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首页> 外文期刊>Acta crystallographica. Section C, Structural chemistry. >Bis(2-{1-[(2,4,6-trimethylphenyl)imino]ethyl}pyrrol-1-ido-κ2N,N′)nickel(II): a supramolecular structure formed by C—H...π(arene) hydrogen bonds
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Bis(2-{1-[(2,4,6-trimethylphenyl)imino]ethyl}pyrrol-1-ido-κ2N,N′)nickel(II): a supramolecular structure formed by C—H...π(arene) hydrogen bonds

机译:双(2- {1-[((2,4,6-三甲基苯基)亚氨基]乙基}吡咯-1-基-κ2N,N')镍(II):由CH-π形成的超分子结构芳烃)氢键

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摘要

Nitrogen-based polydentate ligands are of interest owing to their flexible complexation to transition metal atoms. For the title compound, [Ni(C15H17N2)2], a transition metal complex formed by the coordination of two identical N,N′-bidentate mono(imino)pyrrolyl ligands to an NiII centre, an X-ray crystal diffraction study indicates that the two ligands show an inverted arrangement with respect to one another around the NiII centre, which is located on a crystallographic inversion centre. The planes of the aromatic substituents at the imine N atoms of the ligands show dihedral angles of 85.91?(5)° with respect to the NiN4 plane. The Ni—N bond lengths are in the range 1.9072?(15)–1.9330?(15)?? and the Nimino—Ni—Npyrrole bite angles are 83.18?(6)°. The Ni—Npyrrole bond is substantially shorter than the Ni—Nimino bond. Molecules are linked into an extensive network by means of intermolecular C—H...π(arene) hydrogen bonds in which every molecule acts both as hydrogen-bond donor and acceptor. The supramolecular assembly takes the form of an infinite two-dimensional sheet.
机译:tlsb = -0.2pt>基于氮的多齿配体由于其与过渡金属原子的柔性配合而受到关注。对于标题化合物[Ni(C15H17N2)2],这是一种过渡金属络合物,由两个相同的N,N'-双齿单(亚氨基)吡咯基配体与NiII中心配位形成,X射线晶体衍射研究表明这两个配体在NiII中心周围位于晶体反转中心,相对于彼此显示出反向排列。配位体的亚胺N原子上的芳族取代基的平面相对于NiN4平面具有85.91°(5)°的二面角。 Ni-N键长在1.9072?(15)–1.9330?(15)?范围内。 Nimino-Ni-Npyrrole咬合角为83.18?(6)°。 Ni-N吡咯键实质上比Ni-Nimino键短。分子通过分子间的CHH ...π(芳烃)氢键连接成一个广泛的网络,其中每个分子既充当氢键供体,又充当受体。超分子组装体是无限二维片的形式。

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