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在深共熔溶剂存在下,使用新型钴基金属有机框架将生物质衍生的5-羟甲基糠醛催化转化为5-羟甲基-2-呋喃羧酸。

Catalytic conversion of biomass-derived 5-hydroxymethylfurfural to 5-hydroxymethyl-2-furancarboxylic acid using novel cobalt-based MOF in the presence of deep eutectic solvents.

作者信息

Ashrafi Samaneh Sedigh, Maleki Behrooz

机构信息

Department of Organic Chemistry, Faculty of Chemistry, University of Mazandaran, Babolsar, 47416-95447, Iran.

出版信息

Sci Rep. 2024 Dec 28;14(1):31384. doi: 10.1038/s41598-024-82844-3.

DOI:10.1038/s41598-024-82844-3
PMID:39733148
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11682365/
Abstract

The oxidation of 5-HMF to HMFCA is an important yet complex process, as it generates high-value chemical intermediates. Achieving this transformation efficiently requires the development of non-precious, highly active catalysts derived from renewable biomass sources. In this work, we introduce UoM-1 (UoM, University of Mazandaran), a novel cobalt-based metal-organic framework (Co-MOF) synthesized using a simple one-step ultrasonic irradiation method. The synthesis employed the ligand 4,4'-((1E,1'E)-((5-carboxy-1,3-phenylene)bis(azaneylylidene))bis (methaneylylidene))dibenzoic acid (Hbdda). A comprehensive suite of analytical techniques, including FT-IR, EDX, ICP, XRD, TEM, DLS, FESEM, and BET-BJH, was used to confirm the structural integrity of the synthesized material. The catalytic performance of UoM-1 was investigated for the selective conversion of HMF to HMFCA, demonstrating its effectiveness as a low-cost, accessible catalyst. To promote a more sustainable and environmentally friendly approach, the oxidation reactions were performed in deep eutectic solvents, which offer a green, low-energy alternative to traditional solvents. This study shows that the UoM-1 catalyst not only provides an economical solution but also aligns with modern green chemistry principles, making it a highly promising candidate for future catalytic applications.

摘要

5-羟甲基糠醛(5-HMF)氧化为2,5-二羟甲基呋喃二甲酸(HMFCA)是一个重要但复杂的过程,因为它会生成高价值的化学中间体。要高效实现这种转化,需要开发源自可再生生物质资源的非贵金属、高活性催化剂。在这项工作中,我们介绍了UoM-1(UoM,马赞德兰大学),一种使用简单的一步超声辐照法合成的新型钴基金属有机框架(Co-MOF)。合成过程采用了配体4,4'-((1E,1'E)-((5-羧基-1,3-亚苯基)双(氮烯基亚基))双(亚甲基))二苯甲酸(Hbdda)。使用了一系列综合分析技术,包括傅里叶变换红外光谱(FT-IR)、能量散射X射线光谱(EDX)、电感耦合等离子体质谱(ICP)、X射线衍射(XRD)、透射电子显微镜(TEM)、动态光散射(DLS)、场发射扫描电子显微镜(FESEM)和BET-BJH法,来确认合成材料的结构完整性。研究了UoM-1对HMF选择性转化为HMFCA的催化性能,证明了其作为低成本、易获得催化剂的有效性。为了推动更可持续和环境友好的方法,氧化反应在深共熔溶剂中进行,深共熔溶剂为传统溶剂提供了一种绿色、低能量的替代方案。这项研究表明,UoM-1催化剂不仅提供了一种经济的解决方案,而且符合现代绿色化学原则,使其成为未来催化应用中极具潜力的候选者。

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