The reaction of bis(phenanthroline)metal(ii) cations (M = Mn, Co, Ni, Cu and Zn) with bis(oxalato)chromium(iii) anions in a water/ethanol solution gives rise to a series of compounds with oxalate-bridged cations, [{M(phen)}(μ-CO)][Cr(phen)(CO)]·4HO [MnCr (1), CoCr (2), NiCr (3), CuCr (4) and ZnCr (5)]. Their structural analysis reveals that all the prepared compounds crystallize in the triclinic system, space group P1[combining macron], having similar unit cell parameters, molecular structures and crystal packing features. All metal centres in 1-5 are octahedrally coordinated: M in homodinuclear cations are coordinated with two phen molecules and one bridging oxalate ligand; Cr in anions is coordinated with one phen ligand and two bidentate oxalate groups. The copper atom in CuCr (4) exhibits a Jahn-Teller-distorted octahedral coordination. Owing to the considerable number of pyridyl groups present in 1-5 (from phen ligands) the crystal packing of cations and anions is driven by stacking interactions appearing in offset-face-to-face (OFF) and edge-to-face (EF) orientations. The hydrogen bonds between the anions and water molecules of crystallization form 1D ladder-like motifs. In addition to the single crystal X-ray diffraction studies, the characterization of the new complexes was accomplished by means of IR and UV/Vis spectroscopy and magnetization measurements on a SQUID magnetometer. The temperature dependence of magnetic susceptibility reveals different magnetic super exchange interactions taking place in homodinuclear oxalate-bridged cations depending on the transition metal centre (Mn, Co, Ni and Cu). Oxalate ligands mediate the ferromagnetic coupling of Cu metal cations in CuCr (4), whereas in MnCr (1), CoCr (2) and NiCr (3), antiferromagnetic interactions are observed between Mn, Co and Ni cations, respectively. Also, relatively large zero-field splitting parameters for Cr ions (from mononuclear anions), D ≈ 1 cm, were observed.
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http://dx.doi.org/10.1039/c7dt02522j | DOI Listing |
Acta Crystallogr C Struct Chem
December 2024
Laboratoire de Cristallographie-Themodynamique, Faculté de Chimie, USTHB, BP 32 El-Alia Bab Ezzouar, Algiers, 16111, Algeria.
Inorg Chem
June 2023
Ruđer Bošković Institute, Bijenička Cesta 54, Zagreb 10000, Croatia.
Two heterometallic coordination polymers {[NH(CH)(CH)][MnClCr(CO)]} () and {[NH(CH)-(CH)][MnClCr(CO)]} () were obtained by slow evaporation of an aqueous solution containing the building block [A][Cr(CO)] [A = (CH)(CH)NH or (CH)(CH)NH] and MnCl·2HO. The isostructural compounds comprise irregular two-dimensional (2D) oxalate-bridged anionic layers [MnClCr(CO)] with a Shubnikov plane net topology designated as (4·8), interleaved by the hydrogen-bonded templating cations (CH)(CH)NH () or (CH)(CH)NH (). They exhibit remarkable humidity-sensing properties and very high proton conductivity at room temperature [1.
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November 2022
Ruđer Bošković Institute, Bijenička cesta 54, 10000 Zagreb, Croatia.
Seven novel oxalate-based [CuCr] compounds: [Cu(terpy)Cl][Cr(CO)]·9HO (1; terpy = 2,2':6',2''-terpyridine), {[CrCu(HO)(terpy)(CO)]·10HO} (2), [CrCu(HO)(terpy)(CO)]·12HO (3), [Cu(HO)(terpy)][CrCu(HO)(terpy)(CO)]·9HO (4), [Cu(HO)(terpy)(NO)][CrCu(HO)(terpy)(CO)]·6HO (5), [CrCu(terpy)(CO)(NO)]·1.5HO·CHOH (6) and [CrCu(HO)(terpy)(CO)][CrCu(terpy)(CO)]·9HO·CHOH (7) were obtained from the reaction of an aqueous solution of the building block [Cr(CO)] and a methanol solution containing Cu ions and terpyridine ligand by the layering technique. Interestingly, changing only the anion of the starting salt of copper(II), NO instead of Cl, resulted in an unexpected modification in the bridge type, namely oxalate (compounds 2-7) chloride (compound 1).
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July 2022
Henan Key Laboratory of Polyoxometalate Chemistry, College of Chemistry and Chemical Engineering, Henan University, Kaifeng, Henan 475004, P. R. China.
Oxalate bridged Nd-based arsenotungstate, KNaH[{(AsWO(HO))Nd(HO)}(CO)]·64HO (1), was obtained from the reaction of K[AsWO(HO)], oxalic acid, and NdCl·6HO in mildly acidic aqueous solution. The polyanion exhibits a dimeric structure in which the fully deprotonated oxalate ligands bridge two Nd cations and the arsenotungstate anions act as blocking ligands. The photoluminescence (PL) spectrum of 1 shows the characteristic emission peak of Nd in the near-infrared (NIR) region.
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September 2021
Ruđer Bošković Institute, Bijenička cesta 54, 10000 Zagreb, Croatia.
A novel one-dimensional (1D) oxalate-bridged coordination polymer of iron(III), {[NH(CH)(CH)][FeCl(CO)]} (), exhibits remarkable humidity-sensing properties and very high proton conductivity at room temperature (2.70 × 10 (Ω·cm) at 298 K under 93% relative humidity), in addition to the independent antiferromagnetic spin chains of iron(III) ions bridged by oxalate groups ( = -7.58(9) cm).
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