| Literature DB >> 31436954 |
Weng-Chon Cheong1, Wenjuan Yang1, Jian Zhang1, Yang Li1, Di Zhao1, Shoujie Liu1,2, Konglin Wu1,2, Qinggang Liu1, Chao Zhang1, Dingsheng Wang1, Qing Peng1, Chen Chen1, Yadong Li1.
Abstract
Selective hydrogenation of nitroarenes to arylamines is a great challenge because of the complicated mechanism and competitive hydrogenation of reducible functional groups. Isolated single-atomic site catalysts, benefitting from their uniform and well-defined catalytic sites, are promising to achieve high activity and selectivity. Herein, we prepared an isolated iron single-atomic catalyst supported on ordered mesoporous nitrogen-doped carbon (Fe1/N-C). The as-prepared Fe1/N-C showed excellent activity and tolerance for functional groups in the transfer hydrogenation of nitroarenes over hydrazine hydrate. Density functional theory calculations revealed that the single atomically dispersed, partially positively charged Fe atoms and the lowered energy barrier collectively contribute to the superior hydrogenation performances for nitroarenes.Entities:
Keywords: DFT calculation; hydrazine hydrate; mesoporous; nitroarene; selective hydrogenation; single-atom catalysis
Year: 2019 PMID: 31436954 DOI: 10.1021/acsami.9b09125
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229