首页> 外文期刊>Journal of Organometallic Chemistry >Synthesis and characterization of strongly electron-donating bidentate phosphines containing imidazolin-2-ylidenamino substituents and their electron-rich nickel(0), palladium(II) and gold(I) chelate complexes
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Synthesis and characterization of strongly electron-donating bidentate phosphines containing imidazolin-2-ylidenamino substituents and their electron-rich nickel(0), palladium(II) and gold(I) chelate complexes

机译:含有咪唑啉-2-百苯胺氨基取代基的强电子给磷酸盐的合成与表征及其富含电子镍(0),钯(II)和金(I)螯合物复合物

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摘要

Bidentate phosphines are important ligands in inorganic and organometallic chemistry. However, their electron-donating ability is generally limited by the use of alkyl groups at the phosphorus atoms. Herein, we report two different approaches to strongly electron-donating bidentate phosphines: In the first strategy imidazolin-2-ylidenamino-substituted phosphorus atoms were linked by 1,1'-ferrocene (5) or 1,2-benzene (4) ligand backbones. The second synthetic access is based on linking the imidazolin-2-ylidenamino substituents by an alkyl chain (3). The bidentate phosphines 3-5 were used to synthesize the cationic gold(I) complex [(3)Au][SbF6], the palladium(II) complex [(3)PdCl2], as well as the nickel(0) complexes [(4)Ni(eta(2):eta(2)-cod)] and [(5)(2)Ni-2(mu, eta(2): eta(2)-cod)]. (C) 2020 Elsevier B.V. All rights reserved.
机译:二齿膦是无机和有机金属化学中的重要配体。 然而,它们的电子捐赠能力通常通过在磷原子下使用烷基来限制。 在此,我们报告了两种不同的方法对强电子供应的二齿磷酸酯:在第一策略中,咪唑啉-2- ylidenamino取代的磷原子通过1,1'-二茂铁(5)或1,2-苯(4)配体连接 骨干。 第二合成型基于将咪唑啉-2-甘透苯氨基取代基与烷基链(3)连接。 二齿膦3-5用于合成阳离子金(I)复合物[(3)Au] [SBF6],钯(II)复合物[(3)PdCl 2],以及镍(0)复合物[ (4)NI(ETA(2):ETA(2)-COD)]和[(5)(2)NI-2(MU,ETA(2):ETA(2)-COD)]。 (c)2020 Elsevier B.v.保留所有权利。

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