Suppr超能文献

超细微、分散良好的树枝状大分子接枝磁性氧化石墨烯稳定的 Pd-Ni 双金属催化剂在温和条件下用于选择性还原有毒的硝基芳烃。

Ultrafine and well-dispersed Pd-Ni bimetallic catalyst stabilized by dendrimer-grafted magnetic graphene oxide for selective reduction of toxic nitroarenes under mild conditions.

机构信息

Faculty of Chemistry, Kharazmi University, Tehran, Iran; Research Institute of Green Chemistry, Kharazmi University, Tehran, Iran.

Faculty of Chemistry, Kharazmi University, Tehran, Iran; Research Institute of Green Chemistry, Kharazmi University, Tehran, Iran.

出版信息

J Hazard Mater. 2022 Feb 15;424(Pt D):127717. doi: 10.1016/j.jhazmat.2021.127717. Epub 2021 Nov 11.

Abstract

A facile and efficient strategy is introduced for growing a dendrimer structure on the surface of magnetic graphene oxide by using thiol-ene click reaction. The as-synthesized dendrimer-grafted magnetic graphene oxide was used as a suitable support for bimetallic Pd-Ni nanoparticles. The prepared nanocomposite was utilized for the reduction of toxic nitroarenes to aminoarenes by using sodium borohydride in aqueous medium at room temperature. Various nitroarenes with functional groups like nitrile, halogen, carbonyl, hydroxyl, acid, and heterocycles were converted to their corresponding anilines with good to excellent yields. The enhanced performance of the catalyst could be attributed to the synergistic effect between Ni and Pd which causes the reaction to proceed more efficiently. Moreover, the catalyst could be readily isolated from the reaction mixture by utilizing an external magnet and reused till 5th cycles with marginal loss of activity.

摘要

介绍了一种通过巯基-烯点击反应在磁性氧化石墨烯表面生长树状大分子结构的简便、高效策略。所合成的接枝有树状大分子的磁性氧化石墨烯可用作双金属 Pd-Ni 纳米粒子的合适载体。通过在水相中使用硼氢化钠,在室温下,将制备的纳米复合材料用于将有毒的硝基芳烃还原为氨基芳烃。各种带有腈基、卤素、羰基、羟基、酸和杂环等官能团的硝基芳烃都以良好到优异的收率转化为相应的苯胺。催化剂性能的提高归因于 Ni 和 Pd 之间的协同效应,这使得反应更有效地进行。此外,通过利用外部磁铁,催化剂可以很容易地从反应混合物中分离出来,并在 5 次循环中重复使用,活性略有损失。

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