Thiol-Induced Synthesis of Phosphine-Protected Gold Nanoclusters with Atomic Precision and Controlling the Structure by Ligand/Metal Engineering.

Abstract

Efficient synthesis of atomically precise phosphine-capped gold nanocluster (with >10 metal atoms) is important to deeply understand the relationship between structure and properties. Herein, we successfully utilize the thiol-induced synthesis method and obtain three atomically precise phosphine-protected gold nanoclusters. Single-crystal X-ray structural analysis reveals that the nanoclusters are formulated as [Au13(Dppm)6](BPh4)3, [Au18(Dppm)6Br4](BPh4)2, and [Au20(Dppm)6(CN)6] (where Dppm stands for bis(diphenylphosphino)methane), which are further confirmed by electrospray ionization mass spectrometry, thermogravimetric analysis, and X-ray photoelectron spectroscopy. Meanwhile, [Au18(Dppm)6Br4](BPh4)2 could be converted into [Au13(Dppm)6](BPh4)3 and [Au20(Dppm)6(CN)6] by engineering the surface ligands under excess PPh3 or moderate NaBH3CN, respectively. Furthermore, according to the different binding ability of silver with halogen, we successfully achieved target metal exchange on [Au18(Dppm)6Br4](BPh4)2 with Ag-SAdm (where HS-Adm stands for 1-adamantane mercaptan) complex and obtained [AgxAu18-x(Dppm)6Br4](BPh4)2 (x = 1, 2) alloy nanoclusters. Our work will contribute to more intensive understanding on synthesizing phosphine-protected nanoclusters as well as shedding light on the structure-property correlations in the nanocluster range.