首页> 外文期刊>Acta Crystallographica Section E: Crystallographic Communications >Crystal structure of (μ-trans-1,2-bis­{2-[(2-oxido­phen­yl)methyl­idene]hydrazin-1-yl­idene}ethane-1,2-diolato-κ3O,O′,N)bis­[di-tert-butyl­tin(IV)]
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Crystal structure of (μ-trans-1,2-bis­{2-[(2-oxido­phen­yl)methyl­idene]hydrazin-1-yl­idene}ethane-1,2-diolato-κ3O,O′,N)bis­[di-tert-butyl­tin(IV)]

机译:(μ-反式-1,2-双{2-[((2-氧化苯基)亚甲基]肼-1-亚基}乙烷-1,2-二醇基-κ3O,O',N)双[二叔]的晶体结构-丁基锡(IV)]

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摘要

The binuclear complex, [Sn2(C4H9)4(C16H10N4O4)], contains two Sn4+ ions, connected by doubly N-deprotonated oxalylbis[(2-oxido­benzyl­idene)hydrazide] ligands, and each Sn4+ ion is linked to two tert-butyl groups. The coordination sphere of each Sn atom is best described as a distorted trigonal bipyramid. Each stannic ion in the complex is in a C2O2N environment. The two homologous parts of the doubly deprotonated ligand are located in trans positions with respect to the C—C bond of the oxalamide group. The oxalamide group exhibits an asymmetric coordination geometry, as seen by the slight difference between the C—O and C—N bond lengths. The three-dimensional network is a multilayer of complex mol­ecules with no strong supramolecular inter­actions.
机译:双核络合物[Sn2(C4H9)4(C16H10N4O4)]包含两个Sn4 +离子,它们通过N-去质子化的草酰双[(2-氧化苄叉基)酰肼]配体连接,每个Sn4 +离子均与两个叔丁基连接。每个Sn原子的配位球最好形容为扭曲的三角双锥。络合物中的每个锡离子都处于C2O2N环境中。双去质子化配体的两个同源部分相对于草酰胺基的CC键位于反式位置。草酰胺基团表现出不对称的配位几何形状,如从CO键和CN键长度之间的细微差异所见。三维网络是没有强超分子相互作用的复杂分子的多层。

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