Adsorption of Multiple NO Molecules on Anionic Gold Clusters: Electron Transfer and Disproportionation Enhanced by...

The reactions of Au^- clusters with multiple nitric oxide (NO) molecules are explored at 150 K by utilizing a mini-flow-tube reactor and a time-of-flight mass spectrometer. Adsorption of multiple NO molecules is observed on most Au^-, while disproportionation reactions only occur on even-sized Au^- with n = 4, 6, 8, 20 and odd-sized ones with n = 5 and 7. Theoretical calculations reveal the geometric structures and electronic states of the products containing bimolecular and trimolecular NO units, where two NO molecules typically form dimers. Different from NO monomers that weakly interact with odd-sized Au^- and form electron-sharing covalent bonds with Au₁₀^-(D_3h) and Au₁₆^-, NO dimers can extract significant charge from parent Au^-. Regarding the three NO molecules, a predilection toward condensation into trimers on even-sized Au^- is observed, while the tendency is more toward an adsorption pattern of a dimer plus a monomer on odd-sized Au^-. The NO trimers register even higher charge gain from Au^- as compared with the NO dimers, which leads to an elevated degree of activation and induces the progression of disproportionation reactions. Therefore, when considering the reaction between NO and Au^-, it appears that NO has a propensity to form dimers or trimers on Au^-. This behavior of aggregate formation substantially enhances the ability of NO to absorb negative charges from Au^- although the occurrence of disproportionate dissociation reactions is initiated only for specific sizes.