Zhang Mingkai, Zhang Sai, Ma Yuanyuan
Key Laboratory of Special Functional and Smart Polymer Materials of Ministry of Industry and Information Technology, School of Chemistry and Chemical Engineering, Northwestern Polytechnical University, Xi'an, China.
Frontier Institute of Science and Technology, Xi'an Jiaotong University, Xi'an, China.
Front Chem. 2023 Jan 4;10:1104844. doi: 10.3389/fchem.2022.1104844. eCollection 2022.
Cobalt (Co) as a substitute of noble-metal catalysts shows high catalytic capability for production of the widely used primary amines through the reductive amination. However, the synthesis of Co catalysts usually involves the introduction of organic compounds and the high-temperature pyrolysis, which is complicated and difficult for large-scale applications. Herein, we demonstrated a facile and efficient strategy for the preparation of Co catalysts through the reconstruction of cobalt borate (CoBO) during the reductive amination, delivering a high catalytic activity for production of benzylamine from benzaldehyde and ammonia. Initially, CoBO was transformed into Co(OH) through the interaction with ammonia and subsequently reduced to Co nanoparticles by H under the reaction environments. The generated Co catalysts exhibited a satisfactory activity and selectivity to the target product, which overmatched the commonly used Co/C, Pt or Raney Ni catalysts. We anticipate that such an reconstruction of CoBO by reactants during the reaction could provide a new approach for the design and optimization of catalysts to produce primary amines.
钴(Co)作为贵金属催化剂的替代品,在通过还原胺化反应生产广泛使用的伯胺方面表现出很高的催化能力。然而,钴催化剂的合成通常涉及有机化合物的引入和高温热解,这对于大规模应用来说既复杂又困难。在此,我们展示了一种简便高效的策略,通过在还原胺化过程中对硼酸钴(CoBO)进行重构来制备钴催化剂,该催化剂对由苯甲醛和氨生产苄胺具有高催化活性。最初,CoBO通过与氨相互作用转化为Co(OH),随后在反应环境下被H还原为Co纳米颗粒。生成的钴催化剂对目标产物表现出令人满意的活性和选择性,超过了常用的Co/C、Pt或雷尼镍催化剂。我们预计,反应过程中反应物对CoBO的这种重构可为设计和优化生产伯胺的催化剂提供一种新方法。