首页> 外文期刊>chemistryselect >Receptor-Spacer-Fluorophore Based Coumarin-Thiosemicarbazones as Anion Chemosensors with 'Turn on' Response: Spectroscopic and Computational (DFT) Studies
【24h】

Receptor-Spacer-Fluorophore Based Coumarin-Thiosemicarbazones as Anion Chemosensors with 'Turn on' Response: Spectroscopic and Computational (DFT) Studies

机译:基于受体-间隔区-荧光团的香豆素-氨基硫代脲作为具有“开启”响应的阴离子化学传感器:光谱和计算 (DFT) 研究

获取原文
获取原文并翻译 | 示例

摘要

Anion sensing via small molecules as chemosensor carries unique significance in biological and environmental fields, where it offers several advantages over the traditional methods of ion sensing. In the current study, the receptor-spacerfluorophore based coumarin thiosemicarbazones were synthesized and investigated as chemosensor against different anions. The anion interaction with thiosemicarbazone based receptors (ligands) was observed and investigated with naked-eye and by using UV-Visible, fluorescence and (HNMR)-H-1 spectroscopic techniques. The deprotonation of NH protons upon binding with F was confirmed via (HNMR)-H-1 spectroscopic data. Binding constants and limit of detection was also calculated. Theoretical studies via DFT calculations were also carried to understand the ligand-anion interaction. The theoretical and experimental data was found to be in agreement, confirming the anion mediated NH proton abstraction as the mechanism that is responsible for anion sensing. Furthermore, the reason (and mechanism responsible) for anion selectivity exhibited by these chemosensors was also investigated computationally.
机译:通过小分子作为化学传感器的阴离子传感在生物和环境领域具有独特的意义,与传统的离子传感方法相比,它具有多种优势。在本研究中,合成了基于受体间隔氟基团的香豆素氨基脲,并研究了作为针对不同阴离子的化学传感器。用肉眼和紫外-可见光、荧光和 (HNMR)-H-1 光谱技术观察和研究了阴离子与氨基硫脲基受体(配体)的相互作用。通过(HNMR)-H-1光谱数据证实了NH质子与F结合时的去质子化。还计算了结合常数和检测限。通过DFT计算进行理论研究,了解配体-阴离子相互作用。理论和实验数据是一致的,证实了阴离子介导的NH质子提取是负责阴离子感应的机制。此外,还通过计算研究了这些化学传感器表现出阴离子选择性的原因(和机制)。

著录项

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号