Epoxyethane Methoxycarbonylation over a Heterogeneous Catalyst Based on Functionalized Cobalt Carbonyl

IF 4.7 2区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR
Haoyi Tong, Jiankai Cheng*, Yuntao He, Jiyang Wei, Zhangfeng Zhou, Xinyi Cao, Luyang Qiao, Yong Gao and Yuangen Yao*, 
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Abstract

In this work, we report a new heterogeneous catalyst for the methoxycarbonylation of epoxyethane (EO) to methyl 3-hydroxypropanoate (3-HPM), achieving good yields and recyclability of up to three times with no obvious loss in catalytic activity. The catalysts were prepared through an effective strategy to anchor active cobalt carbonyl species to functionalized silica-based molecular sieves. The successful grafting of functional ligand and cobalt carbonyl cluster was evident through 29Si-MAS NMR and FT-IR studies. Furthermore, an in situ FT-IR study indicates that a binuclear cobalt carbonyl catalyst may undergo a shift from bridged carbonyl to terminal carbonyl in the methoxycarbonylation of EO. According to time-dependent in situ FT-IR spectra in the carbonyl stretching region, the main product and intermediate are both captured, showing a new reaction mechanism different from the previous literature reports. These findings are significant for insight into the relation between the catalytic performance and structure.

Abstract Image

基于功能化羰基钴的异相催化剂上环氧乙烷甲氧羰基化反应
在这项工作中,我们报道了一种新的多相催化剂,用于环氧乙烷(EO)甲氧羰基化为3-羟丙酸甲酯(3-HPM),获得了良好的收率和可回收性高达三次,催化活性没有明显损失。催化剂是通过将活性羰基钴固定在官能化硅基分子筛上的有效策略制备的。29Si-MAS NMR和FT-IR研究表明,功能配体与钴羰基簇成功接枝。此外,原位FT-IR研究表明,双核钴羰基催化剂在EO的甲氧羰基化过程中可能经历从桥接羰基到末端羰基的转变。根据羰基拉伸区随时间变化的原位FT-IR光谱,主产物和中间体都被捕获,显示出不同于以往文献报道的新的反应机理。这些发现对于深入了解催化性能与结构之间的关系具有重要意义。
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来源期刊
Inorganic Chemistry
Inorganic Chemistry 化学-无机化学与核化学
CiteScore
7.60
自引率
13.00%
发文量
1960
审稿时长
1.9 months
期刊介绍: Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.
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