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由单阴离子[N2P2]配体支撑的铝、锌、镓和镉配合物。

Aluminium, zinc, gallium, and cadmium complexes supported by a monoanionic [N2P2] ligand.

作者信息

Minasian Stefan G, Arnold John

机构信息

Department of Chemistry, University of California, Berkeley, CA 94720-1460, USA.

出版信息

Dalton Trans. 2009 Jan 7(1):106-10. doi: 10.1039/b815854a. Epub 2008 Nov 6.

Abstract

Metal-halide complexes of main-group metals Al, Ga, Zn, and Cd supported by the new sterically and electronically versatile monoanionic ligand, (t)BuN(H)SiMe(2)N(CH(2)CH(2)P(i)Pr(2))(2), H[N(2)P(2)], are described. The metal-alkyl complex [N(2)P(2)]AlMe(2) (4) was prepared by two metathesis reactions of [N(2)P(2)]AlCl(2) (1) and 2MeLi, as well as [N(2)P(2)]Li and Me(2)AlCl. All compounds were characterized by standard analytical techniques; in addition, [N(2)P(2)]AlCl(2) (1), [N(2)P(2)]GaCl(2) (3), and [N(2)P(2)]CdCl(2) (6) were characterized by single-crystal X-ray crystallography. The potentially tetradentate ligand enforces a tetrahedral geometry at each metal by adopting two coordination modes: kappa(2)-NP (Al, Ga) and kappa(3)-NP(2) (Cd).

摘要

本文描述了由新型空间位阻和电子性质多样的单阴离子配体(t)BuN(H)SiMe(2)N(CH(2)CH(2)P(i)Pr(2))(2),即H[N(2)P(2)]支撑的主族金属铝、镓、锌和镉的金属卤化物配合物。金属烷基配合物[N(2)P(2)]AlMe(2)(4)通过[N(2)P(2)]AlCl(2)(1)与2MeLi以及[N(2)P(2)]Li和Me(2)AlCl的两个复分解反应制备而成。所有化合物均通过标准分析技术进行表征;此外,[N(2)P(2)]AlCl(2)(1)、[N(2)P(2)]GaCl(2)(3)和[N(2)P(2)]CdCl(2)(6)通过单晶X射线晶体学进行表征。这种潜在的四齿配体通过采用两种配位模式,在每个金属上强制形成四面体几何构型:κ(2)-NP(铝、镓)和κ(3)-NP(2)(镉)。

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