Xueting Liu , Kuayue Li , Wenkui Liu , Peng Cui , Fengyu Wei
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CO<sub>2</sub> cycloaddition reaction with epoxide DMSNs-Cb-1 can convert CO<sub>2</sub> and epoxide to cyclic carbonate at ambient pressure without solvent and co-catalysts (1 bar, 100 °C). The reaction proceeds with high yield and high conversion frequency (TOF = 27.4 h<sup>−1</sup>). The prepared catalyst is easily recovered and still has high activity after five cycles of experiments. The excellent catalytic performance of the obtained catalyst can be attributed to the synergy of hierarchical porous structure and NHC-CO<sub>2</sub> adducts acting as CO<sub>2</sub> adsorption sites as well as zwitterionic catalytic sites. This work demonstrates an efficient strategy for green conversion of CO<sub>2</sub> into cyclic carbonates.</p></div>","PeriodicalId":20056,"journal":{"name":"Phosphorus, Sulfur, and Silicon and the Related Elements","volume":"199 4","pages":"Pages 283-292"},"PeriodicalIF":1.4000,"publicationDate":"2024-04-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Green conversion of CO2 by N-heterocyclic carbene-CO2 adducts grafted hierarchical porous silica microspheres\",\"authors\":\"Xueting Liu , Kuayue Li , Wenkui Liu , Peng Cui , Fengyu Wei\",\"doi\":\"10.1080/10426507.2024.2332891\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The multiphase catalysts DMSNs-Cb-X containing NHC-CO<sub>2</sub> adducts were synthesized by soft template method that is, first preparing dendritic multi-model pore silica nanoparticles (DMSNs) with central-radial structure, and then grafting imidazoline functional groups, and finally allowing to react with dimethyl carbonate to graft NHC-CO<sub>2</sub> adducts. The investigations had the scope to improve the performance and to elucidate the effect of NHC-CO<sub>2</sub> adducts on the CO<sub>2</sub> cycloaddition reaction. The optimum catalyst DMSNs-Cb-1 and the optimum reaction conditions (200 mg, 100 °C, 10 h) were obtained <em>via</em> thermogravimetric analysis. CO<sub>2</sub> cycloaddition reaction with epoxide DMSNs-Cb-1 can convert CO<sub>2</sub> and epoxide to cyclic carbonate at ambient pressure without solvent and co-catalysts (1 bar, 100 °C). The reaction proceeds with high yield and high conversion frequency (TOF = 27.4 h<sup>−1</sup>). The prepared catalyst is easily recovered and still has high activity after five cycles of experiments. The excellent catalytic performance of the obtained catalyst can be attributed to the synergy of hierarchical porous structure and NHC-CO<sub>2</sub> adducts acting as CO<sub>2</sub> adsorption sites as well as zwitterionic catalytic sites. This work demonstrates an efficient strategy for green conversion of CO<sub>2</sub> into cyclic carbonates.</p></div>\",\"PeriodicalId\":20056,\"journal\":{\"name\":\"Phosphorus, Sulfur, and Silicon and the Related Elements\",\"volume\":\"199 4\",\"pages\":\"Pages 283-292\"},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2024-04-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Phosphorus, Sulfur, and Silicon and the Related Elements\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S104265072400011X\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phosphorus, Sulfur, and Silicon and the Related Elements","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S104265072400011X","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0
摘要
采用软模板法合成了含有NHC-CO2加合物的多相催化剂DMSNs-Cb-X,即首先制备具有中心径向结构的树枝状多模孔二氧化硅纳米颗粒(DMSNs),然后接枝咪唑啉官能团,最后与碳酸二甲酯反应接枝NHC-CO2加合物。这些研究旨在提高催化剂的性能,并阐明 NHC-CO2 加合物对 CO2 环化反应的影响。通过热重分析得出了最佳催化剂 DMSNs-Cb-1 和最佳反应条件(200 毫克、100 °C、10 小时)。二氧化碳与环氧化物的环加成反应 DMSNs-Cb-1 可在不使用溶剂和助催化剂的环境压力下(1 巴,100 °C)将二氧化碳和环氧化物转化为环碳酸盐。该反应的产率高,转化率高(TOF = 27.4 h-1)。所制备的催化剂很容易回收,并且在五个实验周期后仍具有很高的活性。所制备催化剂的优异催化性能可归因于分层多孔结构和 NHC-CO2 加合物作为 CO2 吸附位点以及齐聚物催化位点的协同作用。这项工作展示了一种将 CO2 绿色转化为环状碳酸盐的高效策略。
Green conversion of CO2 by N-heterocyclic carbene-CO2 adducts grafted hierarchical porous silica microspheres
The multiphase catalysts DMSNs-Cb-X containing NHC-CO2 adducts were synthesized by soft template method that is, first preparing dendritic multi-model pore silica nanoparticles (DMSNs) with central-radial structure, and then grafting imidazoline functional groups, and finally allowing to react with dimethyl carbonate to graft NHC-CO2 adducts. The investigations had the scope to improve the performance and to elucidate the effect of NHC-CO2 adducts on the CO2 cycloaddition reaction. The optimum catalyst DMSNs-Cb-1 and the optimum reaction conditions (200 mg, 100 °C, 10 h) were obtained via thermogravimetric analysis. CO2 cycloaddition reaction with epoxide DMSNs-Cb-1 can convert CO2 and epoxide to cyclic carbonate at ambient pressure without solvent and co-catalysts (1 bar, 100 °C). The reaction proceeds with high yield and high conversion frequency (TOF = 27.4 h−1). The prepared catalyst is easily recovered and still has high activity after five cycles of experiments. The excellent catalytic performance of the obtained catalyst can be attributed to the synergy of hierarchical porous structure and NHC-CO2 adducts acting as CO2 adsorption sites as well as zwitterionic catalytic sites. This work demonstrates an efficient strategy for green conversion of CO2 into cyclic carbonates.
期刊介绍:
Phosphorus, Sulfur, and Silicon and the Related Elements is a monthly publication intended to disseminate current trends and novel methods to those working in the broad and interdisciplinary field of heteroatom chemistry.