Spontaneous in situ generation of photoemissive aurophilic oligomers in water solution based on the 2-thiocytosine ligand†
Abstract
Complexes [Au(S-2-thiocytosinate)(PMe3)] (2, 2-thiocytosine = 4-amino-2-mercaptopyrimidine) and [Au(S-2-thiocytosine)(PMe3)](CF3CO2) (3) have been prepared by the reaction of [Au(acac)(PMe3)] (1, acac = acetylacetonate) or [Au(OCOCF3)(PMe3)] with 2-thiocytosine, respectively. The equimolecular mixture of complexes 1 and 3 also produces [{Au(PMe3)}2(μ-S,N1-2-thiocytosinate)](CF3CO2) (4), which features two distinct [Au(PMe3)]+ groups coordinated to the S and N1 atoms of the heterocycle. Complex 4 experiences a ligand redistribution process in water solution that liberates [Au(PMe3)2](CF3CO2) and a brightly coloured and luminescent species of [Aun(μ-S,N1-2-thiocytosinate)n] stoichiometry, presumably as a tetraauracycle (n = 4).