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Analytical micelles containing amphiphilic aminoanthraquinone solvatochromic reporter receptor

机译:分析胶束含有两亲氨基氨基属醌溶性多种子胞菌报告器受体

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摘要

The feasibility of using an amphiphilic photoactive derivative of aminoanthraquinone (C18) as both a local solvatochromic probe reporting its position in a micelle and a component of an analytical supramolecular unit in mixed micelles based on a nonionic surfactant, Triton X100, has been considered. The solvatochromism of the 1,8-anthraquinone derivative (C18) has, for the first time, been investigated. Dipole moments of C18 molecules have been determined within the frameworks of the Lippert-Mataga, Kawski, and Reichardt approaches. It has been found that the Delta mu values, as calculated with the help of the first two approaches and the Onsager radius, which is, for C18, equal to 5.8 , are markedly higher than the value obtained in terms of the Reichardt model. Possible reasons for discrepancies, which arise between experimental data and theoretical predictions when analyzing the solvatochromic properties of dyes, have been briefly discussed. C18 has been employed as an example to show that, for chromophores capable of donor-acceptor interactions, the use of protic solvents is more reasonable, because they ensure realization of a wider spectrum of interactions with a probe, among which the van der Waals interactions play an important role. Therewith, polarization effects, rather than charge separation, make a substantial contribution. In the case of amphiphilic chromophores, "enveloping" of polar groups with hydrocarbon chains decreases the local dielectric permittivity and the probability of intermolecular donor-acceptor interactions (hydrogen bonding). The character of the microenvironment of C18 reporter in micelles has been determined with the use of the "relative polarity parameter" proposed in this work. This parameter makes it possible to compare results obtained for different models of solvatochromism. It has been shown that the characteristics of C18 microenvironment in micelles correspond to those of water-alcohol solutions, with the chromophoric moietie
机译:考虑了使用氨基蒽醌(C18)的两亲光学光活性衍生物的可行性作为报告其在胶束中的位置和基于非离子表面活性剂的混合胶束中的分析超分子单元的位置的局部溶解度探针。 1,8-anthraquinnone衍生物(C18)的溶溶色度是首次研究过的。 C18分子的偶极矩已经确定在Lippert-Mataga,Kawski和Reichardt方法的框架内。已经发现,根据前两种方法的帮助和onSager半径计算的Δμ值,即C18,等于5.8的帮助标记明显高于在Reichardt模型中获得的值。已经简要讨论了在分析染料的溶质变色特性时,在实验数据与理论预测之间产生的可能原因。 C18已被用作示例以表明,对于能够受供体 - 受体相互作用的发色团,使用质子溶剂更合理,因为它们确保了实现了与探针的更广泛的相互作用,其中包括van der Wa的相互作用扮演一个重要角色。因此,极化效应,而不是电荷分离,取得了重大贡献。在两亲色团的情况下,具有烃链的极性基团的“包膜”降低了局部介电常数和分子间供体 - 受体相互作用的概率(氢键)。通过使用本工作中提出的“相对极性参数”,确定了C18报道器中C18报道器的微环境的特征。该参数使得可以比较针对不同模型的溶色溶色度的结果进行比较。已经表明,胶束中C18微环境的特性对应于水醇溶液,发色粒子溶液

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  • 来源
    《Colloid journal》 |2017年第6期|共14页
  • 作者

    Ermakova E. V.; Arslanov V. V.;

  • 作者单位

    Russian Acad Sci Frumkin Inst Phys Chem &

    Electrochem Moscow 119071 Russia;

    Russian Acad Sci Frumkin Inst Phys Chem &

    Electrochem Moscow 119071 Russia;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 胶体;
  • 关键词

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