Fujita Shu, Imagawa Kohei, Yamaguchi Sho, Yamasaki Jun, Yamazoe Seiji, Mizugaki Tomoo, Mitsudome Takato
Department of Materials Engineering Science, Graduate School of Engineering Science, Osaka University, 1-3 Machikaneyama, Toyonaka, Osaka, 560-8531, Japan.
Research Center for Ultra-High Voltage Electron Microscopy, Osaka University, 7-1, Mihogaoka, Ibaraki, Osaka, 567-0047, Japan.
Sci Rep. 2021 May 21;11(1):10673. doi: 10.1038/s41598-021-89561-1.
Although transition metal phosphides are well studied as electrocatalysts and hydrotreating catalysts, the application of metal phosphides in organic synthesis is rare, and cooperative catalysis between metal phosphides and supports remains unexplored. Herein, we report that a cerium dioxide-supported nickel phosphide nanoalloy (nano-NiP/CeO) efficiently promoted the C-3 alkylation of oxindoles with alcohols without any additives through the borrowing hydrogen methodology. Oxindoles were alkylated with various alcohols to provide the corresponding C-3 alkylated oxindoles in high yields. This is the first catalytic system for the C-3 alkylation of oxindoles with alcohols using a non-precious metal-based heterogeneous catalyst. The catalytic activity of nano-NiP/CeO was comparable to that reported for precious metal-based catalysts. Moreover, nano-NiP/CeO was easily recoverable and reusable without any significant loss of activity. Control experiments revealed that the NiP nanoalloy and the CeO support functioned cooperatively, leading to a high catalytic performance.
尽管过渡金属磷化物作为电催化剂和加氢处理催化剂已得到充分研究,但金属磷化物在有机合成中的应用却很少见,并且金属磷化物与载体之间的协同催化作用仍未被探索。在此,我们报道了一种二氧化铈负载的磷化镍纳米合金(nano-NiP/CeO),它通过借氢法在无任何添加剂的情况下有效地促进了吲哚酮与醇的C-3烷基化反应。吲哚酮与各种醇发生烷基化反应,以高产率提供相应的C-3烷基化吲哚酮。这是第一个使用非贵金属基多相催化剂实现吲哚酮与醇的C-3烷基化反应的催化体系。nano-NiP/CeO的催化活性与报道的贵金属基催化剂相当。此外,nano-NiP/CeO易于回收和重复使用,且活性没有任何显著损失。对照实验表明,NiP纳米合金和CeO载体协同发挥作用,从而导致了高催化性能。