Chemical transformations of [MAu8(PPh3)8]2+ (M = Pt, Pd) and [Au9(PPh3)8]3+ in methanol induced by irradiation of atmospheric pressure plasma

Abstract

The reaction processes of ligand-protected metal clusters induced by irradiating atmospheric pressure plasma (APP) were investigated using optical spectroscopy, mass spectrometry, and density functional theory (DFT) calculations. The target clusters were phosphine-protected gold-based clusters [MAu8(PPh3)8]2+ (M = Pt, Pd) and [Au9(PPh3)8]3+, which have a crown-shaped M@Au8 (M = Pt, Pd, Au) core with an unligated M site at the central position. The APP irradiation of [MAu8(PPh3)8]2+ (M = Pt, Pd) in methanol resulted in the selective formation of [PtAu8(PPh3)8CO]2+ and [PdAu9(PPh3)8CN]2+ via the addition of a CO molecule and AuCN unit, respectively, generated in situ by the APP irradiation. In contrast, the APP irradiation of [Au9(PPh3)8]3+ in methanol yielded [Au9(PPh3)7(CN)1]2+ and [Au10(PPh3)7(CN)2]2+ as the main products, which were produced by sequential addition of AuCN to reactive [Au8(PPh3)7]2+ formed by dissociation equilibrium of [Au9(PPh3)8]3+. DFT calculations predicted that a unique chain-like {-(CNAu)n-PPh3} (n = 1, 2) ligand was formed via the sequential insertion of -CNAu- units into the Au-PPh3 bond of [PdAu8(PPh3)8]2+ and [Au8(PPh3)7]2+. These findings open up a new avenue for developing novel metal clusters via the chemical transformation of atomically defined metal clusters by APP irradiation.