6533b835fe1ef96bd129ed03
RESEARCH PRODUCT
Isomorphous replacement of MII ions in MII–GdIII dimers (MII = CuII, MnII, NiII, CoII, ZnII): magnetic studies of the products
Belén AbarcaRosa AdamAnastasia N. GeorgopoulouVassilis PsycharisCatherine P. RaptopoulouAthanassios K. BoudalisRafael Ballesterossubject
ManganeseChemistryStereochemistryMolecular ConformationHexacoordinateSpin hamiltonianGadoliniumCobaltCrystallography X-RayMagnetic susceptibilityInductive couplingIonInorganic ChemistryMagneticsZincCrystallographyFerromagnetismCoordination ComplexesMetalsNickelAntiferromagnetismDimerizationCopperMonoclinic crystal systemdescription
Complexes [M(II)Gd(III){pyCO(OEt)pyC(OH)(OEt)py}₃](ClO₄)₂·EtOH [M(II) = Cu(II) (1), Mn(II) (2), Ni(II) (3), Co(II) (4) and Zn(II) (5)] crystallize in the monoclinic Cc space group and contain one hexacoordinate M(II) ion and one enneacoordinate Gd(III) ion, bridged by three {pyCO(OEt)pyC(OH)(OEt)py}⁻ ligands. Magnetic susceptibility measurements indicate a ferromagnetic interaction for 1 and antiferromagnetic interactions for 2-4. Using the Ĥ = -JŜ(Gd(III))Ŝ(M(II)) spin Hamiltonian formalism, fits to the magnetic susceptibility data yielded J values of +0.32 cm⁻¹ for 1, -1.7 cm⁻¹ for 2, and -0.22 cm⁻¹ for 3. In complex 4, the orbital contributions of Co(II) precluded the determination of the magnetic coupling. The complex follows the Curie-Weiss law with θ = -2.07 K (-1.44 cm⁻¹).
year | journal | country | edition | language |
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2011-04-15 | Dalton Transactions |