| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1324367 | Journal of Organometallic Chemistry | 2009 | 7 Pages |
Reactions of metal acetylide complexes M(CCAr)(PP)Cp′ (M = Fe, Ru; Ar = C6H5, C6H4Me-4; PP = (PPh3)2, dppe; Cp′ = Cp, Cp*; not all combinations), or the analogous vinylidene, with cyanogen bromide yield monobromovinylidene complexes [M{CC(Br)Ar}(PP)Cp′]+, isolated as PF6− salts. The trimethylsilyl-capped acetylides M(CCSiMe3)(PP)Cp′ react with cyanogen bromide to give [M(CCBr2)(PP)Cp′]+, the first examples of metal complexes containing a terminal dihalovinylidene ligand, which can be isolated as the BF4− salts. Molecular structures of representative mono- and di-bromovinylidene complexes are reported, together with those of Ru(CCSiMe3)(PPh3)2Cp and Ru(CCSiMe3)(dppe)Cp*.
Graphical abstractReaction of metal acetylide and vinylidene complexes with cyanogen bromide has given access to bromovinylidene complexes, including the first examples of compounds containing a terminal dihalovinylidene ligand.Figure optionsDownload full-size imageDownload as PowerPoint slide
