| Literature DB >> 26214221 |
Renxi Jin1,2, Chong Liu3, Shuo Zhao1, Anindita Das1, Hongzhu Xing2, Chakicherla Gayathri1, Yan Xing2, Nathaniel L Rosi3, Roberto R Gil1, Rongchao Jin1.
Abstract
The [Au37(PPh3)10(SR)10X2](+) nanocluster (where SR = thiolate and X = Cl/Br) was theoretically predicted in 2007, but since then, there has been no experimental success in the synthesis and structure determination. Herein, we report a kinetically controlled, selective synthesis of [Au37(PPh3)10(SC2H4Ph)10X2](+) (counterion: Cl(-) or Br(-)) with its crystal structure characterized by X-ray crystallography. This nanocluster shows a rod-like structure assembled from three icosahedral Au13 units in a linear fashion, consistent with the earlier prediction. The optical absorption and the electrochemical and catalytic properties are investigated. The successful synthesis of this new nanocluster allows us to gain insight into the size, structure, and property evolution of gold nanoclusters that are based upon the assembly of icosahedral units (i.e., cluster of clusters). Some interesting trends are identified in the evolution from the monoicosahedral [Au13(PPh3)10X2](3+) to the bi-icosahedral [Au25(PPh3)10(SC2H4Ph)5X2](2+) and to the tri-icosahedral [Au37(PPh3)10(SC2H4Ph)10X2](+) nanocluster, which also points to the possibility of achieving even longer rod nanoclusters based upon assembly of icosahedral building blocks.Entities:
Keywords: Au37 nanocluster; CO oxidation; clusters of clusters; mixed ligands; structure evolution
Year: 2015 PMID: 26214221 DOI: 10.1021/acsnano.5b03524
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881