四齿氨基吡啶配体钴配合物:二氧化碳和环氧化物环加成反应的单组分高效催化体系

IF 2.7 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Ning Yu, Bowen Zhang, Shuyan Liang, Minghui Shi, Feng Han, Congcong Zhang, Qingfeng Yang and Chengxia Miao
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引用次数: 0

摘要

提出了一种简单可行的由二胺和吡啶组成的四齿氨基吡啶配体的合成路线。随后合成了一系列含有这些四齿氨基吡啶配体的新型钴配合物。对其中一种钴配合物的单晶进行了表征,揭示了四个N原子在顺式α拓扑结构中的配位。该钴配合物成功地作为单组分催化剂,在无溶剂条件下,在2.5 MPa CO2压力下,90℃下由环氧化物和二氧化碳合成环状碳酸盐。红外光谱(IR)和电感耦合等离子体(ICP)分析证实了催化剂具有良好的可回收性和稳定性。此外,利用密度泛函理论(DFT)研究了单co催化环加成反应的机理。值得注意的是,已经提出了一种反应机制,其中环氧化物在钴配合物释放Br -离子后被激活。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cobalt complex with a tetradentate aminopyridine ligand: a single-component and efficient catalytic system for the cycloaddition reactions of CO2 and epoxides†

Cobalt complex with a tetradentate aminopyridine ligand: a single-component and efficient catalytic system for the cycloaddition reactions of CO2 and epoxides†

A simple and commercially viable synthetic route for tetradentate aminopyridine ligands composed of diamine and pyridine has been developed. A series of novel cobalt complexes incorporating these tetradentate aminopyridine ligands were subsequently synthesized. The single crystal of one such cobalt complex was characterized, revealing coordination through four N atoms in a cis-α topology. This cobalt complex was successfully employed as a single-component catalyst for the synthesis of cyclic carbonates from epoxides and carbon dioxide at 90 °C under 2.5 MPa CO2 pressure in solvent-free conditions. The catalyst exhibited excellent recyclability and stability, as confirmed by infrared radiation (IR) spectra and inductively coupled plasma (ICP) analyses. Additionally, a single-Co catalytic mechanism for the cycloaddition reaction was investigated using density functional theory (DFT). Notably, a reaction mechanism has been proposed in which the epoxide is activated following the release of a Br ion from the cobalt complex.

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来源期刊
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in chemistry
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