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首页> 外文期刊>RSC Advances >Extension and functionalization of an encapsulating macrobicyclic ligand using palladium-catalyzed Suzuki-Miyaura and Sonogashira reactions of iron(II) dihalogenoclathrochelates with inherent halogen substituents
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Extension and functionalization of an encapsulating macrobicyclic ligand using palladium-catalyzed Suzuki-Miyaura and Sonogashira reactions of iron(II) dihalogenoclathrochelates with inherent halogen substituents

机译:用铁(II)二卤代菌的钯催化铃木菌和Sonogashira反应与固有卤素取代基的钯 - 催化的铃木菌和Sonogashira反应的延伸和官能化

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摘要

A new approach for performing Suzuki-Miyaura and Sonogashira reactions of iron(ii) dihalogenoclathrochelates, optimizing their reaction conditions (such as temperature, solvent and a palladium-containing catalyst) and the nature of other reagents (such as arylboron components) is elaborated. These palladium-catalyzed reactions are very sensitive to the nature of the macrobicyclic substrates. The reactivity of the leaving halogen atoms correlates with their ability to undergo an oxidative addition, decreasing in the order: I Br Cl, and iron(ii) diiodoclathrochelate underwent these C-C cross-couplings under their classical conditions. Phenylboronic, 4-carboxyphenylboronic and 6-ethoxy-2-naphthylboronic acids, and the diethyl ether of 4-(ethoxycarbonyl)boronic acid were tested as components of Suzuki-Miyaura reactions in DMF and in THF. The highest yields of the target products were obtained in DMF, while the highest activation was observed with sodium and potassium carbonates. The Suzuki-Miyaura reaction of a diiodoclathrochelate with 6-ethoxy-2-naphthylboronic acid gave the mono- and difunctionalized clathrochelates resulting from the tandem hydrodeiodination - C-C cross-coupling and double C-C cross-coupling reactions, respectively. Its Sonogashira reactions with trimethylsilylacetylene and acetylenecarboxylic acid in THF and in DMF were tested. This palladium-catalyzed reaction with a (CH3)(3)Si-containing active component gave the target products in a high total yield. The complexes obtained were characterized using elemental analysis, MALDI-TOF, UV-Vis, H-1 and C-13{H-1} NMR spectroscopy, and by single crystal XRD. Despite the non-equivalence of the ribbed -dioximate fragments of their molecules, the encapsulated iron(ii) ion is situated almost in the centre of its FeN6-coordination polyhedron, the geometry of which is almost intermediate between a trigonal prism and a trigonal antiprism.
机译:阐述了阐述了对铁(II)二卤代菌的苏祖宫菌和Sonoghashira和Sonogashira反应的新方法,优化其反应条件(例如温度,溶剂和含钯催化剂)和其他试剂的性质(例如芳基织物组分)。这些钯催化的反应对大丙二环基衬底的性质非常敏感。离去卤素原子的反应性与其经历氧化添加的能力,按顺序减少:i& BR> CL,铁(II)二碘Clatrochelate在其经典条件下接受了这些C-C的交叉偶联。苯基硼,4-羧基苯硼醌和6-乙氧基-2-萘甲酸,以及4-(乙氧基羰基)硼酸的二乙醚作为DMF和THF中的Suzuki-Miyaura反应的组分。在DMF中获得靶产物的最高产量,同时用钠和碳酸钾观察最高的活化。二碘凝聚叶酸与6-乙氧基-2-萘基硼酸的Suzuki-miyaura反应,得到了由串联加氢碘化 - C-C交叉偶联和双C-C交叉偶联反应产生的单官能化的Clathrochelate。在THF和DMF中三甲基硅烷基与和乙炔基羧酸及其反应的Sonogashira测试。用(CH 3)含Si活性组分此钯催化的反应(3),得到目标产物以高总收率。使用元素分析,MALDI-TOF,UV-VI,H-1和C-13 {H-1} NMR光谱和通过单晶XRD来表征获得的复合物。尽管其分子的罗纹型碎片不等同,但封装的铁(II)离子几乎位于其FEN6协调多面体的中心,其几何形状几乎是间三角棱镜和三角抗抗原之间的中间。

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  • 来源
    《RSC Advances》 |2018年第24期|共10页
  • 作者单位

    Vernadskii Inst Gen &

    Inorgan Chem NASU UA-03142 Kiev Ukraine;

    Vernadskii Inst Gen &

    Inorgan Chem NASU UA-03142 Kiev Ukraine;

    Vernadskii Inst Gen &

    Inorgan Chem NASU UA-03142 Kiev Ukraine;

    Nesmeyanov Inst Organoelement Cpds RAS Moscow 119991 Russia;

    Nesmeyanov Inst Organoelement Cpds RAS Moscow 119991 Russia;

    Nesmeyanov Inst Organoelement Cpds RAS Moscow 119991 Russia;

    Natl Res Ctr Kurchatov Inst Kurchatov Complex Synchrotron &

    Neutron Invest Moscow 123182 Russia;

    Nesmeyanov Inst Organoelement Cpds RAS Moscow 119991 Russia;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
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