Three trinuclear complexes, NiII MnIII NiII, NiII CrIII NiII and Ni(II)3 based on (pyridine-2-aldoximato)nickel(II) units are described. Two of them, and , contain metal-centers in linear arrangement, as is revealed by X-ray diffraction. Complex is a homonuclear complex in which the three nickel(II) centers are disposed in a triangular fashion. The compounds were characterized by various physical methods including cyclic voltammetric and variable-temperature (2-290 K) susceptibility measurements. Complexes and display antiferromagnetic exchange coupling of the neighbouring metal centers, while weak ferromagnetic spin exchange between the adjacent Ni II and Cr III ions in is observed. The experimental magnetic data were simulated by using appropriate models.
Exchange coupling between the radical iminosemiquinone ligands changes from ferromagnetic to antiferromagnetic in l.s. Co(III) complexes, whereas the same coupling in Ga(III) complexes is always antiferromagnetic.
Reaction of a 1 : 1 : 1 molar ratio of NiCl(2), NaN(3) and H(2)L, a tetradentate ligand N-(2-pyridyl)methyl)-N,N-bis(2'-hydroxy-3',5'-dimethylbenzyl)amine in methanol in presence of Et(3)N results in a turquoise precipitate, which affords deep green crystals of [Ni(2)(HL)(2)(N(3))(2)]*1.5CH(2)Cl(2) (1) and [Ni(2)(HL)(2)(N(3))(2)]*H(2)O (2) upon crystallization from CH(2)Cl(2)-MeOH or THF-MeOH, respectively. Both complexes reveal distorted octahedral NiN(4)O(2) coordination environments around the Ni(ii) centers with bis(micro-1,1-azido) bridging ligands. Complex 1 displays an unprecedented small Ni-N-Ni bridge angle of 90.4 degrees , whereas 2 contains the said angle of av. 98.7 degrees lying in the usual range observed for other comparable structures. The variable-temperature magnetic susceptibility together with the variable-field, variable-temperature (VTVH) magnetization measurements discern different ground states of S(t) = 0 for 1 and S(t) = 2 for 2. The magnetic behaviours of these compounds are discussed in the context of the known bis(end-on azido) bridging dinickel(II) complexes.
Two bis(mu-phenoxo)dicopper(II) complexes, [(L(CH3))(2)Cu(2)] (1) and [(L(t-Bu))(2)Cu(2)] (2), where L(CH3) and L(t-Bu) represent the dianions of (methylamino)-N,N-bis(2-methylene-4,6-dimethylphenol) and of (methylamino)-N,N-bis(2-methylene-4,6-di-tert-butylphenol), respectively, are reported to demonstrate the effect of remote substituents on the nature of exchange coupling interactions between the copper(II) centers. In contrast to 1, which is as usual antiferromagnetically coupled, complex 2 is a rare example of a ferromagnetically coupled diphenoxodicopper(II) complex.
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