We are synthesizing stable, crystalline systems containing gold(I) aggregates and exploring their supramolecular structures and interactions in hopes of obtaining molecular sensors.1,2 Colorless, orange-red, luminescent complexes, 2{[μ3-S(AuCNR)3](EF6)} (R = C6H11, C7H13; E = P, As, Sb), are afforded in high yields from treatment of aqueous solutions of Na3[Au(S2O3)2] with [Au(CNR)2](EF6) in acetone. The [Au(S2O3)2]3- anion has the ability to release S2- and facilitate the formation of these new gold(I) sulfido clusters. Single-crystal X-ray diffraction studies showed that 2{[μ3-S(AuCNC7H13)3](SbF6)} undergoes a reversible, polymorphic phase change upon cooling. This temperature-dependent phase change is accompanied by dramatic alterations in the aurophilic (Au∙∙∙Au) separations. In addition, the corresponding photophysical properties are also impacted by the polymorphism, as observed in the solid-state luminescence. These findings will be presented as well as the contrasting behavior uncovered for 2{[μ3-S(AuCNC6H11)3](PF6)}.
Back to Luminescence in Transition Metal Complexes (Invited and Contributed Speakers)
Back to The 61st Northwest Regional Meeting (June 25 - 28, 2006)