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以葡萄糖三糖和低聚乙二醇为端基的自组装单分子层:表面力、润湿性和表面活性剂吸附

Globotriose- and oligo(ethylene glycol)-terminated self-assembled monolayers: surface forces, wetting, and surfactant adsorption.

作者信息

Blomberg Eva, Claesson Per M, Konradsson Peter, Liedberg Bo

机构信息

Department of Chemistry, Surface Chemistry, Royal Institute of Technology, SE-100 44 Stockholm, Sweden.

出版信息

Langmuir. 2006 Nov 21;22(24):10038-46. doi: 10.1021/la061857y.

Abstract

A set of oligo(ethylene glycol)-terminated and globotriose-terminated self-assembled monolayers (SAMs) has been prepared on gold substrates. Such model surfaces are well defined and have good stability due to the strong binding of thiols and disulfides to the gold substrate. They are thus very suitable for addressing questions related to effects of surface composition on wetting properties, surface interactions, and surfactant adsorption. These issues are addressed in this report. Accurate wetting tension measurements have been performed as a function of temperature using the Wilhelmy plate technique. The results show that the nonpolar character of oligo(ethylene glycol)-terminated SAMs increases slightly but significantly with temperature in the range 20-55 degrees C. On the other hand, globotriose-terminated SAMs are fully wetted by water at room temperature. Surface forces measurements have been performed and demonstrated that the interactions between oligo(ethylene glycol)-terminated SAMs are purely repulsive and similar to those determined between adsorbed surfactant layers with the same terminal headgroup. On the other hand, the interactions between globotriose-terminated SAMs include a short-range attractive force component that is strongly affected by the packing density in the layer. In some cases it is found that the attractive force component increases with contact time. Both these observations are rationalized by an orientation- and conformation-dependent interaction between globotriose headgroups, and it is suggested that hydrogen-bond formation, directly or via bridging water molecules, is the molecular origin of these effects.

摘要

在金基底上制备了一组以低聚乙二醇为端基和以三糖为端基的自组装单分子层(SAMs)。这类模型表面定义明确,由于硫醇和二硫化物与金基底的强结合作用而具有良好的稳定性。因此,它们非常适合用于解决与表面组成对润湿性、表面相互作用和表面活性剂吸附的影响相关的问题。本报告探讨了这些问题。使用Wilhelmy板技术进行了精确的润湿热测量,测量结果作为温度的函数。结果表明,在20 - 55摄氏度范围内,以低聚乙二醇为端基的SAMs的非极性特征随温度略有但显著增加。另一方面,以三糖为端基的SAMs在室温下能被水完全润湿。进行了表面力测量,结果表明,以低聚乙二醇为端基的SAMs之间的相互作用完全是排斥性的,与具有相同端基头的吸附表面活性剂层之间的相互作用相似。另一方面,以三糖为端基的SAMs之间的相互作用包括一个短程吸引力分量,该分量受层中堆积密度的强烈影响。在某些情况下,发现吸引力分量随接触时间增加。这两个观察结果都可以通过三糖头基之间取向和构象依赖的相互作用来解释,并且有人提出,直接或通过桥连水分子形成氢键是这些效应的分子起源。

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