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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Cooperative Mn(i)-complex catalyzed transfer hydrogenation of ketones and imines
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Cooperative Mn(i)-complex catalyzed transfer hydrogenation of ketones and imines

机译:合作Mn(i) - 酮催化转移氢化酮和亚胺的催化转移氢化

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摘要

The synthesis and reactivity of Mn(i) complexes bearing bifunctional ligands comprising both the amine N-H and benzimidazole fragments are reported. Among the various ligands, the N-((1H-benzimidazol-2-yl)methyl)aniline ligand containing Mn(i) complex presented higher reactivity in the transfer hydrogenation (TH) of ketones in 2-propanol. Experimentally, it was established that both the benzimidazole and amine N-H proton played a vital role in the enhancement of the catalytic activity. Utilizing this system a wide range of aldehydes and ketones were reduced efficiently. Notably, the TH of several imines, as well as chemoselective reduction of unsaturated ketones, was achieved in the presence of this catalyst. DFT calculations were carried out to understand the plausible reaction mechanism which disclosed that the transfer hydrogenation reaction followed a concerted outer-sphere mechanism.
机译:据报道,Mn(I)络合物的合成和反应性呈现含有胺N-H和苯并咪唑片段的双官能配体。 在各种配体中,含有Mn(I)的N - ((1H-苯并咪唑-2-基)甲基)苯胺配体在2-丙醇中呈递酮的转移氢化(Th)的反应性。 实验,建立苯并咪唑和胺N-H质子在催化活性的增强中发挥着至关重要的作用。 利用该系统,有效地减少了各种醛和酮。 值得注意的是,在该催化剂存在下,在存在的几个亚胺中的几个亚胺以及化学选择性降低的化学选择性。 进行DFT计算以了解所公开的可合理的反应机理,该反应机理公开了转移氢化反应遵循齐全的外球机构。

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