Chandra Sulekh, Pundir Meenakshi
Department of Chemistry, Zakir Husain College, University of Delhi, J.L. Nehru Marg, New Delhi 110002, India.
Spectrochim Acta A Mol Biomol Spectrosc. 2008 Jan;69(1):1-7. doi: 10.1016/j.saa.2007.02.019. Epub 2007 Mar 3.
The complexes of Cr(III), Mn(II) and Ni(II) were synthesized with macrocyclic ligand i.e. 5,11-dimethyl-6,12-diethyl-dione-1,2,4,7,9,10-hexazacyclododeca -1,4,6,10-tetraene. The ligand (L) was prepared by [2+2] condensation reaction of 2,3-pentanedione and semicarbazide hydrochloride. These complexes were found to have the general composition [Cr(L)X(2)]X and [M(L)X(2)] (where M=Mn(II) and Ni(II); X=Cl(-), NO(3)(-), (1/2)SO(4)(2-), NCS(-) and L=ligand [N(6)]). The ligand and its transition metal complexes were characterized by the elemental analysis, molar conductance, magnetic susceptibility, mass, IR, electronic and EPR spectral studies. On the basis of IR, electronic and EPR spectral studies, an octahedral geometry has been assigned for these complexes except sulphato complexes which are of five coordinated geometry.
用大环配体即5,11 - 二甲基 - 6,12 - 二乙基 - 二酮 - 1,2,4,7,9,10 - 六氮杂环十二烷 - 1,4,6,10 - 四烯合成了铬(III)、锰(II)和镍(II)的配合物。配体(L)通过2,3 - 戊二酮与盐酸氨基脲的[2 + 2]缩合反应制备。发现这些配合物具有通式[Cr(L)X₂]X和[M(L)X₂](其中M = 锰(II)和镍(II);X = Cl⁻、NO₃⁻、(1/2)SO₄²⁻、NCS⁻且L = 配体[N(6)])。通过元素分析、摩尔电导率、磁化率、质谱、红外光谱、电子光谱和电子顺磁共振光谱研究对配体及其过渡金属配合物进行了表征。基于红外光谱、电子光谱和电子顺磁共振光谱研究,除了具有五配位几何结构的硫酸根配合物外,这些配合物被指定为八面体几何结构。