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使用表面等离子体共振光谱法测定羧基和氨基封端的烷硫醇的表面pK值。

Determination of the surface pK of carboxylic- and amine-terminated alkanethiols using surface plasmon resonance spectroscopy.

作者信息

Fears Kenan P, Creager Stephen E, Latour Robert A

机构信息

Department of Bioengineering, Clemson University, Clemson, South Carolina, USA.

出版信息

Langmuir. 2008 Feb 5;24(3):837-43. doi: 10.1021/la701760s. Epub 2008 Jan 9.

Abstract

When using self-assembled monolayers (SAMs) with ionizable functional groups, such as COOH and NH2, the dissociation constant (pKd) of the surface is an important property to know, since it defines the charge density of the surface for a given bulk solution pH. In this study, we developed a method using surface plasmon resonance (SPR) spectroscopy for the direct measurement of the pKd of a SAM surface by combining the ability of SPR to detect the change in mass concentration close to a surface and the shift in ion concentration over the surface as a function of surface charge density. This method was then applied to measure the pKd values of both COOH- and NH2-functionalized SAM surfaces using solutions of CsCl and NaBr salts, respectively, which provided pKd values of 7.4 and 6.5, respectively, based on the bulk solution pH. An analytical study was also performed to theoretically predict the shape of the SPR plots by calculating the excess mass of salt ions over a surface as a function of the difference between the solution pH and surface pKd. The analytical relationships show that the state of surface charge also influences the local hydrogen ion concentration, thus resulting in a substantial local shift in pH at the surface compared to the bulk solution as a function of the difference between the bulk solution pH and the pKd of the surface.

摘要

当使用带有可电离官能团(如COOH和NH₂)的自组装单分子层(SAMs)时,表面的解离常数(pKd)是一个需要了解的重要性质,因为它决定了在给定本体溶液pH值下表面的电荷密度。在本研究中,我们开发了一种使用表面等离子体共振(SPR)光谱的方法,通过结合SPR检测靠近表面的质量浓度变化以及表面离子浓度随表面电荷密度变化的能力,直接测量SAM表面的pKd。然后,该方法分别应用于使用CsCl和NaBr盐溶液测量COOH功能化和NH₂功能化SAM表面的pKd值,基于本体溶液pH值,分别得到7.4和6.5的pKd值。还进行了一项分析研究,通过计算表面上盐离子的过量质量作为溶液pH值与表面pKd值之差的函数,从理论上预测SPR图的形状。分析关系表明,表面电荷状态也会影响局部氢离子浓度,从而导致表面pH值相对于本体溶液出现显著的局部偏移,该偏移是本体溶液pH值与表面pKd值之差的函数。

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