Cyclic Bis-alkylidene Complexes of Titanium and Zirconium: Synthesis, Characterization, and Reaction.

Abstract

Transition-metal alkylidenes have exhibited wide applications in organometallic chemistry and synthetic organic chemistry, however, cyclic Schrock-carbene-like bis-alkylidenes of group 4 metals with a four-electron donor from an alkylidene have not been reported. Herein, the synthesis and characterization of five-membered cyclic bis-alkylidenes of titanium (4 a,b) and zirconium (5 a,b) are reported, as the first well-defined group 4 metallacyclopentatrienes, by two-electron reduction of their corresponding titana- and zirconacyclopentadienes. DFT analyses of 4 a show a four-electron donor (σ-donation and π-donation) from an alkylidene carbon to the metal center. The reaction of 4 a with N,N'-diisopropylcarbodiimide (DIC) leads to the [2+2]-cycloaddition product 6. Compound 4 a reacted with CO, affording the oxycyclopentadienyl titanium complex 7. These reactivities demonstrate the multiple metal-carbon bond character. The reactions of 4 a or 5 a with cyclooctatetraene (COT) or azobenzene afforded sandwich titanium complex 8 or diphenylhydrazine-coordinated zirconacyclopentadiene 9, respectively, which exhibit two-electron reductive ability.