Transition‐Metal‐Like Reversible Cycloadditions of [ t BuSP‐W(CO) 5 ] with Alkenes and Alkynes

tert-Butylthiophosphinidene complex [tBuSP-W(CO)5 ] was generated by dissociation of 1-(tert-butylthio)phosphirane-W(CO)5 complex under mild conditions. The formation of transient [tBuSP-W(CO)5 ] was indicated by trapping reactions with 2,3-dimethyl-1,3-butadiene, alkynes, phenanthrene-9,10-dione, and methanol. The LUMO of [MeSP-W(CO)5 ] is significantly lower in energy than those of [Me2 NP-W(CO)5 ], [MeOP-W(CO)5 ], and [Me2 PP-W(CO)5 ]. The HOMO of [MeSP-W(CO)5 ] contains a significant contribution from the in-plane lone pair of P and the LUMO shows a typical π* characteristic. Since stabilized by sulfur lone pair and coordinated by W(CO)5 , [tBuSP-W(CO)5 ] undergoes facile and reversible cycloadditions with alkenes and alkynes.