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Local Cross-Coupling Activity of Azide-Hexa(ethylene glycol)-Terminated Self-Assembled Monolayers Investigated by Atomic Force Microscopy.
Lebitania, Julie Ann; Inada, Natsumi; Morimoto, Masayuki; You, Jiaxun; Shahiduzzaman, Md; Taima, Tetsuya; Hirata, Kaito; Fukuma, Takeshi; Ohta, Akio; Asakawa, Tsuyoshi; Asakawa, Hitoshi.
Afiliación
  • Lebitania JA; Graduate School of Natural Science and Technology, Kanazawa University, Kanazawa 920-1192, Japan.
  • Inada N; Graduate School of Natural Science and Technology, Kanazawa University, Kanazawa 920-1192, Japan.
  • Morimoto M; Nanomaterials Research Institute (NanoMaRi), Kanazawa University, Kanazawa 920-1192, Japan.
  • You J; Graduate School of Frontier Science Initiative, Kanazawa University, Kanazawa 920-1192, Japan.
  • Shahiduzzaman M; Nanomaterials Research Institute (NanoMaRi), Kanazawa University, Kanazawa 920-1192, Japan.
  • Taima T; Nanomaterials Research Institute (NanoMaRi), Kanazawa University, Kanazawa 920-1192, Japan.
  • Hirata K; Graduate School of Frontier Science Initiative, Kanazawa University, Kanazawa 920-1192, Japan.
  • Fukuma T; Graduate School of Natural Science and Technology, Kanazawa University, Kanazawa 920-1192, Japan.
  • Ohta A; Graduate School of Natural Science and Technology, Kanazawa University, Kanazawa 920-1192, Japan.
  • Asakawa T; Nano Life Science Institute (NanoLSI), Kanazawa University, Kanazawa 920-1192, Japan.
  • Asakawa H; Graduate School of Natural Science and Technology, Kanazawa University, Kanazawa 920-1192, Japan.
Langmuir ; 37(50): 14688-14696, 2021 12 21.
Article en En | MEDLINE | ID: mdl-34878277
ABSTRACT
Azide-oligo(ethylene glycol)-terminated self-assembled monolayers (N3-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 N3-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 (N3-EG6-SAMs) were investigated using frequency modulation atomic force microscopy (FM-AFM) in liquid. The N3-EG6-SAMs were prepared on Au(111) substrates through the self-assembly of 11-azido-hexa(ethylene glycol)-undecane-1-thiol (N3-EG6-C11-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 N3-EG6-SAM and its clean surfaces originating from the adsorption resistance property of the terminal EG6 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 N3-EG6-SAMs, which is helpful for the interfacial molecular design based on alkanethiol SAMs in many applications.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Azidas / Glicol de Etileno Tipo de estudio: Prognostic_studies Idioma: En Revista: Langmuir Asunto de la revista: QUIMICA Año: 2021 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Azidas / Glicol de Etileno Tipo de estudio: Prognostic_studies Idioma: En Revista: Langmuir Asunto de la revista: QUIMICA Año: 2021 Tipo del documento: Article País de afiliación: Japón
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