The cobalt(II) containing tungstophosphate [Co(4)(H(2)O)(16)P(8)W(48)O(184)](32-) (1) has been synthesized by addition of Co(2+) ions to an aqueous solution of [H(7)P(8)W(48)O(184)](33-) (P(8)W(48)) and characterized by single-crystal XRD, IR, and UV-vis spectroscopy, elemental analysis, electrochemistry, and magnetochemistry. The novel polyanion 1 is a derivative of the superlacunary P(8)W(48) with four cobalt(II) ions coordinated to the rim of the central cavity and two additional cobalt(II) ions linked on the outside bridging neighboring polyanions. Using similar synthetic procedures, but adding a few drops of H(2)O(2), we isolated the manganese(II) derivative [Mn(4)(H(2)O)(16)(P(8)W(48)O(184))(WO(2)(H(2)O)(2))(2)](28-) (2) and its nickel(II) analogue [Ni(4)(H(2)O)(16)(P(8)W(48)O(184))(WO(2)(H(2)O)(2))(2)](28-) (3). Both polyanions have picked up two equivalents of tungsten resulting in the unprecedented {P(8)W(50)} host framework. We also made the vanadium(V) derivative [(VO(2))(4)(P(8)W(48)O(184))](36-) (4), with four tetrahedral vanadate groups grafted to the P(8)W(48) host. The voltammetric patterns associated with the W-centers in polyanions 1, 2, and 4 display enough distinct features allowing for a qualitative classification according to relative basicity of the reduced polyanions: 2 > P(8)W(48) > 1 > 4. The electrochemistry of 1 offers a new example for detection of the Co(2+) centers in a multicobalt containing polyanion. During a study of the Mn(2+) centers of 2 at pH 5, a film deposition is observed. The vanadium(V) centers of 4 are well-behaved in a pH 0.33 medium. Temperature and magnetic field dependence of the magnetic moment of 1-3 were performed on a SQUID magnetometer over the temperature range 1.8-250 K and field range 0-7 T. The results are consistent with the model of noninteracting 3d metal ions. Variable temperature (4-295 K) and variable frequency (34-413 GHz) EPR measurements support the magnetic susceptibility results. The zero-field splitting D and g values obtained for 1-3 are in agreement with those reported for high-spin Co(2+), Mn(2+), and Ni(2+) ions in axially distorted octahedral environments.
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JACS Au
December 2024
Sorbonne Université, CNRS, Institut Parisien de Chimie Moléculaire, IPCM, F-75005 Paris, France.
Metallogels built in a bottom-up approach by metal coordination and supramolecular interactions have important potential for the elaboration of smart materials. In this context, we present here the formation of supramolecular coordination polymers driven by the complexation of cobalt(II) or zinc(II) ions with polyoxometalate-based hybrids displaying two terpyridine ligands in a linear arrangement. Thanks to the electrostatic interactions between the polyoxometalate cores and metal nodes, the polymer chains self-assemble into fibers that physically cross-link to form gels above a critical concentration.
View Article and Find Full Text PDFInorg Chem
January 2025
Department of Medicinal and Applied Chemistry, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.
Density functional theory (DFT) calculations indicate that [Co(HO)] reacts with two HO molecules to form [(HO)Co(OOH)(HO)] reactant complexes, which decompose through three distinct pathways depending on the relative orientation between the coordinated OOH and HO ligands. The reactive intermediates produced via these activation pathways include hydroperoxyl (OOH)/superoxide (O) radicals, singlet oxygen (O), and Co(III) species [(HO)Co(O)], [(HO)Co(OH)], and [(HO)Co(OH)]. The Co(III) species display from moderate to strong oxidizing abilities that have long been overlooked.
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.
View Article and Find Full Text PDFDalton Trans
December 2024
Dipartimento Scienze Chimiche, Università degli Studi di Catania, and INSTM UdR Catania, Viale Andrea Doria 6, 95125 Catania, Italy.
This work reports the engineering and functional properties of an emerging class of heterobimetallic 3d-4f ionic complexes designed with cobalt and rare-earth (RE) metals. We present a comprehensive examination of the structural, magnetic, optical, and thermal properties of the heterobimetallic ionic complexes with the general formula [Co(hfa)][RE(hfa)tetraglyme] (RE = Dy, Eu, and Y), where the metal centres are coordinated by hexafluoroacetylacetonate (Hhfa = 1,1,1,5,5,5-hexafluoro-2,4-pentanedione), β-diketone and tetraglyme (2,5,8,11,14-pentaoxapentadecane) polyether. Structural analysis reveals an octahedral coordination geometry enveloping the cobalt(II) centre, characterized by inherent symmetry properties consistent across the derivatives, while a capped square-antiprism coordination polyhedron is observed for the RE ions.
View Article and Find Full Text PDFParamagnetic complexes of 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetate (DOTA) derivatives have shown potential for molecular imaging with magnetic resonance. DOTA-tetraglycinate (DOTA-4AmC) coordinated with lanthanide metal ions (Ln) demonstrates pH/temperature sensing with Biosensor Imaging of Redundant Deviation in Shifts (BIRDS) and Chemical Exchange Saturation Transfer (CEST), respectively, detecting nonexchangeable (e.g.
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