Graduate School of Natural Science and Technology, Kanazawa University, Kanazawa 920-1192, Japan.
Nanomaterials Research Institute (NanoMaRi), Kanazawa University, Kanazawa 920-1192, Japan.
Langmuir. 2021 Dec 21;37(50):14688-14696. doi: 10.1021/acs.langmuir.1c02451. Epub 2021 Dec 8.
Azide-oligo(ethylene glycol)-terminated self-assembled monolayers (N-OEG-SAMs) are promising interfacial structures for surface functionalization. Its many potential applications include chemical/bio-sensing and construction of surface models owing to its cross-coupling activity that originates from the azide group and oligo(ethylene glycol) (OEG) units for non-specific adsorption resistance. However, there are only a few studies and limited information, particularly on the molecular-scale structures and local cross-coupling activities of N-OEG-SAMs, which are vital to understanding its surface properties and interfacial molecular design. In this study, molecular-scale surface structures and cross-coupling activity of azide-hexa(ethylene glycol)-terminated SAMs (N-EG-SAMs) were investigated using frequency modulation atomic force microscopy (FM-AFM) in liquid. The N-EG-SAMs were prepared on Au(111) substrates through the self-assembly of 11-azido-hexa(ethylene glycol)-undecane-1-thiol (N-EG-C-HS) molecules obtained from a liquid phase. Subnanometer-resolution surface structures were visualized in an aqueous solution using a laboratory-built FM-AFM instrument. The results show a well-ordered molecular arrangement in the N-EG-SAM and its clean surfaces originating from the adsorption resistance property of the terminal EG units. Surface functionalization by the cross-coupling reaction of copper(I)-catalyzed azide-alkyne cycloaddition was observed, indicating a structural change in the form of fluctuating structures and island-shaped structures depending on the concentration of the alkyne molecules. The FM-AFM imaging enabled to provide information on the relationship between the surface structures and cross-coupling activity. These findings provide molecular-scale information on the functionalization of the N-EG-SAMs, which is helpful for the interfacial molecular design based on alkanethiol SAMs in many applications.
叠氮-聚乙二醇-末端自组装单分子层(N-OEG-SAMs)是一种很有前途的界面结构,可用于表面功能化。由于叠氮基团和聚乙二醇(OEG)单元的交叉偶联活性,它具有抗非特异性吸附的特性,因此在化学/生物传感和表面模型构建等方面具有许多潜在的应用。然而,目前关于 N-OEG-SAMs 的分子尺度结构和局部交叉偶联活性的研究很少,信息也很有限,而这些对于理解其表面性质和界面分子设计至关重要。在这项研究中,我们使用液相结合调频原子力显微镜(FM-AFM)研究了叠氮-六(乙二醇)-末端自组装单分子层(N-EG-SAMs)的分子尺度表面结构和交叉偶联活性。N-EG-SAMs 通过 11-叠氮-六(乙二醇)-十一烷-1-硫醇(N-EG-C-HS)分子在 Au(111)基底上的自组装得到。通过实验室自制的 FM-AFM 仪器,在水溶液中对亚纳米分辨率的表面结构进行了可视化。结果表明,N-EG-SAM 具有良好的有序分子排列,其表面清洁,这归因于末端 EG 单元的抗吸附特性。铜(I)催化的叠氮-炔环加成的交叉偶联反应对表面进行了功能化,这表明表面结构发生了变化,形成了波动结构和岛状结构,这取决于炔烃分子的浓度。FM-AFM 成像提供了表面结构与交叉偶联活性之间关系的信息。这些发现提供了 N-EG-SAMs 功能化的分子尺度信息,这有助于基于烷硫醇 SAM 的界面分子设计在许多应用中得到广泛应用。