Abstract
The tungsten butatrienylidenes [cis-W(CO)(dppe)(2){C=C=C=C(R)(SnMe3)}] (R = SnMe3 (2) and SiMe3 (3); dppe = 1,2-bis(diphenylphosphinoethane)) were prepared from the reactions of [trans-W(CO)(N-2)(dppe)(2)] (1) and the respective butadiynes displaying a 1,4-shift of the respective SnMe3 groups along the butadiyne chains. Stannyl deprotection of 2 with NBu4F center dot 3H(2)O led to the anionic butadiyne derivative [trans-W(CO)(dppe)(2)(C CC CH)][NBu4] (10). The reaction of 1 with stannylated acetylenes gave the vinylidene derivatives [cis-W(CO)(dppe)(2){C=C(SnMe3)(R)}](R = Ph (5) or SnMe3 (6)), which lost a SnMe3 group, yielding W(I) acetylides of the type [trans-W(CO)(dppe)(2)(C CR)] (R = Ph (7), SnMe3 (8), and SiMe3 (9)). They were studied by cyclic voltammetry and EPR spectroscopy.
Original language | English |
---|---|
Pages (from-to) | 6321-6328 |
Number of pages | 8 |
Journal | Organometallics |
Volume | 29 |
Issue number | 23 |
DOIs | |
Publication status | Published - 13 Dec 2010 |