Matsuyama Takehiro, Yatabe Takafumi, Yabe Tomohiro, Yamaguchi Kazuya
Department of Applied Chemistry, School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8656, Japan.
Precursory Research for Embryonic Science and Technology (PRESTO), Japan Science and Technology Agency (JST), 4-1-8 Honcho, Kawaguchi, Saitama, 332-0012, Japan.
Nat Commun. 2025 Feb 7;16(1):1118. doi: 10.1038/s41467-025-56361-4.
The dehydrogenative aromatisation of cyclohexanone derivatives has had a transformative influence on the synthesis of aromatic compounds because functional groups can be easily introduced at desired positions via classic organic reactions without being limited by ortho-, meta- or para-orientations. However, research is still limited on acceptorless dehydrogenative aromatisation, especially with regard to nonprecious-metal catalysts. Ni is a promising candidate catalyst as a congener of Pd, but thermally Ni-catalysed dehydrogenative aromatisation has not been reported even in an oxidative manner because of the difficulty of β-hydride elimination and the fast re-insertion of Ni-H species. Here, we report a CeO-supported Ni(0) nanoparticle catalyst for acceptorless dehydrogenative aromatisation of cyclohexanone derivatives. This catalyst is widely applicable to various compounds such as cyclohexanols, cyclohexylamines, N-heterocycles, enamines and β-heteroatom-substituted ketones. Through various experiments, we demonstrate that the present reaction was achieved by the concerted catalysis utilizing metal ensembles unique to supported metal nanoparticle catalysts.
环己酮衍生物的脱氢芳构化反应对芳香族化合物的合成产生了变革性影响,因为通过经典有机反应可以轻松地将官能团引入到所需位置,而不受邻位、间位或对位取向的限制。然而,关于无受体脱氢芳构化反应的研究仍然有限,特别是在非贵金属催化剂方面。镍作为钯的同系物,是一种有前景的候选催化剂,但由于β-氢消除困难以及镍-氢物种的快速重新插入,即使在氧化方式下,热催化的镍催化脱氢芳构化反应也尚未见报道。在此,我们报道了一种用于环己酮衍生物无受体脱氢芳构化反应的氧化铈负载镍(0)纳米颗粒催化剂。该催化剂广泛适用于各种化合物,如环己醇、环己胺、氮杂环、烯胺和β-杂原子取代的酮。通过各种实验,我们证明了本反应是通过利用负载型金属纳米颗粒催化剂特有的金属团簇协同催化实现的。