Abstract

The dinuclear (Fe(II), Gd(III)) complexes studied in this report derive from hexadentate Schiff base ligands abbreviated H(2)L(i)() (i = 1, 2, 3). H(2)L(1) = N,N'-bis(3-methoxysalicylidene)-1,3-diamino-2,2'-dimethyl-propane, H(2)L(2) = N,N'-bis(3-methoxysalicylidene)-1,2-diamino-2-methylpropane, and H(2)L(3) = N,N'-bis(3-methoxysalicylidene)-1,2-diaminoethane. The crystal and molecular structures of three complexes have been determined at 160 K. Depending on the solvent used in the preparation, L(1)Fe(CH(3)OH)Gd(NO(3))(3)(CH(3)OH)(2), 1, or L(1)Fe((CH(3))(2)CO)Gd(NO(3))(3), 1', is obtained from H(2)L(1). A similar complex, L(2)Fe((CH(3))(2)CO)Gd(NO(3))(3), 2, is obtained from H(2)L(2). Complex 1 crystallizes in the orthorhombic space group Pca2(1) (No. 29): a = 22.141(3) A, b = 9.4159(16) A, c = 15.2075(17) A, V = 3170.4(7) A(3), Z = 4. Complexes 1' and 2 crystallize in the monoclinic space group P2(1)/c (No. 14): 1', a = 9.6264(17) A, b = 19.662(3) A, c = 16.039(3) A, beta = 95.15(2) degrees, V = 3023.6(9) A(3), Z = 4; 2, a = 9.7821(13) A, b = 18.7725(17) A, c = 16.100(2) A, beta = 96.497(16) degrees, V = 2937.5(6) A(3), Z = 4. Complexes 1, 1', and 2 possess an Fe(O(phenoxo))(2-)Gd core. The mononuclear L(3)Fe complex could be prepared from H(2)L(3) but not the related dinuclear (Fe, Gd) species. Mössbauer spectroscopy evidences that the iron center is in the +2 oxidation state for the six complexes. The experimental magnetic susceptibility and magnetization data of complexes 1, 1', and 2 indicate the occurrence of weak Fe(II)-Gd(III) ferromagnetic interactions. Single ion zero-field splitting of the iron(II) must be taken into account for satisfactorily fitting the data by exact calculation of the energy levels associated to the spin Hamiltonian through diagonalization of the full matrix for axial symmetry (1, J = 0.50 cm(-1), D = 2.06 cm(-1); 1', J = 0.41 cm(-1), D = 3.22 cm(-1); 2, J = 0.08 cm(-1), D = 4.43 cm(-1)).

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