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Preparation of Alkanethiolate-Functionalized Core/Shell Fe_(3)O_(4)@Au Nanoparticles and Its Interaction with Several Typical Target Molecules

机译:硫烷酸酯官能化的核/壳Fe_(3)O_(4)@Au纳米粒子的制备及其与几种典型目标分子的相互作用

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This paper reports the synthesis of alkanethiolate-functionalized core/shell Fe_(3)O_(4)/Au nanoparticles (Fe_(3)O_(4)@Au NPs) that combine the advantages of core/shell magnetic nanoparticles with self-assembled monolayers (SAMs). The alkanethiolates, having carboxylic acid (COOH) and methyl (CH_(3)) terminal groups, can be easily self-assembled on the Fe_(3)O_(4)@Au NPs substrates. The surface composition and structure of 11-mercaptoundecanoic acid (11-MUA) and 1-dodecanethiol (11-DDT) SAMs were characterized in detail using energy-dispersive spectroscopy (EDS), Fourier transform infrared spectroscopy (FT-IR), and X-ray photoelectron spectroscopy (XPS). To further study the surface properties of the SAMs, hydrophobic, ionic, and nonionic organic compounds were selected as probe molecules. The results indicated that the hydrophobic interaction caused strong retention of analytes, whereas the repulsive electrostatic interaction between the negatively charged 11-MUA SAMs surface and the negatively charged probe molecule would lead to the decrease of adsorption affinity.
机译:本文报道了硫代烷烃官能化的核/壳Fe_(3)O_(4)/ Au纳米颗粒(Fe_(3)O_(4)@Au NPs)的合成,这些颗粒结合了核/壳磁性纳米颗粒的优点和自组装的优点单层(SAM)。具有羧酸(COOH)和甲基(CH_(3))端基的链烷硫醇盐可以轻松地自组装在Fe_(3)O_(4)@Au NPs基板上。使用能量色散光谱(EDS),傅里叶变换红外光谱(FT-IR)和X对11-巯基十一酸(11-MUA)和1-十二烷硫醇(11-DDT)SAM的表面组成和结构进行了详细表征射线光电子能谱(XPS)。为了进一步研究SAM的表面特性,选择了疏水,离子和非离子有机化合物作为探针分子。结果表明,疏水相互作用导致被分析物的强烈保留,而带负电荷的11-MUA SAMs表面与带负电荷的探针分子之间的排斥性静电相互作用将导致吸附亲和力的降低。

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