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首页> 外文期刊>Journal of Fluorescence >Spectroscopic Studies of Fluorescence Effects in Bioactive 4-(5-Heptyl-1,3,4-Thiadiazol-2-yl)Benzene-1,3-Diol and 4-(5-Methyl-1,3,4-Thiadiazol-2-yl)Benzene-1,3-Diol Molecules Induced by pH Changes in Aqueous Solutions
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Spectroscopic Studies of Fluorescence Effects in Bioactive 4-(5-Heptyl-1,3,4-Thiadiazol-2-yl)Benzene-1,3-Diol and 4-(5-Methyl-1,3,4-Thiadiazol-2-yl)Benzene-1,3-Diol Molecules Induced by pH Changes in Aqueous Solutions

机译:生物活性4-(5-庚基-1,3,4-噻二唑-2-基)苯-1,3-二醇和4-(5-甲基-1,3,4-噻唑-2的荧光效应的光谱研究 - 苯-1,3-二醇分子通过pH变化致水溶液诱导

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This paper presents the results of stationary fluorescence spectroscopy and time-resolved spectroscopy analyses of two 1,3,4-thiadiazole analogues, i.e. 4-(5-methyl-1,3,4-thiadiazol-2-yl)benzene-1,3-diol (C1) and 4-(5-heptyl-1,3,4-thiadiazol-2-yl)benzene-1,3-diol (C7) in an aqueous medium containing different concentrations of hydrogen ions. An interesting dual florescence effect was observed when both compounds were dissolved in aqueous solutions at pH below 7 for C1 and 7.5 for C7. In turn, for C1 and C7 dissolved in water at pH higher than the physiological value (mentioned above), single fluorescence was only noted. Based on previous results of investigations of the selected 1,3,4-thiadiazole compounds, it was noted that the presented effects were associated with both conformational changes in the analysed molecules and charge transfer (CT) effects, which were influenced by the aggregation factor. However, in the case of C1 and C7, the dual fluorescence effects were visible in a higher energetic region (different than that observed in the 1,3,4-thiadiazoles studied previously). Measurements of the fluorescence lifetimes in a medium characterised by different concentrations of hydrogen ions revealed clear lengthening of the excited-state lifetime in a pH range at which dual fluorescence effects can be observed. An important finding of the investigations presented in this article is the fact that the spectroscopic effects observed not only are interesting from the cognitive point of view but also can help in development of an appropriate theoretical model of molecular interactions responsible for the dual fluorescence effects in the analysed 1,3,4-thiadiazoles. Furthermore, the study will clarify a broad range of biological and pharmaceutical applications of these compounds, which are more frequently used in clinical therapies.
机译:本文介绍了静止荧光光谱的结果和两种1,3,4-噻二唑类似物的时间分辨光谱分析,即4-(5-甲基-1,3,4-噻二唑-2-基)苯-1,在含有不同浓度的氢离子的水性介质中,3-二醇(C1)和4-(5-庚基-1,3,4-噻二唑-2-基)苯-1,3-二醇(C7)。当将两个化合物在低于7的pH下溶解在水溶液中的C1和7.5时,将两种化合物溶解在水溶液中的溶解中的有趣的双重荧光效果。反过来,对于将pH溶解在水中的C1和C7高于生理值(上述),仅注意到单荧光。基于所选择的1,3,4-噻二唑化合物的研究结果,注意到所提出的效果与分析的分子和电荷转移(CT)效应的构象变化有关,其受到聚集因子的影响。然而,在C1和C7的情况下,在更高的能量区域(比以前研究的1,3,4-噻唑在噻唑中观察到的不同)中可见双荧光效应。以不同浓度的氢离子的介质中的荧光寿命的测量显示出在可以观察到双荧光效应的pH范围内激发态寿命的清晰延长。重要的发现本条中提出的调查是观察到的光谱效应不仅是来自认知观点的有趣,而且可以帮助开发负责双重荧光影响的适当理论模型的分子相互作用分析了1,3,4-噻唑。此外,该研究将阐明这些化合物的广泛的生物学和药物应用,这些化合物在临床疗法中更常用。

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