ABSTRACT
An Au(25) cluster protected by azobenzene derivative thiolates (S-Az) ([Au(25)(S-Az)(18)](-)) was synthesized with the aim of producing a photoresponsive Au(25) cluster. The matrix-assisted laser desorption/ionization mass spectrum of the product revealed that [Au(25)(S-Az)(18)](-) was synthesized in high purity. Optical absorption spectra of [Au(25)(S-Az)(18)](-) obtained before and after photoirradiation suggest that the azobenzenes in the ligands of Au(25)(S-Az)(18) isomerize with an efficiency of nearly 100%, both from the trans to cis conformation and from the cis to trans conformation. Furthermore, the redox potential and optical absorption of Au(25)(S-Az)(18) were found to change reversibly due to photoisomerization of azobenzenes.
ABSTRACT
We report the isolation and structural characterization of an octaneselenolate-protected Au(25) cluster ([Au(25)(SeC(8)H(17))(18)](-)). Isolated [Au(25)(SeC(8)H(17))(18)](-) was characterized by various analytical techniques. The results strongly suggest that [Au(25)(SeC(8)H(17))(18)](-) possesses a similar geometric structure to the well-studied thiolate (RS)-protected Au(25) cluster ([Au(25)(SR)(18)](-)) and that the charge transfer between the metal atoms and ligands in [Au(25)(SeC(8)H(17))(18)](-) is lower than that in [Au(25)(SR)(18)](-). To the best of our knowledge, this is the first report of the isolation of a selenolate-protected gold cluster. [Au(25)(SeC(8)H(17))(18)](-) is an ideal compound for determining how changing the ligand from thiolate to selenolate affects the fundamental properties of a cluster.
