Oxidative acetylenic coupling reactions as a surface chemistry tool
dc.contributor.author | Ciampi, S | en_AU |
dc.contributor.author | James, M | en_AU |
dc.contributor.author | Darwish, N | en_AU |
dc.contributor.author | Luais, E | en_AU |
dc.contributor.author | Guan, B | en_AU |
dc.contributor.author | Harper, JB | en_AU |
dc.contributor.author | Gooding, JJ | en_AU |
dc.date.accessioned | 2011-11-22T05:09:54Z | en_AU |
dc.date.available | 2011-11-22T05:09:54Z | en_AU |
dc.date.issued | 2011-09-14 | en_AU |
dc.date.statistics | 2011-11-22 | en_AU |
dc.description.abstract | A novel method to prepare redox monolayers on silicon electrodes has been developed that employs CuI-catalyzed oxidative acetylenic coupling reactions for molecular electronic type applications. As the first case study, ethynylferrocene was covalently immobilized onto an acetylene-terminated monolayer on a Si(100) surface to give a 1,3-diyne (C[triple bond, length as m-dash]C-C[triple bond, length as m-dash]C-) linked redox assembly. The derivatization process requires no protection/de-protection steps, nor activation procedures. The effect of the conjugated diyne linkage on the rate of electron transfer between tethered ferrocenyl units and the silicon electrode is benchmarked against well-established "click" products (i.e. 1,2,3-triazole linkage). The surfaces, after each step, are characterized thoroughly using X-ray reflectivity (XRR), X-ray photoelectron spectroscopy (XPS), electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). The coupling chemistry provides a useful strategy for functionalizing silicon surfaces and contributes to an expanding repertoire of wet chemistry routes for the functionalization of solid substrates.© 2011, Royal Society of Chemistry | en_AU |
dc.identifier.citation | Ciampi, S., James, M., Darwish, N., Luais, E., Guan, B., Harper, J. B., & Gooding, J. J. (2011). Oxidative acetylenic coupling reactions as a surface chemistry tool. Physical Chemistry Chemical Physics, 13(34), 15624-15632. doi:10.1039/c1cp21450k | en_AU |
dc.identifier.govdoc | 3790 | en_AU |
dc.identifier.issn | 1463-9076 | en_AU |
dc.identifier.issue | 34 | en_AU |
dc.identifier.journaltitle | Physical Chemistry Chemical Physics | en_AU |
dc.identifier.pagination | 15624-15632 | en_AU |
dc.identifier.uri | http://dx.doi.org/10.1039/c1cp21450k | en_AU |
dc.identifier.uri | http://apo.ansto.gov.au/dspace/handle/10238/3880 | en_AU |
dc.identifier.volume | 13 | en_AU |
dc.language.iso | en | en_AU |
dc.subject | Silicon | en_AU |
dc.subject | X-ray photoelectron spectroscopy | en_AU |
dc.subject | Electrodes | en_AU |
dc.subject | Acetylene | en_AU |
dc.subject | Couplings | en_AU |
dc.subject | Solids | en_AU |
dc.title | Oxidative acetylenic coupling reactions as a surface chemistry tool | en_AU |
dc.type | Journal Article | en_AU |
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