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首页> 外文期刊>Zeitschrift fur Anorganische und Allgemeine Chemie >Synthesis and X-ray Crystal Structures of Zinc Complexes Supported by Chelating Ligands: Various Reactions of -Iminopyridines with ZnEt2
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Synthesis and X-ray Crystal Structures of Zinc Complexes Supported by Chelating Ligands: Various Reactions of -Iminopyridines with ZnEt2

机译:通过螯合配体支持的锌络合物的合成和X射线晶体结构:Znet2的-Iminopyridines的各种反应

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摘要

alpha-Iminopyridine (-IP) is an important redox-noninnocent ligand. The substituents on the imino function of -IPs have important impact on the reaction selectivity with diethylzinc. For the -IPs with a hydrogen substituent on the imino carbon, reduction occurred for the non-bulky N-substituents phenyl and 2-methylphenyl groups, whereas alkyl addition and coupling reactions can be selectively achieved for the sterically bulky N-substituents 2,6-dimethylphenyl or 2,4,6-trimethylphenyl group. However, for the -IPs with a CH3 substituent on the imino carbon, the deprotonation reaction happened regardless of the N-substituents of 2-methylphenyl or 2,6-dimethylphenyl group. All the products were isolated and characterized by single-crystal X-ray diffraction. The possible mechanisms of these reactions were also discussed.
机译:α-亚氨基吡啶(-IP)是一种重要的氧化还原非损伤配体。IPs亚氨基上的取代基对与二乙基锌的反应选择性有重要影响。对于亚氨基碳上带有氢取代基的-IPs,非大块N-取代基苯基和2-甲基苯基发生还原,而对于空间大块N-取代基2,6-二甲基苯基或2,4,6-三甲基苯基,可以选择性地实现烷基加成和偶联反应。然而,对于亚氨基碳上带有CH3取代基的-IPs,无论2-甲基苯基或2,6-二甲基苯基的N-取代基是什么,都会发生脱质子反应。所有产物均经分离,并用单晶X射线衍射进行了表征。并对这些反应的可能机理进行了讨论。

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