Yuan Ning, Gudmundsson Arnar, Gustafson Karl P J, Oschmann Michael, Tai Cheuk-Wai, Persson Ingmar, Zou Xiaodong, Verho Oscar, Bajnóczi Éva G, Bäckvall Jan-E
Department of Materials and Environmental Chemistry, Arrhenius Laboratory, Stockholm University, SE-106 91 Stockholm, Sweden.
Department of Molecular Sciences, Swedish University of Agricultural Sciences, P.O. Box 7015, SE-750 07 Uppsala, Sweden.
ACS Catal. 2021 Mar 5;11(5):2999-3008. doi: 10.1021/acscatal.0c04374. Epub 2021 Feb 22.
A well-studied heterogeneous palladium(II) catalyst used for the cycloisomerization of acetylenic acids is known to be susceptible to deactivation through reduction. To gain a deeper understanding of this deactivation process and to enable the design of a reactivation strategy, X-ray absorption spectroscopy (XAS) was used. With this technique, changes in the palladium oxidation state and coordination environment could be studied in close detail, which provided experimental evidence that the deactivation was primarily caused by triethylamine-promoted reduction of palladium(II) to metallic palladium nanoparticles. Furthermore, it was observed that the choice of the acetylenic acid substrate influenced the distribution between palladium(II) and palladium(0) species in the heterogeneous catalyst after the reaction. From the mechanistic insight gained through XAS, an improved catalytic protocol was developed that did not suffer from deactivation and allowed for more efficient recycling of the catalyst.
一种用于炔酸环异构化的经过充分研究的多相钯(II)催化剂已知易通过还原而失活。为了更深入地了解这种失活过程并设计一种再活化策略,使用了X射线吸收光谱(XAS)。通过该技术,可以详细研究钯氧化态和配位环境的变化,这提供了实验证据,表明失活主要是由三乙胺促进钯(II)还原为金属钯纳米颗粒引起的。此外,观察到炔酸底物的选择会影响反应后多相催化剂中钯(II)和钯(0)物种之间的分布。基于通过XAS获得的机理见解,开发了一种改进的催化方案,该方案不会失活,并允许更有效地循环使用催化剂。