Molecular copper complexes embedded within porous polymer macroligands for the heterogeneously catalyzed aerobic oxidative formation of N–N bonds†

IF 2.7 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Rémi Beucher, Emmanuel Lacôte, Jérôme Canivet and David Farrusseng
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引用次数: 0

Abstract

Here we report the synthesis of series of bipyridine-based porous polymers as macroligands for molecular copper complexes. The resulting Cu@N-POP solids efficiently catalyze the dehydrogenative N–N coupling of di-p-tolylamine into the corresponding hydrazine using oxygen as the oxidant. The heterogenization of the Cu-based catalyst within porous macroligands improved the catalytic activity with regard to previously reported Cu-based molecular homogeneous systems. Increasing the availability of the bipyridine sites to Cu coordination led to enhanced catalytic performances.

Abstract Image

嵌入多孔聚合物大配体的分子铜复合物,用于异构催化 N-N 键的有氧氧化形成†。
我们在此报告了一系列双吡啶基多孔聚合物作为分子铜络合物的大配体的合成过程。由此得到的 Cu@N-POP 固体能高效催化二对甲苯胺以氧作为氧化剂脱氢 N-N 偶联成相应的肼。与之前报道的铜基分子均相体系相比,铜基催化剂在多孔大载体中的异质化提高了催化活性。增加双吡啶位点与铜的配位可提高催化性能。
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来源期刊
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in chemistry
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