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RESEARCH PRODUCT
Magneto-structural correlations in asymmetric oxalato-bridged dicopper(II) complexes with polymethyl-substituted pyrazole ligands
Giovanni De MunnoIsabel CastroM. Luisa CalatayudNadia MarinoRafael Ruiz-garcíaMiguel JulveFrancesc LloretMarta Orts-arroyosubject
010405 organic chemistrychemistry.chemical_elementCrystal structurePyrazole ligandsPyrazole010402 general chemistry01 natural sciencesCopperSquare pyramidal molecular geometryAntiferromagnetic coupling0104 chemical sciencesIonCrystallographychemistry.chemical_compoundTrigonal bipyramidal molecular geometrychemistryMaterials ChemistryPhysical and Theoretical Chemistrydescription
Two oxalato-bridged dinuclear copper(II) complexes, [{Cu(Hdmpz)3}2(μ-ox)](ClO4)2·2H2O (1) and [{Cu(Htmpz)3}2(μ-ox)](ClO4)2·2H2O (2) (Hdmpz = 3,5-dimethyl-1H-pyrazole and Htmpz = 3,4,5-trimethyl-1H-pyrazole), have been synthesized and structurally and magnetically characterized. The crystal structures of 1 and 2 consist of asymmetric bis-bidentate μ-oxalatodicopper(II) complex cations with two short [Cu–O = 1.976(2) (1) and 1.973(2) Å (2)] and two long copper–oxygen bonds [Cu–O = 2.122(2) (1) and 2.110(2) Å (2)]. The environment at each CuII ion in 1 and 2 is closer to the trigonal bipyramidal geometry than to the square pyramidal [τ = 0.633 (1) and 0.711 (2)]. The magnetic properties of 1 and 2 show moderate antiferromagnetic coupling between the CuII ions through the oxalato bridge [J = −129 (1) and 161 cm−1 (2); H = −JS1 · S2 with S1 = S2 = SCu = ½]. A thorough magneto-structural analysis has been carried out for the family of asymmetric μ-oxalatodicopper(II) complexes with different terminal ligands to determine the influence on the sign and strength of the magnetic coupling of subtle structural factors, such as the trigonal distortion of the metal geometry and the lengthening or the asymmetry of the metal-oxalato bond distances.
year | journal | country | edition | language |
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2018-01-12 |