State Key Laboratory of Molecular Reaction Dynamics, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian 116023, China.
J Chem Phys. 2012 Aug 14;137(6):064318. doi: 10.1063/1.4745000.
A set of silver-doped lead Zintl anions, Ag@Pb(n)(-) (n = 5-12), have been studied using photoelectron velocity-map imaging spectroscopy and quantum chemical calculation. The structures of Ag@Pb(n)(-) (n = 7-9, 11) built upon a square pyramid base, hitherto not considered, were assigned. Overall agreement between the experimental and calculated photoelectron spectra as well as vertical detachment energies allows for structural evolution to be established. The silver atom prefers to stay outside in the n ≤ 6 clusters and intends to be encapsulated by the lead atoms in n > 6. A stable endohedral cage with bicapped square antiprism structure is formed at n = 10, the endohedral structure of which persists for the larger clusters. Especially, these Ag@Pb(n)(-) anions have been found to undergo a transition between square pyramid and pentagonal pyramid molecular structures at n = 11.
采用光电子速度成像光谱和量子化学计算研究了一组掺银的铅 Zintl 负离子 Ag@Pb(n)(-)(n = 5-12)。基于此前未考虑的四方锥基底,分配了 Ag@Pb(n)(-)(n = 7-9、11)的结构。实验和计算光电子能谱以及垂直离解能之间的整体一致性允许确定结构演变。银原子更喜欢留在 n ≤ 6 簇的外部,并打算被 n > 6 的铅原子包裹。在 n = 10 时形成具有双帽四方反棱柱结构的稳定包合物,其包合物结构在较大的簇中仍然存在。特别是,在 n = 11 时,这些 Ag@Pb(n)(-) 负离子被发现经历了从四方锥到五方锥分子结构的转变。