一种新型杂环硫代氨基脲的合成、表征及离子传感的初步研究

ECSOC-25 Pub Date : 2021-11-14 DOI:10.3390/ecsoc-25-11760
Maria Lene F. Jardim, M. Raposo, S. Costa
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引用次数: 0

摘要

在过去的几十年里,人们对与生物和/或环境相关的分子和离子的快速、灵敏的识别和检测越来越感兴趣。因此,寻找能够协调这些分析物的新分子是一个重要的研究课题,特别是那些具有光学响应(通过颜色或荧光变化)的分子。硫代氨基脲类化合物具有广泛的生物活性和有趣的光学、电子和氧化还原性质,是一种用途广泛的有机化合物。此外,它们具有不同的结合位点,其络合能力可以通过引入不同电子特征的取代基来调节。考虑到这一点,我们报道了一种新的含氮杂环功能化的硫代氨基脲衍生物的合成。通过1h和13c核磁共振、紫外-可见吸收和荧光光谱对化合物进行了表征。此外,在具有生物、医学和环境相关性的相关离子存在的乙腈溶液中进行了初步的化学感觉研究,表明该受体具有作为荧光化学传感器的潜在应用。紫外-可见吸收和荧光光谱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Novel Heterocyclic Thiosemicarbazone: Synthesis, Characterization and Preliminary Sensing Studies for Ions
: Over the past decades, the interest in the fast and sensitive recognition and detection of molecules and ions with biological and/or environmental relevance has increased. Therefore, the search of new molecules capable of coordinating these analytes is an important topic of investiga-tion, especially those with an optical response (via color or fluorescence changes). Thiosemicarbazones are versatile organic compounds due to their wide range of biological activities and interesting optical, electronic and redox properties. Also, they possess various binding sites, whose com-plexing ability can be tuned by the introduction of substituents of different electronic character. Having this in mind, we report the synthesis of a new thiosemicarbazone derivative functionalized with a nitrogen heterocyclic moiety. The new compound was characterized by 1 H and 13 C NMR, UV-Vis absorption and fluorescence spectroscopies. Moreover, a preliminary chemosensory study was undertaken in acetonitrile solutions in the presence of relevant ions with biological, medicinal and environmental relevance showing that this receptor has potential application as a fluorimetric chemosensor. UV-Vis absorption and fluorescence spectroscopies.
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