Structural diversity of transition-metal coordination polymers derived from isophthalic acid and bent bis(imidazole) ligands |
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Authors: | Jin-ming Hao Ying-na Zhao Bao-yi Yu Kristof Van Hecke Guang-hua Cui |
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Affiliation: | 1. College of Chemical Engineering, Hebei United University, 46 West Xinhua Road, Tangshan, 063009, Hebei, People’s Republic of China 2. Department of Inorganic and Physical Chemistry, Ghent University, Krijgslaan 281 S3, 9000, Ghent, Belgium
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Abstract: | Four coordination polymers associated with bent bis(imidazole) 1,3-bis(imidazol-l-yl-methyl)benzene (mbix) and isophthalic acid (H2ip) or 5-methylisophthalic acid (H2mip) ligands, formulated as {[Cd(mbix)(mip)]·H2O} n (1), {[Co(mbix)(mip)]·0.4H2O} n (2) [Ni(mbix)(mip)H2O] n (3) and [Ni(mbix)(ip)] n (4), were synthesized under hydrothermal conditions and characterized by physico-chemical and spectroscopic methods. Complexes 1 and 2 are isomorphous and exhibit a 1D loop-like chain. Complex 3 features a 2D (4,4) layer, which further extends into an unusual 2D (3,5)-connected 3,5L2 double-layered supramolecular network via classical O–H···O hydrogen bonding interactions. Complex 4 is a 3D network, which shows a rare binodal (3,5)-connected 3,5T1 framework. Moreover, the luminescence and catalytic properties of the complexes for the degradation of methyl orange by sodium persulfate in a Fenton-like process are reported. |
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