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二水双(5-羧基-2-甲基-1H-咪唑-4-羧基合-κN,O)钴(II)二甲基甲酰胺溶剂化物

Diaqua-bis(5-carb-oxy-2-methyl-1H-imidazole-4-carboxyl-ato-κN,O)cobalt(II) dimethyl-formamide disolvate.

作者信息

Tang Si-Ping

机构信息

Department of Chemistry and Material Science, Hengyang Normal University, Hengyang, Hunan 421008, People's Republic of China .

出版信息

Acta Crystallogr Sect E Struct Rep Online. 2009 Apr 10;65(Pt 5):m504. doi: 10.1107/S1600536809012902.

DOI:10.1107/S1600536809012902
PMID:21583752
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2977566/
Abstract

In the title compound, [Co(C(6)H(5)N(2)O(4))(2)(H(2)O)(2)]·2C(3)H(7)NO, the Co(II) ion lies on an inversion center and adopts a slightly distorted CoN(2)O(4) octa-hedral geometry binding two bidentate chelating 5-carb-oxy-2-methyl-1H-imidazole-4-carboxyl-ate (H(2)MIDA(-)) monoanionic ligands and two axial aqua ligands. In the crystal structure, inter-molecular O-H⋯O hydrogen bonds link neighboring mol-ecules, generating a two-dimensional framework containing eight-membered H(4)O(4) rings. In addition, the dimethyl-formamide solvent mol-ecules are hydrogen bonded to the two-dimensional framework via the NH groups of the H(2)MIDA(-) ligands.

摘要

在标题化合物[Co(C₆H₅N₂O₄)₂(H₂O)₂]·2C₃H₇NO中,Co(II)离子位于一个对称中心上,采用略微扭曲的CoN₂O₄八面体几何构型,与两个双齿螯合的5-羧基-2-甲基-1H-咪唑-4-羧酸根(H₂MIDA⁻)单阴离子配体以及两个轴向水配体配位。在晶体结构中,分子间的O—H⋯O氢键连接相邻分子,形成了包含八元H₄O₄环的二维框架。此外,二甲基甲酰胺溶剂分子通过H₂MIDA⁻配体的NH基团与二维框架形成氢键。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49e1/2977566/c42b83ec7e17/e-65-0m504-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49e1/2977566/8de806d90923/e-65-0m504-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49e1/2977566/c42b83ec7e17/e-65-0m504-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49e1/2977566/8de806d90923/e-65-0m504-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49e1/2977566/c42b83ec7e17/e-65-0m504-fig2.jpg

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本文引用的文献

1
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Acta Crystallogr Sect E Struct Rep Online. 2008 Feb 15;64(Pt 3):m476. doi: 10.1107/S160053680800411X.
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A short history of SHELX.SHELX简史。
Acta Crystallogr A. 2008 Jan;64(Pt 1):112-22. doi: 10.1107/S0108767307043930. Epub 2007 Dec 21.