The structural characterization of the distorted octahedral complex Tc
O(HAF)(PAC), containing the terdentate ONS2- donor Schiff base ligand
HAF(2-) and the bidentate NS- donor ligand PAC(-), is reported. The ox
ygen donor atom of the terdentate ligand occupies the coordination sit
e trans to the Tc=O bond, with the N2S2 donors in the equatorial plane
. It was previously implicated that, complexes of this type could not
be formed. The complex ReOCl3(PPh(3))(HMEC), formed by the reaction of
trans-ReOCl3(PPh(3))(2) with the potentially bidentate NS- donor liga
nd l-2-(N-ethylamino)-1-cyclopentenedithiocarboxylate (HMEC) in aceton
e, was also structurally characterized. It was found that the ligand H
MEC coordinates to the rhenium(V) in an unexpected monodentate manner
through the neutral thiocarbonyl sulfur atom.