Affiliation:
1. Department of Chemistry Sapienza University of Rome P.le Aldo Moro 5 00185 Rome Italy
2. Department of Sciences Roma Tre University Via della Vasca Navale 79 00146 Rome Italy
3. Department of Anatomical Histological Forensic and Orthopaedic Sciences Section of Human Anatomy Sapienza University of Rome Via A. Borelli 50 00161 Rome Italy
Abstract
AbstractRod‐like organometallic dithiol containing square‐planar Pt(II) centers, i. e., trans,trans‐[(H3COCS)Pt(PBu3)2(C≡C−C6H4−C6H4−C≡C)(PBu3)2Pt(SCOCH3)] was used as bifunctional stabilizing agent for the synthesis of Pd‐, Au‐, and AgNPs (MNPs). All the MNPs showed diameters of about 4 nm, which can be controlled by carefully modulating the synthesis parameters. Covalent MNPs stabilization occurred through a single S bridge between Pt(II) and the noble metal nanocluster surfaces, leading to a network of regularly spaced NPs with the formation of dyads, as supported by SR‐XPS data and by TEM imaging analysis. The chemical nature of NPs systems was also confirmed by EDS and NMR. Comparison between SR‐XPS data of MNPs and self‐assembled monolayers and multilayers of pristine rod‐like dithiols deposited onto polycrystalline gold surfaces revealed an electronic interaction between Pt(II) centers and biphenyl moieties of adjacent ligands, stabilizing the organic structure of the network. The possibility to obtain networks of regularly spaced MNPs opens outstanding perspectives in optoelectronics.
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