Synthesis and Characterization of Group 4 Permethylpentalene Dichloride Complexes

Abstract

We report the high-yield syntheses of the (η8-Pn*)MCl2 complexes (η8-Pn* = C8Me6; M = Ti, Zr, Hf), utilizing the cis-(SnMe3)2Pn* or cis-Li2Pn*(TMEDA)x synthons. Stereoselective synthesis of the appropriate Pn* precursor [cis-Li2Pn* and cis-(SnMe3)2Pn*] can be achieved by the appropriate choice of solvent. Treatment of cis-(SnMe3)2Pn* with TiCl4·2THF enabled the first high-yielding synthesis of a group 4 η8-Pn* complex, [η8-Pn*TiCl(μ-Cl)]2 (1). Analogous complexes for the remaining group 4 congeners have been synthesized via the reaction of Li2Pn*(TMEDA)x with MCl4·2THF (M = Zr, Hf). These have been found to incorporate LiCl, resulting in the chemical formula [η8-Pn*M(μ-Cl)3/2]2(μ-Cl)2Li·THFx [M = Zr (2), Hf (3)]. 1, 2, and 3 have all been fully characterized in the solution phase and in the solid state via single-crystal X-ray diffraction, revealing all three to be dimeric; 3 is the first structurally elucidated hafnium pentalene compound. The solid-state structure of trans-(SnMe3)2Pn* has also been reported. All three compounds have been produced in sufficiently high yields to act as excellent entry points to further group 4 η8-Pn* species via salt metathesis reactions.