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双-[四-(四氢呋喃-κ)锂]双[μ-2,2',2''-甲烷三基三(4,6-二叔丁基苯酚根)-κ,':','']-二镁配合物的晶体结构

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

作者信息

Zhou Hongyan, Wang Lei

机构信息

College of Science, Gansu Agricultural University, Lanzhou 730070, People's Republic of China.

College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou 730070, People's Republic of China.

出版信息

Acta Crystallogr E Crystallogr Commun. 2017 Jun 13;73(Pt 7):1026-1028. doi: 10.1107/S2056989017008337. eCollection 2017 Jul 1.

Abstract

The title ion-association metal complex, [Li(CHO)][Mg(CHO)], has been synthesized from the tridentate phenolic ligand tris-(3,5-di--butyl-2-hy-droxy-phen-yl)methane in tetra-hydro-furan (THF). The aryl-oxo magnesiate complex anion is binuclear with each MgO 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 LiO 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.

摘要

标题离子缔合金属配合物[Li(CHO)][Mg(CHO)]是由三齿酚配体三-(3,5-二叔丁基-2-羟基苯基)甲烷在四氢呋喃(THF)中合成的。芳基氧镁酸根配合物阴离子是双核的,每个MgO配合物单元通过配体的两个三齿螯合酚盐O供体反演相关并桥连。配合物中心具有扭曲的四面体立体化学结构[Mg-O范围为1.8796 (17)-2.0005 (16) Å],Mg⋯Mg间距为2.9430 (14) Å]。阳离子的LiO配位球包含四个THF O供体原子,具有略微扭曲的四面体构象[Li-O范围为1.899 (5)-1.953 (5) Å]。在晶体中存在许多稳定的阴离子内C-H⋯O氢键相互作用,但未发现物种间缔合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baa5/5499282/1106008458ce/e-73-01026-fig1.jpg

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