The characterization and deprivatization of catenane gold nanoparticles

Cardinal Scholar

Show simple item record

dc.contributor.advisor Lang, Patricia L. en_US
dc.contributor.author Kern, Eric R. en_US
dc.date.accessioned 2011-06-03T19:40:43Z
dc.date.available 2011-06-03T19:40:43Z
dc.date.created 2005 en_US
dc.date.issued 2005
dc.identifier LD2489.Z78 2005 .K47 en_US
dc.identifier.uri http://cardinalscholar.bsu.edu/handle/handle/188011
dc.description.abstract We plan to form and characterize surface-attached catenane gold nanoparticles. The proposed catenane self-assembles when a pi-electron-rich bis(thiol)hydroquinone derivative (hereby referred to as the dithiol) threads through a pi-electron-deficient inorganic molecular square forming a charge-transfer complex in solution and then attaches itself to a particle via two gold-sulfur covalent bonds.In preparation of this goal, an inorganic molecular square had to be synthesized. We synthesized, recrystallized, and characterized a cationic, tetranuclear, Pd(II)-based macrocyclic square according to the procedures published by Stang2.Then various methods of synthesis and derivatization of gold nanoparticles were investigated. Using a two-phase method published in the literature, dodecanethiolderivatized nanoparticles were synthesized,8 and attachment of the dodecanethiol was confirmed by NMR, IR, and UV/Vis spectroscopy. After the confirmation of the model compound, the reaction scheme was scaled-down for the derivatization of the nanoparticle with the dithiol alone which will be one of the components that will form the proposed catenane.Upon the derivatization of the nanoparticle with the dithiol, there was great difficulty in dissolving the nanoparticles in any polar or non-polar solvent. This led us to believe that nanoparticles are cross-linking with each other and therefore not dissolving. However, the attachment of the dithiol to the nanoparticle was confirmed by infrared spectroscopy. To solve the cross-linking problem an exchange reaction was conducted between the dodecanethiol-derivatized gold nanoparticles and the dithiol in a modified procedure from the literature.18 Although a successful exchange was confirmed by infrared spectroscopy, the dithiol-derivatized gold nanoparticles were still not soluble in any suitable solvent.
dc.description.sponsorship Department of Chemistry
dc.format.extent vi, 58 leaves : ill. ; 28 cm. en_US
dc.source Virtual Press en_US
dc.subject.lcsh Nanoparticles. en_US
dc.subject.lcsh Catenanes. en_US
dc.subject.lcsh Gold. en_US
dc.title The characterization and deprivatization of catenane gold nanoparticles en_US
dc.description.degree Thesis (M.S.)
dc.identifier.cardcat-url http://liblink.bsu.edu/catkey/1314331 en_US


Files in this item

Files Size Format View

There are no files associated with this item.

This item appears in the following Collection(s)

  • Master's Theses [5510]
    Master's theses submitted to the Graduate School by Ball State University master's degree candidates in partial fulfillment of degree requirements.

Show simple item record

Search Cardinal Scholar


Browse

My Account