Design of halogen-free hyper-crosslinked porous ionic polymers for efficient CO2 capture and conversion†

IF 9.2 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Green Chemistry Pub Date : 2025-01-20 DOI:10.1039/d4gc05351f
Xiaoqing Yang , Jinshan Zhao , Junfeng Zeng , Bihua Chen , Liang Tang , Jun Zhang , Akif Zeb , Zhiyong Li , Shiguo Zhang , Yan Zhang
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Abstract

Hyper-crosslinked porous ionic polymers (HCPIPs) are important materials for CO2 capture and catalytic conversion. In this work, we used ion exchange to combine the cross-linking-active tetraphenylborate anion (BPh4) with a guanidine-based (Gua) ionic liquid (IL), forming a halogen-free IL ([Gua][BPh4]). Using different proportions of formaldehyde dimethyl acetal (FDA), we successfully constructed a series of halogen-free guanidine-functionalized HCPIPs (Gua-HCPIP-x) and achieved efficient CO2 capture and conversion. Specifically, Gua-HCPIP-4, which had rich porosity and a high specific surface area, achieved a CO2 adsorption capacity of up to 3.2 mmol g−1. Gua-HCPIP-x, with guanidine and BPh4 groups, exhibited higher efficiency and selectivity in the catalytic N-formylation reaction of CO2. Under mild conditions (3 bar, 80 °C), Gua-HCPIP-4 achieved a 94% yield in the CO2N-formylation reaction and maintained catalytic activity after 5 cycles. This study provides new insights into enhancing the catalytic activity of the CO2N-formylation reaction and offers practical guidance for synthesizing halogen-free HCPIPs.

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无卤超交联多孔离子聚合物的设计,用于高效的CO2捕获和转化†
超交联多孔离子聚合物(HCPIPs)是二氧化碳捕获和催化转化的重要材料。在这项工作中,我们使用离子交换将具有交联活性的四苯基硼酸盐阴离子(BPh4−)与胍基离子液体(Gua)结合,形成无卤离子液体([Gua][BPh4])。采用不同比例的甲醛缩二甲基缩醛(FDA),成功构建了一系列无卤胍功能化的hcpip (Gua-HCPIP-x),实现了高效的CO2捕获和转化。其中,具有丰富孔隙度和高比表面积的Gua-HCPIP-4的CO2吸附量可达3.2 mmol g−1。Gua-HCPIP-x具有胍基和BPh4 -基团,在CO2的n -甲酰化反应中表现出更高的效率和选择性。在温和条件下(3 bar, 80°C), Gua-HCPIP-4在co2n -甲酰化反应中获得了94%的产率,并在5个循环后保持了催化活性。该研究为提高co2n -甲酰化反应的催化活性提供了新的见解,并为合成无卤hcpps提供了实践指导。
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来源期刊
Green Chemistry
Green Chemistry 化学-化学综合
CiteScore
16.10
自引率
7.10%
发文量
677
审稿时长
1.4 months
期刊介绍: Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.
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