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以钙钛矿型氧化物MgMnO纳米颗粒为催化剂的烷基芳烃碱辅助需氧C-H氧化反应

Base-Assisted Aerobic C-H Oxidation of Alkylarenes with a Murdochite-Type Oxide MgMnO Nanoparticle Catalyst.

作者信息

Hayashi Eri, Tamura Takatoshi, Aihara Takeshi, Kamata Keigo, Hara Michikazu

机构信息

Laboratory for Materials and Structures, Institute of Innovative Research, Tokyo Institute of Technology, Yokohama, Kanagawa 226-8503, Japan.

出版信息

ACS Appl Mater Interfaces. 2022 Feb 9;14(5):6528-6537. doi: 10.1021/acsami.1c20080. Epub 2022 Jan 26.

DOI:10.1021/acsami.1c20080
PMID:35080862
Abstract

Heterogeneously catalyzed aerobic oxidative C-H functionalization under mild conditions is a chemical process to obtain desired oxygenated products directly. Nanosized murdochite-type oxide MgMnO (MgMnO-MA) was successfully synthesized by the sol-gel method using malic acid. The specific surface area reached up to 104 m g, which is about 7 times higher than those (2-15 m g) of MgMnO synthesized by previously reported methods. MgMnO-MA exhibited superior catalytic performance to those of other Mn- and Mg-based oxides, including manganese oxides with Mn-O-Mn active sites for the oxidation of fluorene with molecular oxygen (O) as the sole oxidant under mild conditions (40 °C). The present catalytic system was applicable to the aerobic oxidation of various substrates. The catalyst could be recovered by simple filtration and reused several times without obvious loss of its high catalytic performance. The correlation between the reactivity and the p of the substrates, basic properties of catalysts, and kinetic isotope effects suggest a basicity-controlled mechanism of hydrogen atom transfer. The O-labeling experiments, kinetics, and mechanistic studies showed that H abstraction of the hydrocarbon proceeds a mechanism involving O activation. The structure of MgMnO consisting of isolated Mn species located in a basic MgO matrix plays an important role in the present oxidation.

摘要

温和条件下的多相催化需氧氧化C-H官能团化是一种直接获得所需氧化产物的化学过程。采用苹果酸通过溶胶-凝胶法成功合成了纳米级默多克石型氧化物MgMnO(MgMnO-MA)。其比表面积高达104 m²/g,约为先前报道方法合成的MgMnO(2-15 m²/g)的7倍。在温和条件(40°C)下,以分子氧(O₂)作为唯一氧化剂,MgMnO-MA对芴的氧化表现出优于其他基于锰和镁的氧化物的催化性能,包括具有Mn-O-Mn活性位点的锰氧化物。本催化体系适用于各种底物的需氧氧化。催化剂可通过简单过滤回收,并可重复使用多次,而其高催化性能无明显损失。底物的反应活性与pKa、催化剂的碱性以及动力学同位素效应之间的相关性表明了氢原子转移的碱度控制机制。O₂标记实验、动力学和机理研究表明,烃类的H提取通过涉及O₂活化的机制进行。由位于碱性MgO基质中的孤立Mn物种组成的MgMnO结构在当前氧化过程中起着重要作用。

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