Coordination chemistry of gold(II) with amidinate, thiolate and ylide ligands

Abstract

Various reagents such as Cl 2, Br 2, I 2, benzoyl peroxide and CH 3I add to the dinuclear gold(I) amidinate complex [Au 2(2,6-Me 2Ph-form) 2] to form oxidative-addition gold(II) metal–metal bonded complexes. The gold–gold distance in the dinuclear complex decreases upon oxidative-addition with halogens from 2.7 to 2.5 Å, similar to observations made with dithiolate and ylide ligands. The sodium salt of the guanidinate Hhpp ligand, Hhpp = 1,3,4,6,7,8-hexahydro-2 H-pyrimido[1,2-a]pyrimidine reacts with (THT)AuCl in THF or CH 2Cl 2 to form a Au(II) complex, [Au 2(hpp) 2Cl 2], either by solvent oxidation or disproportionation of the Au(I) to Au(II) and the metal. Density functional theory (DFT) and MP2 calculations on [Au 2(hpp) 2Cl 2] find that the highest occupied molecular orbital (HOMO) is predominately hpp and chlorine-based with some Au–Au δ* character. The lowest unoccupied molecular orbital (LUMO) has metal-to-ligand (M–L) and metal-to-metal (M–M) σ* character (approximately 50% hpp/chlorine, and 50% gold). The charge-transfer character of the deeply colored solutions is observed in all the oxidative-addition products of the dinuclear gold(II) nitrogen ligands. This contrasts with the colors of the gold(II) ylide oxidative-addition products which are pale yellow. The colors of the crystalline gold(II) nitrogen complexes are dark orange to brown. This review will focus on the chemistry of gold(II) with nitrogen ligands and compare this with the well reviewed chemistry of gold(II) thiolate and ylide complexes.