首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Controlling substitution chemistry in ruthenium(II) systems. Synthesis of heteroleptic complexes incorporating the [Ru([9]aneS(3))](2+) metal center
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Controlling substitution chemistry in ruthenium(II) systems. Synthesis of heteroleptic complexes incorporating the [Ru([9]aneS(3))](2+) metal center

机译:控制钌(II)系统中的取代化学。合成[[Ru([9] aneS(3))](2+)金属中心的杂配物

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The complex [Ru(py)(3)([9]aneS(3))][PF6](2), 1 (py = pyridine), has proved to be a suitable starting material for the synthesis of heteroleptic Ru(ZI) complexes. By exploiting unfavorable steric interactions between 2-H and 6-H hydrogens of coordinated pyridyl ligands, we have synthesized half-sandwich complexes incorporating the thiocrown [9]aneS(3) and a variety of facially coordinated N-donor ligands. Such complexes are easily prepared: Stirring 1 at room temperature in the presence of a suitable nitrile ligand leads to the exclusive substitution of one py ligand to produce complexes such as [([9]aneS(3))Ru(py)(2)(NCMe)] [PF6](2), 2. However, if the same reaction is carried out at higher temperatures, two py ligands are substituted, leading to complexes such as [([9]aneS(3))Ru(py)(NCMe)(2)][PF6](2), 3. An alternative approach to such heteroleptic species has also been developed which exploits the restricted ability of thioethers to neutralize positive charges through a-donation. This phenomenon allows the synthesis of heteroleptic complexes in a two-step procedure via monocationic species. By variation of the donor/acceptor properties of ligands incorporated into the [Ru([9]aneS(3))](2+) metal center, it is possible to tune the Ru(III)/Ru(II) redox couple over a range of >700 mV. The solid-state structures of 1-3 were confirmed by X-ray crystallography studies. Crystal data: C22H30F12N4O2P2RuS3 (1.CH3NO2), monoclinic, Cc, a = 23.267(5) Angstrom, b = 11.5457(18) Angstrom, c = 26.192(5) Angstrom, alpha = 90 degrees, beta = 114.836(10)degrees, gamma = 90 degrees, Z = 8; C18H25F12N3P2RuS3 (2), triclinic, P1, a = 11.3958(19) Angstrom, b = 11.4280(19) Angstrom, c = 11.930(2) Angstrom, alpha = 100.518(3)degrees, beta = 100.542(3)degrees, gamma = 112,493(3)degrees, Z = 2; C15H23F12N3P2RuS3 (3), orthorhombic, Pna2(1), a = 14.748(5) Angstrom, b = 18.037(18) Angstrom, c = 10.341(5) Angstrom, alpha = 90 degrees, beta = 90 degrees, gamma = 90 degrees, Z = 4. [References: 30]
机译:络合物[Ru(py)(3)([9] aneS(3))] [PF6](2),1(py =吡啶),已证明是合成杂合Ru(ZI)的合适原料)复合体。通过利用吡啶基配位体的2-H和6-H氢之间不利的空间相互作用,我们合成了半三明治复合体,其中掺入了硫冠[9] aneS(3)和多种面部配合的N-供体配体。此类配合物易于制备:在室温下在合适的腈配体存在下搅拌1会导致一个py配体的排他性取代,从而生成诸如[[[[9] aneS(3))Ru(py)(2)等配合物。 (NCMe)] [PF6](2),2。但是,如果在较高温度下进行相同的反应,则两个py配体会被取代,从而形成复合物,例如[([9] aneS(3))Ru(py )(NCMe)(2)] [PF6](2),3.还开发出了另一种替代方法,可利用硫醚通过a捐赠中和正电荷的有限能力。这种现象允许通过单阳离子物质在两步过程中合成杂配物。通过改变并入[Ru([9] aneS(3))](2+)金属中心的配体的供体/受体性能,可以调节Ru(III)/ Ru(II)氧化还原对范围> 700 mV。 X射线晶体学研究证实了1-3的固态结构。晶体数据:C22H30F12N4O2P2RuS3(1.CH3NO2),单斜晶,Cc,a = 23.267(5)埃,b = 11.5457(18)埃,c = 26.192(5)埃,α= 90度,beta = 114.836(10)度,γ= 90度,Z = 8; C18H25F12N3P2RuS3(2),三斜晶系,P1,a = 11.3958(19)埃,b = 11.4280(19)埃,c = 11.930(2)埃,alpha = 100.518(3)度,beta = 100.542(3)度,γ = 112,493(3)度,Z = 2; C15H23F12N3P2RuS3(3),正交,Pna2(1),a = 14.748(5)埃,b = 18.037(18)埃,c = 10.341(5)埃,alpha = 90度,beta = 90度,γ= 90度,Z =4。[参考:30]

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