Suppr超能文献

基于三嗪的有机聚合物在环境压力的一氧化碳作用下催化环氧化物转化为环状碳酸酯

Triazine-based Organic Polymer-catalysed Conversion of Epoxide to Cyclic Carbonate under Ambient CO Pressure.

作者信息

Biswas Tanmoy, Halder Arjun, Paliwal Khusboo S, Mitra Antarip, Tudu Gouri, Banerjee Rahul, Mahalingam Venkataramanan

机构信息

Department of Chemical Sciences, Indian Institute of Science Education and Research (IISER) Mohanpur, Kolkata, West Bengal 741252, India.

Department of Chemistry, University of California, Berkeley, California 94720, United States.

出版信息

Chem Asian J. 2020 Jun 2;15(11):1683-1687. doi: 10.1002/asia.201901277. Epub 2020 Apr 20.

Abstract

In this work we have achieved epoxide to cyclic carbonate conversion using a metal-free polymeric catalyst under ambient CO pressure (1.02 atm) using a balloon setup. The triazine containing polymer (CYA-ANIS) was prepared from cyanuric chloride (CYA-Cl) and o-dianisidine (ANIS) in anhydrous DMF as solvent by refluxing under the N gas environment. The presence of triazine and amine functional groups in the polymer results in the adsorption of CO up to 7 cc/g at 273 K. This inspired us to utilize the polymer for the conversion of a series of functionalised epoxides into their corresponding cyclic carbonates in the presence of tetrabutyl ammonium iodide (TBAI) as co-catalyst. The product has wide range of applications like solvent in lithium ion battery, precursor for polycarbonate, etc. The catalyst was efficient for the conversion of different mono and di-epoxides into their corresponding cyclic carbonates under atmospheric pressure in the presence of TBAI as co-catalyst. The study indicates that epoxide attached with electron withdrawing groups (like, CH Cl, glycidyl ether, etc.) displayed better conversion compared to simple alkane chain attached epoxides. This is mainly due to the stabilization of electron rich intermediates produced during the reaction (e. g. epoxide ring opening or CO incorporation into the halo-alkoxide anion). This catalyst mixture was capable to maintain its reactivity up to five cycles without losing its activity. Post catalytic characterization clearly supports the heterogeneous and recyclable nature of the catalyst.

摘要

在本工作中,我们使用无金属聚合物催化剂,在环境CO压力(1.02 atm)下,通过气球装置实现了环氧化物向环状碳酸酯的转化。含三嗪聚合物(CYA-ANIS)由三聚氯氰(CYA-Cl)和邻联茴香胺(ANIS)在无水N,N-二甲基甲酰胺(DMF)中作为溶剂,在氮气环境下回流制备而成。聚合物中三嗪和胺官能团的存在导致在273 K下对CO的吸附量高达7 cc/g。这启发我们在四丁基碘化铵(TBAI)作为助催化剂的存在下,利用该聚合物将一系列官能化环氧化物转化为其相应的环状碳酸酯。该产物具有广泛的应用,如锂离子电池中的溶剂、聚碳酸酯的前体等。在TBAI作为助催化剂存在下,该催化剂在大气压下能有效地将不同的单环氧化物和二环氧化物转化为其相应的环状碳酸酯。研究表明,与简单的烷烃链连接的环氧化物相比,连接有吸电子基团(如CH₂Cl、缩水甘油醚等)的环氧化物表现出更好的转化率。这主要是由于反应过程中产生的富电子中间体(例如环氧化物开环或CO掺入卤代醇盐阴离子)的稳定性。这种催化剂混合物能够在五个循环中保持其反应活性而不丧失活性。催化后表征清楚地支持了催化剂的非均相和可循环性质。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验