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Cation-Assisted Laser Desorption/Ionization for Matrix-Free Surface Mass Spectrometry of Alkanethiolate Self-Assembled Monolayers on Gold Substrates and Nanoparticles

机译:阳离子辅助激光解吸/电离的金基质和纳米粒子上硫代烷烃自组装单分子膜的无基质表面质谱

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摘要

We propose a new scheme of matrix-free laser desorption/ionization with cation assistance for surface mass spectrometry of self-assembled monolayers (SAMs) of alkanethiolates on gold substrates and gold nanoparticles (NPs). In a proof-of-concept experiment, a simple treatment using an aqueous salt solution such as NaI(aq) was shown to lead to a significant laser desorption/ionization, producing the characteristic (disulfide) ions of alkanethiolate molecules from the monolayers. Further efforts to understand the mechanism were also given, including laser power and salt concentration dependence studies. In the power dependence study, the characteristic ions were found to be produced at low laser power where no gold substrate species was seen. At high laser power, the generation of gold species, Au~(+)-Au_(5~(+)), resulted in a saturation behavior in the characteristic mass peak for alkanethiolate molecules. In addition, characteristic ions with gold adducts were not observed at any laser power. With increasing salt concentration, the characteristic mass peak was gradually increased. The results suggest that the adduct formation of a cation with alkanethiolates in the monolayers provide a facile pathway to supply a charge to UV laser-desorbed secondary neutrals for mass spectrometric detection. This cation-assisted laser desorption/ionization (CALDI) mass spectrometry was further examined with the SAMs and mixed SAMs with various terminals such as -OH, -OCH_(3), -NH_(2), -ethylene (-CH(velence)CH_(2)), and -acetylene (-C(ident to)CH). The CALDI method was also successfully applied to surface mass spectrometry of monolayer-protected gold NPs (approx16 nm diameter) with OH- and COOH-terminated SAMs. The unique advantages of the matrix-free CALDI method may extend our capability in investigations of interfacial chemistry at SAMs as well as mass spectrometric applications using biochips and nanoparticles.
机译:我们提出了一种新的无基质激光解吸/离子化和阳离子辅助的新方案,该方案用于在金基底和金纳米颗粒(NP)上链烷硫醇盐的自组装单分子层(SAM)进行表面质谱分析。在概念验证实验中,使用诸如NaI(aq)的盐水溶液进行的简单处理显示出显着的激光解吸/电离作用,从而从单层生成链烷硫醇分子的特征(二硫键)离子。还进行了进一步的理解机理的努力,包括激光功率和盐浓度依赖性研究。在功率相关性研究中,发现特征离子是在低激光功率下产生的,没有看到金底物。在高激光功率下,金的生成Au〜(+)-Au_(5〜(+))导致硫代烷烃分子的特征质量峰出现饱和行为。另外,在任何激光功率下均未观察到具有金加合物的特征离子。随着盐浓度的增加,特征质量峰逐渐增加。结果表明,在单层中阳离子与链烷硫醇盐的加合物形成提供了一种简便的途径,可将电荷提供给紫外激光解吸的次级中性离子进行质谱检测。使用SAM和带有各种末端(例如-OH,-OCH_(3),-NH_(2),-乙烯(-CH(velence))的混合SAM进一步检查了这种阳离子辅助激光解吸/电离(CALDI)质谱CH_(2))和-乙炔(-C(与CH相同))。 CALDI方法也已成功应用于具有OH和COOH封端的SAM的单层保护金纳米颗粒(直径约16 nm)的表面质谱分析。无基质CALDI方法的独特优势可能会扩展我们在SAM界面化学研究以及使用生物芯片和纳米颗粒进行质谱分析应用方面的能力。

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