ABSTRACT
Dinuclear Ru(III) complexes, [Ru(III)(acac)(2)(dabe)Ru(III)(acac)(2)] (acacH = acetylacetone; dabeH(2) = 1, 2-diacetyl-1,2-dibenzoylethane) and [Ru(III)(acac)(2)(tbet)Ru(III)(acac)(2)] (tbetH(2) = 1,1,2,2-tetrabenzoylethane) were synthesized by reacting [Ru(acac)(2)(CH(3)CN)(2)]PF(6) with dabeH(2) and tbetH(2) respectively, in toluene. The X-ray structural analysis of a meso-type dinuclear Ru(III) complex, ΔΛ-[Ru(III)(acac)(2)(dabe)Ru(III)(acac)(2)], showed that the bridging part became chiral due to the orthogonal twisting of two non-symmetrical ß-diketonato moieties. To confirm this conclusion, the complex was resolved chromatographically to provide a pair of optical antipodes. Such chirality in the bridging part was not generated for [Ru(III)(acac)(2)(tbet)Ru(III)(acac)(2)], because the ß-diketonato moieties in tbet(2-) are symmetrical.
