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Origins of Catalyst Inhibition in the Manganese‐Catalysed Oxidation of Lignin Model Compounds with H2O2

机译:木质素模型化合物与H2O2的锰催化氧化中催化剂抑制作用的起源

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摘要

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 H2O2 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.
机译:通过解聚,复杂的生物可再生原料(如木质纤维素)的升级得益于关键官能团的选择性反应。干扰组分的存在挑战了将为选择性有机氧化转化而开发的均相催化剂应用于木质素等复杂原料的挑战。选择合适的模型化合物对于应用新的催化系统和识别此类干扰至关重要。在此,以含有H 2 O 2的β-O-4键的模型基质和原位制备的锰基催化剂的氧化为例进行了说明,该催化剂能够有效地氧化苄醇,从而不受释放出的化合物的干扰在反应过程中可以防止其应用于木质纤维素解聚。

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