Abstract
Binuclear complexes [M2Cl4(μ-bpym)], where M = VO2+, FeII, CoII or CuII and bpym = 2,2′-bipyrimidine, and [M2(hfacac)4(μ-bpym)] complexes, where hfacac = hexafluoroacetylacetonate and M = FeII, NiII or CoII have been synthesized and characterized by chemical analysis, conductance measurements, i.r., electronic and e.p.r spectroscopies and by magnetic susceptibility measurements (in the 4.2–291 K range). CoII and FeII are in a high spin state. [(VO)2Cl4(μ-bpym)] is paramagnetic, without significant interactions. [Fe2Cl4(μ-bpym)] shows a singular behaviour explained by an antiferromagnetic intradimer exchange and a ferromagnetic interdimer interaction. All other complexes are antiferromagnetic, with an intramolecular exchange parameter, J, varying from −3.3 cm−1 for CoII/math> to −109 cm−1 for CuII.
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Barquín, M., Garmendia, M.J.G. & Bellido, V. Synthesis, spectroscopic studies and magnetic properties of binuclear complexes of the first transition series cations bridged by 2,2′-bipyrimidine. Transition Metal Chemistry 24, 584–588 (1999). https://doi.org/10.1023/A:1006940930679
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DOI: https://doi.org/10.1023/A:1006940930679