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Base-Free Methanol Dehydrogenation Using a Pincer-Supported Iron Compound and Lewis Acid Co-catalyst

机译:使用夹钳式铁化合物和路易斯酸助催化剂进行无碱甲醇脱氢

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摘要

Hydrogen is an attractive alternative energy vector to fossil fuels if effective methods for its storage and release can be developed. In particular, methanol, with a gravimetric hydrogen content of 12.6%, is a promising target for chemical hydrogen storage. To date, there are relatively few homogeneous transition metal compounds that catalyze the aqueous phase dehydrogenation of methanol to release hydrogen and carbon dioxide. In general, these catalysts utilize expensive precious metals and require a strong base. This paper shows that a pincer-supported Fe compound and a co-catalytic amount of a Lewis acid are capable of catalyzing base-free aqueous phase methanol dehydrogenation with turnover numbers up to 51 000. This is the highest turnover number reported for either a first-row transition metal or a base-free system. Additionally, this paper describes preliminary mechanistic experiments to understand the reaction pathway and propose a stepwise process, which requires metal ligand cooperativity. This pathway is supported by DFT calculations and explains the role of the Lewis acid co-catalyst.
机译:如果可以开发出有效的存储和释放氢的方法,氢将是化石燃料的一种有吸引力的替代能源。特别地,重量氢含量为12.6%的甲醇是化学氢存储的有希望的目标。迄今为止,催化甲醇的水相脱氢以释放氢和二氧化碳的均相过渡金属化合物相对较少。通常,这些催化剂利用昂贵的贵金属并且需要强碱。本文表明,夹钳式负载的Fe化合物和助催化量的路易斯酸能够催化无碱水相甲醇脱氢,其转换数最高为51000。这是首次报道的最高转换数。行过渡金属或无碱体系。此外,本文描述了初步的机械实验,以了解反应途径并提出逐步过程,该过程需要金属配体的协同作用。 DFT计算支持该途径,并解释了路易斯酸助催化剂的作用。

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