首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Making connections with molecular wires: extending tri-nickel chains with axial cyanide, dicyanamide, and phenylacetylide ligands
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Making connections with molecular wires: extending tri-nickel chains with axial cyanide, dicyanamide, and phenylacetylide ligands

机译:与分子线建立连接:通过轴向氰化物,双氰胺和苯乙炔配体扩展三镍链

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摘要

New chemistry needed to facilitate the replacement of axial ligands (X) in Ni_3(dpa)_4X_2 complexes (dpa = the anion of dipyridylamine) has been explored and used to replace X = Cl by X = CN, NCNCN, and C≡CPh. The resulting compounds, 3, 4 and 5, respectively, have been characterized by X-ray crystallography and cyclic voltammetry, inter alia. It is found that both the mean Ni…Ni separations (D), and the magnitude of the antiferromagnetic coupling (J) between the terminal, high spin (S = 1) Ni(II) atoms vary in a correlated way, with |J| decreasing with increasing D. The relationship is nearly linear over the available ranges of parameters, suggesting that the coupling may proceed mainly through the central, diamagnetic Ni(II) ion.
机译:已经探索了促进Ni_3(dpa)_4X_2配合物(dpa =二吡啶胺的阴离子)中轴向配体(X)取代所需的新化学方法,并用于通过X = CN,NCNCN和C≡CPh取代X = Cl。所得的化合物3、4和5分别通过X射线晶体学和循环伏安法表征。结果发现,平均Ni…Ni间距(D)和末端高自旋(S = 1)Ni(II)原子之间的反铁磁耦合(J)的幅度均呈| J |随D的增加而减小。这种关系在可用参数范围内几乎是线性的,这表明该耦合可能主要通过中心的抗磁性Ni(II)离子进行。

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