Synthesis, crystal structures and magnetic behaviors of two dicyanamide bridged di- and polynuclear complexes of cobalt(II) derived from 2,4,6-tris(2-pyridyl)1,3,5-triazine and imidazole (original) (raw)

Synthesis, crystal structures and magnetic behaviors of two dicyanamide bridged di-and polynuclear complexes of cobalt(II) derived from 2,4,6-tris(2-pyridyl)1,3,5-triazine and imidazole a b s t r a c t Two new dicyanamido-bridged di-and polynuclear complexes of Co(II), [Co(dca)(tptz)(H 2 O)] 2 Á2(ClO 4 ) (1) and [Co(dca) 2 (imz) 2 ] n (2) [dca, dicyanamide; tptz, 2,4,6-tris(2-pyridyl)1,3,5-triazine; and imz, imidazole] have been synthesized and characterized structurally, as well as magnetically. The X-ray single crystal structure determination of complex 1 shows that two symmetry related octahedral Co(II) ions are separated by dca ligand and other coordination sites are satisfied by tptz and aquo ligands. Each dinuclear unit is associated with each other by intramolecular hydrogen bonding interactions, giving rise to a 1D chain structure. On the other hand complex 2 is a 1D coordination polymer having [Co(II)(imz) 2 ] units connected by double bridging dca ligands. These 1D chains interact through face-to-face p-p stacking interactions of the imz rings extending the dimensionality to a 2D supramolecular network. The variable temperature (300-2 K) magnetic measurements of both compounds reveal that dicyanamide exhibits a weak antiferromagnetic interaction between the metal centers. S(A) = 1 S(B) = 3/2 g = -Aκ g e = 2.00 L, S J L-S = Aκλ J Co-Co S(A) = 1 S(B) = 3/2 g = -Aκ g e = 2.00 J L-S = Aκλ Real system Model system Δ Δ J Co-Co Fig. 6. Schematic representation of the spin-orbit coupling and exchange coupling parameter (J CoÀCo ) in a dinuclear Co(II) complex.

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