In situ ligand reactions under hydrothermal conditions afford a novel zinc-substituted polyoxovanadate dimer

Shou Tian Zheng, Ming Hui Wang, Guo Yu Yang*

*此作品的通讯作者

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摘要

A novel polyoxovanadate (POV), [Zn(2,2′-bpy)3] 4[(ppz){{Zn(tepa)}2ZnAs8V13O 41(H2O)}2][As8V14O 42(0.5H2O)]2·4H2O (1, 2,2′-bpy = 2,2′-bipyridine, ppz = piperazine, tepa = tetraethylenepentamine), has been hydrothermally synthesized and structurally characterized by elemental analysis, IR spectra, thermogravimetric analysis, magnetic measurement, and single-crystal X-ray diffraction analysis. Crystal data for 1: orthorhombic, Aba2, a = 28.3414(14) Å, b = 27.9995(16) Å, c = 41.5819(16) Å, V = 32997(3) Å3, Z = 4, ρ = 2.264 mg·cm-3. X-ray structure analysis shows that the structure of 1 consists of one unique zinc-substituted POV dimer and two POV monomers. Interestingly, the formation of the zinc-substituted POV dimer involves two new in situ ligand reactions under hydrothermal conditions, the intermolecular and intramolecular deamination coupling reactions of dien. Magnetization measurement revealed the presence of antiferromagnetic interaction between VIV ions in 1.

源语言英语
页(从-至)9503-9508
页数6
期刊Inorganic Chemistry
46
22
DOI
出版状态已出版 - 29 10月 2007
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Zheng, S. T., Wang, M. H., & Yang, G. Y. (2007). In situ ligand reactions under hydrothermal conditions afford a novel zinc-substituted polyoxovanadate dimer. Inorganic Chemistry, 46(22), 9503-9508. https://doi.org/10.1021/ic700562m