摘要
By employing two mer-tricyanidoiron(III) precursors [Ph4P] [Fe-III(pcq)(CN)(3)] and [Ph4P] [Fe-III (pzq)(CN)(3)] as building blocks and a salen-tpye Schiff-base manganese (III) compound as assembling segment, two tetranuclear cyanide- and phenoxo- bridged heterobimetallic Fe(III)-Mn(III) complexes {[Mn(saltmen)] [Fe(pcq)(CN)(3)]}(2)center dot 2CH(3)OH (1) and {[Mn(saltmen)] [Fe(pzq)(CN)(3)]}(2)center dot 2CH(3)OH (2) (pcq = 8-(pyridine-2-carboxamido, pzq = 8-(pyrazine-2-carboxamido, saltmen(2-) = N, N'-(1,1,2,2-tetramethylethylene)bis(salicylideneaminato)dianion) have been synthesized and characterized by elemental analysis, IR spectroscopy and X-ray structure determination. Single x-ray analysis reveals their isostructural cyanide-bridged Fe(III)-Mn(III) binuclear structure. The binuclear entity is self-complementary through phenoxo oxygen from the neighbouring complex, giving cyanide- and phenoxo- bridged tetranuclear structure. Furthermore, under the help of the intermolecular pi-pi interaction, these two complexes can be constructed into 1D infinite chain supramolecular structure. Investigation over magnetic susceptibilities reveals the overall ferromagnetic coupling between the adjacent Fe(III) and Mn(III) ions bridged by cyanide group with J = 5.34 cm(-1) and 5.55 cm(-1) for complexes 1 and 2, respectively.
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单位山东理工大学