Phase transfer of large gold nanoparticles to organic solvents with increased stability

Jeffrey M McMahon; Steven R Emory

doi:10.1021/la0617560

Phase transfer of large gold nanoparticles to organic solvents with increased stability

Langmuir. 2007 Jan 30;23(3):1414-8. doi: 10.1021/la0617560.

Authors

Jeffrey M McMahon¹, Steven R Emory

Affiliation

¹ Department of Chemistry, Western Washington University, 516 High Street, Bellingham, WA 98225, USA.

PMID: 17241067
DOI: 10.1021/la0617560

Abstract

In this paper, we describe a new procedure to phase transfer large gold nanoparticles (diameters > 45 nm) from aqueous solution to organic solvents. This is accomplished using a covalent amide coupling reaction that incorporates dicyclohexylamine (DCHA) headgroups on the surface of mercaptoacetic acid (MAA) functionalized gold nanoparticles. Gold nanoparticles are first synthesized in aqueous solution by the citrate-reduction method, and nanoparticle size is controlled by the molar ratio of the reducing agent (sodium citrate) and the gold precursor (KAuCl4). MAA is then adsorbed to the surface of the gold nanoparticles followed by an amide-coupling reaction to covalently attach DCHA to the surface-immobilized MAA. The bulky dicyclohexyl groups entropically stabilize gold nanoparticles in organic solvents. This procedure was used to reliably transfer gold nanoparticles with diameters between 45 and 100 nm from aqueous solution to organic solvents such as dimethyl sulfoxide and chloroform.