电子顺磁共振
化学
离子
铜
四方晶系
结晶学
八面体
超精细结构
顺磁性
金属
超精细耦合
价(化学)
分子
晶体结构
核磁共振
原子物理学
凝聚态物理
物理
有机化学
作者
Luciana da Silva,Jaílson B. de Andrade,Antônio S. Mangrich
标识
DOI:10.1590/s0103-50532007000300018
摘要
An evaluation was made of the presence of paramagnetic ions in the host lattice of CuI2SO3.CdII SO3.2H2O by the electron paramagnetic resonance (EPR) technique, using copper(II) ions as paramagnetic probes. The existing M I and M II complexation sites in the double sufite structure were successfully differentiated. The results indicate that the CuI2SO3.CdII SO3.2H2O structure was doped with CuII ions in the two metal ion substitutional positions. The low g||/A|| ratio for the CuII probe in the distorted octahedral site resulted from the interaction of copper ions with oxygen donor atoms in a distorted tetragonal environment, with elongation of the molecule in the z direction. The very low value of the A33 hyperfine coupling constant was explained considering the admixture of the d x² -y² and d z² orbitals and the almost trigonal pyramidal structure of the other site.
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