利用可回收锰基催化系统进行一氧化碳制甲醇的液相加氢反应†。

IF 9.3 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Green Chemistry Pub Date : 2024-06-07 DOI:10.1039/D4GC01050G
Sebastian Stahl, Niklas Wessel, Andreas J. Vorholt and Walter Leitner
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引用次数: 0

摘要

建立了一种简单且可回收的均相催化系统,用于将一氧化碳氢化为甲醇。该反应由分子锰络合物催化,使用高沸点醇作为催化剂固定的溶剂。在催化量的 NaOMe 作为碱的介导下,通过形成甲酸甲酯或十二烷基甲酸酯中间体,一氧化碳加氢反应得到了产物本身和溶剂的帮助。这样就可以在醇中催化形成甲醇,并通过蒸馏方便地分离产物和回收催化剂。在以 1-十二醇/甲醇为反应介质(T = 160 °C,p(H2/CO) = 80/10 bar)的优化条件下,初始转化率 (TOF) 达到 2250 h-1。通过 6 次分批循环运行,总周转次数 (TTON) 达到 12 000,与相同条件下的单次分批运行相比,性能提高了五倍以上,从而使性能趋于稳定。在蒸馏产品分离过程中,有机金属催化剂成分的浸出极少,通过重新添加碱 NaOMe 可以完全恢复催化剂活性。
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Liquid-phase hydrogenation of carbon monoxide to methanol using a recyclable manganese-based catalytic system†

A simple and recyclable homogeneous catalytic system for the hydrogenation of carbon monoxide to methanol was established. The reaction is catalyzed by a molecular manganese complex using a high-boiling alcohol as the solvent for catalyst immobilization. The CO hydrogenation is assisted by the product itself and the solvent through the formation of a methyl or dodecyl formate ester intermediate mediated by catalytic amounts of NaOMe as the base. This allows the catalytic formation of methanol in alcohols combined with facile product separation and catalyst recycling via distillation. Initial turnover frequencies (TOF) of 2250 h−1 were reached under optimized conditions in 1-dodecanol/methanol as the reaction medium (T = 160 °C, p(H2/CO) = 80/10 bar). The performance was stabilized in batch-wise recycling over 6 runs achieving a total turnover number (TTON) of >12 000 corresponding to an enhancement of more than five times compared to single batch operation under identical conditions. Minimal leaching of the components of the organometallic catalyst was observed during distillative product separation and catalyst activity could be fully restored by re-addition of the base NaOMe.

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来源期刊
Green Chemistry
Green Chemistry 化学-化学综合
CiteScore
16.10
自引率
7.10%
发文量
677
审稿时长
1.4 months
期刊介绍: Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.
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