The location of the Pd atoms in Pd₂Au₃₆(SC₂H₄Ph)₂₄, is studied both experimentally and theoretically. X-ray photoelectron spectroscopy (XPS) indicates oxidized Pd atoms. Palladium K-edge extended X-ray absorption fine-structure (EXAFS) data clearly show Pd-S bonds, which is supported by far infrared spectroscopy. By comparing theoretical EXAFS spectra in R space and circular dichroism spectra of the staple, surface and core doped structures with experimental spectra.

We investigate the distinctly different interaction of thiolate-protected cluster Au₃₈(SC₂H₄Ph)₂₄with two diverse support materials Al₂O₃ and CeO₂. The catalytic surfaces have been heated in different atmospheres, and the removal of the thiolate ligands has been studied. Thermogravimetry (TG), temperature-programmed process coupled with mass spectrometer (TPRDO-MS), and X-ray absorption spectroscopy (XAFS) studies were performed to understand the desorption of thiol ligands depending on conditions and support material. Depending on the atmosphere and the support material the fate of the thiol ligands is different upon heating, leading to metallic Au in the case of Al₂O₃ and to cationic Au with CeO₂. The thiolate removal seems to be a two-step procedure. The catalytic activity of these Au₃₈-supported clusters was studied for the aerobic oxidation of cyclohexane. Conversion was higher for the gold clusters supported on CeO₂. Surprisingly, a significant amount of cyclohexanethiol was found, revealing the active participation of the thiolate ligand in catalytic reactions. The observation also indicates that breaking and formation of C–S bonds can be catalyzed by the gold clusters.

A palladium catalyzed intermolecular asymmetric Heck reaction with cyclic trisubstituted olefins is reported. The use of two different chiral ligands provides access to valuable 2,3- and 2,5-dihydrofurans with a fully substituted C2 stereocenter with high levels of regio- and enantiocontrol.