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Spectroscopic study of the ground and excited state prototropic equilibria of 4-azaindole

机译:4-氮杂吲哚基态和激发态质子平衡的光谱研究

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The ground and singlet excited state prototropism of 4-azaindole, 4AI, in acid and basic aqueous solutions, inside and outside the pH range, has been systematically studied by using absorption and fluorescence spectroscopic techniques. These studies have thrown light on some interesting aspects on the nature and the photophysics of the 4-AI prototropic species. Thus, the changes of the 4AI absorption spectra reveal the existence of four ground state species; the pyridinic protonated cation, C (pKaC=7.5±0.1), the neutral molecule, N (pKaN=15.5±0.5), the pyrrolic deprotonated anion, A, and a previously unnoticed dication, DC (pKaDC=-4.6±0.4). Besides the emissions of these species, a new fluorescence profile appears in alkaline solutions at around 500 nm. This extra band has been ascribed to the neutral phototautomer, NT. What is more relevant to this study is the fact that the position and the intensity of the emission band assigned to the monoprotonated cation are very different from those observed for the normal cation of the 7-azaindole, 7-AI. This together with the fact that for the formation of the DC species a cationic precursor with a quinoid structure must be invoked, have prompted us to assign this cationic emission to the isomeric CI cations. Finally, the excited-state pK _as of the prototropic species of 4AI have been theoretically estimated by using the F?rster-Weller cycle.
机译:已通过吸收和荧光光谱技术系统研究了4-氮杂吲哚4AI在酸性和碱性水溶液中(pH值范围内外)的基态和单重激发态质子性。这些研究为4-AI质子变种的性质和光物理提供了一些有趣的方面。因此,4AI吸收光谱的变化揭示了四种基态物种的存在。吡啶甲酸质子化阳离子C(pKaC = 7.5±0.1),中性分子N(pKaN = 15.5±0.5),吡咯酸去质子化阴离子A和以前未被注意的指示剂DC(pKaDC = -4.6±0.4)。除了这些物质的发射外,碱性溶液中约500 nm处还出现了新的荧光特征。该额外的带归因于中性光互变异构体NT。与这项研究更相关的是,分配给单质子化阳离子的发射带的位置和强度与对7-氮杂吲哚,7-AI的正阳离子所观察到的那些不同。这与为形成DC物种而必须调用具有醌型结构的阳离子前体这一事实一起,促使我们将这种阳离子发射分配给异构CI阳离子。最后,理论上已经使用F?rster-Weller周期估算了4AI的质子态物种的激发态pK _as。

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