Li Boyang, Fang Jian, Xu Dan, Zhao Hong, Zhu Hanghang, Zhang Fengwei, Dong Zhengping
State Key Laboratory of Applied Organic Chemistry, Laboratory of Special Function Materials and Structure Design of the Ministry of Education College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, 730000, P. R. China.
Institute of Crystalline Materials, Shanxi University, Taiyuan, 030006, P. R. China.
ChemSusChem. 2021 Oct 20;14(20):4536-4545. doi: 10.1002/cssc.202101330. Epub 2021 Sep 20.
The catalytic dehydrogenation of readily available alcohols to high value-added carbonyl compounds is a research hotspot with scientific significance. Most of the current research about this reaction is performed with noble metal-based homogeneous catalysts of high price and poor reusability. Herein, highly dispersed Co-cluster-decorated N-doped carbon nanotubes (Co/N-CNTs) were fabricated via a facile strategy and used for the dehydrogenation of alcohols with high efficiency. Various characterization techniques confirmed the presence of metallic Co clusters with almost atomic dispersion, and the N-doped carbon supports also enhanced the catalytic activity of Co clusters in the dehydrogenation reaction. Aldehydes as dehydrogenation products were further transformed in situ to carboxylic acids through a Cannizzaro-type pathway under alkaline conditions. The reaction pathway of the dehydrogenation of alcohols was clearly confirmed by theoretical calculations. This work should provide an effective and simple approach for the accurate design and synthesis of small Co-clusters catalysts for the efficient dehydrogenation-based transformation of alcohols to carboxylic acids under mild reaction conditions.
将易得的醇催化脱氢转化为高附加值的羰基化合物是一个具有科学意义的研究热点。目前关于该反应的大多数研究是使用价格高昂且可重复使用性差的贵金属基均相催化剂进行的。在此,通过一种简便的策略制备了高度分散的钴簇修饰的氮掺杂碳纳米管(Co/N-CNTs),并将其用于高效催化醇的脱氢反应。各种表征技术证实了几乎呈原子分散的金属钴簇的存在,并且氮掺杂的碳载体也增强了钴簇在脱氢反应中的催化活性。在碱性条件下,作为脱氢产物的醛通过坎尼扎罗型途径进一步原位转化为羧酸。醇脱氢反应的途径通过理论计算得到了明确证实。这项工作应为在温和反应条件下高效脱氢将醇转化为羧酸的小型钴簇催化剂的精确设计和合成提供一种有效且简便的方法。