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锆掺杂二氧化铈催化剂用于苯胺甲氧羰基化反应的性能增强

Enhanced Performance of Zirconium-Doped Ceria Catalysts for the Methoxycarbonylation of Anilines.

作者信息

Núñez-Rico José Luis, Rellán-Piñeiro Marcos, Puértolas Begoña, Vidal-Ferran Anton, López Núria, Pérez-Ramírez Javier, Wershofen Stefan

机构信息

Department of Inorganic and Organic Chemistry, University of Barcelona, C. Martí i Franquès 1-11, 08028, Barcelona, Spain.

Institute of Chemical Research of Catalonia (ICIQ) and The Barcelona Institute of Science and Technology, Avgda. Països Catalans 16, 43007, Tarragona, Spain.

出版信息

Chemistry. 2020 Dec 4;26(68):16129-16137. doi: 10.1002/chem.202003201. Epub 2020 Nov 3.

Abstract

The methoxycarbonylation of anilines stands as an attractive method for the phosgene-free production of carbamates. Despite the high yields obtained for ceria catalysts, the reduction of the amount of side products and the prevention of catalyst deactivation still represent major hurdles in this chemistry. One advantage of ceria is the possibility of tuning its reactivity by doping its lattice with other metals. In the present work, a series of doped ceria-based materials, prepared by substitution with metals, are evaluated in the methoxycarbonylation of 2,4-diaminotoluene with dimethyl carbonate. Among all catalysts, containing Eu, Hf, La, Pr, Sm, Tb, Y or Zr, ceria promoted with 2 mol % Zr exhibited 96 % selectivity towards the desired carbamates, improving the pure CeO catalyst. Density functional theory demonstrates that two descriptors are needed: 1) a geometric factor that governs the reduction of energy barriers for carbamate formation through ureas; 2) catalyst basicity as N-H bonds need to be activated. Assessment in subsequent reaction cycles revealed that the CeO -ZrO catalyst is more stable than bulk CeO , along with the reduction of fouling processes.

摘要

苯胺的甲氧羰基化是一种颇具吸引力的、用于无光气生产氨基甲酸酯的方法。尽管二氧化铈催化剂能获得高产率,但减少副产物的量以及防止催化剂失活仍是该化学过程中的主要障碍。二氧化铈的一个优点是可以通过用其他金属掺杂其晶格来调节其反应活性。在本工作中,通过金属取代制备的一系列掺杂二氧化铈基材料,在2,4 - 二氨基甲苯与碳酸二甲酯的甲氧羰基化反应中进行了评估。在所有含有铕、铪、镧、镨、钐、铽、钇或锆的催化剂中,用2 mol%锆促进的二氧化铈对所需氨基甲酸酯的选择性为96%,比纯CeO₂催化剂有所提高。密度泛函理论表明需要两个描述符:1)一个几何因子,它通过脲控制氨基甲酸酯形成的能垒降低;2)催化剂碱性,因为N - H键需要被活化。后续反应循环中的评估表明,CeO₂ - ZrO₂催化剂比块状CeO₂更稳定,同时污垢形成过程减少。

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