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Detecting Important Intermediates in Pd Catalyzed Depolymerization of a Lignin Model Compound by a Combination of DFT Calculations and Constrained Minima Hopping
Stockholm University, Faculty of Science, Department of Organic Chemistry.
Stockholm University, Faculty of Science, Department of Organic Chemistry.
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Number of Authors: 5
2016 (English)In: The Journal of Physical Chemistry C, ISSN 1932-7447, E-ISSN 1932-7455, Vol. 120, no 41, 23469-23479 p.Article in journal (Refereed) Published
Abstract [en]

Density functional theory (DFT) calculations, combined with a constrained minima hopping algorithm (global minimum search while preserving the molecular identity), have been performed to investigate important reaction intermediates for the heterogeneously catalyzed beta-O-4' bond cleavage in lignin derivatives. More specifically, we have studied the adsorption properties of a keto tautomer (1-methoxypropan-2-one) and its enol form on a catalytically active Pd(111) surface. In agreement with experiments, we find that for the gas phase molecules the keto tautomer is the most stable. Interestingly, the enol tautomer has a higher affinity to the Pd catalyst than the keto form, and becomes the most stable molecular form when adsorbed on the catalyst surface. The global minimum complex found on the metal surface corresponds to an enolate structure formed when the enol tautomer chemisorbs onto the surface and donates its pi-electrons from the C=C region to two adjacent palladium atoms. The actual formation of a chemical bond to the surface in the case of the enol molecule could be the key to understanding why the enol derivative is needed for an efficient beta-O-4' bond cleavage.

Place, publisher, year, edition, pages
2016. Vol. 120, no 41, 23469-23479 p.
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Chemical Sciences Nano Technology Materials Engineering
Identifiers
URN: urn:nbn:se:su:diva-136052DOI: 10.1021/acs.jpcc.6b05622ISI: 000386107600018OAI: oai:DiVA.org:su-136052DiVA: diva2:1058741
Available from: 2016-12-21 Created: 2016-11-29 Last updated: 2016-12-21Bibliographically approved

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Galkin, Maxim V.Samec, Joseph S. M.
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