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[强酸性溶液中氧氟沙星的荧光光谱与质子化作用]

[Fluorescence spectra and protonation of ofloxacin in strong acidic solutions].

作者信息

Li Hui-zhen, Zhang Cheng-feng, Gao Xiu-xiang, Huang Kun, Zhai Yu-jing, Xu Yi-zhuang, Wu Jin-guang

机构信息

The State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China.

出版信息

Guang Pu Xue Yu Guang Pu Fen Xi. 2009 May;29(5):1308-12.

Abstract

Fluorescence and UV-Vis spectra of ofloxacin (OFL) in sulfuric acid were studied. In the present paper, a new protonation state of OFL was observed. In hydrochloric acid, OFL produced bright green fluorescence upon excitation by UV radiation. The maximal emission wavelength of OFL is about 505 nm. However, OFL produces violet fluorescence when dissolved in concentrated sulfuric acid. The maximal emission wavelength changes into 400 nm. Further analysis demonstrated that the above changes arise from the variation of protonation states of OFL molecule. In dilute sulfuric acid, OFL accepted one proton, resulting in a protonation state that is similar to the OFL molecule dissolved HCl solution. The corresponding fluorescence band occurs at 505 nm. In concentrated sulfuric acid solution, OFL might accept additional protons. As a result, the size of the conjugated system is reduced and the fluorescence band exhibits a blue shift. In sulfuric acid of moderate concentrations, two bands at 505 and 400 nm respectively were found in the fluorescence emission spectra, indicating that OFL in two different protonation states coexists in the solution. In addition, both excitation band in excitation spectra and absorption bands in UV-Vis spectra exhibit red-shifted with the decrease in the concentration of sulfuric acid. Based on the above result, OFL can be used as a spectral probe to reflect the variation of H+ in strong acid environment.

摘要

研究了硫酸中氧氟沙星(OFL)的荧光光谱和紫外可见光谱。在本文中,观察到OFL的一种新的质子化状态。在盐酸中,OFL在紫外辐射激发下产生亮绿色荧光。OFL的最大发射波长约为505nm。然而,OFL溶解在浓硫酸中时产生紫色荧光。最大发射波长变为400nm。进一步分析表明,上述变化源于OFL分子质子化状态的改变。在稀硫酸中,OFL接受一个质子,形成与溶解在HCl溶液中的OFL分子相似的质子化状态。相应的荧光带出现在505nm处。在浓硫酸溶液中,OFL可能接受额外的质子。结果,共轭体系的尺寸减小,荧光带出现蓝移。在中等浓度的硫酸中,荧光发射光谱中分别在505和400nm处发现两条谱带,表明溶液中存在两种不同质子化状态的OFL共存。此外,激发光谱中的激发带和紫外可见光谱中的吸收带均随着硫酸浓度的降低而出现红移。基于上述结果,OFL可作为光谱探针来反映强酸环境中H+的变化。

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