Aryl sulfonate anion stabilized aromatic triangular cation [Pd3]+: syntheses, structures and properties

Abstract

A series of sulfonate anions paired aromatic triangular palladium clusters 3–7, abbreviated as [Pd₃]⁺[ArSO₃]⁻, were synthesized using a simple “one pot” method, and gave excellent isolated yields (90–95%). Their structures and properties have been fully characterized and further investigated by fluorescence, single crystal X-ray Diffraction (XRD) and X-ray Photoelectron Spectroscopy (XPS). In varying organic solvents, they presented apparently stronger absorption and emission in MeOH, driven by the combined interactions of hydrogen bonds and polarity. The crystallographic data demonstrated that the methyl orange ion stabilized complex 7 possessed a D_3h symmetric metallic core which was still coplanar and almost equilateral, jointly influenced by the giant hindrance and milder donating effect from the sulfonate. The binding energies for Pdⁿ⁺ 3d_5/2 and Pdⁿ⁺ 3d_3/2 measured by XPS presented at 336.55 and 342.00 eV, respectively. These data were much lower than that of a usual Pd²⁺ 3d and significantly higher than that of a Pd⁰ species, further proving the unified palladium valence state (+4/3) in the tri-palladium core and its aromaticity featured by the cyclic electron delocalization.