کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1334734 | 979446 | 2012 | 5 صفحه PDF | دانلود رایگان |
The synthesis of two [Hg(L1)2] and [Hg(L2)2] complexes using asymmetric triazenes as ligands are reported. The triazene ligands are substituted with cyano and chloride groups in the ortho positions of the aryl rings (where HL1 and HL2 are 1-(2-ethoxyphenyl)-3-(2-cyanophenyl)triazene and 1-(2-ethoxyphenyl)-3-(2-chlorophenyl) triazene, respectively). These complexes were prepared by the reaction of corresponding triazenes with Hg(NO3)2 and were characterized by FT-IR, NMR, elemental and single crystal X-ray analyses. Both triazene ligands were found to deprotonate on coordination and act as tridentate chelating ligands forming distorted N4O2 octahedral geometry around HgII atoms. Hydrogen bonds, π⋯π and C–H⋯π stacking interactions help to the stabilization of the resulted frameworks.
Here two HgII complexes using asymmetric triazenes (substituted with cyano and chloride groups in the ortho positions of the aryl rings) are reported. Both triazene ligands were found to deprotonate on coordination and act as tridentate chelating ligands forming distorted N4O2 octahedral geometry around HgII atoms. Hydrogen bonds, π⋯π and C–H⋯π stacking interactions help to the stabilization of the resulted frameworks.Figure optionsDownload as PowerPoint slide
Journal: Polyhedron - Volume 44, Issue 1, 31 August 2012, Pages 138–142