Jinpeng Liang, Chenglei Xiao, Zhaoxi Cai, Kongqian Liang, Yayun Pang, Zhonghai Liu, Prof. Jinliang Song
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引用次数: 0
Abstract
Catalytic transfer hydrogenolysis (CTH) of aromatic ether bonds provides a promising strategy for sustainably converting lignin into useful chemicals. Design of innovative catalysts with high activity is the key for this route. Herein, we constructed the hexagonal boron nitride (h-BN)-supported Ru nanoparticles (Ru/h-BN) as the heterogeneous catalyst for the CTH of aromatic ether bonds. Notably, the fabricated Ru/h-BN catalyst could efficiently catalyze CTH of various types of aromatic ether bonds contained in lignin (i.e., 4-O-5, α-O-4, β-O-4, and aryl-O-CH3) employing 2-propanol as the hydrogen resource without using extra acidic or basic additives. Besides, the Ru/h-BN catalyst demonstrated superior performance compared to commercial Ru/C. Systematic investigation revealed that electron-enriched Ru sites and the B atoms on h-BN collaboratively promoted the CTH reaction. Besides, a mechanism study indicated that the direct cleavage of aromatic ether bonds was the primary reaction pathway over Ru/h-BN.
芳香醚键催化转移氢解(CTH)为木质素可持续转化为有用的化学物质提供了一种有前途的策略。创新的高活性催化剂的设计是这条路线的关键。本文构建了六方氮化硼(h-BN)负载的Ru纳米颗粒(Ru/h-BN)作为芳香醚键CTH的非均相催化剂。值得注意的是,制备的Ru/h-BN催化剂可以在不使用额外的酸性或碱性添加剂的情况下,以2-丙醇为氢源,高效催化木质素中含有的各种芳香醚键(4-O-5、α-O-4、β-O-4和芳基- o - ch3)的CTH。此外,与商用Ru/C相比,Ru/h-BN催化剂表现出更优越的性能。系统的研究表明,富电子的Ru位点和h-BN上的B原子共同促进了CTH反应。机理研究表明,Ru/h-BN的主要反应途径是直接裂解芳醚键。
期刊介绍:
With an impact factor of 4.495 (2018), ChemCatChem is one of the premier journals in the field of catalysis. The journal provides primary research papers and critical secondary information on heterogeneous, homogeneous and bio- and nanocatalysis. The journal is well placed to strengthen cross-communication within between these communities. Its authors and readers come from academia, the chemical industry, and government laboratories across the world. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies, and is supported by the German Catalysis Society.