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dc.contributor.authorEggers, P.
dc.contributor.authorDa Silva, P.
dc.contributor.authorDarwish, Nadim
dc.contributor.authorZhang, Y.
dc.contributor.authorTong, Y.
dc.contributor.authorYe, S.
dc.contributor.authorPaddon-Row, M.
dc.contributor.authorGooding, J.
dc.date.accessioned2017-01-30T11:59:07Z
dc.date.available2017-01-30T11:59:07Z
dc.date.created2016-09-12T08:37:07Z
dc.date.issued2010
dc.identifier.citationEggers, P. and Da Silva, P. and Darwish, N. and Zhang, Y. and Tong, Y. and Ye, S. and Paddon-Row, M. et al. 2010. Self-assembled monolayers formed using zero net curvature norbornylogous bridges: The influence of potential on molecular orientation. Langmuir. 26 (19): pp. 15665-15670.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/17017
dc.identifier.doi10.101/la101590b
dc.description.abstract

A new class of electroactive norbornylogous bridges, with no net curvature, that form self-assembled monolayers on gold electrodes were studied by electrochemistry and in situ infrared spectroscopy. The influence of the electrode potential on the structure and conformation of the self-assembled monolayers (SAMs) was investigated. This was performed using two different lengths of rigid norbornylogous bridges with terminal ferrocene moieties and ?-hydroxyalkanethiols. It was found that single component monolayers of the rigid norbornylogous bridges changed their tilt angle with their transition from the ferrocene to ferricinium. However, when the norbornylogous SAMs were diluted with?-hydroxyalkanethiols the tilt angle remained unchanged upon oxidation of ferrocene to ferricinium. It was also observed that the tilt angle of the diluent, ?-hydroxyalkanethiols changed at potentials exceeding 500 mV. © 2010 American Chemical Society.

dc.publisherAmerican Chemical Society
dc.titleSelf-assembled monolayers formed using zero net curvature norbornylogous bridges: The influence of potential on molecular orientation
dc.typeJournal Article
dcterms.source.volume26
dcterms.source.number19
dcterms.source.startPage15665
dcterms.source.endPage15670
dcterms.source.issn0743-7463
dcterms.source.titleLangmuir
curtin.departmentNanochemistry Research Institute
curtin.accessStatusFulltext not available


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