The effect of the solvent nature on the quinoline derivatives physicochemical characteristics

V. V. Shcherbakov, S. Kurbatova, M. Zemtsova
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Abstract

The influence of the solvent nature on some physicochemical parameters of the quinoline derivatives molecules is investigated. It was noted that a variety of intermolecular interactions arising between the dissolved substance and the solvent and often accompanied by the phenomena of solvation, association, etc. leads to a variety of structural and energy changes in such systems and complicating their description. The most urgent problems of solutions include issues related to the solubility and bioavailability of biologically active compounds and drugs, the study of their ability to dissolve, the permeability of biological barriers, targeted delivery, etc., as well as the problems associated with the study of sorption of organic compounds from aqueous-organic eluents, for example, in liquid chromatography. Derivatives of quinoline (4-carboxy- and 4-aminoquinoline), known as potential drugs with various types of pharmacological action, were used as research objects. Using quantum chemical calculations, the dipole moment of the amino and carboxy derivatives of quinoline was determined, and the data obtained for vacuum and in solvents of various chemical nature were compared. A significant effect of solvent polarity on the dipole moment of quinoline derivatives dissolved in these solvents was found. The values of the solvation energy of quinoline derivatives in solvents of various chemical nature are calculated. It is shown that a change in the solvation energy is determined both by the structure of the molecules of the quinoline derivatives and by the polarity of the solvent. A nonlinear change in the energy of solvation with a change in the polarity of the solvent is established. A comparison is made of the values of the quinoline derivatives molecules polar surface area in solvents of various chemical nature. It was found that the polar surface area of the studied compounds changes slightly with a change in the nature of the solvent.
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溶剂性质对喹啉衍生物理化性质的影响
研究了溶剂性质对喹啉衍生物分子理化参数的影响。有人指出,溶解物质与溶剂之间产生的各种分子间相互作用,往往伴随着溶剂化、缔合等现象,导致这种体系中各种结构和能量的变化,并使其描述复杂化。解决方案中最紧迫的问题包括与生物活性化合物和药物的溶解度和生物利用度有关的问题,它们的溶解能力的研究,生物屏障的渗透性,靶向递送等,以及与从水-有机洗脱液中吸附有机化合物的研究相关的问题,例如,在液相色谱中。喹啉衍生物(4-羧基喹啉和4-氨基喹啉)被认为是具有多种药理作用的潜在药物。采用量子化学计算方法,测定了喹啉氨基和羧基衍生物的偶极矩,并比较了真空和不同化学性质溶剂中的偶极矩。溶剂极性对喹啉衍生物在溶剂中的偶极矩有显著影响。计算了喹啉衍生物在不同化学性质的溶剂中的溶剂化能。结果表明,溶剂化能的变化既取决于喹啉衍生物的分子结构,也取决于溶剂的极性。建立了溶剂化能量随溶剂极性变化的非线性变化。比较了喹啉衍生物分子在不同化学性质溶剂中的极性表面积值。研究发现,所研究化合物的极性表面积随着溶剂性质的变化而略有变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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