Please use this identifier to cite or link to this item: https://doi.org/10.1021/jp049006r
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dc.titleThree-dimensional self-assembled monolayer (3D SAM) of n-alkanethiols on copper nanoclusters
dc.contributor.authorAng, T.P.
dc.contributor.authorWee, T.S.A.
dc.contributor.authorChin, W.S.
dc.date.accessioned2014-10-16T08:46:21Z
dc.date.available2014-10-16T08:46:21Z
dc.date.issued2004-07-29
dc.identifier.citationAng, T.P., Wee, T.S.A., Chin, W.S. (2004-07-29). Three-dimensional self-assembled monolayer (3D SAM) of n-alkanethiols on copper nanoclusters. Journal of Physical Chemistry B 108 (30) : 11001-11010. ScholarBank@NUS Repository. https://doi.org/10.1021/jp049006r
dc.identifier.issn15206106
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/95314
dc.description.abstractThree-dimensional self-assembled monolayer (3D SAM) of 1-octanethiol, 1-decanethiol, and 1-dodecanethiol has been formed on copper nanoclusters. The morphology and spectroscopy of the nanoparticles were characterized while the conformation of the 3D SAMs was investigated with thermal and variable-temperature analyses. TEM results suggest the copper clusters consist of a spherical shape of ∼3-5 nm. IR, XPS, and 13C CPMAS NMR results confirm that alkanethiols are chemisorbed via the -SH group and the packing density of the alkanethiols on copper nanoclusters increases with the alkyl chain lengths. The thiol chain is deduced to adopt the all-trans zigzag conformation through the analysis by IR and 13C CPMAS NMR. Low-angle peaks observed in XRD further suggest strong interdigitation among these chains to form superlattice structures. On increasing temperature, VT-FTIR and VT- 13C CPMAS NMR depict the disruption of lateral interaction between the chains. This melting of crystalline packing is endothermic but an exothermic peak was observed upon reheating in DSC. We attribute this exothermic "crystallization" to the conformational memory effect of the compact chains. We have found that much higher melting points and enthalpies are obtained on copper nanoclusters as compared to earlier reports on gold and silver clusters.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/jp049006r
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.contributor.departmentPHYSICS
dc.description.doi10.1021/jp049006r
dc.description.sourcetitleJournal of Physical Chemistry B
dc.description.volume108
dc.description.issue30
dc.description.page11001-11010
dc.description.codenJPCBF
dc.identifier.isiut000222864200056
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