Abstract
The crystal structure analyses of copper(II) and iron(II) complexes of 3,6-dicarboxypyridazine (H 2DCP) have shown the role of this ligand to form binuclear complexes. However, the reaction with manganese(II) chloride in an aqueous medium led to the formation of a new mononuclear complex, [Mn(HDCP) 2(H 2O)] · 2H 2O, which has been characterised by X-ray crystallography. The 3,6-dicarboxypyridazine plays the role of a bidentate ligand with a trans coordination mode. The complex has crystallographic C i symmetry. The Mn(II) ion has slightly deformed octahedral geometry and is coordinated to two oxygens of the deprotonated carboxylic acid functions (MnO 2.150 Å), two equivalent nitrogen atoms of the pyridazine rings [MnN 2.298(2) Å)] and two water molecules [MnO(W) 2.160(2) Å].
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