Magnetism, IR and Raman spectra of a tetracoordinate and hexacoordinate Co(II) complexes derived from aminopyrimidine

被引:12
作者
Idesicova, M. [1 ]
Boca, R. [1 ]
机构
[1] Univ SS Cyril & Methodius, FPV, Dept Chem, Trnava 91701, Slovakia
关键词
Co(II) complexes; Magnetism; Far-IR spectra; Heterocyclic ligands; Zero-field splitting; HIGH-SPIN COBALT(II); ZERO-FIELD; AB-INITIO; AQUEOUS-SOLUTION; HYDRATION; RELAXATION; NICKEL(II); EPR;
D O I
10.1016/j.ica.2013.09.002
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two mononuclear Co(II) complexes of the [CoCl2L2] and [CoCl2L4] family, with L being a heterocyclic Ndonor ligand-2-aminopyrimidine were prepared and subjected to magnetochemical investigation. Temperature dependence of the magnetic susceptibility and the field dependence of magnetization have been analyzed simultaneously in terms of the spin Hamiltonian formalism. The magnetic parameters obtained by a fitting procedure show a considerable magnetic anisotropy measured by the g-factor difference and the zero-field splitting parameter 2D, which splits the ground B-4(1)(D-2d) term and/or (4)A(1)g(D-4h) term. The temperature dependence of the Far-IR spectra for the centrosymmetric hexacoordinate complex shows variable-temperature absorption peaks which yield the value of the zero-field energy gap DIR = 455 cm(-1). Raman spectra, ab initio and DFT calculations assist in an accurate assignment of the absorption peaks. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:162 / 171
页数:10
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