Abstract
A project related to the crystal engineering of hydrogen-bonded coordination complexes has been initiatied and some of our first results are presented here. The compounds [Mn(DMU)6](ClO4)2(1), [Ni(DMU)6](ClO4)2(2), [Cu(OClO3)2(DMU)4] (3) and [Zn(DMU)6](ClO4)2(4) have all been prepared from the reaction of N,N′-dimethylurea (DMU) and the appropriate hydrated metal perchlorate salt. Crystal structure determinations of the four compounds demonstrate the existence of [M(DMU)6]2+ cations and ClO4− counterions in (1), (2) and (4), whereas in (3) monodentate coordination of the perchlorate groups leads to molecules. The [M(DMU)6]2+ cations and ClO4− anions self-assemble to form a hydrogen-bonded one-dimensional (1D) architecture in (1) and different 2D hydrogen-bonded networks in (2) and (4). The hydrogen bonding functionalities on the molecules of (3) create a 2D structure. The complexes were also characterised by room-temperature effective magnetic moments and i.r. studies. The data are discussed in terms of the nature of bonding and the known structures.
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