一些TUTTON盐体系的电子顺磁共振研究

Q3 Multidisciplinary Malaysian journal of science Pub Date : 2020-10-31 DOI:10.22452/mjs.vol39no3.7
N. Pant, A. L. Verma, S. Pandey
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引用次数: 0

摘要

采用电子顺磁共振(EPR)研究了钒基掺杂的混合塔顿盐(Zn 0.25 Mg 0.75 (nh4) 2 (so4) 2.6 h2o)体系。从我们的研究中得到的“g”和“A”参数与其他钒基掺杂的Tutton盐进行了比较,并提出了一个关键的分析。由于EPR结果依赖于掺杂V=O离子在基体中v4 +的位置,我们的研究得到的“g”和“A”参数反映了Tutton盐基体中v4 +的畸变八面体环境,并建立了两种主要的金属-水键。我们的发现得到了x射线研究和早期工作的电场辅助脱水研究的支持。临界分析和结果对比表明,水分子氧与塔顿盐中二价阳离子之间的赤道键和轴向键性质不同,证实了水分子围绕塔顿盐中二价离子形成的八面体是扭曲的。
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ELECTRON PARAMAGNETIC RESONANCE STUDIES ON SOME TUTTON SALT SYSTEMS
Electron paramagnetic resonance (EPR) studies were carried out on a vanadyl doped mixed Tutton salt (Zn 0.25 Mg 0.75 (NH 4 ) 2 (SO 4 ) 2 .6H 2 O) system. The “g” and “A” parameters obtained from our studies were compared with other vanadyl doped Tutton salts and a critical analysis is presented. As the EPR results depend upon the vicinity of V 4+ of doped V=O ion in the host, the ‘g’ and ‘A’ parameters obtained from our studies reflect distorted octahedral surroundings of V 4+ in the Tutton salt host and two major types of metal –water linkages are established. Our findings are supported by the X-ray studies and electric field assisted de-aquation studies on Tutton salts by the earlier works. Critical analysis and correlation of the results indicate that the equatorial bonds and axial bonds between the oxygen of water molecules and the divalent cation in Tutton salts are of different nature, confirming that the octahedron formed by water molecules around the divalent ion in Tutton salts is distorted.
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来源期刊
Malaysian journal of science
Malaysian journal of science Multidisciplinary-Multidisciplinary
CiteScore
1.10
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0.00%
发文量
36
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