Carboxylation and Decarboxylation of Aluminum Oxide Nanoparticles Using Bifunctional Carboxylic Acids and Octylamine

dc.citation.articleNumber7950876en_US
dc.citation.journalTitleJournal of Nanomaterialsen_US
dc.citation.volumeNumber2016en_US
dc.contributor.authorAlexander, Shirinen_US
dc.contributor.authorGomez, Virginiaen_US
dc.contributor.authorBarron, Andrew R.en_US
dc.date.accessioned2017-03-07T17:07:15Zen_US
dc.date.available2017-03-07T17:07:15Zen_US
dc.date.issued2016en_US
dc.description.abstractThe carboxylation of alumina nanoparticles (NPs), with bifunctional carboxylic acids, provides molecular anchors that are used for building more complexed structures via either physisorption or chemisorption. Colloidal suspensions of the NPs may be prepared by covalently bonding a series of carboxylic acids with secondary functional groups (HO2C-R-X) to the surface of the NPs: lysine (X = NH2), p-hydroxybenzoic acid (X = OH), fumaric acid (X = CO2H), and 4-formylbenzoic acid (X = C(O)H). Subsequent reaction with octylamine at either 25°C or 70°C was investigated. Fourier transform IR-attenuated reflectance spectroscopy (FTIR-ATR), thermogravimetric analysis (TGA), and scanning electron microscopy (SEM) along with energy dispersive X-ray (EDX) analysis were used to characterize the bifunctionalized monolayers and/or multilayer corona surrounding the alumina NPs and investigate the reaction mechanism of octylamine with the functional groups (X) of the NPs. Except for the fumaric functionalized NPs, addition of octylamine to the functionalized NPs leads to removal of excess carboxylic acid corona from the surface via an amide formation. The extent of the multilayer is dependent on the strength of the acid⋯acid interaction.en_US
dc.identifier.citationAlexander, Shirin, Gomez, Virginia and Barron, Andrew R.. "Carboxylation and Decarboxylation of Aluminum Oxide Nanoparticles Using Bifunctional Carboxylic Acids and Octylamine." <i>Journal of Nanomaterials,</i> 2016, (2016) Hindawi: http://dx.doi.org/10.1155/2016/7950876.en_US
dc.identifier.doihttp://dx.doi.org/10.1155/2016/7950876en_US
dc.identifier.urihttps://hdl.handle.net/1911/94019en_US
dc.language.isoengen_US
dc.publisherHindawien_US
dc.rightsThis is an open access article distributed under theᅠCreative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.titleCarboxylation and Decarboxylation of Aluminum Oxide Nanoparticles Using Bifunctional Carboxylic Acids and Octylamineen_US
dc.typeJournal articleen_US
dc.type.dcmiTexten_US
dc.type.publicationpublisher versionen_US
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