Picture of a sphere with binary code

Making Strathclyde research discoverable to the world...

The Strathprints institutional repository is a digital archive of University of Strathclyde research outputs. It exposes Strathclyde's world leading Open Access research to many of the world's leading resource discovery tools, and from there onto the screens of researchers around the world.

Explore Strathclyde Open Access research content

Dialkyl sulfides : novel passivating agents for gold nanoparticles

Shelley, Elwyn J. and Ryan, Declan and Johnson, Simon R. and Couillard, Martin and Fitzmaurice, Donald and Nellist, Peter D. and Chen, Yu and Palmer, Richard E. and Preece, Jon A. (2002) Dialkyl sulfides : novel passivating agents for gold nanoparticles. Langmuir, 18 (5). pp. 1791-1795. ISSN 0743-7463

Full text not available in this repository. (Request a copy from the Strathclyde author)

Abstract

Gold nanoparticles passivated with symmetrical and unsymmetrical dialkyl sulfides (H21C10SC10H21 and H37C18SC10H21) have been synthesized via the borohydride reduction of HAuCl4 and characterized by H-1 NMR, FTIR, UV-vis, Auger Electron, XPS spectroscopies, and TEM. Under equivalent conditions of formation, the size and polydispersity of the gold cores obtained was greater for dialkyl sulfide ligands (d(C10SC10) = 5.3 +/- 0.8 nm; d(C18SC10) = 6.3 +/- 1.1 nm) than alkanethiol ligands (d(C10H22SH) = 2.2 +/- 0.1 nm). Edge-edge interparticle spacing of 2-D arrays of the nanoparticles is found to be dependent on the length of the longest alkyl chain passivating the nanoparticles and is independent of the asymmetry of the alkyl chains in the dialkyl sulfide.