环己醇
木质素
键裂
愈创木酚
催化作用
分子内力
纳米颗粒
选择性
化学
氢键
化学工程
劈理(地质)
材料科学
光化学
有机化学
分子
工程类
断裂(地质)
复合材料
作者
Sheng Wang,Peng Zhou,Ximing Yan,Hu Li,Hongguo Wu,Zehui Zhang
标识
DOI:10.1016/j.jechem.2022.12.020
摘要
In this work, a dual-size MOF-derived Co catalyst (0.2Co1-NPs@NC) composed of single atoms (Co1) and highly dispersed nanoparticles (Co NPs) was prepared by in-situ Zn evaporation for the high-performance conversion of lignin-derived o-methoxyphenols (lignin oil) to cyclohexanols (up to 97% yield) via cascade demethoxylation and dearomatization. Theoretical calculations elaborated that the dual-size Co catalyst exhibited a cooperative effect in the selective demethoxylation process, in which the Co NPs could initially dissociate hydrogen at lower energies while Co1 remarkably facilitated the cleavage of the CAr − OCH3 bond. Moreover, the intramolecular hydrogen bonds formed in the o-methoxy-containing phenols were found to result in a decrease in the bond energy of the CAr − OCH3 bond, which was more prone to be activated by the dual-size Co sites. Notably, the pre-hydrogenated intermediate (e.g., 2-methoxycyclohexanol from guaiacol) is difficult to undergo demethoxylation, indicating that the selective CAr − OCH3 bond cleavage is a prerequisite for the synthesis of cyclohexanols. The 0.2Co1-NPs@NC catalyst was highly recyclable with a neglect decline in activity during five consecutive cycles. This cooperative catalytic strategy based on the metal size effect opens new avenues for biomass upgrading via enhanced C O bond cleavage of high selectivity.
科研通智能强力驱动
Strongly Powered by AbleSci AI