An Intermetallic Au24Ag20 Superatom Nanocluster Stabilized by Labile Ligands

An intermetallic nanocluster containing 44 metal atoms, Au24Ag20(2-SPy)4­(PhCC)20Cl2, was successfully synthesized and structurally characterized by single-crystal analysis and density funtional theory computations. The 44 metal atoms in the cluster are arranged as a concentric three-shell Au12@​Ag...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of the American Chemical Society 2015-04, Vol.137 (13), p.4324-4327
Hauptverfasser: Wang, Yu, Su, Haifeng, Xu, Chaofa, Li, Gang, Gell, Lars, Lin, Shuichao, Tang, Zichao, Häkkinen, Hannu, Zheng, Nanfeng
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:An intermetallic nanocluster containing 44 metal atoms, Au24Ag20(2-SPy)4­(PhCC)20Cl2, was successfully synthesized and structurally characterized by single-crystal analysis and density funtional theory computations. The 44 metal atoms in the cluster are arranged as a concentric three-shell Au12@​Ag20@​Au12 Keplerate structure having a high symmetry. For the first time, the co-presence of three different types of anionic ligands (i.e., phenyl­alkynyl, 2-pyridyl­thiolate, and chloride) was revealed on the surface of metal nanoclusters. Similar to thiolates, alkynyls bind linearly to surface Au atoms using their σ-bonds, leading to the formation of two types of surface staple units (PhCC-Au-L, L = PhCC– or 2-pyridylthiolate) on the cluster. The co-presence of three different surface ligands allows the site-specific surface and functional modification of the cluster. The lability of PhCC– ligands on the cluster was demonstrated, making it possible to keep the metal core intact while removing partial surface capping. Moreover, it was found that ligand exchange on the cluster occurs easily to offer various derivatives with the same metal core but different surface functionality and thus different solubility.
ISSN:0002-7863
1520-5126
DOI:10.1021/jacs.5b01232