4.8 Article

Iridium supported on porous polypyridine-oxadiazole as high-activity and recyclable catalyst for the borrowing hydrogen reaction

期刊

GREEN CHEMISTRY
卷 24, 期 6, 页码 2602-2612

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2gc00190j

关键词

-

资金

  1. National Natural Science Foundation of China [21861039]
  2. State Key Laboratory of Pulp and Paper Engineering [202001]
  3. Central Laboratory, School of Chemical and Material Engineering, Jiangnan University

向作者/读者索取更多资源

Homogenization of heterogeneous catalysts is a valuable and interesting research topic. In this study, a porous polypyridine-oxadiazole iridium catalyst was designed and synthesized, and it exhibited high catalytic activity in various reactions. The catalyst also showed the potential for recycling and reuse, indicating its promising application value. Mechanism explorations were conducted to understand the catalytic mechanism.
Homogenization of heterogeneous catalysts is a valuable and interesting research topic. Porous polypyridine-oxadiazole (PPO), as not only a carrier but also a ligand, was designed and synthesized from pyridine-oxadiazole and 1-iodo-4-vinylbenzene. Iridium was anchored onto the skeleton of this polymer (ligand) through coordination bonds. This porous polypyridine-oxadiazole iridium catalyst (PPO-Ir) was clearly characterized by XRD, BET, EDS, HRTEM, SEM, and XPS, and revealed high catalytic activity for the reaction of dimethyl-6-aminouracil with benzyl alcohols, 1,3-dimethylbarbituric acid with benzyl alcohols and 2-aminobenzylamine and benzyl alcohols through dehydrogenation and the borrowing hydrogen strategy with alcohol or water as the solvent. In addition, this PPO-Ir catalyst could be recycled and reused without a manifest loss of catalytic activity for at least five times and revealed potential application value. The mechanism explorations were further conducted to clarify this PPO-Ir and these transformations.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据