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A Simple Method for the Size Controlled Synthesis of Stable Oligomeric Clusters of Gold Nanoparticles under Ambient Conditions
Published on: February 5, 2016
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Size-Controlled Synthesis of Modifiable Glycine-Terminated Au Nanoclusters as a Platform for Further
Maryam Alyari1, Robert W J Scott1
1Department of Chemistry, University of Saskatchewan, 110 Science Place, Saskatoon S7N 5C9, Canada.
Langmuir : the ACS Journal of Surfaces and Colloids
|November 5, 2021
Summary
Researchers developed a simple method to create stable, narrow-sized glycine-cystamine (Gly-CSA)-functionalized gold nanoclusters (Au NCs). The size of these Au NCs is controllable by adjusting the reducing agent concentration, showing potential for biomedical applications.
Area of Science:
- Nanomaterials Science
- Chemical Synthesis
- Biomedical Engineering
Background:
- Gold nanoclusters (Au NCs) offer unique optical and electronic properties.
- Functionalization of Au NCs is crucial for targeted applications.
- Controlling Au NC size and surface chemistry is an ongoing challenge.
Purpose of the Study:
- To develop a simple and improved synthetic method for producing stable, narrow-sized glycine-cystamine (Gly-CSA)-functionalized Au NCs.
- To investigate the size control of Au NCs based on reducing agent concentration.
- To explore the functionalization of Au NCs via Michael addition for potential biomedical applications.
Main Methods:
- Synthesis of Fmoc-Gly-CSA-functionalized Au NCs.
- Size control using varying concentrations of sodium borohydride (NaBH4).
- Characterization using UV-vis spectroscopy, 1H NMR, and TEM.
- Functionalization of amine groups via Michael addition with methyl acrylate.
Main Results:
- A simple synthetic route to stable, narrow-sized Gly-CSA-functionalized Au NCs was established.
- Au NC size was directly controllable by NaBH4 concentration, yielding smaller diameters at higher concentrations.
- Formation of atom-precise Au25(SR)18 NCs was confirmed, with successful ester-termination via Michael addition.
- Functionalization did not alter the size of the Au NCs, confirmed by TEM.
Conclusions:
- The developed method allows for controllable synthesis of Gly-CSA-functionalized Au NCs.
- The functionalized Au NCs exhibit stability and tunable size.
- These Au NCs show promise as scaffolds for diverse biomedical applications due to their facile functionalization and controllable properties.

