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Divergent Coupling of Alcohols and Amines Catalyzed by Isoelectronic Hydride Mn-I and Fe-II PNP Pincer Complexes

机译:等电子氢化物Mn-I和Fe-II PNP钳形配合物催化的醇和胺的发散偶联

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摘要

Herein, we describe an efficient coupling of alcohols and amines catalyzed by well-defined isoelectronic hydride Mn-I and Fe-II complexes, which are stabilized by a PNP ligand based on the 2,6-diaminopyridine scaffold. This reaction is an environmentally benign process implementing inexpensive, earth-abundant non-precious metal catalysts, and is based on the acceptorless alcohol dehydrogenation concept. A range of alcohols and amines including both aromatic and aliphatic substrates were efficiently converted in good to excellent isolated yields. Although in the case of Mn selectively imines were obtained, with Feexclusively monoalkylated amines were formed. These reactions proceed under base-free conditions and required the addition of molecular sieves.
机译:在这里,我们描述了由明确定义的等电子氢化物Mn-I和Fe-II配合物催化的醇和胺的有效偶联,这些配合物由基于2,6-二氨基吡啶骨架的PNP配体稳定。该反应是一种环境友好的方法,使用廉价的,富含地球的非贵金属催化剂,并且基于无受体醇脱氢的概念。包括芳族和脂族底物在内的多种醇和胺都以良好的分离效率得到了有效的转化。尽管在Mn的情况下选择性地获得了亚胺,但是Fexclusively形成了单烷基化的胺。这些反应在无碱条件下进行,需要添加分子筛。

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