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首页> 外文期刊>European journal of inorganic chemistry >A Mononuclear Manganese Complex of a Tetradentate Nitrogen Ligand - Synthesis, Characterizations, and Application in the Asymmetric Epoxidation of Olefins
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A Mononuclear Manganese Complex of a Tetradentate Nitrogen Ligand - Synthesis, Characterizations, and Application in the Asymmetric Epoxidation of Olefins

机译:四齿氮配体的单核锰配合物-合成,表征及其在烯烃不对称环氧化中的应用

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摘要

A new chiral manganese complex (C1) bearing a tetradentate nitrogen ligand containing chiral bipyrrolidine and benzimidazole moieties was prepared. The structure of C1 was confirmed by ESI-MS and crystallography. This manganese complex is an active catalyst for the asymmetric epoxidation of various olefins with excellent conversion (up to 99%) and high enantiomeric excess (up to 96%ee) with hydrogen peroxide as the oxidant in the presence of 2-ethylhexanoic acid or acetic acid. Compared with previous structurally similar manganese complexes with different diamine backbones (C2, cyclohexanediamine; C3, diamine from L-proline), C1 showed improved asymmetric induction, especially for simple olefins such as styrene derivatives and substituted chromene. The possible reasons for the improvement of the ee values are discussed in the text on the basis of the crystal structures of the manganese complexes.
机译:制备了一种新的手性锰配合物(C1),其带有包含手性联吡咯烷和苯并咪唑部分的四齿氮配体。 C1的结构通过ESI-MS和晶体学确认。该锰配合物是一种活性催化剂,用于在2-乙基己酸或乙酸存在下用过氧化氢作为氧化剂,具有优异的转化率(最高99%)和高对映体过量(最高96%ee)的各种烯烃不对称环氧化。酸。与以前具有不同二胺骨架的结构相似的锰配合物(C2,环己二胺; C3,来自L-脯氨酸的二胺)相比,C1表现出更好的不对称诱导性,特别是对于简单的烯烃(如苯乙烯衍生物和取代的色烯)。本文根据锰配合物的晶体结构讨论了提高ee值的可能原因。

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