Abstract
A series of [(C9H7)2ZrL]+[RR′NCS2]− complexes (where L is the conjugate base of acetylacetone and R = R′ = C2H5 or i-C3H7; R = CH3, R′ = C6H5CH2; R = C2H5, R′ = C6H4.CH3; R = C2H5, R′ = C6H11; RR′ = C6H12) have been synthesised in aqueous solution by the reaction of [(C9H7)2ZrL]+Cl− with RR′NCS2 −Na+. Conductivity measurements indicate that these complexes are 1:1 electrolytes in nitrobenzene. IR and 1H NMR spectral studies demonstrate that the acetylacetone ligand is chelating in all these complexes. Consequently, tetrahedral coordination about the zirconium atom is proposed.