Synthesis, Characterization, and Norbornene Polymerization Behavior of the Half-Sandwich Complexes [Cp*<sub>3</sub>M<sub>3</sub>(μ<sub>3</sub>-L)Cl<sub>3</sub>] and [Cp*M(2-SPyH)Cl<sub>2</sub>] (M = Ir, M = Rh, [L]<sup>3−</sup> = 1,3,5-Triazine-2,4,6-trithiolato, 2-SPy = 2-Pyridinethione)
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The trinuclear complexes [Cp*3M3(μ3-L)Cl3] (3a, M = Ir; 3b, M = Rh; [L]3− = 1,3,5-triazine-2,4,6-trithiolato) have been synthesized via the reactions of the bridging oxalato complexes [Cp*2M2(μ-C2O4)Cl2] (2a, M = Ir; 2b, M = Rh) with the trisodium salt of 1,3,5-triazine-2,4,6-trithiol (Na3L), respectively. The reactions of half-sandwich iridium and rhodium complexes [Cp*MCl(μ-Cl)]2 with 2-pyridinethione gave the corresponding mononuclear complexes [Cp*M(2-SPyH)Cl2] (4a, M = Ir; 4b, M = Rh). All complexes have been characterized by elemental analyses and NMR and IR spectroscopy. The molecular structures of 3a,b and 4a,b have been determined by X-ray crystallography. The trinuclear iridium complex 3a shows catalytic activities for the polymerization of norbornene in the presence of methylaluminoxane (MAO) as cocatalyst.
