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Facile synthesis of new divergent imidazole-containing ligands for a 1-D cobalt(II) coordination polymer

A new divergent ligand containing a triaryl core and two imidazole side-arms has been designed and synthesized through a two-step strategy which allows facile ligand modification. The ability of this type of ligands in forming unique metal coordination networks has been proved by the observation of...

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Bibliographic Details
Published in:Polyhedron 2017-05, Vol.127, p.355-360
Main Authors: Liu, E, Xiong, Hangxing, Li, Li, Yang, Chengxiong, Yin, Zhiwei, Chang, Anthony, Manke, David R., Golen, James A., Zhang, Guoqi
Format: Article
Language:English
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Summary:A new divergent ligand containing a triaryl core and two imidazole side-arms has been designed and synthesized through a two-step strategy which allows facile ligand modification. The ability of this type of ligands in forming unique metal coordination networks has been proved by the observation of a 1-D looped cobalt(II) coordination polymer. [Display omitted] A new divergent ligand (3a) containing a triaryl core and two imidazole side-arms has been designed and synthesized. The synthetic procedure utilizes a two-step strategy, i.e. the Kröhnke condensation, followed by a Cu-catalyzed Ullman-type coupling. This synthetic strategy allows the facile introduction of various substituents on the 4-position of the central pyridine in the ligands, which was proved by the synthesis of a ligand analog (3b). The new ligands were well characterized by spectroscopic methods and X-ray structural analysis was carried out for 3a. Reaction of 3a with Co(NCS)2 by a layering method afforded single crystals of a coordination polymer 5, which was structurally characterized by X-ray diffraction. 5 is composed of two ligands and one Co(NCS)2 in its asymmetric unit and features a 1-D coordination polymer with nano-scale metallomacrocyles. The structure of 5 is found to be quite different from all known coordination networks composed of Co(NCS)2 and closely related divergent ligands.
ISSN:0277-5387
DOI:10.1016/j.poly.2017.02.028