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首页> 外文期刊>Acta crystallographica. Section C, Structural chemistry. >Homoleptic 2,2′-bi-pyridine metal-ates(-I) of iron and cobalt, one cocrystallized with an anthracene radical anion and the other with neutral anthracene
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Homoleptic 2,2′-bi-pyridine metal-ates(-I) of iron and cobalt, one cocrystallized with an anthracene radical anion and the other with neutral anthracene

机译:铁和钴的同型2,2'-联吡啶金属盐(-I),一个与蒽自由基阴离子共结晶,另一个与中性蒽共结晶

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摘要

Homoleptic 2,2′-bi-pyridine (bipy) metalates of iron and cobalt have been synthesized directly from the corresponding homo-leptic anthracene metalates. In the iron structure, bis-[([2.2.2]cryptand)potassium(I)] tris-(2,2′-bi-pyridine)-fer-rate(-I) anthracene(-I), [K(C18H36N2O6)] 2[Fe(C10H8N2)3](C14H10), the asymmetric unit contains one potassium complex cation in a general position, the Fe center and one and a half bipy ligands of the ferrate complex on a crystallographic twofold axis that includes the Fe atom, and one half of an anthracene radical anion whose other half is generated by a crystallographic inversion center. The cations and anions are well separated and the geometry about the Fe center is essentially octa-hedral. In the cobalt structure, ([2.2.2]cryptand)potassium(I) bis-(2,2′-bi-pyridine) -cobaltate(-I) anthracene hemisolvate tetra-hydro-furan (THF) disolvate, [K(C18H36N2O6)][Co(C10H8N2)2]·0.5C14H10·2C4H8O, the asymmetric unit contains the cation, anion, and both cocrystallized THF solvent mol-ecules in general positions, and one half of a cocrystallized anthracene mol-ecule whose other half is generated by a crystallographic inversion center. The cation and anion are well separated and the ligand planes in the cobaltate anion are periplanar. Each anthracene mol-ecule is midway between and is oriented perpendicular to a pair of symmetry-related bipy ligands such that aromatic donor-acceptor inter-actions may play a role in the packing arrangement. The lengths of the bonds that connect the bipy rings support the assertion that the ligands are bipy radical anions in the iron structure. However, in the case of cobalt, these lengths are between the known ranges for a bipy radical anion and a bipy dianion, and therefore no conclusion can be made from the crystallography alone. One cocrystallized THF solvent mol-ecule in the cobalt structure was modeled as disordered over three positions with appropriate geometric and thermal restraints, which resulted in a refined component mass ratio of 0.412 (4):0.387 (3):0.201 (3).
机译:铁和钴的同质2,2'-联吡啶(bipy)金属盐已直接从相应的同金属蒽金属盐中合成。在铁结构中,双-[([[2.2.2] cryptand)钾(I)] tris-(2,2'-双吡啶)-铁-速率(-I)蒽(-I),[K( C18H36N2O6)] 2 [Fe(C10H8N2)3](C14H10),该不对称单元的一个基本位置包含一个钾配位阳离子,Fe中心和高铁酸盐配合物的一个半Bipy配体在结晶双轴上,包括Fe原子和蒽自由基阴离子的一半,另一半由晶体学反演中心生成。阳离子和阴离子被很好地分开,并且围绕Fe中心的几何形状基本上是八面体。在钴结构中,([2.2.2] cryptand)钾(I)双-(2,2'-联吡啶)-钴(-I)蒽半溶剂合物四氢呋喃(THF)脱溶剂,[K( C18H36N2O6)] [Co(C10H8N2)2]·0.5C14H10·2C4H8O,该不对称单元在一般位置上包含阳离子,阴离子和两个共结晶的THF溶剂分子,以及另一半的共结晶的蒽分子分子。由晶体反转中心产生。阳离子和阴离子被很好地分开,钴酸根阴离子中的配体平面是平面的。每个蒽分子位于两个对称相关的双联配体之间,并且垂直于一对对称相关联的双配体取向,从而芳族供体-受体相互作用可在堆积结构中起作用。连接双联环的键的长度支持这样的说法,即配体是铁结构中的双联自由基阴离子。然而,在钴的情况下,这些长度在联吡啶自由基阴离子和联吡啶二阴离子的已知范围之间,因此不能仅从晶体学上得出结论。将钴结构中的一个共结晶的THF溶剂分子建模为在三个位置上无序,并具有适当的几何和热约束,从而使精制组分的质量比为0.412(4):0.387(3):0.201(3)。

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