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过氧钒酸根与2-(2'-吡啶基)咪唑配合物的研究

Investigation on the complex of diperoxovanadate with 2-(2'-pyridyl)-imidazole.

作者信息

Yu Xian-Yong, Cai Shu-Hui, Chen Zhong

机构信息

Department of Physics, State Key Laboratory of Physical Chemistry of Solid Surface, Xiamen University, Xiamen, Fujian, 361005, PR China.

出版信息

J Inorg Biochem. 2005 Oct;99(10):1945-51. doi: 10.1016/j.jinorgbio.2005.06.007.

Abstract

A novel diperoxovanadate complex NH4[OV(O2)2{2-(2'-pyridyl)-imidazole}] x 4H2O was synthesized in aqueous solution under physiological conditions. The solution structure of the complex was characterized by multinuclear (1H, 13C, 14N, and 51V) as well as multi-dimensional (DOSY and C-H COSY) NMR techniques in the interaction system of NH4VO3/H2O2/2-(2'-pyridyl)-imidazole at room temperature. The crystal structure of the complex was determined at 173K by single-crystal X-ray diffraction method. It belongs to the monoclinic space group P21/c with a = 13.048(4), b = 6.984(2), c = 17.814(5) A, beta = 104.695(5), V = 1570.3(8) A3 and Z = 4. The crystal is composed of ammonium ions, {2-(2'-pyridyl)-imidazole}oxodiperoxovanadate(V) ions, and water molecules, which are held together by ionic and hydrogen bond forces. The metal atom in the complex is seven-coordinated with a distorted pentagonal bipyramidal geometry. It is the first mononuclear diperoxovanadate complex with a N, N'-chelating biheteroaromatic ligand and its 51V chemical shift is at the highest field among the known mononuclear diperoxovanadate(V) complexes.

摘要

在生理条件下于水溶液中合成了一种新型双过氧钒酸盐配合物NH4[OV(O2)2{2-(2'-吡啶基)-咪唑}]·4H2O。在室温下,通过多核(1H、13C、14N和51V)以及多维(DOSY和C-H COSY)核磁共振技术对NH4VO3/H2O2/2-(2'-吡啶基)-咪唑相互作用体系中该配合物的溶液结构进行了表征。通过单晶X射线衍射法在173K下测定了该配合物的晶体结构。它属于单斜空间群P21/c,a = 13.048(4),b = 6.984(2),c = 17.814(5) Å,β = 104.695(5),V = 1570.3(8) Å3,Z = 4。该晶体由铵离子、{2-(2'-吡啶基)-咪唑}氧代双过氧钒(V)离子和水分子组成,它们通过离子键和氢键作用力结合在一起。配合物中的金属原子为七配位,具有扭曲的五角双锥几何构型。它是第一个具有N,N'-螯合双杂芳族配体的单核双过氧钒酸盐配合物,其51V化学位移在已知的单核双过氧钒(V)配合物中处于最高场。

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