Aminophosphine PNH complexes of Mn(i), Fe(ii), and Co(ii) and evaluation of their activities in the transfer hydrogenation of nitriles†

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-09-27 DOI:10.1039/D4DT02442G
Ainur Slamova, Ayazhan Bizhanova, Ofeliya Talimonyuk, Kristina A. Gudun, Samat Tussupbayev, Anton Dmitrienko, Aishabibi Kassymbek, Konstantin A. Lyssenko and Andrey Y. Khalimon
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Abstract

A series of Mn(I), Fe(II), and Co(II) complexes with PNH ligands bearing secondary amine functionality were prepared and tested in the catalytic transfer hydrogenation of nitriles using ammonia borane as a hydrogen source. Among all tested complexes, a tetracoordinate Fe(II) bromide, (PNH)FeBr2, proved the most effective, representing a rare example of a highly active iron-based catalytic system for transfer hydrogenation reactions beyond carbonyl compounds and the first example of the iron catalyst for the transfer hydrogenation of nitriles to the corresponding primary amines. Mechanistic studies point out a metal–ligand cooperative mechanism enabled by the secondary amine moiety of the PNH ligand.

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锰(I)、铁(II)和钴(II)的氨基膦 PNH 复合物及其在腈的转移加氢反应中的活性评估
研究人员制备了一系列带有仲胺官能团的 PNH 配体的 Mn (I)、Fe(II) 和 Co(II) 复合物,并在以硼烷氨为氢源的腈催化转移加氢反应中进行了测试。在所有测试的配合物中,四配位溴化铁((PNH)FeBr2)被证明是最有效的,它代表了一个罕见的高活性铁基催化体系,可用于羰基化合物以外的转移加氢反应,也是第一个铁催化剂用于将腈转移加氢为相应伯胺的实例。机理研究指出,PNH 配体的仲胺分子促成了一种金属-配体合作机理
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