Ag-13-Centered Cuboctahedral Architecture in Inorganic Cluster Chemistry: A DFT Investigation

作者：Kahlal Samia; Liu C W; Saillard Jean Yves^*

来源：Inorganic Chemistry, 2017, 56(3): 1209-1215.

DOI：10.1021/acs.inorgchem.6b02207

The bonding in the [Ag-13{mu(3)-Fe(CO)(4)}(8)](3-/5-) clusters, which exhibit an Ag-13-centered cuboctahedral core, has been analyzed and rationalized by DFT calculations. Not considering the interaction with its encapsulated atom, the empty [Ag-12{mu(3)-Fe(CO)(4)}(8)](4-) cage can be considered as the assembly of 12 linearly coordinated 14-electron AgI metal centers. Adding a supplementary Ag+ at the center allows some covalent delocalized bonding which to some extent tends to reduce the electron deficiency of the 14-electron centers. Adding now two electrons strengthens the delocalized bonding between the encapsulated atom and its host, making [Ag-13{mu(3)-Fe(CO)(4)}(8)](5-) a superatom with two jellium (5s-type) electrons. TDDFT calculations predict near-IR absorption for this penta-anion, because of the presence of an a1g HOMO in the middle of an energy gap. Luminescence in the same optical range is also suggested. Other related cubococtahedral species, such as [Ag-23(SH)(16)](-), a model for the known 8-electron [Au-23(SR)(16)](-) species which exhibits a bicapped centered dodecahedral kernel structure, have also been investigated.

• 出版日期2017-2-6
• 单位东华大学