کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1303006 | 974728 | 2010 | 5 صفحه PDF | دانلود رایگان |
Three hydrogen-bonded nanotubular zinc(II) complexes of a monodentate ligand N-(9-anthracenyl)-N′-(4-pyridyl)urea (L), [Zn(OAc)2L2]∙H2O (1), [ZnBr(OAc)L2]∙H2O (2) and [ZnCl(OAc)L2]∙4H2O (3), were synthesized and structurally characterized. In the complexes, the central metal ion is tetrahedrally coordinated by the pyridyl nitrogen atoms of two ligands and different anions, while the urea groups of the ligands self-associate into the typical urea tape through R21(6) hydrogen bonds, which are essential for the formation of the nanotubes. The fluorescence properties of ligand L and the complexes were studied in the solid state at room temperature.
Graphical AbstractWe report three nanotubular zinc(II) complexes [Zn(OAc)2 L2]∙H2O (1), [ZnBr(OAc)L2]∙H2O (2) and [ZnCl(OAc)L2]∙4H2O (3) of a monodentate ligand N-(9-anthracenyl)-N′-(4-pyridyl)urea (L). The metal ion is four-coordinated by two ligands and different anions, thus forming a half square which aligns with each other through the typical N–H⋯O hydrogen bonding of urea groups to form the nanotubes.Figure optionsDownload as PowerPoint slide
Journal: Inorganic Chemistry Communications - Volume 13, Issue 7, July 2010, Pages 873–877