Crystal structure of bis-[tetra-kis-(tetra-hydro-furan-κO)lithium] bis[μ-2,2',2''-methanetriyltris(4,6-di-tert-butylphenolato)-κ4O,O':O',O'']-dimagnesiate.

Hongyan Zhou, Lei Wang
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Abstract

The title ion-association metal complex, [Li(C4H8O)4]2[Mg2(C43H61O3)2], has been synthesized from the tridentate phenolic ligand tris-(3,5-di-tert-butyl-2-hy-droxy-phen-yl)methane in tetra-hydro-furan (THF). The aryl-oxo magnesiate complex anion is binuclear with each Mg2O4 complex unit inversion-related and bridged through the two tridentate chelating phenolate O-donors of the ligand. The complex centres have a distorted tetra-hedral stereochemistry [Mg-O range 1.8796 (17)-2.0005 (16) Å] and an Mg⋯Mg separation of 2.9430 (14) Å]. The LiO4 coodination sphere of the cation comprises four THF O-donor atoms and has a slightly distorted tetra-hedral conformation [Li-O range 1.899 (5)- 1.953 (5) Å]. In the crystal, a number of stabilizing intra-anion C-H⋯O hydrogen-bonding inter-actions are present but no inter-species associations are found.

Abstract Image

Abstract Image

Abstract Image

双-[四氢呋喃四氢呋喃-κO]锂]双[μ-2,2',2 " -甲烷三基三(4,6-二叔丁基苯酚)-κ O,O':O',O "]-二镁酸盐的晶体结构。
以四氢呋喃(THF)为原料,以三-(3,5-二叔丁基-2-羟基苯基)甲烷为配体,合成了标题离子结合金属配合物[Li(c4h80)4]2[Mg2(c43h6103)2]。芳基氧化镁配合阴离子是双核的,每个Mg2O4配合物单元反转相关,并通过配体的两个三齿螯合酚酸o给体桥接。配合物中心具有扭曲的四面体立体化学[Mg- o范围为1.8796 (17)-2.0005 (16)Å]和Mg⋯Mg分离为2.9430 (14)Å]。阳离子的LiO4配位球由4个THF o给体原子组成,具有轻微畸变的四面体构象[Li-O范围1.899 (5)- 1.953 (5)Å]。在晶体中,存在许多稳定阴离子内C-H⋯O氢键相互作用,但没有发现物种间的相互作用。
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