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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Metal and ligand substitution of the aluminium tris-pyridyl ligands [RAl(2-py ')(3)](-) (R = Et, Bu-n, Bu-s, Bu-t; 2-py '=2-pyridyl, 3-methyl-2-pyridyl, 5-methyl-2-pyridyl, 6-methyl-2-pyridyl)
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Metal and ligand substitution of the aluminium tris-pyridyl ligands [RAl(2-py ')(3)](-) (R = Et, Bu-n, Bu-s, Bu-t; 2-py '=2-pyridyl, 3-methyl-2-pyridyl, 5-methyl-2-pyridyl, 6-methyl-2-pyridyl)

机译:铝三吡啶基配体[RAl(2-py')(3)](-)的金属和配体取代(R = Et,Bu-n,Bu-s,Bu-t; 2-py'= 2-吡啶基,3-甲基-2-吡啶基,5-甲基-2-吡啶基,6-甲基-2-吡啶基)

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摘要

A series of tris-pyridyl complexes [RAl(2-py)(3)]Li center dot thf[2-py = 2-pyridyl; R = Et (1); Bu-n (2); Bu-s (3), Bu-t (4)] were prepared by the sequential reaction of AlCl3 with RLi then 2-Li-py in thf. The related complexes [MeAl{2-(3-Me)py}(3)]Li(mu-Br)Li(thf)(3) (5), [MeAl{2-(5-Me)py}(3)] Li center dot thf (6) and [MeAl{2-(6-Me)py}(3)]Li center dot thf (7) are obtained similarly from MeAlCl2 and the appropriate lithio-pyridine (2-Li-py '). The synthetic approaches used provide the means for extensive elaboration of the [RAl(2-py ')(3)](-) ligand frameworks, and potentially broad access to a large range of new anionic tris-pyridyl ligands of this type. Fundamental insights into how the ligand bites and coordination environments offered are modified by substituents at the Al bridgehead and pyridyl rings are given by the solid-state structures of 1-7.
机译:一系列的三吡啶基配合物[RAl(2-py)(3)] Li中心点thf [2-py = 2-吡啶基; R = Et(1);布恩(2); Bu-s(3),Bu-t(4)]是通过AlCl3与RLi然后2-Li-py依次反应制得的。相关配合物[MeAl {2-(3-Me)py}(3)] Li(mu-Br)Li(thf)(3)(5),[MeAl {2-(5-Me)py}(3 )] Li中心点thf(6)和[MeAl {2-(6-Me)py}(3)] Li中心点thf(7)相似地从MeAlCl2和适当的硫代吡啶(2-Li-py ')。所使用的合成方法为[RAl(2-py')(3)](-)配体构架的广泛修饰提供了手段,并潜在地广泛使用了这种新型新的阴离子型三吡啶基配体。 1-7的固态结构给出了关于如何通过Al桥头和吡啶环上的取代基修饰配体咬合和配位环境的基本见解。

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