{"title":"Multi-amino functionalized triazine-based polymers as the catalyst for cycloaddition of CO2 to epoxides","authors":"Chaokun Yang , Xin Wang , Xin Zhao","doi":"10.1016/j.mcat.2024.114724","DOIUrl":null,"url":null,"abstract":"<div><div>Designing efficient catalysts for CO<sub>2</sub> cycloaddition to reduce CO<sub>2</sub> emission is one of crucial for environmental issues technology. Herein, the multiple-amino functionalized triazine-based polymer (MAFTP) was prepared through the nucleophilic reaction of cyanuric chloride with melamine and ethylenediamine by a conventional heating method, which are favorable for CO<sub>2</sub> adsorption due to their nitrogen-rich structure. MAFTP was characterized entirely, the CO<sub>2</sub> adsorption capacity of MAFTP showed the CO<sub>2</sub> uptake performance with the values of 5.73 cm<sup>3</sup> <em>g</em><sup>−1</sup> at 273 K and 1 bar. MAFTP/KI catalyst exhibited efficient catalytic activity for CO<sub>2</sub> fixation to epoxides. 99 % propylene carbonate yield and 99 % selectivity were obtained under 120 °C, 2.0 MPa for 2.0 h without organic solvent. Additionally, the catalysts could be recycled easily from the products after reaction by centrifugation and then reused 5 times efficiently. Meanwhile, the catalytic activity of MAFTP/KI to other substituted epoxides was discussed. Moreover, DFT calculation was adopted to analyze the possible cycloaddition reaction mechanism. The MAFTP/KI system is a promising candidate for CO2 chemical fixation attributing to the low cost, abundant availability, easy separation and high catalytic activity for CO<sub>2</sub> chemical fixation.</div></div>","PeriodicalId":393,"journal":{"name":"Molecular Catalysis","volume":"572 ","pages":"Article 114724"},"PeriodicalIF":3.9000,"publicationDate":"2024-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Catalysis","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2468823124009064","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Designing efficient catalysts for CO2 cycloaddition to reduce CO2 emission is one of crucial for environmental issues technology. Herein, the multiple-amino functionalized triazine-based polymer (MAFTP) was prepared through the nucleophilic reaction of cyanuric chloride with melamine and ethylenediamine by a conventional heating method, which are favorable for CO2 adsorption due to their nitrogen-rich structure. MAFTP was characterized entirely, the CO2 adsorption capacity of MAFTP showed the CO2 uptake performance with the values of 5.73 cm3g−1 at 273 K and 1 bar. MAFTP/KI catalyst exhibited efficient catalytic activity for CO2 fixation to epoxides. 99 % propylene carbonate yield and 99 % selectivity were obtained under 120 °C, 2.0 MPa for 2.0 h without organic solvent. Additionally, the catalysts could be recycled easily from the products after reaction by centrifugation and then reused 5 times efficiently. Meanwhile, the catalytic activity of MAFTP/KI to other substituted epoxides was discussed. Moreover, DFT calculation was adopted to analyze the possible cycloaddition reaction mechanism. The MAFTP/KI system is a promising candidate for CO2 chemical fixation attributing to the low cost, abundant availability, easy separation and high catalytic activity for CO2 chemical fixation.
期刊介绍:
Molecular Catalysis publishes full papers that are original, rigorous, and scholarly contributions examining the molecular and atomic aspects of catalytic activation and reaction mechanisms. The fields covered are:
Heterogeneous catalysis including immobilized molecular catalysts
Homogeneous catalysis including organocatalysis, organometallic catalysis and biocatalysis
Photo- and electrochemistry
Theoretical aspects of catalysis analyzed by computational methods