State Key Laboratory of Applied Organic Chemistry (SKLAOC), Gansu Provincial Engineering Laboratory for Chemical Catalysis, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, PR China.
State Key Laboratory of Applied Organic Chemistry (SKLAOC), Gansu Provincial Engineering Laboratory for Chemical Catalysis, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, PR China.
J Colloid Interface Sci. 2019 Mar 7;538:709-719. doi: 10.1016/j.jcis.2018.11.092. Epub 2018 Nov 24.
Four types of core-shell materials with magnetic FeO microparticles as the core were prepared through different approaches using dopamine, glucose, tetrabutyl orthotitanate (TBOT), and tetraethyl orthosilicate (TEOS) as the shell precursor, respectively. CeO nanoparticles (NPs) was successfully immobilized onto these supports to fabricate efficient catalysts for the tandem catalytic synthesis of imines from benzyl alcohols and anilines at low temperature under air atmosphere. The as-prepared catalysts were detailedly characterized by TEM, EDX, XRD, FT-IR, XPS VSM, ICP, and CO-TPD. Interestingly, these prepared catalysts showed higher catalytic activity than reported CeO catalysts. Most attractively, the catalyst with a shell ofnitrogen-doped-carbon derived from dopamine exhibited the best catalytic property, and outstanding stability and recyclability in the cycle experiment. According to the XPS and CO-TPD characterization, the enhanced performance of FeO@CN@CeO composites can be attributed to two reasons as follows: (1) the immobilization of CeO improved its alkalinity at low reaction temperature, and alkalinity is beneficial to promote the oxidation of alcohols to benzaldehyde, which is the rate-determining step for this tandem reaction; (2) the doped nitrogen generated Lewis basic site could satisfactorily stabilize Ce/Ce pair of CeO, which determined the catalytic activity and stability of CeO based catalysts for this tandem reaction. Moreover, the prepared catalysts could be facilely recovered from the reaction mixture with an external magnet. This work may provide a useful strategy for constructing CeO based catalysts for green and sustainable catalysis.
四种核壳材料均以磁性 FeO 微球为核,通过不同方法制备,壳前体分别为多巴胺、葡萄糖、钛酸四丁酯(TBOT)和正硅酸乙酯(TEOS)。成功地将 CeO 纳米颗粒(NPs)固定在这些载体上,制备了高效的催化剂,用于在空气气氛下低温串联催化合成苯甲醇和苯胺的亚胺。通过 TEM、EDX、XRD、FT-IR、XPS VSM、ICP 和 CO-TPD 对所制备的催化剂进行了详细的表征。有趣的是,这些制备的催化剂表现出比报道的 CeO 催化剂更高的催化活性。最吸引人的是,由多巴胺衍生的氮掺杂碳壳的催化剂表现出最好的催化性能,在循环实验中具有出色的稳定性和可回收性。根据 XPS 和 CO-TPD 表征,FeO@CN@CeO 复合材料性能的增强归因于以下两个原因:(1)CeO 的固定提高了其在低反应温度下的碱性,碱性有利于促进醇氧化为苯甲醛,这是串联反应的速率决定步骤;(2)掺杂氮产生的路易斯碱性位可以充分稳定 CeO 中的 Ce/Ce 对,这决定了 CeO 基催化剂在该串联反应中的催化活性和稳定性。此外,所制备的催化剂可以通过外部磁铁从反应混合物中方便地回收。这项工作可能为构建用于绿色可持续催化的 CeO 基催化剂提供了一种有用的策略。