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Fluorescent 1,8-naphthalimide dyes as photochemical sensors for the detection of transition metal ion concentrations in non-aqueous solutions.

机译:荧光1,8-萘二甲酰亚胺染料作为光化学传感器,用于检测非水溶液中的过渡金属离子浓度。

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摘要

Designing molecules that combine a fluorophore and receptor in a modular fashion is a growing field used for chemical sensing. The photoactive supramolecule N-butyl-4(2'-aninoethyl)amino-1,8-naphthalimide is shown to be capable of considerable tuning to satisfy the requirements of a versatile sensing system. In this research it is shown that efficient through-space intramolecular photoinduced electron transfer (PET) between the fluorophore and amino group (used here as a receptor for the metals and protons) is responsible for the photoreactive signaling pathway. There exists an intramolecular charge transfer reaction leading from a locally excited (LE) state to a charge transfer state in the singlet excited state which causes the fluorescence to exhibit dual emission. The normal or planar conformation (LE) occurs at the shorter wavelength due to coupling of the lone pair of electrons on the proximal amine with the electrons on the p-orbital of the aromatic naphthalimide. The other conformation exists as the longer wavelength, or anomalous band, is described as the twisted intramolecular charge transfer (TICT) state, arising from the decoupling of the electron pairs.; The phenomenon of molecular fluorescence possesses many features that make it suitable for real-time monitoring and responding to atomic and molecular species. It is shown in this work that this naphthalinide is an efficient system where measurable spectral changes in the locally excited state and TICT state are dependent upon transition metal complexation, pH, and temperature. It is observed that a fluorescence enhancement of the LE state occurs at acidic pH, high temperatures, or in the presence of complexing metal ions, whereas the TICT state predominates at basic pH levels, lower temperatures or the absence of complexing metal ions. Because these environmental changes affect the naphthalimide's equilibrium between the TICT excited state and LE excited state, the ratio of the TICT and LE excited states can be used to measure physical properties of the naphthalimide such as the metal binding affinity and pKa values. The photophysical properties of this sensor and its fluorescence response toward the changing environment of metal complexation, pH and temperature are reported here.
机译:设计以模块化方式结合荧光团和受体的分子是用于化学传感的一个不断发展的领域。显示了光活性超分子N-丁基-4(2'-氨基乙基)氨基-1,8-萘二甲酰亚胺能够进行相当大的调节以满足通用传感系统的要求。在这项研究中表明,荧光团和氨基(在此用作金属和质子的受体)之间的有效空间内分子内光诱导电子转移(PET)负责光反应信号通路。存在分子内电荷转移反应,该分子内电荷转移反应从局部激发(LE)状态变为单重激发态的电荷转移状态,这导致荧光表现出双重发射。由于近端胺上的孤对电子与芳族萘二甲酰亚胺对位轨道上的电子偶合,因此正常或平面构象(LE)在较短的波长处发生。存在另一种构象,因为更长的波长或异常谱带被描述为扭曲的分子内电荷转移(TICT)状态,这是由于电子对的去耦引起的。分子荧光现象具有许多特征,使其适合于实时监视和响应原子和分子种类。这项工作表明,这种萘化物是一种有效的系统,其中局部激发态和TICT态的可测量光谱变化取决于过渡金属的络合物,pH和温度。观察到,在酸性pH,高温或存在络合金属离子的情况下,LE状态的荧光增强,而在碱性pH值,较低温度或不存在络合金属离子的情况下,TICT状态占主导。由于这些环境变化会影响TICT激发态和LE激发态之间的萘二甲酰亚胺平衡,因此TICT和LE激发态的比率可用于测量萘二甲酰亚胺的物理性质,例如金属结合亲和力和pKa值。本文报道了该传感器的光物理特性及其对金属络合,pH和温度变化环境的荧光响应。

著录项

  • 作者

    Kidder, Michelle Kelly.;

  • 作者单位

    South Dakota State University.;

  • 授予单位 South Dakota State University.;
  • 学科 Chemistry Organic.; Chemistry Inorganic.; Chemistry Analytical.
  • 学位 Ph.D.
  • 年度 2000
  • 页码 187 p.
  • 总页数 187
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 有机化学;无机化学;化学;
  • 关键词

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