首页> 外文期刊>Journal of Catalysis >Stable chiral salen Mn(III) complexes with built-in phase-transfer capability for the asymmetric epoxidation of unfunctionalized olefins using NaOCl as an oxidant
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Stable chiral salen Mn(III) complexes with built-in phase-transfer capability for the asymmetric epoxidation of unfunctionalized olefins using NaOCl as an oxidant

机译:稳定的手性Salen Mn(III)配合物,具有内置相转移能力,可使用NaOCl作为氧化剂对未官能化烯烃进行不对称环氧化

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摘要

A series of novel chiral salen Mn(III) complexes with inherent phase-transfer capability were prepared by covalent linkage of the limidazolium IL moieties containing various PEG chains with chiral salen ligand at two sides of 5,5′-position. Technologies of characterization well suggested the presence of polyether chain, the IL linker, and the intact active sites in the complexes. The amphipathic nature of the PEG chain allowed the PEG-based catalysts to undergo built-in phase transfer, which in turn increased the reaction rates in water/organic biphasic systems. Enantioselective epoxidation of styrene, α-methylstyrene, indene, 1,2-dihydronaphthalene, 6-cyano-2,2-dimethylchromene, and 6-nitro-2,2-dimethylchromene catalyzed by the complexes with NaOCl gave >99% conversions within 60 min. The enantiomeric excess (ee) for the epoxides was in the range of 68-93%, except for styrene (ee, 35%) and α-methylstyrene (ee, 42%). Furthermore, the PEG-based complexes were stable and could be separated from the reaction mixture by control of the solvent.
机译:通过将含有各种PEG链的咪唑类IL部分与5,5'-位两侧的手性Salen配体共价连接,制备了一系列具有固有相转移能力的新型手性Salen Mn(III)配合物。表征技术很好地表明了复合物中存在聚醚链,IL接头和完整的活性位点。 PEG链的两亲性质使PEG基催化剂可以进行内置相转移,从而提高了水/有机双相系统中的反应速率。 NaOCl配合物催化的苯乙烯,α-甲基苯乙烯,茚,1,2-二氢萘,6-氰基-2,2-二甲基色烯和6-硝基-2,2-二甲基色烯的对映选择性环氧化在60℃内的转化率> 99%分钟除苯乙烯(ee,35%)和α-甲基苯乙烯(ee,42%)外,环氧化物的对映体过量(ee)为68-93%。此外,基于PEG的复合物是稳定的,并且可以通过控制溶剂与反应混合物分离。

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