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Structural and luminescent properties of a series of Cd(II) pyridyl benzimidazole complexes that exhibit extended three-dimensional hydrogen bonded networks
Authors:Jin-Hua Wang  Ting-Xiao Qin  Yue-Zhi Cui  Seik Weng Ng
Institution:1. Department of Chemical Engineering, Shandong Provincial Key Laboratory of Fine Chemicals, Qilu?University?of?Technology, Jinan, P.R. China;2. Faculty of Science, Chemistry Department, King Abdulaziz University, Jeddah, Saudi Arabia
Abstract:Five new coordination complexes, CdI2(3-PyBim)](H2O)3 (1), Cd(SO4)(3-PyBim)(H2O)4] (2), CdCl2(4-PyBim)2(H2O)2] (3), CdBr2(4-PyBim)2(H2O)2] (4) and CdI2(4-PyBim)2(H2O)2] (5) 3-PyBim=2-Pyridin-3-yl-1H-benzoimidazole, 4-PyBim=2-Pyridin-4-yl-1H-benzoimidazole], were obtained under hydrothermal conditions and characterized by single crystal X-ray diffraction, IR, elemental analysis, and powder X-ray diffraction. All of the complexes have mononuclear structures. Among the crystal structures of these complexes, there exist a variety of intermolecular hydrogen bonding interactions and π?π interactions, which further extend to a 3-D supramolecular architecture. The solid state photoluminescent properties of 15 vary with the electronegativity of the coordination anion. Additionally, the thermogravimetric analyses of these complexes are discussed.
Keywords:Metal coordination complexes  N-heterocyclic ligand  self-assembly  tunable luminescence  cadmium  anions
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