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阳离子辅助激光解吸/电离用于金基底和纳米颗粒上硫醇盐自组装单分子层的无基质表面质谱分析。

Cation-assisted laser desorption/ionization for matrix-free surface mass spectrometry of alkanethiolate self-assembled monolayers on gold substrates and nanoparticles.

作者信息

Ha Tae Kyung, Lee Tae Geol, Song Nam Woong, Moon Dae Won, Han Sang Yun

机构信息

Nanobio Fusion Research Center, Korea Research Institute of Standards and Science, Daejeon 305-340, Republic of Korea.

出版信息

Anal Chem. 2008 Nov 15;80(22):8526-31. doi: 10.1021/ac801405k. Epub 2008 Oct 11.

Abstract

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(+)-Au5(+), 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, -OCH3, -NH2, -ethylene (-CH=CH2), and -acetylene (-C[triple bond]CH). The CALDI method was also successfully applied to surface mass spectrometry of monolayer-protected gold NPs (approximately 16 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.

摘要

我们提出了一种新的无基质激光解吸/电离方案,借助阳离子辅助对金基底和金纳米颗粒(NPs)上的链烷硫醇盐自组装单分子层(SAMs)进行表面质谱分析。在一个概念验证实验中,使用诸如碘化钠水溶液(NaI(aq))的简单处理被证明会导致显著的激光解吸/电离,从单分子层产生链烷硫醇盐分子的特征(二硫化物)离子。还进一步努力去理解其机制,包括激光功率和盐浓度依赖性研究。在功率依赖性研究中,发现特征离子在低激光功率下产生,此时未观察到金基底物种。在高激光功率下,金物种Au(+)-Au5(+)的生成导致链烷硫醇盐分子特征质量峰出现饱和行为。此外,在任何激光功率下均未观察到带有金加合物的特征离子。随着盐浓度增加,特征质量峰逐渐增大。结果表明,单分子层中阳离子与链烷硫醇盐的加合物形成提供了一条便捷途径,为紫外激光解吸的二次中性粒子提供电荷以进行质谱检测。这种阳离子辅助激光解吸/电离(CALDI)质谱法进一步用于研究具有各种末端如 -OH、-OCH3、-NH2、-乙烯(-CH=CH2)和 -乙炔(-C≡CH)的SAMs以及混合SAMs。CALDI方法还成功应用于具有OH - 和COOH末端SAMs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SAMs界面化学研究以及使用生物芯片和纳米颗粒的质谱应用方面的能力。

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