| Literature DB >> 27662338 |
Maria Şologan, Domenico Marson, Stefano Polizzi1, Paolo Pengo, Silvia Boccardo, Sabrina Pricl, Paola Posocco, Lucia Pasquato.
Abstract
The spontaneous self-organization of dissimilar ligands on the surface of metal nanoparticles is a very appealing approach to obtain anisotropic "spherical" systems. In addition to differences in ligand length and end groups, a further thermodynamic driving force to control the self-assembled monolayer organization may become available if the ligands are inherently immiscible, as is the case of hydrogenated (H-) and fluorinated (F-) species. Here, we validate the viability of this approach by combining 19F NMR experiments and multiscale molecular simulations on large sets of mixed-monolayer-protected gold nanoparticles (NPs). The phase segregation of blends of F- and H-thiolates grafted on the surface of gold NPs allows a straightforward approach to patterned mixed monolayers, with the shapes of the monolayer domains being encoded in the structure of the F/H-thiolate ligands. The results obtained from this comprehensive study offer molecular design rules to achieve a precise control of inorganic nanoparticles protected by specifically patterned monolayers.Entities:
Keywords: NMR; anisotropic nanoparticles; gold nanoparticles; multiscale molecular modeling; phase segregation; self-assembly
Year: 2016 PMID: 27662338 DOI: 10.1021/acsnano.6b03931
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881