Simple Catalyst Based on Zinc(II) Iodide for the Synthesis of Cyclic Carbonates

IF 1.1 3区 化学 Q4 CHEMISTRY, INORGANIC & NUCLEAR
M. D. Tugushev, D. D. Strunin, A. A. Dan’shina, Yu. V. Nelyubina, I. A. Nikovskii
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引用次数: 0

Abstract

The reaction of tridentate ligand 2,6-bis(5-(tert-butyl)-1H-pyrazol-3-yl)pyridine (L) and zinc(II) iodide affords a new zinc(II) complex LZnI2. The compound is isolated in the individual state and characterized by NMR spectroscopy, and its single crystal LZnI2∙2C3H7NO is characterized by X-ray diffraction (XRD) (CIF file CCDC no. 2447394). The synthesized complex demonstrates a catalytic activity in the reactions of CO2 with substituted oxiranes with the formation of cyclic carbonates. This is due to the simultaneous presence in the catalyst of the metal Lewis acidic site capable of coordinating epoxide, nitrogen Lewis basic site providing CO2 fixation, and nucleophilic iodide ion that activates epoxide ring opening. The development of the proposed approach to the design of catalysts will possibly simplify the preparation of efficient systems for the reactions of carbon oxide with three-membered heterocycles.

Abstract Image

基于碘化锌的简单催化剂合成环状碳酸盐
三齿配体2,6-二(5-(叔丁基)- 1h -吡唑-3-基)吡啶(L)与碘化锌(II)反应生成新的锌(II)配合物LZnI2。该化合物在单体状态下得到分离,并通过NMR进行了表征,其单晶LZnI2∙2C3H7NO通过x射线衍射(XRD)进行了表征(CIF文件CCDC no. 7)。2447394)。所合成的配合物在CO2与取代氧环烷的反应中具有催化活性,并形成环状碳酸盐。这是由于催化剂中同时存在能够配位环氧化物的金属路易斯酸性位点、提供CO2固定的氮路易斯碱性位点和激活环氧化物开环的亲核碘离子。所提出的催化剂设计方法的发展可能会简化氧化碳与三元杂环反应的高效体系的制备。
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来源期刊
Russian Journal of Coordination Chemistry
Russian Journal of Coordination Chemistry 化学-无机化学与核化学
CiteScore
2.40
自引率
15.80%
发文量
85
审稿时长
7.2 months
期刊介绍: Russian Journal of Coordination Chemistry is a journal that publishes reviews, original papers, and short communications on all aspects of theoretical and experimental coordination chemistry. Modern coordination chemistry is an interdisciplinary science that makes a bridge between inorganic, organic, physical, analytical, and biological chemistry.
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