Electric Literature of 101-84-8, Chemo-enzymatic cascade processes are invaluable due to their ability to rapidly construct high-value products from available feedstock chemicals in a one-pot relay manner. 101-84-8, Name is Diphenyl oxide, SMILES is C1(OC2=CC=CC=C2)=CC=CC=C1, belongs to ethers-buliding-blocks compound. In a article, author is Lu, Qiang, introduce new discover of the category.
A novel interaction mechanism in lignin pyrolysis: Phenolics-assisted hydrogen transfer for the decomposition of the beta-O-4 linkage
Pyrolysis of lignin involves complex unimolecular decomposition and bimolecular interaction mechanisms. Unimolecular decomposition of lignin model compounds has been widely investigated, while bimolecular interactions are far from well elucidated. Currently, only two radical reaction-based interactions, i.e., hydrogen abstraction and hydrogen-bond-induced homolysis mechanisms, have been proposed to explain the interactions in the lignin pyrolysis process, which ignores the concerted reaction-based interactions involving the pyrolytic products of lignin. Particularly, a large number of phenolics are produced in the pyrolysis of lignin, which can further affect the concerted pyrolysis reactions of lignin. In the present work, a novel interaction mechanism, phenolics-assisted hydrogen transfer (phenolics-AHT) pro cess for the concerted reactions, is confirmed and carefully investigated. Phenylethyl phenyl ether (PPE), a typical beta-O-4 lignin dimer, is used as the model compound to reveal the phenolics-AHT mechanism in the lignin pyrolysis system. Density functional theory (DFT) calculation, electrostatic potential (ESP) analysis, and fast pyrolysis experiment results are combined to reveal that the phenolic products participate in the hydrogen transfer process of the concerted Maccoll elimination reaction by means of their phenolic hydroxyl structures and significantly reduce the energy barrier, thus promoting the cleavage of the beta-O-4 linkage. On the contrary, phenolics-AHT has no obvious effect on the concerted retro-ene fragmentation. At medium pyrolysis temperatures, the hydrogen transfer processes induced by phenolic products play a more significant role in the dissociation of the beta-O-4 linkage than the hydrogen abstraction induced by radicals, due to the limited amount of free radicals. In addition, DFT calculation results further suggest that decarbonylation, decarboxylation, dehydration, tautomerism, and other concerted reactions can also be promoted by phenolics-AHT. (C) 2020 The Combustion Institute. Published by Elsevier Inc. All rights reserved.
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