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    Preparation of thiol-terminated monolayers on silicon(100) surfaces using thioacetyl-protected alkynethiol

    Access Status
    Fulltext not available
    Authors
    Ng, C.
    Le Saux, G.
    Chockalingam, M.
    Ciampi, Simone
    Harper, J.
    Gooding, J.
    Date
    2010
    Type
    Conference Paper
    
    Metadata
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    Citation
    Ng, C. and Le Saux, G. and Chockalingam, M. and Ciampi, S. and Harper, J. and Gooding, J. 2010. Preparation of thiol-terminated monolayers on silicon(100) surfaces using thioacetyl-protected alkynethiol, pp. 244-247.
    Source Title
    ICONN 2010 - Proceedings of the 2010 International Conference on Nanoscience and Nanotechnology
    DOI
    10.1109/ICONN.2010.6045195
    ISBN
    9781424452620
    School
    Nanochemistry Research Institute
    URI
    http://hdl.handle.net/20.500.11937/42676
    Collection
    • Curtin Research Publications
    Abstract

    The attachment of acetyl-protected alkynethiol groups onto silicon(100) surfaces was achieved using a hydrosilylation methodology. Subsequent deprotection of the thiols using either hydrochloric acid or ammonia solution was investigated using X-ray photoelectron spectroscopy (XPS), and compared with similar reaction in solution. It was found that ammonia solution was more efficient than hydrochloric acid for the deprotection step. However, the deprotection was much less efficient on the surface than in solution. © 2010 IEEE.

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