Journal
ACS CATALYSIS
Volume 9, Issue 5, Pages 4054-4064Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acscatal.9b00556
Keywords
lignin; hydrogenolysis; base-dependent; Ru/C; mechanism
Categories
Funding
- National Natural Science Foundation of China [21776020]
- Fundamental Research Funds for the Central Universities [2018BLRD12]
- National Program for Thousand Young Talents of China
Ask authors/readers for more resources
Substantial attention has been given to depolymerization of lignin into monomeric phenols in recent years because lignin is a renewable and CO2-netural aromatic resource. Recent results indicated that the base can shift the selectivity from C3-fragmented phenols to C2-fragmented phenols partially in transition metal-catalyzed lignin hydogenolysis, while reaction mechanisms have remained elusive. Using a series of dimeric, trimeric, and polymeric beta-O-4 lignin mimics, as well as their deuterated analogues, we now report an in-depth experimental study on the mechanism of Ru/C-catalyzed hydogenolysis lignin. Experimental evidence based on substrate probes, reactivity examination of possible intermediates, and isotopic labeling experiments confirmed that the reported pathways, such as enol ether generated via alpha,beta-dehydration reaction or C-alpha carbonyl compounds generated via dehydrogenation or consecutive C-beta-O and C-gamma-OH bonds hydrogenolysis, are irrelevant to current reactions. For C3-fragmented phenols with Ru/C catalyst under neutral condition, we deduced that the monolignol such as coniferyl alcohol is formed primarily through a concerted hydrogenolysis process, where C-alpha-O and C-beta-O bonds are ruptured synchronously. For C2-fragmented phenols generated by the combination of Ru/C and Cs2CO3, the reaction should start from quinone methide specie generated from the dehydration (or demethanolization) reaction between phenolic proton and C-alpha-OH (or C-alpha-OMe). The followed deprotonation of C-gamma-OH and the coordination of oxygen with Ru results in a Ru specie, which undergoes C-beta-H, C-beta-O, and C-beta-C-gamma bonds cleavage to release 4-vinylphenol. In the case of Ru/C- catalyzed hydrogenolysis of an enzymatic mild acidolysis lignin (EMAL) derived from birch tree, the effects of some key parameters such as temperature, reaction time, as well as the type and dosage of base were also examined in terms of monomer yields and selectivity. We found the formation of C2-phenols is a base-dependent process, which is in line with the proposed mechanism. Under optimized conditions, a high proportion of C2-phenols (44%) could be obtained with 26.6 wt % total monomers yield.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available