Department of Chemistry (FPV), University of SS. Cyril and Methodius, SK-917 01 Trnava, Slovakia.
Inorg Chem. 2013 Aug 19;52(16):9409-17. doi: 10.1021/ic400980b. Epub 2013 Aug 7.
Six pseudotetrahedral cobalt(II) complexes of the type [CoL2Cl2], with L = heterocyclic N-donor ligand, have been studied in parallel by magnetometry, and high-frequency and -field electron paramagnetic resonance (HFEPR). HFEPR powder spectra were recorded in a 50 GHz < ν < 700 GHz range in a 17 T superconducting and 25 T resistive magnet, which allowed constructing of resonance field vs frequency diagrams from which the fitting procedure yielded the S = 3/2 spin ground state Hamiltonian parameters. The sign of the axial anisotropy parameter D was determined unambiguously; the values range between -8 and +11 cm(-1) for the given series of complexes. These data agree well with magnetometric analysis. Finally, quantum chemical ab initio calculations were performed on the whole series of complexes to probe the relationship between the magnetic anisotropy, electronic, and geometric structure.
六例四配位钴(II)配合物,类型为[CoL2Cl2],其中 L 为杂环 N-供体配体,已通过磁测量法和高频/强磁场电子顺磁共振(HFEPR)进行了平行研究。在 17 T 超导和 25 T 电阻磁体中记录了 HFEPR 粉末光谱,范围为 50 GHz < ν < 700 GHz,从中构建了共振场与频率图,拟合程序得出 S = 3/2 自旋基态哈密顿参数。轴向各向异性参数 D 的符号被明确确定;对于给定的一系列配合物,其值范围在-8 到+11 cm(-1)之间。这些数据与磁测量分析吻合良好。最后,对整个系列的配合物进行了量子化学从头计算,以探究磁各向异性、电子和几何结构之间的关系。