Building a Co-Salen-Immobilized Porous Organic Polymer Catalyst for CO2 Cycloaddition.

IF 4.2 3区 化学 Q2 POLYMER SCIENCE
Shuai Gu, Lei Li, Lingling Hu, Shuyu Guo, Yi Feng, Huicong Zhang, Guipeng Yu, Juntao Tang
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引用次数: 0

Abstract

The CO2-epoxide addition to cyclic carbonate is of great significance but usually requires high temperatures and CO2 pressures. Herein, a spirobifluorene-based porous organic polymer catalyst is designed with a Co-salen complex immobilized on the backbone (ST-CoSalen-POP) to enable CO2 fixation under mild conditions. ST-CoSalen-POP possesses a high Co-loading content (9.35 wt%), a large pore volume, and high CO2 adsorption capacity. This catalyst achieves a 96% yield in the cycloaddition of CO2 with epoxides at 25 °C and 0.1 MPa CO2 pressures. Moreover, ST-CoSalen-POP also offers the advantages of wide adaptability over epoxide substrates and high structural stability for three consecutive cycles. This study presents a novel catalytic approach for promoting CO2 fixation, offering a significant advancement in the efficient synthesis of fine chemicals.

co - salen固定化多孔有机聚合物CO2环加成催化剂的构建。
环氧化二氧化碳加入环状碳酸盐具有重要意义,但通常需要较高的温度和CO2压力。本文设计了一种螺芴基多孔有机聚合物催化剂,其骨架上固定了Co-salen配合物(ST-CoSalen-POP),可在温和条件下固定CO2。ST-CoSalen-POP具有高共载含量(9.35 wt%)、大孔隙体积和高CO2吸附能力。该催化剂在25°C和0.1 MPa CO2压力下与环氧化物进行CO2环加成反应,收率为96%。此外,ST-CoSalen-POP还具有对环氧化物衬底的广泛适应性和连续三次循环的高结构稳定性的优点。本研究提出了一种新的促进CO2固定的催化方法,为精细化学品的高效合成提供了重要的进展。
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来源期刊
Macromolecular Rapid Communications
Macromolecular Rapid Communications 工程技术-高分子科学
CiteScore
7.70
自引率
6.50%
发文量
477
审稿时长
1.4 months
期刊介绍: Macromolecular Rapid Communications publishes original research in polymer science, ranging from chemistry and physics of polymers to polymers in materials science and life sciences.
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