Abstract
Ligand shells of gold nanoclusters play important roles in regulating their molecular and electronic structures. However, the similar but distinct impacts of the homologous analogues of the protecting ligands remain elusive. The C(2v) symmetric monoarsine-protected cluster [Au(13)(AsPh(3))(8)Cl(4)](+) (Au(13)As(8)) was facilely prepared by direct reduction of (Ph(3)As)AuCl with NaBH(4). This cluster is isostructural with its previously reported stibine analogue [Au(13)(SbPh(3))(8)Cl(4)](+) (Au(13)Sb(8)), enabling a comparative study between them. Au(13)As(8) exhibits a blue-shifted electronic absorption band, and this is probably related to the stronger π-back donation interactions between the Au(13) core and AsPh(3) ligands, which destabilize its superatomic 1P and 1D orbitals. In comparison to the thermodynamically less stable Au(13)Sb(8), Au(13)As(8) achieves a better trade-off between catalytic stability and activity, as demonstrated by its excellent catalytic performance towards the aldehyde-alkyne-amine (A(3)) coupling reaction. Moreover, the ligand exchange reactions between Au(13)As(8) with phosphines, as exemplified by PPh(3) and Ph(2)P(CH(2))(2)PPh(2), suggest that Au(13)As(8) may be a good precursor cluster for further cluster preparation through the "cluster-to-cluster" route.