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Metal Triflates for the Production of Aromatics from Lignin.
Deuss, Peter J; Lahive, Ciaran W; Lancefield, Christopher S; Westwood, Nicholas J; Kamer, Paul C J; Barta, Katalin; de Vries, Johannes G.
Afiliação
  • Deuss PJ; Stratingh Institute for Chemistry, University of Groningen, Nijenborgh 4, 9747 AG, Groningen, The Netherlands.
  • Lahive CW; School of Chemistry and Biomedical Science Research Complex, University of St Andrews and EaStCHEM, North Haugh, St Andrews, Fife, KY16 9ST, United Kingdom.
  • Lancefield CS; School of Chemistry and Biomedical Science Research Complex, University of St Andrews and EaStCHEM, North Haugh, St Andrews, Fife, KY16 9ST, United Kingdom.
  • Westwood NJ; School of Chemistry and Biomedical Science Research Complex, University of St Andrews and EaStCHEM, North Haugh, St Andrews, Fife, KY16 9ST, United Kingdom.
  • Kamer PC; School of Chemistry and Biomedical Science Research Complex, University of St Andrews and EaStCHEM, North Haugh, St Andrews, Fife, KY16 9ST, United Kingdom.
  • Barta K; Stratingh Institute for Chemistry, University of Groningen, Nijenborgh 4, 9747 AG, Groningen, The Netherlands. k.barta@rug.nl.
  • de Vries JG; Stratingh Institute for Chemistry, University of Groningen, Nijenborgh 4, 9747 AG, Groningen, The Netherlands. j.g.devries@rug.nl, johannes.devries@catalysis.de.
ChemSusChem ; 9(20): 2974-2981, 2016 Oct 20.
Article em En | MEDLINE | ID: mdl-27650221
ABSTRACT
The depolymerization of lignin into valuable aromatic chemicals is one of the key goals towards establishing economically viable biorefineries. In this contribution we present a simple approach for converting lignin to aromatic monomers in high yields under mild reaction conditions. The methodology relies on the use of catalytic amounts of easy-to-handle metal triflates (M(OTf)x ). Initially, we evaluated the reactivity of a broad range of metal triflates using simple lignin model compounds. More advanced lignin model compounds were also used to study the reactivity of different lignin linkages. The product aromatic monomers were either phenolic C2-acetals obtained by stabilization of the aldehyde cleavage products by reaction with ethylene glycol or methyl aromatics obtained by catalytic decarbonylation. Notably, when the method was ultimately tested on lignin, especially Fe(OTf)3 proved very effective and the phenolic C2-acetal products were obtained in an excellent, 19.3±3.2 wt % yield.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Lignina / Metais Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Lignina / Metais Idioma: En Ano de publicação: 2016 Tipo de documento: Article