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十六烷基三甲基溴化铵(CTAB)和十二烷基硫酸钠(SDS)胶束对某些吲哚探针激发态平衡的影响。

Effect of CTAB and SDS micelles on the excited state equilibria of some indole probes.

作者信息

Sharma Neera, Jain Sapan K, Rastogi Ramesh C

机构信息

Department of Chemistry, University of Delhi, Delhi, India.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2007 Nov;68(3):927-41. doi: 10.1016/j.saa.2007.01.014. Epub 2007 Jan 23.

Abstract

The absorption and fluorescence spectral characteristics of some biologically active indoles have been studied as a function of acidity and basicity (H_/pH/H(o)) in cationic (cetyltrimethylammonium bromide, CTAB), anionic (sodium dodecylsulphate, SDS) and aqueous phases at a given surfactant concentration. The prototropic equilibrium reactions of these probes have been studied in aqueous and micellar phases and apparent excited state acidity constant (pK(a)()) values are calculated. The probes show formation of different species on changing pH. Various species present in water, CTAB and SDS have been identified and the equilibrium constants have been determined by Fluorimetric Titration method. The fluorescence spectral data suggest the formation of oxonium ion through the excited state proton transfer reaction in highly acidic media and formation of photoproducts due to the base catalyzed auto-oxidative reaction in basic aqueous solutions. Variations in the apparent pK(a)() value have been observed in different media. The change in the apparent pK(a) values depends upon the solubilising power of the micelles, as well as on the location of the protonating site in the molecule. The observation about increase in pK(a)(*) values in SDS and decrease in CTAB compared to pure water for various equilibria is consistent with the pseudophase ion-exchange (PIE) model.

摘要

在给定表面活性剂浓度下,研究了一些生物活性吲哚在阳离子(十六烷基三甲基溴化铵,CTAB)、阴离子(十二烷基硫酸钠,SDS)和水相中的吸收光谱和荧光光谱特性随酸度和碱度(H⁺/pH/H(o))的变化。在水相和胶束相中研究了这些探针的质子转移平衡反应,并计算了表观激发态酸度常数(pK(a)())值。这些探针在改变pH值时显示出不同物种的形成。通过荧光滴定法鉴定了存在于水、CTAB和SDS中的各种物种,并确定了平衡常数。荧光光谱数据表明,在高酸性介质中通过激发态质子转移反应形成了氧鎓离子,在碱性水溶液中由于碱催化的自氧化反应形成了光产物。在不同介质中观察到了表观pK(a)()值的变化。表观pK(a)值的变化取决于胶束的增溶能力,以及分子中质子化位点的位置。与纯水相比,各种平衡在SDS中pK(a)(*)值增加而在CTAB中降低的观察结果与假相离子交换(PIE)模型一致。

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