Formation of an alkyne during degradation of metal-alkylidyne complexes.

The compound [(Ot-Bu)3W≡Ct-Bu] (1) (t-Bu = C(CH3)3) decomposes upon contact with water and several organic products are formed, including di-tert-butylacetylene, t-BuC≡Ct-Bu. This process is reminiscent of the degradation of trinuclear metal-alkylidyne complexes in which free carbynes are ejected into solution, couple and form alkynes along with many other products. The reactivity pattern of the resulting t-BuC carbynes that includes extensive hydrogen abstraction, cleavage of alkynes and lack of reactivity towards alkenes is indicative of a quartet (S = 3/2) spin state. A similar spin state was assigned to other RC (R = alkyl) species that were produced by degrading M3-alkylidyne (M = transition metal) complexes in water. t-BuC≡Ct-Bu is also produced during thermal decomposition of solid 1. In 1977 Fischer and co-workers reported a very similar process in which solids of Br(CO)4Cr≡CR(1) and Br(CO)4Cr≡CR(2) were co-thermolyzed to produce R(1)C≡CR(2), R(1)C≡CR(1), and R(2)C≡CR(2). Fischer had considered the involvement of free carbynes in the making of the alkynes but later resorted to other explanations. The current results suggest that his original proposal is indeed valid.