Solvent-Free Coupling Reaction of Carbon Dioxide and Epoxides Catalyzed by Quaternary Ammonium Functionalized Schiff Base Metal Complexes under Mild Conditions

Author:

Wen Qin1,Yuan Xuexin1,Zhou Qiqi1,Yang Hai-Jian1,Jiang Qingqing1,Hu Juncheng1ORCID,Guo Cun-Yue2ORCID

Affiliation:

1. Key Laboratory of Catalysis and Energy Materials Chemistry of Education & Hubei Key Laboratory of Catalysis and Materials Science, College of Chemistry and Materials Science, South-Central Minzu University, Wuhan 430074, China

2. School of Chemical Sciences, University of Chinese Academy of Sciences, Beijing 100049, China

Abstract

A series of bifunctional Schiff base metal catalysts (Zn-NPClR, Zn-NPXH, and M-NPClH) with two quaternary ammonium groups were prepared for carbon dioxide (CO2) and epoxide coupling reactions. The effects of the reaction variables on the catalytic activity were systematically investigated, and the optimal reaction conditions (120 °C, 1 MPa CO2, 3 h) were screened. The performances of different metal-centered catalysts were evaluated, and Co-NPClH showed excellent activity. This kind of bifunctional catalyst has a wide range of substrate applicability, excellent stability, and can be reused for more than five runs. A relatively high TOF could reach up to 1416 h−1 with Zn-NPClH as catalyst by adjusting reaction factors. In addition, the kinetic study of the coupling reaction catalyzed by three catalysts (Zn, Co, and Ni) was carried out to obtain the activation energy (Ea) for the formation of cyclic carbonates. Finally, a possible mechanism for this cyclization reaction was proposed.

Publisher

MDPI AG

Subject

General Materials Science

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