In the centrosymmetric polymeric title compound, {[CoEr(2)(C(14)H(8)N(2)O(5))(4)(H(2)O)(4)]·4H(2)O}(n), the Er(III) cation has a coordination number of eight and is surrounded by seven carboxyl-ate O atoms from four 5-(pyridine-4-carboxamido)-isophthalate (L) ligands and one water mol-ecule, forming a distorted square-anti-prismatic arrangement. The Co(II) cation is located on an inversion center and is coordinated by two pyridine N atoms, two carboxyl-ate O atoms and two water mol-ecules in a distorted octa-hedral geometry. The asymmetric unit contains two anionic L ligands. One bridges two Er(III) cations and one Co(II) cation through two carboxyl-ate groups and one pyridine N atom, while the other bridges two Er(III) cations and one Co(II) cation through two carboxyl-ate groups. Extensive O-H⋯O, O-H⋯N and N-H⋯O hydrogen-bonding inter-actions are present in the crystal, involving all uncoordinated water mol-ecules and the uncoordinated pyridine N atom of one of the ligands bonded to an adjacent coordinated water mol-ecule. The title compound is isotypic with the gadolinium analogue.
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http://dx.doi.org/10.1107/S1600536811039948 | DOI Listing |
Acta Crystallogr E Crystallogr Commun
January 2025
Institut für Anorganische Chemie, Universität Kiel, Max-Eyth.-Str. 2, 24118 Kiel, Germany.
Reaction of Co(NCS) with 4-methyl-pyridine in water leads to the formation of single crystals of the title compound, [Co(NCS)(CHN)] . The asymmetric unit consists of two crystallographically independent thio-cyanate anions and two crystallographically independent 4-methyl-pyridine coligands in general positions, as well as of two different Co cations, of which one is located on a twofold rotational axis, whereas the second occupies a center of inversion. The methyl H atoms in both 4-methyl-pyridine ligands are disordered and were refined using a split model.
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 Sci Pollut Res Int
December 2024
Cellulose, Paper and Advanced Water Treatments Research Group, Department of Chemical Engineering, Complutense University of Madrid, Avda. Complutense S/N, Madrid, Spain.
The recovery of Co(II), Mn(II), Ni(II), and Cu(II) from black mass e-waste solutions through cellulose nanofibers (CNFs) and nanocrystals (CNCs) was investigated. These materials were synthetized by TEMPO-oxidation followed by high-pressure homogenization, and acid hydrolysis, respectively. The NC characterization included the measurement of consistency, cationic demand, carboxylic content, dissolved amorphous cellulose, and transmittance at λ = 600 nm.
View Article and Find Full Text PDFEnviron Sci Pollut Res Int
December 2024
Department of Chemistry, Faculty of Science, Arak University, Arak, 38156-8-8349, Iran.
This research utilized tetraethylenepentamine-functionalized HY cubic zeolite as an adsorbent to effectively remove heavy metals from aqueous solutions. The adsorbent was characterized using FT-IR, XRD, TGA, FE-SEM, and EDS-MAP techniques. The synthesis aimed to optimize and evaluate the removal efficiency of Pb(II), Cr(III), Co(II), and Cu(II) from aqueous solutions by investigating key parameters, including initial pH, concentration, adsorbent dosage, and contact time.
View Article and Find Full Text PDFInt J Mol Sci
November 2024
Faculty of Chemistry and Pharmacy, Sofia University "St. Kliment Ohridski", 1164 Sofia, Bulgaria.
Monensic acid is a natural polyether ionophore and is a therapeutic of first choice in veterinary medicine for the control of coccidiosis. Although known as a sodium-binding ligand, it can also form a variety of coordination species depending on experimental conditions applied. In this study, we present the crystal structures and properties of Co(II) and Mn(II) complexes of sodium monensinate (MonNa) derived from the reaction of MonNa with cobalt or manganese dinitrates.
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