Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433, China.
School of Materials Science and Engineering, Northwestern Polytechnical University, Xi'an, Shaansi 710072, China.
Nat Commun. 2017 Mar 28;8:14881. doi: 10.1038/ncomms14881.
The ability of Au catalysts to effect the challenging task of utilizing molecular oxygen for the selective epoxidation of cyclooctene is fascinating. Although supported nanometre-size Au particles are poorly active, here we show that solubilized atomic Au clusters, present in ng ml concentrations and stabilized by ligands derived from the oxidized hydrocarbon products, are active. They can be formed from various Au sources. They generate initiators and propagators to trigger the onset of the auto-oxidation reaction with an apparent turnover frequency of 440 s, and continue to generate additional initiators throughout the auto-oxidation cycle without direct participation in the cycle. Spectroscopic characterization suggests that 7-8 atom clusters are effective catalytically. Extension of work based on these understandings leads to the demonstration that these Au clusters are also effective in selective oxidation of cyclohexene, and that solubilized Pt clusters are also capable of generating initiators for cyclooctene epoxidation.
金催化剂能够利用分子氧来实现挑战性的任务,即选择性环氧化环辛烯,这令人着迷。尽管负载的纳米尺寸金颗粒活性较差,但我们在这里表明,在氧化烃产物衍生的配体稳定下,存在于纳克毫升浓度的溶解原子金团簇是活性的。它们可以由各种金源形成。它们生成引发剂和传播剂,以触发自动氧化反应的开始,其表观周转率为 440 s,并在自动氧化循环中继续生成额外的引发剂,而无需直接参与循环。光谱表征表明,7-8 原子团簇具有有效的催化作用。基于这些理解的扩展工作表明,这些 Au 团簇在环己烯的选择性氧化中也是有效的,并且溶解的 Pt 团簇也能够为环辛烯环氧化生成引发剂。