Phungpanya Chalida, Sodpiban Ounjit, Gobbo Silvano Del, Arayachukiat Sunatda, Piromchart Taradon, D'Elia Valerio
Department of Material Science and Engineering, School of Molecular Science and Engineering, Vidyasirimedhi Institute of Science and Technology (VISTEC), 21210, Payupnai, WangChan, Rayong, Thailand.
PTT Exploration and Production Company Limited, Energy Complex Building A, Floors 6, 19 - 36, 555/1 Vibhavadi Rangsit Road, Chatuchak, Bangkok 10900, Thailand.
Data Brief. 2021 Jun 1;37:107190. doi: 10.1016/j.dib.2021.107190. eCollection 2021 Aug.
The cycloaddition of CO to epoxides under mild conditions is a growing field of research and a viable strategy to recycle CO in the form of cyclic carbonates as useful intermediates, solvents, and additives. This target requires readily accessible and recyclable catalysts whose synthesis does not involve expensive monomers, multistep procedures, coupling reagents, etc. Additionally, the catalysts should be active under atmospheric pressure and tolerate impurities such as methane and HS. In a recent manuscript ( 422 (2021) 129930) we have developed strategies to prepare efficient heterogeneous catalysts for the cycloaddition reaction of CO to epoxides. Such materials consist of dispersions of metal halides (ZnCl or SnCl) on silica support that is further functionalized with ionic liquids bearing nucleophilic halide moieties for cooperative epoxide activation and ring-opening. Herein, we provide useful complementary data for the characterization of the prepared materials in the form of: SEM images of materials (SEM: scanning electron microscope), SEM-EDS images of materials (EDS: Energy-dispersive X-ray spectroscopy), TEM images of materials (TEM: transmission electron microscope); XPS (X-ray photoelectron spectroscopy) survey spectra of most active catalysts and related high-resolution spectra in spectral regions of interest, BET (Brunauer-Emmett-Teller) physisorption isotherms of materials, raw H NMR spectra of catalytic reactions to verify the reproducibility of the reaction outcome and identify the reaction products.
在温和条件下,一氧化碳与环氧化合物的环加成反应是一个不断发展的研究领域,也是一种可行的策略,可将一氧化碳以环状碳酸酯的形式回收利用,环状碳酸酯可作为有用的中间体、溶剂和添加剂。这一目标需要易于获得且可回收的催化剂,其合成不涉及昂贵的单体、多步程序、偶联试剂等。此外,催化剂应在大气压下具有活性,并能耐受甲烷和硫化氢等杂质。在最近的一篇论文(《422 (2021) 129930》)中,我们开发了制备高效非均相催化剂的策略,用于一氧化碳与环氧化合物的环加成反应。这类材料由金属卤化物(ZnCl或SnCl)在二氧化硅载体上的分散体组成,二氧化硅载体进一步用带有亲核卤化物部分的离子液体进行功能化,以协同活化环氧化物并使其开环。在此,我们以以下形式提供了用于表征所制备材料的有用补充数据:材料的扫描电子显微镜(SEM)图像、材料的扫描电子显微镜 - 能量色散X射线光谱(SEM - EDS)图像、材料的透射电子显微镜(TEM)图像;最具活性催化剂的X射线光电子能谱(XPS)全谱以及感兴趣光谱区域的相关高分辨率光谱、材料的布鲁诺尔 - 埃米特 - 泰勒(BET)物理吸附等温线、催化反应的原始核磁共振氢谱,以验证反应结果的可重复性并鉴定反应产物。