首页> 外文期刊>Inorganica Chimica Acta >Cobalt and iron complexes of chiral C1- and C2-terpyridines: Synthesis, characterization and use in catalytic asymmetric cyclopropanation of styrenes
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Cobalt and iron complexes of chiral C1- and C2-terpyridines: Synthesis, characterization and use in catalytic asymmetric cyclopropanation of styrenes

机译:手性C1-和C2-三联吡啶的钴和铁配合物:苯乙烯的催化不对称环丙烷化反应的合成,表征和应用

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摘要

Optically pure C_1- and C_2-terpyridine ligand.(L) form cobalt(II) and iron(lI) complexes of formula [Co(L)Cl_2] and [Fe(L)Cl_2], respectively, and Iron(III) complexes of formulas [Fe(L)C1_31. Structures of three new chiral cobalt(II) and one iron(III) complexes were analysed using X-ray crystal structure analysis. These complexes were shown to be precursor of efficient catalyst for cyclopropanation. Reaction with AgOTf converted the complex to active catalyst, which gave enantioselectivities of up to 76% ee for the trans-isomers and 83% ee for the cis-isomers of styrene cyclopropanes with ethyl diazoacetate. Hammett studies showed the active species for both cobalt and iron complexes to have a non-linear relationship to constant.
机译:光学纯的C_1-和C_2-吡啶基配体。(L)分别形成式[Co(L)Cl_2]和[Fe(L)Cl_2]的钴(II)和铁(II)配合物,以及铁(III)配合物式[Fe(L)C1_31。使用X射线晶体结构分析了三种新的手性钴(II)和一种铁(III)配合物的结构。这些络合物被证明是有效的环丙烷化催化剂的前体。与AgOTf的反应将络合物转化为活性催化剂,与重氮乙酸乙酯反应,苯乙烯环丙烷的反式异构体的对映选择性高达76%ee,顺式异构体的对映选择性高达83%ee。 Hammett研究表明,钴和铁配合物的活性物种均与常数具有非线性关系。

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