| Literature DB >> 32319978 |
Vera Truttmann1, Christopher Herzig2, Ivonne Illes2, Andreas Limbeck2, Ernst Pittenauer2, Michael Stöger-Pollach3, Günter Allmaier2, Thomas Bürgi4, Noelia Barrabés1, Günther Rupprechter1.
Abstract
The properties of gold nanoclusters, apart from being size-dependent, are strongly related to the nature of the protecting ligand. Ligand exchange on Au nanoclusters has been proven to be a powerful tool for tuning their properties, but has so far been limited to dissolved clusters in solution. By supporting the clusters previously functionalized in solution, it is uncertain that the functionality is still accessible once the cluster is on the surface. This may be overcome by introducing the desired functionality by ligand exchange after the cluster deposition on the support material. We herein report the first successful ligand exchange on supported (immobilized) Au11 nanoclusters. Dropcast films of Au11(PPh3)7Br3 on planar oxide surfaces were shown to react with thiol ligands, resulting in clusters with a mixed ligand shell, with both phosphines and thiolates being present. Laser ablation inductively coupled plasma mass spectrometry and infrared spectroscopy confirmed that the exchange just takes place on the cluster dropcast. Contrary to systems in solution, the size of the clusters did not increase during ligand exchange. Different structures/compounds were formed depending on the nature of the incoming ligand. The feasibility to extend ligand engineering to supported nanoclusters is proven and it may allow controlled nanocluster functionalization.Entities:
Year: 2020 PMID: 32319978 DOI: 10.1039/c9nr10353h
Source DB: PubMed Journal: Nanoscale ISSN: 2040-3364 Impact factor: 7.790