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含吡啶的 14 元大环镍(II)配合物完整卤化物系列的结构和磁性性质

Structural and magnetic properties of a complete halide series of Ni(II) complexes with a pyridine-containing 14-membered macrocycle.

作者信息

Tamayo Abel, Escriche Lluis, Lodeiro Carlos, Ribas-Ariño Jordi, Ribas Joan, Covelo Berta, Casabó Jaume

机构信息

Departament de Química, Universitat Autonoma de Barcelona, 08193 Bellaterra, Barcelona, Spain.

出版信息

Inorg Chem. 2006 Sep 18;45(19):7621-7. doi: 10.1021/ic060231s.

Abstract

The complete halide series of Ni(II) complexes containing the tetradentate macrocyclic ligand 3,11-dithia-7,17-diazabicyclo[11.3.1]heptadeca-1(17),13,15-triene (L), was fully characterized by X-ray diffraction. The fluoro, chloro, and bromo complexes are dinuclear species with formula [{Ni(L)}2(mu-X)2]2+ (X = halide), whereas only mononuclear species with formula [Ni(Y)(solv)(L)]n+ (Y = halide or solvent molecule), were obtained with I. To date, the fluoro derivative is the first nonorganometallic coordination compound containing the Ni(mu-F)2Ni core. The magnetic properties of these halo complexes have been studied. Intramolecular interactions were observed in the three dinuclear complexes, being antiferromagnetic in the fluoro derivative and ferromagnetic in both the chloro and bromo ones. The two iodo derivatives are paramagnetic species, as would be expected for mononuclear octahedral Ni(II) complexes. Density functional theory calculations led us to relate the magnetic behaviors of these compounds to the values of the corresponding Ni-X-Ni(i) angle. The analysis of the singly occupied molecular orbitals gave a clear comprehension of the different magnetic exchange interactions found in these Ni(II) complexes.

摘要

含有四齿大环配体3,11 - 二硫杂 - 7,17 - 二氮杂双环[11.3.1]十七碳 - 1(17),13,15 - 三烯(L)的镍(II)配合物的完整卤化物系列通过X射线衍射进行了全面表征。氟、氯和溴配合物是具有化学式[{Ni(L)}2(μ - X)2]2 +(X = 卤化物)的双核物种,而用碘得到的只有化学式为[Ni(Y)(solv)(L)]n +(Y = 卤化物或溶剂分子)的单核物种。迄今为止,氟衍生物是第一个含有Ni(μ - F)2Ni核心的非有机金属配位化合物。已经研究了这些卤代配合物的磁性。在三种双核配合物中观察到了分子内相互作用,氟衍生物中为反铁磁性,氯和溴衍生物中为铁磁性。两种碘衍生物是顺磁性物种,这对于单核八面体镍(II)配合物来说是预期的。密度泛函理论计算使我们能够将这些化合物的磁性行为与相应的Ni - X - Ni(i)角的值联系起来。对单占据分子轨道的分析清楚地理解了在这些镍(II)配合物中发现的不同磁交换相互作用。

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