首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >Solvation and Rotational Dynamics of Coumarin-153 in Ethylammonium Nitrate Containing γ-Cyclodextrin
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Solvation and Rotational Dynamics of Coumarin-153 in Ethylammonium Nitrate Containing γ-Cyclodextrin

机译:香豆素153在含γ-环糊精的硝酸乙酯中的溶解和旋转动力学

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Carbohydrates are known to serve as an abundant, diverse, and reusable source of carbon, but their derivatization for industrial applications is still a challenging task because of their low solubility in solvents other than water; they are only sparingly soluble in common organic solvents as well as in weakly coordinating ionic liquids, such as l-butyl-3-methylimidazolium tetrafluoroborate (bmimBF4). In this manuscript, we have shown that the solubility of cyclodextrins (CDs) in ethylammonium nitrate (EAN), at 298 K is comparable to that in water. This combination of EAN and γ-CD can be useful in many ways: (i) combination of both γ-CD and EAN can provide selectivity and resolution for separations that otherwise are not possible (vide infra); (ii) the combination of these two can find interesting applications in protein-detergent systems (vide infra), and (iii) they can improve chiral resolutions in simultaneous enantioseparation by capillary electrophoresis method (vide infra). In this study, we have characterized thissystem using the following techniques: By the use of the competitive fluorescence method we have shown that there is no inclusion complex formation between EAN and γ-CD. Using the Benesi Hildebrand equation, we have shown the variation of binding constant of the C- 153/γ-CD complex with temperature. The negative entropy and enthalpy changes indicated that the formation of the above C-153/γ-CD complex is entropically unfavorable and enthalpy-driven. We have also investigated the effect of temperature on the fluorescence anisotropy decays and the solvation dynamics of coumarin-153 (C-153) using picosecond time-resolved spectroscopy. Finally, we have shown that the aggregation behavior of γ-CD in EAN is entirely different from that in water, and the increase in average solvation time on going from neat EAN to EAN containing γ-CD is very small compared to the increase in solvation time on going from pure water to water containing γ-CD.
机译:已知碳水化合物可作为丰富,多样且可重复使用的碳源,但由于它们在水以外的溶剂中溶解度低,因此将其衍生化用于工业应用仍然是一项艰巨的任务。它们仅微溶于普通的有机溶剂以及弱配位的离子液体中,例如1-丁基-3-甲基咪唑四氟硼酸酯(bmimBF4)。在本手稿中,我们显示了在298 K的条件下,环糊精(CDs)在硝酸乙基铵(EAN)中的溶解度与在水中的溶解度相当。 EAN和γ-CD的这种组合可以在许多方面有用:(i)γ-CD和EAN的组合可以为原本不可能的分离提供选择性和分离度(见下文); (ii)两者的结合可以在蛋白质洗涤剂系统中找到有趣的应用(见下文),并且(iii)在通过毛细管电泳方法同时对映分离时,可以提高手性拆分度(见下文)。在这项研究中,我们使用以下技术对该系统进行了表征:通过使用竞争荧光方法,我们表明EAN和γ-CD之间没有形成包合物。使用Benesi Hildebrand方程,我们显示了C-153 /γ-CD复合物的结合常数随温度的变化。熵和焓的负变化表明上述C-153 /γ-CD络合物的形成在熵上是不利的,并且是由焓驱动的。我们还使用皮秒时间分辨光谱技术研究了温度对香豆素153(C-153)的荧光各向异性衰减和溶剂化动力学的影响。最后,我们表明γ-CD在EAN中的聚集行为与水中的聚集行为完全不同,并且从纯EAN到含有γ-CD的EAN的平均溶剂化时间的增加与溶剂化的增加相比很小。从纯净水到含有γ-CD的水的时间。

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