Mild Heterogeneous Palladium‐Catalyzed Cleavage of β‐O‐4′‐Ether Linkages of Lignin Model Compounds and Native Lignin in Air. Issue 1 (4th November 2013)

• Record Type: Journal Article
• Authors: Galkin, Maxim V.; Sawadjoon, Supaporn; Rohde, Volker; Dawange, Monali; Samec, Joseph S. M.
• Is Part Of: ChemCatChem. Volume 6:Issue 1(2014:Jan.)
• Page Start: 179
• Page End: 184
• Publication Date: 2013-11-04
• Subjects: Catalysis -- Periodicals; 541.39505
• DOI: 10.1002/cctc.201300540
• Languages: English
• ISSNs: 1867-3880

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>A mild and robust heterogeneous palladium‐catalyzed CO bond cleavage of 2‐aryloxy‐1‐arylethanols using formic acid as reducing agent in air was developed. The cleaved products were isolated in 92–98 % yield; and by slightly varying the reaction conditions, a ketone, an alcohol, or an alkane can be generated in near‐quantitative yield. This reaction is applicable to cleaving the β‐<italic>O</italic>‐4′‐ether bond found in lignin polymers of different origin. The reaction was performed on a lignin polymer model to generate either the monomeric aryl ketone or alkane in a quantitative yield. Moderate depolymerization was achieved with native lignin at similar reaction conditions. Mechanistic studies under kinetic control indicate that an initial palladium‐catalyzed dehydrogenation of the alcohol is followed by insertion of palladium to an enol equivalent. A palladium–formato complex reductively cleaves the palladium–enolate complex to generate the ketone.</p> </abstract>