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Four Complexes derived from a Benzimidazole‐thioether Derivative Ligand: Syntheses, Crystal Structures and Luminescent Properties
Author(s) -
Li Linke,
Fan Liyan,
Wei Lulu,
Li Yanyan,
Hou Hongwei
Publication year - 2014
Publication title -
zeitschrift für anorganische und allgemeine chemie
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.354
H-Index - 66
eISSN - 1521-3749
pISSN - 0044-2313
DOI - 10.1002/zaac.201300375
Subject(s) - benzimidazole , thioether , ligand (biochemistry) , chemistry , luminescence , supramolecular chemistry , hydrogen bond , crystallography , crystal structure , intermolecular force , pyridine , derivative (finance) , infrared spectroscopy , solvent , stereochemistry , molecule , medicinal chemistry , materials science , organic chemistry , receptor , biochemistry , optoelectronics , financial economics , economics
Four complexes based on a benzimidazole‐thioether derivative ligand 2‐[(4‐pyridine)sulfydryl]‐ethyl‐1H‐benzimidazole (pteHb), namely, {[CdCl 2 (pteHb) 2 ] 2 · 2DMF} n ( 1 ), [CdI 2 (pteHb)] 2 ( 2 ), {[CoCl 2 (pteHb)] 2 · DMF} ( 3 ), and {[ZnCl 2 (pteHb)] 2 · DMF} ( 4 ), were prepared under solvothermal and solvent evaporation conditions. X‐ray diffraction analysis reveals that the Cl – ions of complex 1 act as μ 2 bridge to connect the Cd II ions resulting in a dinuclear unit. The units are bridged by the ligand pteHb to give a 1D double‐looped chain. Complexes 2 – 4 are dinuclear and further assembled into a 3D supramolecular architecture via π–π interactions, hydrogen bonding interactions, and intermolecular forces. Complexes 1 – 4 were characterized by elemental analyses and IR spectroscopy. Furthermore, solid‐state luminescent properties of complexes 1 , 4 , and ligand pteHb were also investigated.