Xiaoqing Yang , Jinshan Zhao , Junfeng Zeng , Bihua Chen , Liang Tang , Jun Zhang , Akif Zeb , Zhiyong Li , Shiguo Zhang , Yan Zhang
{"title":"Design of halogen-free hyper-crosslinked porous ionic polymers for efficient CO2 capture and conversion†","authors":"Xiaoqing Yang , Jinshan Zhao , Junfeng Zeng , Bihua Chen , Liang Tang , Jun Zhang , Akif Zeb , Zhiyong Li , Shiguo Zhang , Yan Zhang","doi":"10.1039/d4gc05351f","DOIUrl":null,"url":null,"abstract":"<div><div>Hyper-crosslinked porous ionic polymers (HCPIPs) are important materials for CO<sub>2</sub> capture and catalytic conversion. In this work, we used ion exchange to combine the cross-linking-active tetraphenylborate anion (BPh<sub>4</sub><sup>−</sup>) with a guanidine-based (Gua) ionic liquid (IL), forming a halogen-free IL ([Gua][BPh<sub>4</sub>]). Using different proportions of formaldehyde dimethyl acetal (FDA), we successfully constructed a series of halogen-free guanidine-functionalized HCPIPs (Gua-HCPIP-<em>x</em>) and achieved efficient CO<sub>2</sub> capture and conversion. Specifically, Gua-HCPIP-4, which had rich porosity and a high specific surface area, achieved a CO<sub>2</sub> adsorption capacity of up to 3.2 mmol g<sup>−1</sup>. Gua-HCPIP-<em>x</em>, with guanidine and BPh<sub>4</sub><sup>−</sup> groups, exhibited higher efficiency and selectivity in the catalytic <em>N</em>-formylation reaction of CO<sub>2</sub>. Under mild conditions (3 bar, 80 °C), Gua-HCPIP-4 achieved a 94% yield in the CO<sub>2</sub><em>N</em>-formylation reaction and maintained catalytic activity after 5 cycles. This study provides new insights into enhancing the catalytic activity of the CO<sub>2</sub><em>N</em>-formylation reaction and offers practical guidance for synthesizing halogen-free HCPIPs.</div></div>","PeriodicalId":78,"journal":{"name":"Green Chemistry","volume":"27 6","pages":"Pages 1729-1739"},"PeriodicalIF":9.3000,"publicationDate":"2025-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Green Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1463926225000251","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
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.
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.