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Materials Chemistry

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Expanding The Scope Of Clickable Azide-Functionalized Nanoclusters To Include Au144, Johanna A. De Jong Nov 2022

Expanding The Scope Of Clickable Azide-Functionalized Nanoclusters To Include Au144, Johanna A. De Jong

Electronic Thesis and Dissertation Repository

Thiolate-protected Au144 nanoclusters (NCs) are an intriguing member of the gold NC family. Their geometric structure, distinct electrochemical features, and susceptibility to structural rearrangement under the duress of ligand exchange have been studied. However, there are currently no established protocols for surface modification or tuning of their ligand shells post synthesis. Here, the direct synthesis of three regioisomers of azide-modified Au144 NCs with 60 azide moieties, i.e., Au144(SC2H4C6H4-N3)60, is reported, in which the azide functionality is located at the ortho-, meta-, or …


Nanoorthogonal Surface Modifications Of Gold Nanoparticles And Nanoclusters Through Strain-Promoted Cycloaddition Chemistry, Praveen N. Gunawardene Jul 2021

Nanoorthogonal Surface Modifications Of Gold Nanoparticles And Nanoclusters Through Strain-Promoted Cycloaddition Chemistry, Praveen N. Gunawardene

Electronic Thesis and Dissertation Repository

This thesis explores the preparation of thiolated gold nanoparticles (AuNPs) and thiolated gold nanoclusters (AuNCs) capable of undergoing post-assembly surface modifications using two common “bioorthogonal” click reactions: the strain-promoted alkyne-azide cycloaddition (SPAAC) reaction (which occurs between a strained-alkyne and an azide) and the strain-promoted alkyne-nitrone cycloaddition (SPANC) reaction (which occurs between a strained-alkyne and a nitrone). Due to their rapid and modifiable reaction kinetics, high chemoselectivity, and stability of the reactive partners, these reactions were originally designed to tether functional substrates to biologically sensitive biomolecules, without altering their structure or perturb the biologically sensitive environments in which they …


Development Of Bioorthogonal Molecular Tools On Gold Nanoparticles, Wilson Luo Jun 2019

Development Of Bioorthogonal Molecular Tools On Gold Nanoparticles, Wilson Luo

Electronic Thesis and Dissertation Repository

This thesis describes the development of bioorthogonal chemical tools — originally designed to form bonds cleanly and selectively in living systems — on gold nanoparticles (AuNPs) as a model reactive nanomaterial template to showcase chemical modifications in a facile and robust manner. To achieve this goal, new methodologies to cleanly incorporate strained alkyne (SA) and cargo-bearing triarylphosphine derivatives onto AuNPs were developed. The protocols described herein provide well-defined reactive AuNP interfaces that undergo bioorthogonal bond-forming and breaking reactions cleanly, selectively, and rapidly to enable chemical tuning of their properties and function.

In order to circumvent the high reactivity of SAs, …


Click And Bioorthogonal Chemistry For The Chemical Modification Of Nanomaterials, Pierangelo Gobbo Mar 2016

Click And Bioorthogonal Chemistry For The Chemical Modification Of Nanomaterials, Pierangelo Gobbo

Electronic Thesis and Dissertation Repository

The goal of this Ph.D. thesis work is the development of novel reactive nanomaterial templates that can be chemically modified in a facile and robust (i.e., formation of covalent bonds) way for the further modification of the nanomaterial’s physical-chemical properties by the reaction partner molecular system. This type of technology was employed to further expand the application of nanomaterials in nanomedicine, chemical biology and materials science.

In order to reach this goal, as a proof of concept, small (d = 3nm) gold nanoparticles (AuNPs) and carbon nanotubes (CNT) were used as the nanomaterial substrates. Innovative synthetic strategies …