Abstract
The crystal structures have been determined and the magnetic properties investigated for four novel [MII(A)(H2O)m]n polymeric complexes, where MII = CdII, CuII or NiII, m = 2–4 and A = adipate dianion. In [Cd(A)(H2O)2]n1, [Cu(A)(H2O)2]n2 and [Ni(A)(H2O)4]n4 the combination of the metal cation with the dicarboxylate ligand leads to the formation of infinitive chains; still the co-ordinated water molecules and the carboxylate oxygen atoms collaborate to hydrogen-bond the chains into 3-D structures. Each cadmium(II) and nickel(II) ion in 1 and 4 is coordinated in an octahedral geometry to carboxylate and water molecules. The coordination sphere around copper(II) ions in 2 is square planar. The structure of 3, [Cu3(A)2(OH)2(H2O)4]n, is made up of ribbons linked to neighboring ones by hydrogen bonds. Each ribbon is composed of 2 crystallographically independent metal centers, Cu(1) and Cu(2), which exhibit octahedral and square pyramidal coordination geometries, respectively. Weak antiferromagnetic interactions were observed for 2, and 3 (singlet–triplet energy gap values of −2.3 and −54.5 cm−1, respectively) and isolated nickel(II) ions for 4. An interpretation of the magnetic behavior was attempted. The strategy for the assembly of 1-D metal–organic chains into 3-D structures, with the use of coordinated water molecules as hydrogen bond donors and carboxylate oxygens as hydrogen bond acceptors, is also discussed.
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