School of Chemistry and Chemical Technology, Shanghai Jiao Tong University, Shanghai, 200240, China.
J Mol Model. 2010 Mar;16(3):505-12. doi: 10.1007/s00894-009-0566-2. Epub 2009 Aug 7.
The phosphane-stabilized gold cluster Au(13)(PMe(2)Ph)(10)Cl(2) was studied using density functional theory. The extraordinary stability of the cluster has been attributed to the stability of the gold core and the protection conferred by ligands. Here, five stability factors of the gold core were explained and verified by investigating the Au (13) (5+) core in detail. Interactions between the gold core and several PR(3) ligands (R = Me, H, I, Br, Cl, F) were investigated according to the different electron donor abilities of each ligand; bonding energy between the ligand and the gold core was found to increase with the electronegativity of the R substituent. Furthermore, two other aspects of the ligands were clarified: how the ligand stabilizes the Au (13) (5+) core, and which kind of ligand provides the best stabilization for the cluster.
采用密度泛函理论研究了膦稳定的金簇Au(13)(PMe(2)Ph)(10)Cl(2)。该簇的非凡稳定性归因于金核的稳定性和配体的保护作用。在此,通过详细研究 Au(13)(5+)核,解释并验证了五个金核稳定性因素。根据每个配体的不同电子给体能力,研究了金核与几个 PR(3)配体(R = Me、H、I、Br、Cl、F)之间的相互作用;发现配体与金核之间的键合能随 R 取代基的电负性增加而增加。此外,还澄清了配体的另外两个方面:配体如何稳定 Au(13)(5+)核,以及哪种配体为该簇提供最佳稳定性。