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Origins of Catalyst Inhibition in the Manganese‐Catalysed Oxidation of Lignin Model Compounds with H(2)O(2)

The upgrading of complex bio‐renewable feedstock, such as lignocellulose, through depolymerisation benefits from the selective reactions at key functional groups. Applying homogeneous catalysts developed for selective organic oxidative transformations to complex feedstock such as lignin is challenge...

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Detalles Bibliográficos
Autores principales: Barbieri, Alessia, Kasper, Johann B., Mecozzi, Francesco, Lanzalunga, Osvaldo, Browne, Wesley R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6617720/
https://www.ncbi.nlm.nih.gov/pubmed/31001914
http://dx.doi.org/10.1002/cssc.201900689
Descripción
Sumario:The upgrading of complex bio‐renewable feedstock, such as lignocellulose, through depolymerisation benefits from the selective reactions at key functional groups. Applying homogeneous catalysts developed for selective organic oxidative transformations to complex feedstock such as lignin is challenged by the presence of interfering components. The selection of appropriate model compounds is essential in applying new catalytic systems and identifying such interferences. Here, it was shown by using as an example the oxidation of a model substrate containing a β‐O‐4 linkage with H(2)O(2) and an in situ‐prepared manganese‐based catalyst, capable of efficient oxidation of benzylic alcohols, that interference from compounds liberated during the reaction can prevent its application to lignocellulose depolymerisation.