探索了与CN -的相互作用。
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