The title compound, {[Co(H(2)O)(6)][Co(SO(4))(C(10)H(8)N(2))(H(2)O)(3)][Co(SO(4))(2)(C(10)H(8)N(2))(H(2)O)(2)]}(n), contains three crystallographically unique Co(II) centres, all of which are in six-coordinated environments. One Co(II) centre is coordinated by two bridging 4,4'-bipyridine (4,4'-bipy) ligands, one sulfate ion and three aqua ligands. The second Co(II) centre is surrounded by two N atoms of two 4,4'-bipy ligands and four O atoms, i.e. two O atoms from two monodentate sulfate ions and two from water molecules. The third Co(II) centre forms part of a hexaaquacobalt(II) ion. In the crystal structure, there are two different one-dimensional chains, one being anionic and the other neutral, and adjacent chains are arranged in a cross-like fashion around the mid-point of the 4,4'-bipy ligands. The structure features O-H···O hydrogen-bonding interactions between sulfate anions and water molecules, resulting in a three-dimensional supramolecular network.
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http://dx.doi.org/10.1107/S0108270112034385 | DOI Listing |
Environ Sci Pollut Res Int
January 2025
Centre de Recherche Scientifique Et Technique en Analyses Physico-Chimiques, CP 42004, Bou-Ismail, Tipaza, Algeria.
ZnO-CoO material was successfully synthesized by the co-precipitation method and used as a catalyst for the removal of diclofenac sodium (DCF). ZnO-CoO exhibited higher catalytic activity in the catalytic process compared to the photocatalytic processes. Under optimum conditions, the activation of peroxymonosulfate (PMS) by ZnO-CoO achieved approximately 99% removal of DCF, confirming the effective adsorption and activation of PMS.
View Article and Find Full Text PDFInorg Chem
January 2025
Department of Inorganic Chemistry, Faculty of Science, University of Maragheh, Maragheh 55181-83111, Iran.
Clean energy conversion and storage require simple, economical, and effective electrode materials to achieve promising results. The development of high-performance electrocatalysts with adequate stability and cost-effectiveness is essential to ensure low overpotentials toward the oxygen evolution reaction (OER). Herein, a cobalt-based metal-organic framework with 4,4,4-6T14 topology in combination with various ratios of NiMn-layered double hydroxide (Co-MOF@%NiMn-LDH, = 5, 10, 20, and 40%) is applied as an effective electrocatalyst for the oxidation of water.
View Article and Find Full Text PDFSmall
December 2024
Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, India.
A mixed-ligand-based thermo-chemically robust and undulated metal-organic framework (MOF) is developed that embraces carboxamide moiety-grafted porous channels and activation-induced generation of open-metal site (OMS). The guest-free MOF acts as an outstanding heterogeneous catalyst in Hantzsch condensation for electronically assorted substrates with low catalyst loading and short duration under greener conditions than the reported materials. Besides Lewis acidic OMS, the carboxamide group activates the substrate via two-point hydrogen bonding, highlighting the effectiveness of custom-made functionalities in this multi-component reaction.
View Article and Find Full Text PDFChem Sci
December 2024
Chemistry and Bioengineering, Graduate School of Engineering, Osaka Metropolitan University Sugimoto, Sumiyoshi-ku Osaka 558-8585 Japan
[This corrects the article DOI: 10.1039/D4SC04390A.].
View Article and Find Full Text PDFEnviron Res
December 2024
Yanshan Earth Critical Zone and Surface Fluxes Research Station, College of Resources and Environment, University of Chinese Academy of Sciences, Beijing, 100049, China. Electronic address:
N-termini Cyano group (CN) in metal hexacyanoferrates (MHCF) have been identified as specific-affinity sites for palladium (Pd), but C-termini CN do not effectively serve as Pd adsorption sites due to their stronger bonds with the metal ligands (M), which reduces the activity and density of CN. Herein, the optimization of directional coordination of cyano group C/N-termini by modulating the electronic structure of the M (Fe, Co, and Ni) in MHCF was investigated to reinforce the Pd recovery. Spectroscopic analyses and DFT calculations revealed that NiHCF exhibited N-site mono-coordination, whereas CoHCF displayed C-site mono-coordination due to spin-exchange interactions, leading to the strengthened N-Co bonds and weakened Fe-C bonds.
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