We report a photocatalyst composed of a diphenylanthracene core appended with two lipophilic thioether side-chains that binds gold(III) chloride. Upon excitation using visible light, the Au III ions are smoothly reduced to Au I which, in the presence of water, lead to the formation of crystalline gold nanoparticles of 20–50 nm diameter that are devoid of sulfur-containing capping agents. Ultrafast transient absorption spectroscopy shows that the anthracene excited state is quenched with a rate k = 3.5 × 10 10 s –1, assigned to intramolecular energy transfer to the bound gold ions, which then oxidizes the solvent to produce an intermediate low-valency gold(I) species. In the absence of water, the latter is stable and can be used as a homogeneous Au I catalyst. When employed in a biphasic reactor, the photocatalyst shows average turnover numbers of 150 atoms of Au III reduced to Au 0 per molecule of photocatalyst.
No takes yet. Share an insight, caveat, or question.
Mongin et al. (2014) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: