Martina Casciotti, Guillermo Romo, María Álvarez, Francisco Molina, José M Muñoz Molina, Tomás R. Belderrain and Laura Rodríguez. Dalton Transactions, 2022 https://doi.org/10.1039/D2DT02429B
The synthesis and characterization of two dinuclear and five tetranuclear gold(I) complexes bearing the 2,6(diphenylphosphinomethyl)pyridine diphosphane ligand (DPPMPY) are herein reported. The reaction between the dinuclear complexes, DPPMPY(AuCl)2 (1) or DPPMPY(AuBr)2 (2), with 1 or 2 equivalents of Ag salts yielded five tetranuclear gold(I) complexes, DPPMPY2Au4X2 (3-7), differing on the terminal ancillary ligands (X = Cl, Br, acetonitrile) and the counter ions (SbF6- or BF4-). The structures of complexes 1, 2, 3, and 5 were confirmed by single-crystal X-ray diffraction studies. The Au···Au distances found in complexes 3 and 5 are in the range of aurophilic interactions and the disposition of Au atoms varies from a linear arrangement in complex 3 to a zigzag arrangement in complex 5. The photophysical characterization of the compounds was performed both in solution and in the solid state. Very high emission quantum yields were observed for the acetonitrile complexes 4 and 6 in the solid state. The use of this family of gold(I) complexes as catalyst for lactone synthesis via oxidative heteroarylation of alkenes was investigated and yields up to ca 65% were obtained. Dicationic halide complexes 3 and 5 showed a slight enhancement of the yield of the catalytic reaction, indicating that there is no influence of the counter ion employed in the reaction outcome. Luminescence techniques have been also used to follow the progress of the catalytic reaction.