Abstract

Three gold(I) saccharinate complexes of the type M[Au(Sac)₂] (M = Na, K and NH4) have been prepared by treatment of Au(tht)Cl (tht = tetrahydrothiophene) with saccharine and MOH in MeOHacetone. The compounds are very stable in the solid state but moderately soluble and of limited stability in water. Single crystal X-ray diffraction analysis of the three compounds revealed a linear coordination of the gold atom by the two N-bonded saccharinato ligands. ForM = Na, the two heterobicyclic ligands are roughly coplanar with a cis orientation of the two carbonyl groups which allows for a chelation of the sodium cation. For M = K, NH₄, the ligands form large dihedral angles with a trans orientation of the donor sites out of which the potassium cations are coordinated in bridging positions between neighboring anions, and the ammonium ions are hydrogen-bonded, respectively.

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