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An lcy-topology amino acid MOF as eco-friendly catalyst for cyclic carbonate synthesis from CO2: Structure-DFT corroborated study

机译:Lcy-topology氨基酸MOF作为从CO2合成环状碳酸酯的环保催化剂:Structure-DFT确证研究

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The concept of bio-metal-organic framework (bio-MOF) catalysts for CO2 transformation was devised using L-glutamic acid as the natural surrogate for synthetic ligands, and demonstrated their catalytic efficacy for the first time, in the cycloaddition of CO2 with epoxides, supplemented with the structure-DFT correlation. The water stable amino acid bio-MOF, zinc-glutamate-MOF (ZnGlu), with a rare 3D topology (3(3).5(9).6(3))-lcy was synthesized as single crystals and bulk, through an ecofriendly protocol in aqueous medium, from zinc and the proteinogenic amino acid, L-glutamic acid. Amino acid MOFs (AA-MOFs), owing to their economic and environmental factors, are expected to be the future of MOF chemistry at industrial levels. The ZnGlu catalyst with open metal sites was successfully demonstrated as the first bio-MOF catalyst for cyclic carbonate synthesis from CO2 and epoxides, and its efficiency was compared with those of prominent synthetic MOFs reported so far in the process. The as-synthesized catalyst operated even under moist conditions, was thermally and chemically stable; heterogeneous, easily separable (due to its high selectivity, absence of synthesis solvents, and easy catalyst recovery by filtration) and was recycled up to four times. Mechanistic aspects, possible intermediates, transition states and pathways were portrayed using a combination of the experimental inferences, previous reports and ab initio quantum mechanical calculations (DFT techniques) by its correlation with the single crystal XRD structure and topology.
机译:以L-谷氨酸为合成配体的天然替代物,设计了用于CO2转化的生物金属有机骨架(bio-MOF)催化剂的概念,并首次证明了其在环氧与环氧化物加环中的催化功效。 ,并辅以结构-DFT相关性。通过稀有的3D拓扑结构(3(3).5(9).6(3))-lcy合成的水稳定性氨基酸生物MOF,谷氨酸锌MOF(ZnGlu)通过锌和蛋白氨基酸L-谷氨酸在水介质中的一种环保协议。由于其经济和环境因素,氨基酸MOF(AA-MOF)有望成为MOF化学工业的未来。具有开放金属位点的ZnGlu催化剂已成功证明是首个用于从CO2和环氧化物合成环状碳酸酯的生物MOF催化剂,并将其效率与迄今为止报道的主要合成MOF进行了比较。合成后的催化剂即使在潮湿条件下也能保持热和化学稳定性。多相的,易于分离的(由于其高选择性,不存在合成溶剂以及易于通过过滤回收催化剂),最多可循环使用四次。通过与单晶XRD结构和拓扑的相关性,结合了实验推论,先前的报道和从头算起的量子力学计算(DFT技术),描绘了机械方面,可能的中间体,过渡态和途径。

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