首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Toward an Understanding of How the Optical Property of Water-Soluble Cationic Polythiophene Derivative Is Altered by the Addition of Salts: The Hofmeister Effect
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Toward an Understanding of How the Optical Property of Water-Soluble Cationic Polythiophene Derivative Is Altered by the Addition of Salts: The Hofmeister Effect

机译:理解如何通过添加盐来改变水溶性阳离子聚噻吩衍生物的光学性质:霍夫迈斯特效应

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摘要

Hofmeister ion-specific effects on optical properties of a water-soluble cationic polymer, poly(3-alkoxy-4-methylthiophene) (PMNT), are investigated by means of absorption, resonance Raman spectroscopy, and molecular dynamic simulations. It is found that the ionochromism of conjugated polyelectrolytes PMNT obeys Hofmeister series with high optical sensitivity, while the spectral changes result from the different electrostatic interactions and the conformational change of the cationic PMNT in different salt solutions. As a result, UV— vis absorption spectra exhibit almost no shift of absorption of PMNT in the presence of SO_4~(2-), F~-, etc., whereas a red-shifted absorption of PMNT with I~-, SCN~ is clearly observed. To gain a deeper understanding of the nature of these anion-dependent chromic phenomena, ab initio calculations and molecular dynamics (MD) simulations are carried out to present the microscopic insights, that the Hofmeister effect occurs at the PMNT/water interface through the direct (hydrophobic, hydrophilic, and electrostatic) interactions between the anions and PMNT backbone. It is found that the salting-in anions like I~- strongly suppress the hydrophobic collapse of PMNT backbone, leading to more extended and ordered PMNT backbone with red-shifted absorption, and the salting-out anions like F~- strongly avoid the hydrophobic PMNT backbone, keeping a random-coiled configuration of PMNT backbone without obvious absorption changes in KP solution. The existence of ordered and disordered backbone configurations is further verified by monitoring the main in-plane skeleton Raman modes (C=C and C—C stretch) of PMNT in various salt solutions. The results presented here could provide a fundamental understanding of salt effects on chemical and biological processes occurring at the macromolecular/water interface, and then may potentially stimulate many chemical and biological applications.
机译:通过吸收,共振拉曼光谱和分子动力学模拟研究了霍夫迈斯特离子对水溶性阳离子聚合物聚(3-烷氧基-4-甲基噻吩)(PMNT)光学性质的特定影响。研究发现,共轭聚电解质PMNT的电离变色服从Hofmeister系列,具有较高的光敏性,而光谱变化则是由不同盐溶液中阳离子PMNT的不同静电相互作用和构象变化引起的。结果,在SO_4〜(2-),F〜-等存在下,UV-vis吸收光谱几乎不显示PMNT的吸收位移,而在I〜-,SCN〜下PMNT的红移吸收清楚地观察到。为了更深入地了解这些与阴离子有关的铬现象的性质,我们进行了从头算和分子动力学(MD)模拟,以提供微观见解,即霍夫迈斯特效应通过直接(阴离子和PMNT主链之间的疏水,亲水和静电相互作用。结果发现,像I〜-的盐溶阴离子强烈抑制了PMNT主链的疏水塌陷,导致PMNT主链具有更多的扩展和有序吸收,并发生了红移吸收;而像F〜-的盐析阴离子则强烈避免了疏水性PMNT骨架,保持PMNT骨架的无规卷曲结构,而KP溶液中吸收没有明显变化。通过监测各种盐溶液中PMNT的主要面内骨架拉曼模式(C = C和CC拉伸),可以进一步验证有序和无序的骨架结构的存在。此处给出的结果可以提供对盐对大分子/水界面处发生的化学和生物过程的影响的基本理解,然后可能潜在地刺激许多化学和生物学应用。

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