Self-assembled coordination thioether silver(I) macrocyclic complexes for homogeneous catalysis.

The bis--thioether 9,10-bis[(-methylthio)phenyl]anthracene was synthesized as a atropisomer, as revealed by X-ray diffraction. This alkylaryl thioether ligand (L) formed different macrocyclic complexes by coordination with silver(I) salts depending on the nature of the anion: ML for AgOTf and AgOTFA, ML for AgNO. A discrete ML complex was obtained in the presence of bulky PPhAgOTf. These silver(I) complexes adopted similar structures in solution and in the solid state. As each sulfur atom in the ligand is prochiral, macrocycles LM were obtained as mixtures of diastereoisomers, depending on the configurations of the sulfur atoms coordinated to silver cations. The X-ray structures of the two L·(AgOTf) stereoisomers highlighted their different geometry. The catalytic activity of all silver(I) complexes was effective under homogeneous conditions in two tandem addition/cycloisomerization of alkynes using 0.5-1 mol % of catalytic loading.