| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1327016 | Journal of Organometallic Chemistry | 2010 | 5 Pages |
Reaction of [(η5-C5Me5)MCl4], 1–2 (1: M = Mo and 2: W) with six fold excess of [LiBH4·thf] followed by thermolysis with excess chalcogen powders (S, Se and Te) yielded dichalcomolybda- and tungstaboranes, [(η5-C5Me5M)2B4H4E2], 5–8 (5: M = Mo, E = S; 6: M = Mo, E = Se; 7: M = Mo, E = Te; 8: M = W, E = Se) in modest yields. The geometry of 5–8 resembles a hexagonal bipyramid with a missing connectivity of two chalcogen vertices and a very short cross cage metal–metal bonding. All these new dichalcometallaboranes have been characterized by mass, 1H, 11B, 13C NMR spectroscopy, and the structural types were unequivocally established by crystallographic analysis of compound 6.
Graphical abstractReaction of [(η5-C5Me5)MCl4] (M = Mo or W) with sixfold excess of [LiBH4·thf] followed by thermolysis with excess chalcogen powders (S, Se or Te) yielded dichalcomolybda- and tungstaboranes, [(η5-C5Me5M)2B4H4E2] (M = Mo or W; E = S, Se or Te) in modest yields.Figure optionsDownload full-size imageDownload as PowerPoint slide
